Heterocyclic compounds, their preparation, pharmaceutical compositions containing them and their use in medicine

[0001] This application is a continuation application of U.S. patent application Ser. No. 09/928,242 filed on Aug. 10, 2001 now U.S. Pat. No. 6,987,123, from which priority is claimed, which is herein incorporated by reference.

[0002] The present invention relates to novel hypolipidaemic and hypocholesterolemic compounds, their derivatives, their analogs, their tautomeric forms, their stereoisomers, their polymorphs, their pharmaceutically acceptable salts, their pharmaceutically acceptable solvates and pharmaceutically acceptable compositions containing them. More particularly, the present invention relates to novel β-aryl-α-substituted propanoic acids of the general formula (I), their derivatives, their analogs, their tautomeric forms, their stercoisomers, their polymorphs, their pharmaceutically acceptable salts, their pharmaceutically acceptable solvates, pharmaceutical compositions containing them, use of these compounds in medicine and the intermediates involved in their preparation.

[0003]

[0004] The present invention also relates to a process for the preparation of the above said novel compounds, their derivatives, their analogs, their tautomeric forms, their stereoisomers, their polymorphs, their pharmaceutically acceptable salts, their pharmaceutically acceptable solvates, and pharmaceutical compositions containing them.

[0005] The compounds of general formula (I) are useful in lowering elevated levels of cholesterol (TC), low-density lipoproteins (LDL), triglycerides, free fatty acids, glucose, insulin and the like; while increasing high-density lipoproteins, which results in beneficial effect in the mammals.

[0006] The compounds of the general formula (I) lower or modulate triglyceride levels and/or cholesterol levels and/or low-density lipoproteins (LDL) and raise HDL plasma levels and hence are useful in combating different medical conditions, where such lowering (and raising) is beneficial. Thus, it could be used in the treatment and/or prophylaxis of obesity, hyperlipidaemia, hypercholesteremia, hypertension, atherosclerotic disease events, vascular restenosis, diabetes and many other related conditions.

[0007] The compounds of general formula (I) are useful to prevent or reduce the risk of developing atherosclerosis, which leads to diseases and conditions such as arteriosclerotic cardiovascular diseases, stroke, coronary heart diseases, cerebrovascular diseases, peripheral vessel diseases and related disorders. These compounds of general formula (I) are useful for the treatment and/or prophylaxis of metabolic disorders loosely defined as Syndrome X. The characteristic features of Syndrome X include initial insulin resistance followed by hyperinsulinemia, dyslipidemia and impaired glucose tolerance. The glucose intolerance can lead to non-insulin dependent diabetes mellitus (NIDDM, Type 2 diabetes), which is characterized by hyperglycemia, which if not controlled may lead to diabetic complications or metabolic disorders caused by insulin resistance. Diabetes is no lodger considered to be associated only with glucose metabolism, but it affects anatomical and physiological parameters, the intensity of which vary depending upon stages/duration and severity of the diabetic state. The compounds of this invention are also useful in prevention, halting or slowing progression or reducing the risk of the above mentioned disorders along with the resulting secondary diseases such as cardiovascular diseases, like arteriosclerosis, atherosclerosis; diabetic retinopathy, diabetic neuropathy and renal disease including diabetic nephropathy, glomerulonephritis, glomerular sclerosis, nephrotic syndrome, hypertensive nephrosclerosis and end stage renal diseases, like microalbuminuria and albuminuria, which may be result of hyperglycemia or hyperinsulinemia.

[0008] The compounds of the present invention can be useful as aldose reductase inhibitors; for improving cognitive functions in dementia, and in the treatment and/or prophylaxis of disorders such as psoriasis, polycystic ovarian syndrome (PCOS), cancer, osteoporosis, leptin resistance, inflammation and inflammatory bowel diseases, xanthoma, pancreatitis, myotonic dystrophy, endothelial cell dysfunction and hyperlipidemia.

[0009] The compounds of the present invention are useful in the treatment of the diseases mentioned herein, alone or in combination one or more hypoglycemic, antihyperglycemic, hypolipidaemic, hypolipoproteinemic agents, antioxidants, antihypertensives, such as HMG CoA reductase inhibitor, fibrate, statins, glitazones, sulfonyl ureas, insulin, α-glycosidase inhibitors, nicotinic acid, cholestyramine, cholestipol or probucol, and the like.

[0010] Hyperlipidaemia has been recognized as the major risk factor in causing cardiovascular diseases due to atherosclerosis. Atherosclerosis and other such peripheral vascular diseases affect the quality of life of a large population in the world. The emphasis during the therapy is laid on lowering the elevated plasma LDL cholesterol, low-density lipoprotein and plasma triglycerides in order to prevent or reduce the risk of occurrence of cardiovascular diseases. The details of etiology in atherosclerosis and coronary artery diseases is discussed by Ross and Glomset [New Engl. J. Med., 295, 369-377 (1976)]. Plasma cholesterol is generally esterified with various serum lipoproteins and numerous studies suggest an inverse relation between serum HDL-cholesterol level and risk for occurrence of cardiovascular disease. Many studies have suggests an increased risk of coronary artery diseases (CAD) due to elevated LDL and VLDL-cholesterol levels [Stampfer et al., N. Engl. J. Med., 325, 373-381(1991)]. The other studies illustrate protective effects of HDL against progression of atherosclerosis. Thus, HDL has become a crucial factor in treating diseases with increased levels of cholesterol [Miller et. al., Br. Med. J. 282, 1741-1744(1981); Picardo et al., Arteriosclerosis, 6, 434-441 (1986); Macikinnon et al., J. Biol. Chem. 261, 2548-2552 (1986)].

[0011] Diabetes is associated with a number of complications and also affects a large population. Usually, the disease is closely associated with other diseases such as obesity, hyperlipidemia, hypertension and angina. It is a well recognized that improper treatment aggravates impaired glucose tolerance and insulin resistance, leading to frank diabetes. Further, patients with insulin resistance and type 2 diabetes often have raised triglycerides and low HDL-cholesterol concentrations and therefore, have greater risk of cardiovascular diseases. The present therapy mostly includes sulfonylureas and biguanides along with insulin. This drug therapy have limitations such as mild to severe hypoglycemia, which may lead to coma or in some cases may lead to death. The later mainly results due to unsatisfactory glycaemic control. The recent addition of thiazolidinediones, drugs having insulin-sensitizing action. Thiazolidinediones are prescribed alone or in combination with other anti-diabetic agents like troglitazone, rosiglitazone and pioglitazone. These are useful in treating diabetes, affects lipid metabolism but are suspected to have tumor-inducing potential and cause hepatic dysfunction, which may lead to liver failure. Further, serious undesirable side-effects have occurred in animal and/or human studies including cardiac hypertrophy, hema dilution and liver toxicity in a few glitazones progressing to advanced human trials. The drawback is considered to be idiosyncratic. Presently, there is need for a safe and an effective drug, to treat insulin resistance, diabetes and hyperlipidemia.

[0012] Obesity is another major health problem being associated with increased morbidity and mortality. It is a metabolic disorder, in which excess of fat is accumulated in the body. Although, its etiology is unclear, the general feature includes excess of calorie intake than it is consumed. Various therapies such as dieting, exercise, appetite suppression, inhibition of fat absorption etc. have been used to combat obesity. However, more efficient therapies to treat this abnormality is essential as obesity is closely related to several diseases such as coronary heart disease, stroke, diabetes, gout, osteoarthritis, hyperlipidaemia and reduced fertility. It also leads to social and psychological problems.

[0013] Peroxisome Proliferator Activated Receptor (PPAR) is a member of the steroid/retinoid/thyroid hormone receptor family. PPAR∝, PPARγand PPARδ have been identified as subtypes of PPARs. Extensive reviews regarding PPAR, their role in different diseased conditions are widely published [Endocrine Reviews, 20(5), 649-688 (1999); J. Medicinal Chemistry, 43(4), 58-550 (2000); Cell, 55, 932-943 (1999); Nature, 405, 421-424 (2000); Trends in pharmacological Sci., 469-473 (2000)]. PPARγ activation has been found to play a central role in initiating and regulating adipocyte differentiation [Endocrinology 135, 798-800, (1994)] and energy homeostasis, [Cell, 83, 803-812 (1995); Cell, 99, 239-242 (1999)]. PPARγ agonists would stimulate the terminal differentiation of adipocyte precursors and cause morphological and molecular changes characteristic of a more differentiated, less malignant state. During adipocyte differentiation, several highly specialized proteins are induced, which are being involved in lipid storage and metabolism. It is accepted that PPARγ activation leads to expression of CAP gene [Cell biology, 95, 14751-14756, (1998)], however, the exact link from PPARγ activation to changes in glucose metabolism and decrease in insulin resistance in muscle has not been clear. PPARα is involved in stimulating β-oxidation of fatty acids [Trends Endocrine. Metabolism, 4, 291-296 (1993)] resulting in plasma circulating free fatty acid reduction [Current Biol., 5, 618-621 (1995)]. Recently, role of PPARγ activation in the terminal differentiation of adipocyte precursors has been implicated in the treatment of cancer. [Cell, 79, 1147-1156 (1994); Cell, vol. No., 377-389 (1996); Molecular Cell, 465-470 (1998); Carcinogenesis, 1949-1953 (1998); Proc. Natl. Acad. Sci., 94, 237-241 (1997); Cancer Research, 58, 3344-3352 (1998)]. Since PPARγ is expressed in certain cells consistently, PPARγ agonists would lead to nontoxic chemotherapy. There is growing evidence that PPAR agonists may also influence the cardiovascular system through PPAR receptors as well as directly by modulating vessel wall function [Med. Res. Rev., 20 (5), 350-366 (2000)].

[0014] PPAR α agonists have been found useful in the treatment of obesity (WO 97/36579). Dual PPAR α and γ agonists have been suggested to be useful for Syndrome X (WO 97/25042). PPAR γ agonists and HMG-CoA reductase inhibitors have exhibited synergism and indicated the usefulness of the combination in the treatment of atherosclerosis and xanthoma (EP 0753 298).

[0015] Leptin is a protein when bound to leptin receptors is involved in sending satiety signal to the hypothalamus. Leptin resistance would therefore lead to excess food in-take, reduced energy expenditure, obesity, impaired glucose tolerance and diabetes. It has been reported that insulin sensitizers lower plasma leptin concentration [Proc. Natl. Acad. Sci. 93, 5793-5796 (1996): WO 98/02159)].

[0016] A number of compounds have been reported to be useful in the treatment of hyperlipidemia, hypercholesterolemia and hyperglycemia [U.S. Pat. No. 5,306,726, U.S. Pat. No. 5,985,884, U.S. Pat. No. 6,054,453, EP 90 3343, PCT publications Nos. WO 91/19702, WO 94/01420, WO 94/13650, WO 95/03038, WO 95/17394, WO 96/04260, WO 96/04261, WO 96/33998, WO 97/25042, WO 97/36579, WO 98/28534, WO 99/08501, WO 99/16758, WO 99/19313, WO99/20614, WO 00/23417, WO 00/23445, WO 00/23451].

[0017] A few β-aryl-α-hydroxypropanoic acids, their derivatives, and their analogs have been reported to be useful in the treatment of hyperglycemia and hypercholesterolemia. Some of such compounds described in the prior art are outlined below:

• • [0018] 1. U.S. Pat. No. 5,306,726 and U.S. Pat. No. 5,089,514 disclose several 3-aryl-2-hydroxypropionic acid derivatives of general formulae (II) and (III) as hypolipidaemic and hypoglycemic agents. Examples of these compounds are shown in the formulae (IV) and (V).

[0019]

• • [0020] 2. International Patent Applications, U.S. Pat. No. 6,166,049 and WO 96/04260 disclose compounds of general formula (VI) wherein, R^a represents 2-benzoxazolyl or 2-pyridyl and R^b represent CF₃, CH₂OCH₃ or CH₃. A typical example is (S)-3-[4-[2-[N-(2-benzoxazolyl)N-methylamino]ethoxy]phenyl]-2-(2,2,2,-trifluoro ethoxy)propanoic acid (VII).

[0021]

• • [0022] 3. International patent applications, WO 94/13650, WO 94/29302, U.S. Pat. No. 6,048,883, WO 95/17394 and WO 97/31970 disclose the compounds of general formula (VIII) wherein,
    A¹—X—(CH₂)_n —O-A²-A³-YR²   (VIII)
    A¹ represents aromatic heterocycle moiety, A² represents substituted benzene ring and A³ represents moiety of formula (CH₂)_m—CH—(OR¹), where R¹ represents alkyl groups, m is integer of the range of 1-5; X represents substituted or unsubstituted N; Y represents C═O or C═S and R² represents OR³ where R³ may be hydrogen, alkyl, aralkyl, or aryl group and n is integer in the range of 2-6. An example of these compounds is shown in formula (IX).

[0023]

• • [0024] 4. International patent application, WO 00/23,445, WO 00/23,417 and WO 00/23,451 disclose cyclic compounds of the general formula (X) useful in treatment of diabetes and obesity. A typical example of these compounds is shown formulae (XI) and (XII).

[0025]

• • [0026] 5. International patent application, WO 99/08501 and WO 97/319707, disclose cyclic compounds of the formulae (XIII) and (XIV) active as PPAR-gamma agonist. A typical examples of these compounds is shown formulae (XV) and (XVI).

[0027]

• • [0028] 6. U.S. Pat. No. 6,054,453 and WO 99/16758 reports compounds of general formulae (XVII), (XVIII), which reduce glucose, cholesterol and triglycerides exemplified by compounds of formula (XIX).

[0029]

• • [0030] 7. WO 99/19,313, U.S. Pat. No. 6,130,214 and WO 99/38850 reports compounds of general formula (XX) and (XXI) and (XXII) which reduce glucose, cholesterol and triglycerides.

[0031]

[0032] The objective of this invention is to develop novel compounds represented by the general formula (I) used as hypocholesterolemic, hypolipidaemic, hypolipoproteinemic, anti-obesity and antihyperglycemic agents which may have additional body weight lowering effect and beneficial effect in the treatment and/or prophylaxis of diseases caused by hyperlipidaemia, diseases classified under syndrome X and atherosclerosis.

[0033] The main objective of the present invention is to provide novel β-aryl-α-substituted propanoic acids represented by the general formula (I), their derivatives, their analogs, their tautomeric forms, their stereoisomers, their polymorphs, their pharmaceutically acceptable salts, their pharmaceutically acceptable solvates, and pharmaceutical compositions containing them or their mixtures thereof

[0034] Another objective of the present invention is to provide novel β-aryl-α-substituted propanoic acids represented by the general formula (I), their derivatives, their analogs, their tautomeric forms, their stereoisomers, their polymorphs, their pharmaceutically acceptable salts, their pharmaceutically acceptable solvates, and pharmaceutical compositions containing them or their mixtures thereof having enhanced activities, without toxic effects or with reduced toxic effect.

[0035] Yet another objective of this invention is to provide a process for the preparation of novel β-aryl-α-substituted propanoic acids represented by the general formula (I), their derivatives, their analogs, their tautomeric forms, their stereoisomers, their polymorphs, their pharmaceutically acceptable salts, their pharmaceutically acceptable solvates.

[0036] Still another objective of the present invention is to provide pharmaceutical compositions containing compounds of the general formula (I), their derivatives, their analogs, their tautomeric forms, their stereoisomers, their polymorphs, their pharmaceutically acceptable salts, their pharmaceutically acceptable solvates or their mixtures in combination with suitable carriers, solvents, diluents and other media normally employed in preparing such compositions.

[0037] A further objective of the present invention is to provide process for preparation of intermediates involved in the process.

[0038] Accordingly, the present invention relates to compounds of the general formula (I),

[0039]
their derivatives, their analogs, their tautomeric forms, their stereoisomers, their polymorphs, their pharmaceutically acceptable salts, their pharmaceutically acceptable solvates, wherein one or more groups R¹, R², R³, R⁴ may be same or different and represent hydrogen, halogen, perhaloalkyl, hydroxy, thio, amino, nitro, cyano, formyl, amidino, guanidino, substituted or unsubstituted groups selected from linear or branched (C₁-C₁₂)alkyl, linear or branched (C₂-C₁₂)alkenyl, (C₃-C₇)cycloalkyl, (C₃-C₇)cycloalkenyl, bicycloalkyl, bicycloalkenyl, (C₁-C₁₂)alkoxy, cyclo(C₃-C₇)alkoxy, aryl, aryloxy, aralkyl, ar(C₁-C₁₂)alkoxy, heterocyclyl, heteroaryl, heterocyclyl(C₁-C₁₂)alkyl, heteroar(C₁-C₁₂)alkyl, heteroaryloxy, heteroar(C₁-C₁₂)alkoxy, heterocyclyloxy, heterocyclylalkyloxy, acyl, acyloxy, acylamino, monoalkylamino, dialkylamino, arylamino, aralkylamino, alkoxycarbonyl, aryloxycarbonyl, aralkoxycarbonyl, heterocyclylalkoxycarbonyl, heteroaryloxycarbonyl, heteroaralkoxycarbonyl, heterocyclyloxycarbonyl, hydroxyalkyl, aminoalkyl, monoalkylaminoalkyl, dialkylaminoalkyl, alkoxyalkyl, aryloxyalkyl, aralkoxyalkyl, (C₁-C₁₂)alkylthio, thio(C₁-C₁₂)alkyl, arylthio, (C₁-C₁₂)alkoxycarbonylamino, aryloxycarbonylamino, aralkyloxycarbonylamino, aminocarbonylamino, alkylaminocarbonylamino, alkylamidino, alkylguanidino, dialkylguanidino, hydrazino, alkyl hydrazino, alkoxyamino, hydroxylamino, derivatives of sulfenyl and sulfonyl groups, carboxylic acid and its derivatives, sulfonic acid and its derivatives, phosphonic acid and its derivatives; or the adjacent groups R² and R³ together may form a five or a six membered ring, optionally containing one or more double bonds and optionally containing one or more heteroatoms selected from O, N, or S; n is an integer ranging from 1 to 8; W represents O, S or NR⁹ where R⁹ represents hydrogen, (C₁-C₁₂)alkyl or aryl; Ar represents a substituted or unsubstituted divalent single or fused aromatic, heteroaromatic or heterocyclic group; R⁵ and R⁶ represent both hydrogen or together represent a bond; R⁵ and R⁶ may also represent a hydroxy, (C₁-C₁₂)alkyl, (C₁-C₁₂)alkoxy, halogen, acyl, substituted or unsubstituted aralkyl group; X represents O or S; R⁷ represents hydrogen, perfluoro(C₁-C₁₂)alkyl; substituted or unsubstituted groups selected from (C₁-C₁₂)alkyl, cyclo(C₁-C₁₂)alkyl, aryl, ar(C₁-C₁₂)alkyl, heteroaryl, heteroar(C₁-C₁₂)alkyl, heterocyclyl, alkoxyalkyl, aryloxyalkyl, alkoxycarbonyl, aryloxycarbonyl, cycloalkyloxycarbonyl, alkylaminocarbonyl, arylaminocarbonyl, acyl groups; Y represents O or S; Z represents oxygen, sulfur or NR¹⁰, where R¹⁰ represents hydrogen or substituted or unsubstituted groups selected from (C₁-C₁₂)alkyl, aryl, ar(C₁-C₁₂)alkyl, hydroxy(C₁-C₁₂)alkyl, amino(C₁-C₁₂)alkyl, heteroaryl, heteroar(C₁-C₁₂)alkyl groups; R⁸ represents hydrogen, substituted or unsubstituted groups selected from (C₁-C₁₂)alkyl, aryl, ar(C₁-C₁₂)alkyl, heteroaryl, heteroar(C₁-C₁₂)alkyl, heterocyclyl, heterocyclylalkyl, hydroxyalkyl, alkoxyalkyl, alkylaminoalkyl groups; R¹⁰ and R⁸ together may form a 5 or 6 membered substituted or unsubstituted cyclic ring structure containing carbon atoms or containing one or more heteroatoms selected from O, N and S

[0040] Suitable groups represented by R¹, R², R³ and R⁴may be selected from hydrogen, halogen atom such as fluorine, chlorine, bromine or iodine; perhaloalkyl particularly, perfluoro(C₁-C₆)alkyl such as fluoromethyl, difluoromethyl, trifluoromethyl, trifluoroethyl, fluoroethyl, difluoroethyl, mono or polyhalo substituted methyl, ethyl, propyl, butyl, pentyl or hexyl groups and the like; hydroxy, thio, amino, nitro, cyano, formyl, amidino, guanidino groups; substituted or unsubstituted (C₁-C₁₂) alkyl group, especially, linear or branched (C₁-C₈)alkyl group, such as methyl, ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl, t-butyl, n-pentyl, iso-pentyl, hexyl, iso-hexyl, heptyl, octyl and the like; cyclo(C₃-C₇)alkyl group such as cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, the cycloalkyl group may be substituted; cyclo(C₃-C₇)alkenyl group such as cyclopropenyl, cyclobutenyl, cyclopentenyl, cyclohexenyl, cycloheptenyl, cycloheptadienyl, cycloheptatrienyl and the like, the cycloalkenyl group may be substituted; (C₁-C₁₂)alkoxy, especially, (C₁-C₆)alkoxy group such as methoxy, ethoxy, propyloxy, iso-propyloxy, butyloxy, iso-butyloxy, pentyloxy, hexyloxy and the like, which may be substituted; cyclo(C₃-C₇)alkoxy group such as cyclopropyloxy, cyclobutyloxy, cyclopentyloxy, cyclohexyloxy, cycloheptyloxy and the like, the cycloalkoxy group may be substituted; aryl group such as phenyl or naphthyl, the aryl group may be substituted; aryloxy group such as phenoxy, naphthyloxy, the aryloxy group may be substituted; aralkyl group such as benzyl, phenethyl, C₆H₅CH₂CH₂CH₂, naphthylmethyl and the like, the aralkyl group may be substituted; aralkoxy group such as benzyloxy, phenethyloxy, naphthylmethyloxy, phenylpropyloxy and the like, the aralkoxy group may be substituted; heterocyclyl groups such as aziridinyl, pyrrolidinyl, morpholinyl, thiomorpholinyl, oxazolinyl, piperidinyl, piperazinyl and the like, the heterocyclyl group may be substituted; heteroaryl group such as pyridyl, thienyl, furyl, pyrrolyl, oxazolyl, thiazolyl, imidazolyl, isoxazolyl, oxadiazolyl, tetrazolyl, benzopyranyl, benzofuranyl, indolinyl, indolyl, quinolinyl, pyrimidinyl, pyrazolyl, quinazolinyl, pyrimidonyl, benzoxazinyl, benzothiazinyl, benzoxazolyl, benzothiazolyl, benzimidazolyl and the like, the heteroaryl group may be substituted; heterocyclyl(C₁-C₆)alkyl, such as pyrrolidinealkyl, piperidinealkyl, morpholinealkyl, thiomorpholinealkyl, oxazolinealkyl and the like, the heterocyclyl(C₁-C₆)alkyl group may be substituted; heteroar(C₁-C₅)alkyl group, wherein heteroaryl group is as defined earlier and the heteroaralkyl group may be substituted; heteroaryloxy, heteroaralkoxy, heterocyclylalkoxy, heterocyclylalkoxy wherein heteroaryl, heteroaralkyl, heterocyclylalkyl and heterocyclylalkyl moieties are as defined earlier and may be substituted; acyl group such as acetyl, propanoyl, butanoyl, pentanoyl, hexanoyl, iso-butyroyl, or benzoyl, the acyl group may be substituted and may be branched; acyloxy group wherein acyl moiety is as defined earlier, may be MeCOO, EtCOO, PrCOO, BuCOO, PhCOO and the like, which may optionally be substituted; acylamino groups, wherein acyl moiety is as defined earlier, may be CH₃CONH, C₂H₅CONH, C₃H₇CONH, C₄H₉CONH, C₆H₅CONH which may be substituted; (C₁-C₆)monoalkylamino group such as CH₃NH, C₂H₅NH, C₃H₇NH, C₄H₉NH, C₅H₁₁NH, C₆H₁₃NH and the like, which may be substituted; (C₁-C₆)dialkylamino group such as N(CH₃)₂, N(Et)₂, CH₃(C₂H₅)N and the like, which may be substituted; arylamino group such as C₆H₅NH, CH₃(C₆H₅)N, C₆H₄(CH₃)NH, NHC₆H₄—Hal and the like, which may be substituted; aralkylamino group wherein aralkyl group is as defined earlier, may be such as C₆H₅CH₂NH, C₆H₅CH₂CH₂NH, C₆H₅CH₂NCH₃ and the like, which may be substituted; hydroxy(C₁-C₆)alkyl which may be substituted; amino(C₁-C₆)alkyl which may be substituted; mono(C₁-C₆)alkylamino(C₁-C₆)alkyl, di(C₁-C₆)alkylamino(C₁-C₆)alkyl group which may be substituted; alkoxyalkyl group such as methoxymethyl, ethoxymethyl, methoxyethyl, ethoxyethyl and the like, which may be substituted; aryloxyalkyl group such as C₆H₅OCH₂, C₆H₅OCH₂CH₂, naphthyloxymethyl and the like, which may be substituted; aralkoxyalkyl group such as C₆H₅CH₂OCH₂, C₆H₅CH₂OCH₂and the like, which may be substituted; (C₁-C₆)alkylthio, thio(C₁-C₆)alkyl which may be substituted; arylthio which may be substituted alkoxycarbonylamino group such as C₂H₅OCONH, CH₃OCONH and the like which may be substituted; aryloxycarbonylamino group such as C₆H₅OCONH, C₆H₅OCONCH₃, C₆H₅OCONC₂H₅, C₆H₄CH₃OCONH, C₆H₄(OCH₃)OCONH and the like which may be substituted; aralkoxycarbonylamino group such as C₆H₅CH₂OCONH, C₆H₅CH₂CH₂OCONH, C₆H₅CH₂OCONCH₃, C₆H₅CH₂OCONC₂H₅, C₆H₄(CH₃)CH₂OCONH, C₆H₄(OCH₃)CH₂OCONH and the like, which may be substituted; aminocarbonylamino group, which may optionally be substituted; (C₁-C₆)alkylaminocarbonylamino group, di(C₁-C₆)alkylaminocarbonyl amino group, (C₁-C₆)alkylamidino group, (C₁-C₆)alkylguanidino group, di(C₁-C₆)alkylguanidino groups, hydrazino, (C₁-C₆)alkyl hydrazino groups, (C₁-C₆)alkoxyamino and hydroxylamino groups, which may optionally be substituted; carboxylic acid or its derivatives such as amides, like CONH₂, alkylaminocarbonyl like MeNHCO, Me₂NCO, EtNHCO, Et₂NCO, arylaminocarbonyl like PhNHCO, NapthNHCO and the like, which may be substituted; aralkylaminocarbonyl such as PhCH₂NHCO, PhCH₂CH₂NHCO and the like, which may be substituted; heteroarylaminocarbonyl and heteroaralkylamino carbonyl groups where the heteroaryl groups are as defined earlier, which may be substituted; heterocyclylaminocarbonyl where the heterocyclyl group is as defined earlier, which may be substituted; carboxylic acid derivatives such as esters, wherein the ester moieties are alkoxycarbonyl such as methoxycarbonyl or ethoxycarbonyl, which may be substituted; aryloxycarbonyl group such as unsubstituted or substituted phenoxycarbonyl, naphthyloxycarbonyl and the like; aralkoxycarbonyl group such as benzyloxycarbonyl, phenethyloxycarbonyl, naphthylmethoxycarbonyl and the like, which may be substituted; heteroaryloxycarbonyl, heteroaralkoxycarbonyl, wherein the heteroaryl group is as defined earlier, which may be substituted; heterocyclyloxycarbonyl where heterocycle is as defined earlier and may be substituted; sulfinyl or its derivatives like CH₃SO and RSO, wherein R is substituted or unsubstituted alkyl, aryl, heteroaryl, heterocycyl and the like; sulfones or its derivatives like RSO₂, wherein R is substituted or unsubstituted groups selected from alkyl, aryl, heteroaryl, heterocyclyl and the like; sulfonic acid or its derivatives such as SO₂NH₂, SO₂NHMe, SO₂NMe₂, SO₂NHCF₃, SO₂NHCO(C₁-C₆)alkyl, SO₂NHCOaryl where the aryl group is as defined earlier and the sulfonic acid derivatives may be substituted; phosphonic acid and its derivatives such as P(O)(OH)₂, P(O)(O C₁-C₆ alkyl)₂, P(O)(O aryl)₂, P(O)(OH) (O C₁-C₆ alkyl)and the like.

[0041] When the groups represented by R¹, R², R³ and R⁴ are substituted by one or more than one, same or different groups, the substituents are selected from halogen, hydroxy, nitro, oxo, thio or unsubstituted or substituted groups selected from (C₁-C₁₂)alkyl, cyclo(C₁-C₁₂)alkyl, (C₁-C₁₂)alkoxy, cyclo(C₁-C₂)alkoxy, aryl, ar(C₁-C₁₂)alkyl, aralkoxy(C₁-C₁₂)alkyl, heterocyclyl, heteroaryl, heteroar(C₁-C₁₂)alkyl, acyl, acyloxy, hydroxy(C₁-C₁₂)alkyl, amino, acylamino, arylamino, amino(C₁-C₁₂)alkyl, aryloxy, aralkoxy, (C₁-C₁₂)alkylamino, alkoxy(C₁-C₁₂)alkyl, (C₁-C₁₂)alkylthio, thio(C₁-C₁₂)alkyl, aryl thio groups, carboxylic acid or its derivatives, or sulfenyl or its derivatives or sulfones or its derivatives or sulfonic acid or its derivatives or phosphonic acid or its derivatives.

[0042] Preferably the substituents on the pyrrole namely, R¹ to R⁴ represent halogen atom such as fluorine, chlorine, bromine; hydroxy group, formyl, nitro, oxo, thio, also linear or branched alkyl such as methyl, ethyl, propyl, iso-propyl, butyl, iso-butyl, pentyl, hexyl, heptyl, octyl groups, which may be substituted; cycloalkyl group such as cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl which may be substituted; aryl group such as phenyl or naphthyl, which may be substituted; aralkyl group such as benzyl, or naphthylmethyl, which may be substituted; (C₁-C₆)alkoxy, benzyloxy, acyl or acyloxy groups; heteroaryl group such as pyridyl, thienyl, furyl, pyrrolyl, oxazolyl, thiazolyl, imidazolyl, isoxazolyl, oxadiazolyl, tetrazolyl, benzopyranyl, benzofuranyl, indolinyl, indolyl, quinolinyl, pyrimidinyl, pyrazolyl, quinazolinyl, pyrimidonyl, benzoxazinyl, benzothiazinyl, benzoxazolyl, benzothiazolyl, benzimidazolyl and the like, the heteroaryl group may be substituted; heterocyclyl groups such as aziridinyl, pyrrolidinyl, morpholinyl, thiomorpholinyl, oxazolinyl, piperidinyl, piperazinyl and the like, the heterocyclyl group may be substituted; carboxylic acid and its derivatives; alkylaminocarbonyl or arylaminocarbonyl groups which may be substituted; thioalkyl, alkylsulfenyl, arylthio, alkylsulfonyl, arylsulfenyl, arylsulfonyl, which may be optionally halogenated.

[0043] Suitable cyclic structures formed by the two adjacent groups R² and R³ together with the carbon atoms to which they are attached contain 5 to 6 ring atoms which may optionally contain one or more heteroatoms selected from oxygen, nitrogen or sulfur and optionally contain one or more double bonds. The cyclic structure may further be optionally substituted phenyl, pyridyl, furanyl, thienyl, pyrrolyl, imidazolyl, isoxazolyl, pyrimidinyl, pyrazinyl and the like. Suitable substituents on the cyclic structure formed by R² and R³ together with the adjacent carbon atoms to which they are attached include oxo, hydroxy, halogen atom such as chlorine, bromine and iodine; nitro, cyano, amino, formyl, (C₁-C₃)alkyl, (C₁-C₆)alkoxy, thioalkyl, arylthio, alkylthio, phenyl or benzyl groups.

[0044] The R¹, R², R³ and R⁴ groups on the pyrrole, when further substituted preferable substitutents are halogen, hydroxy, formyl, nitro, oxo, thio, or unsubstituted or substituted groups selected from alkyl, cycloalkyl, alkoxy, cycloalkoxy, aryl, aralkyl, aralkoxyalkyl, heterocyclyl, heteroaryl, heteroaralkyl, acyl, acyloxy, hydroxyalkyl, amino, acylamino, arylamino, aminoalkyl, aryloxy, aralkoxy, alkylamino, alkoxyalkyl, alkylthio, thioalkyl, arylthio, alkylsulfenyl, alkylsulfonyl, arylsulfenyl, arylsulfonyl, carboxylic acid or its derivatives, or sulfonic acid or its derivatives or phosphonic acid or its derivatives.

[0045] n is an integer in the range of 1 to 8. It is preferred that n be 1 to 4.

[0046] Suitable groups represented by Ar include substituted or unsubstituted groups selected from divalent moieties selected from phenylene, naphthylene, pyridyl, quinolinyl, benzofuryl, dihydrobenzofuryl, benzopyranyl, indolyl, indolinyl, azaindolyl, azaindolinyl, pyrazolyl, benzothiazolyl, benzoxazolyl and the like.

[0047] The substituents on the group represented by Ar may be selected from substituted or unsubstituted linear or branched (C₁-C₆)alkyl, (C₁-C₆)alkoxy, halogen, haloalkyl, haloalkoxy, acyl, amino, acylamino, oxo, thio, thioalkyl, arylthio or carboxylic or sulfonic acids and their derivatives or phosphonic acid and their derivatives.

[0048] It is preferred that Ar represents substituted or unsubstituted divalent phenylene, naphthylene, benzofuryl, indolyl, indolinyl, quinolinyl, azaindolyl, azaindolinyl, benzothiazolyl or benzoxazolyl groups.

[0049] It is more preferred that Ar is represented by divalent phenylene or naphthylene, which may be unsubstituted or substituted by halogen, methyl, halomethyl, methoxy or halomethoxy groups.

[0050] Suitable R⁵ includes hydrogen, lower alkyl groups such as methyl, ethyl or propyl; hydroxy, (C₁-C₆)alkoxy, halogen atom such as fluorine, chlorine, bromine, or iodine; aralkyl such as benzyl, phenethyl, which may be unsubstituted or substituted or R⁵ together with R⁶ represent a bond.

[0051] Suitable R⁶ may be hydrogen, lower alkyl groups such as methyl, ethyl or propyl; hydroxy, (C₁-C₆)alkoxy; halogen atom such as fluorine, chlorine, bromine, iodine; acyl group such as linear or branched (C₂-C₁₀) acyl group such as acetyl, propanoyl, butanoyl, pentanoyl, benzoyl and the like; aralkyl such as benzyl, phenethyl, which may be unsubstituted or substituted or together with R⁵ forms a bond.

[0052] When R⁵ or R⁶ represent substituted aralkyl, the preferred substituents are hydroxy, halogen, alkyl and alkoxy.

[0053] It is preferred that R⁵ or R⁶ represent hydrogen atom or R⁵ and R⁶ together represent a bond.

[0054] Suitable groups represented by R⁷ may be selected from hydrogen, substituted or unsubstituted, linear or branched (C₁-C₁₆)alkyl, preferably (C₁-C₁₂)alkyl group such as methyl, ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl, pentyl, hexyl, octyl and the like; (C₃-C₇)cycloalkyl group such as cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl and the like, the cycloalkyl group may be substituted; aryl group such as phenyl, naphthyl, the aryl group may be substituted; heteroaryl group such as pyridyl, thienyl, furyl, pyrrolyl, oxazolyl, thiazolyl, imidazolyl, isoxazolyl, oxadiazolyl, tetrazolyl, benzopyranyl, benzofuranyl, indolinyl, indolyl, quinolinyl, pyrimidinyl, pyrazolyl, quinazolinyl, pyrimidonyl, benzoxazinyl, benzothiazinyl, benzoxazolyl, benzothiazolyl, benzimidazolyl and the like, the heteroaryl group may be substituted; heteroar(C₁-C₆)alkyl group wherein the heteroaryl groups are as defined earlier and the heteroar(C₁-C₆)alkyl group may be substituted; aralkyl group wherein the alkyl moiety may contain C₁-C₆ atoms such as benzyl and phenethyl etc, wherein the aryl moiety may be substituted; heterocyclyl groups such as aziridinyl, pyrrolidinyl, morpholinyl, thiomorpholinyl, oxazolinyl, piperidinyl, piperazinyl and the like, the heterocyclyl group may be substituted; (C₁-C₆)alkoxy(C₁-C₆)alkyl group such as methoxymethyl, ethoxymethyl, methoxyethyl, ethoxypropyl and the like, the alkoxyalkyl group may be substituted; substituted or unsubstituted, linear or branched (C₂-C₁₆)acyl group such as acetyl, propanoyl, butanoyl, benzoyl, octanoyl, decanoyl and the like; (C₁-C₆)alkoxycarbonyl, the alkyl group may be substituted; aryloxycarbonyl such as phenoxycarbonyl, naphthyloxycarbonyl, the aryl group may be substituted; (C₁-C₆)alkylaminocarbonyl, the alkyl group may be substituted; arylaminocarbonyl such as PhNHCO, or naphthylaminocarbonyl, the aryl moiety may be substituted. The substituents on R⁷ may be selected from the group consisting of halogen, hydroxy, nitro, oxo, thio or unsubstituted/substituted groups selected from alkyl, cycloalkyl, alkoxy, cycloalkoxy, aryl, aralkyl, aryloxy, aryloxy, alkyl, aralkoxyalkyl, heterocyclyl, heteroaryl, heteroaryloxy, heteroaralkyl, acyl, acyloxy, hydroxyalkyl, amino, acylamino, arylamino, aminoalkyl, alkoxycarbonyl, alkylamino, alkoxyalkyl, alkylthio, thioalkyl, arylthio groups, carboxylic acid or its derivatives, or sulfonic acid or its derivatives.

[0055] Suitable groups represented by R⁸ may be selected from hydrogen, substituted or unsubstituted, linear or branched (C₁-C₁₆)alkyl, preferably (C₁-C₁₂)alkyl group such as methyl, ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl, pentyl, hexyl, octyl and the like; (C₃-C₇)cycloalkyl such as cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl and the like, the cycloalkyl group may be substituted; aryl group such as phenyl, naphthyl, the aryl group may be substituted; heteroaryl group such as pyridyl, thienyl, furyl, pyrrolyl, oxazolyl, thiazolyl, imidazolyl, isoxazolyl, oxadiazolyl, tetrazolyl, benzopyranyl, benzofuranyl, indolinyl, indolyl, quinolinyl, pyrimidinyl, pyrazolyl, quinazolinyl, pyrimidonyl, benzoxazinyl, benzothiazinyl, benzoxazolyl, benzothiazolyl, benzimidazolyl and the like, the heteroaryl group may be substituted; heteroaralkyl group such as furanemethyl, pyridinemethyl, oxazolemethyl, oxazolethyl and the like, the heteroaralkyl group may be substituted; aralkyl group such as benzyl and phenethyl, the aralkyl group may be substituted; heterocyclyl groups such as aziridinyl, pyrrolidinyl, morpholinyl, thiomorpholinyl, oxazolinyl, piperidinyl, piperazinyl and the like, the heterocyclyl group may be substituted. The substituents on R⁸ may be selected from halogen, hydroxy, nitro formyl, oxo, thio or unsubstituted or substituted groups selected from alkyl, cycloalkyl, alkoxy, cycloalkoxy, aryl, aralkyl, aralkoxyalkyl, heterocyclyl, heteroaryl, heteroaralkyl, acyl, acyloxy, hydroxyalkyl, amino, acylamino, arylamino, aminoalkyl aryloxy, aralkoxy, alkoxycarbonyl, alkylamino, alkoxyalkyl, alkylthio, thioalkyl, arylthio, carboxylic acid or its derivatives, or sulfonic acid or its derivatives.

[0056] Z represents oxygen, sulfur or NR¹⁰.

[0057] Suitable groups represented by R¹⁰ may be selected from hydrogen, substituted or unsubstituted, linear or branched (C₁-C₁₆)alkyl, preferably (C₁-C₁₂)alkyl; hydroxy(C₁-C₆)alkyl; aryl group such as phenyl, naphthyl; aralkyl group such as benzyl and phenethyl; heterocyclyl groups such as aziridinyl, pyrrolidinyl, morpholinyl, thiomorpholinyl, oxazolinyl, piperidinyl, piperazinyl and the like, the heterocyclyl group may be substituted; heteroaryl group such as pyridyl, thienyl, furyl, pyrrolyl, oxazolyl, thiazolyl, imidazolyl, isoxazolyl, oxadiazolyl, tetrazolyl, benzopyranyl, benzofuranyl, indolinyl, indolyl, quinolinyl, pyrimidinyl, pyrazolyl, quinazolinyl, pyrimidonyl, benzoxazinyl, benzothiazinyl, benzoxazolyl, benzothiazolyl, benzimidazolyl and the like, the heteroaryl group may be substituted.

[0058] The cyclic structure formed by R⁸ and R¹⁰ together with the carbon atoms to which they are attached may be a substituted or unsubstituted 5 or 6 membered cyclic structure containing carbon atoms which may optionally contain one or two heteroatoms selected from oxygen, nitrogen or sulfur. The cyclic structure may contain one or more double bonds.

[0059] Suitable ring structures formed by R⁸ and R¹⁰ together may be selected from pyrrolidinyl, piperidinyl, morpholinyl, thiomorpholinyl, piperazinyl, oxazolinyl, diazolinyl and the like. Suitable substituents on the cyclic structure formed by R⁸ and R¹⁰ taken together may be selected from halogen, hydroxy, alkyl, oxo, thio, aryl, aralkyl and the like.

[0060] For any R¹, R², R³, R⁴, R⁵, R⁶, R⁷, R⁸, R⁹, R¹⁰ and Ar that may be substituted, the substituents are as defined anywhere in this specification.

[0061] Suitable n is an integer ranging from 1 to 6, preferably n represents an integer 2 to 4.

[0062] Pharmaceutically acceptable salts forming part of this invention are intended to define but not limited to salts of the carboxylic acid moiety such as alkali metal salts like Li, Na, and K salts; alkaline earth metal salts like Ca and Mg salts; salts of organic bases such as lysine, arginine, guanidine and its derivatives, which may be optionally substituted, diethanolamine, choline, tromethamine and the like; ammonium or substituted ammonium salts and aluminium salts. Salts may be acid addition salts which defines but not limited to sulfates, bisulfates, nitrates, phosphates, perchlorates, borates, hydrohalides, acetates, tartrates, maleates, fumarates, maleiates, citrates, succinates, palmoates, methanesulfonates, benzoates, salicylates, hydroxynaphthoates, benzenesulfonates, ascorbates, glycerophosphates, ketoglutarates and the like. Pharmaceutically acceptable solvates may be hydrates or comprising other solvents of crystallization such as alcohols.

[0063] Particularly useful compounds according to the present invention includes

• [0064] (±)Ethyl 3-{4-[2-(pyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoate;
• [0065] (+)Ethyl 3-{4-[2-(pyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoate;
• [0066] (−)Ethyl 3-{4-[2-(pyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoate;
• [0067] (±)Ethyl 3-{4-[2-(2,5-dimethylpyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoate;
• [0068] (+)Ethyl 3-{4-[2-(2,5-dimethylpyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoate;
• [0069] (−)Ethyl 3-{4-[2-(2,5-dimethylpyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoate;
• [0070] (±)Ethyl 3-{4-[2-(2,4-dimethylpyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoate;
• [0071] (+)Ethyl 3-{4-[2-(2,4-dimethylpyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoate;
• [0072] (−)Ethyl 3-{4-[2-(2,4-dimethylpyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoate;
• [0073] (±)Ethyl 3-{4-[2-(2-formylpyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoate;
• [0074] (+)Ethyl 3-{4-[2-(2-formylpyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoate;
• [0075] (−)Ethyl 3-{4-[2-(2-formylpyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoate;
• [0076] (±)Ethyl 3-{4-[2-(2-acetylpyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoate;
• [0077] (+)Ethyl 3-{4-[2-(2-acetylpyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoate;
• [0078] (−)Ethyl 3-{4-[2-(2-acetylpyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoate;
• [0079] (±)Ethyl 3-{4-[2-(2-ethylpyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoate;
• [0080] (+)Ethyl 3-{4-[2-(2-ethylpyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoate;
• [0081] (−)Ethyl 3-{4-[2-(2-ethylpyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoate;
• [0082] (±)Ethyl 3-{4-[2-(2-ethyl-5-methylpyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoate;
• [0083] (+)Ethyl 3-{4-[2-(2-ethyl-5-methylpyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoate;
• [0084] (−)Ethyl 3-{4-[2-(2-ethyl-5-methylpyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoate;
• [0085] (±)Ethyl 3-{4-[2-(5-methyl-2-propylpyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoate;
• [0086] (+)Ethyl 3-(4-[2-(5-methyl-2-propylpyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoate;
• [0087] (−)Ethyl 3-{4-[2-(5-methyl-2-propylpyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoate;
• [0088] (±)Ethyl 3-{4-[2-(5-methyl-2-n-butylpyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoate;
• [0089] (+)Ethyl 3-{4-[2-(5-methyl-2-n-butylpyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoate;
• [0090] (−)Ethyl 3-{4-[2-(5-methyl-2-n-butylpyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoate;
• [0091] (±)Ethyl 3-{4-[2-(5-methyl-2-phenylpyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoate;
• [0092] (+)Ethyl 3-{4-[2-(5-methyl-2-phenylpyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoate;
• [0093] (−)Ethyl 3-{4-[2-(5-methyl-2-phenylpyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoate;
• [0094] (±)Ethyl 3-{4-[2-(5-methyl-3-phenylpyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoate;
• [0095] (+)Ethyl 3-{4-[2-(5-methyl-3-phenylpyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoate;
• [0096] (−)Ethyl 3-{4-[2-(5-methyl-3-phenylpyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoate;
• [0097] (±)Ethyl 3-{4-[2-(5-methyl-2-phenylpyrrol-1-yl)ethoxy]phenyl}-2-methoxypropanoate;
• [0098] (+)Ethyl 3-{4-[2-(5-methyl-2-phenylpyrrol-1-yl)ethoxy]phenyl}-2-methoxypropanoate;
• [0099] (−)Ethyl 3-{4-[2-(5-methyl-2-phenylpyrrol-1-yl)ethoxy]phenyl}-2-methoxypropanoate
• [0100] (±)Methyl 3-{4-[2-(5-methyl-2-phenylpyrrol-1-yl)ethoxy]phenyl}-2-methoxypropanoate;
• [0101] (+)Methyl 3-{4-[2-(5-methyl-2-phenylpyrrol-1-yl)ethoxy]phenyl}-2-methoxypropanoate;
• [0102] (−)Methyl 3-{4-[2-(5-methyl-2-phenylpyrrol-1-yl)ethoxy]phenyl}-2-methoxypropanoate;
• [0103] (±)Ethyl 3-{4-[2-(5-methyl-2-phenylpyrrol-1-yl)ethoxy]phenyl}-2-propoxypropanoate;
• [0104] (+)Ethyl 3-{4-[2-(5-methyl-2-phenylpyrrol-1-yl)ethoxy]phenyl}-2-propoxypropanoate;
• [0105] (−)Ethyl 3-{4-[2-(5-methyl-2-phenyl)pyrrol-1-yl)ethoxy]phenyl}-2-propoxypropanoate;
• [0106] (±)Propyl 3-{4-[2-(5-methyl-2-phenylpyrrol-1-yl)ethoxy]phenyl}-2-propoxypropanoate;
• [0107] (+)Propyl 3-{4-[2-(5-methyl-2-phenylpyrrol-1-yl)ethoxy]phenyl}-2-propooxypropanoate;
• [0108] (−)Propyl 3-{4-[2-(5-methyl-2-phenylpyrrol-1-yl)ethoxy]phenyl}-2-propoxypropanoate;
• [0109] (±)Ethyl 3-{4-[2-(5-methyl-2-(4-methylphenyl)pyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoate;
• [0110] (+)Ethyl 3-{4-[2-(5-methyl-2-(4-methylphenyl)pyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoate;
• [0111] (−)Ethyl 3-{4-[2-(5-methyl-2-(4-methylphenyl)pyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoate;
• [0112] (±)Ethyl 3-(4-[2-(5-methyl-2-(3-methylphenyl)pyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoate;
• [0113] (+)Ethyl 3-{4-[2-(5-methyl-2-(3-methylphenyl)pyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoate;
• [0114] (−)Ethyl 3-{4-[2-(5-methyl-2-(3-methylphenyl)pyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoate;
• [0115] (±)Ethyl 3-{4-[2-(5-methyl-2-(2-methylphenyl)pyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoate;
• [0116] (+)Ethyl 3-{4-[2-(5-methyl-2-(2-methylphenyl)pyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoate;
• [0117] (−)Ethyl 3-{4-[2-(5-methyl-2-(2-methylphenyl)pyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoate;
• [0118] (±)Ethyl 3-{4-[2-(5-methyl-2-(4-methoxyphenyl)pyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoate;
• [0119] (+)Ethyl 3-{4-[2-(5-methyl-2-(4-methoxyphenyl)pyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoate;
• [0120] (−)Ethyl 3-{4-[2-(5-methyl-2-(4-methoxyphenyl)pyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoate;
• [0121] (±)Ethyl 3-{4-[2-(5-methyl-2-(4-bromophenyl)pyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoate;
• [0122] (+)Ethyl 3-{4-[2-(5-methyl-2-(4-bromophenyl)pyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoate;
• [0123] (−)Ethyl 3-{4-[2-(5-methyl-2-(4-bromophenyl)pyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoate;
• [0124] (±)Ethyl 3-{4-[2-(5-methyl-2-(4-fluorophenyl)pyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoate;
• [0125] (+)Ethyl 3-{4-[2-(5-methyl-2-(4-fluorophenyl)pyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoate;
• [0126] (−)Ethyl 3-{4-[2-(5-methyl-2-(4-fluorophenyl)pyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoate;
• [0127] (±)Ethyl 3-{4-[2-(5-methyl-2-(4-chlorophenyl)pyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoate;
• [0128] (+)Ethyl 3-{4-[2-(5-methyl-2-(4-chlorophenyl)pyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoate;
• [0129] (−)Ethyl 3-{4-[2-(5-methyl-2-(4-chlorophenyl)pyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoate;
• [0130] (±)Ethyl 3-{4-[2-(4-methyl-2-phenylpyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoate;
• [0131] (+)Ethyl 3-{4-[2-(4-methyl-2-phenylpyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoate;
• [0132] (−)Ethyl 3-{4-[2-(4-methyl-2-phenylpyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoate;
• [0133] (±)Ethyl 3-{4-[2-(5-methyl-2,3diphenylpyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoate;
• [0134] (+)Ethyl 3-{4-[2-(5-methyl-2,3diphenylpyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoate;
• [0135] (−)Ethyl 3-{4-[2-(5-methyl-2,3diphenylpyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoate;
• [0136] (±)Ethyl 3-{4-[2-(2-isopropyl-5-methylpyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoate;
• [0137] (+)Ethyl 3-{4-[2-(2-isopropyl-5-methylpyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoate;
• [0138] (−)Ethyl 3-{4-[2-(2-isopropyl-5-methylpyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoate;
• [0139] (±)Ethyl 3-{4-[2-(2,5-diisopropylpyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoate;
• [0140] (+)Ethyl 3-{4-[2-(2,5-diisopropylpyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoate;
• [0141] (−)Ethyl 3-{4-[2-(2,5-diisopropylpyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoate;
• [0142] (±)Ethyl 3-{4-[2-(5-isopropyl-2-phenylpyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoate;
• [0143] (+)Ethyl 3-{4-[2-(5-isopropyl-2-phenylpyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanotae;
• [0144] (−)Ethyl 3-{4-[2-(5-isopropyl-2-phenylpyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoate;
• [0145] (+)Ethyl 3-{4-[2-(2,5-diisopropyl-3-phenylpyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoate;
• [0146] (+)Ethyl 3-{4-[2-(2,5-diisopropyl-3-phenylpyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoate;
• [0147] (−)Ethyl 3-{4-[2-(2,5-diisopropyl-3-phenylpyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoate;
• [0148] (+)Ethyl 3-(4-{2-[5-isopropyl-2-(4-methoxyphenyl)pyrrol-1-yl]ethoxy}phenyl)-2-ethoxypropanoate;
• [0149] (+)Ethyl 3-(4-{2-[5-isopropyl-2-(4-methoxyphenyl)pyrrol-1-yl]ethoxy}phenyl)-2-ethoxypropanoate;
• [0150] (−)Ethyl 3-(4-{2-[5-isopropyl-2-(4-methoxyphenyl)pyrrol-1-yl]ethoxy}phenyl)-2-ethoxypropanoate;
• [0151] (±)Ethyl 3-(4-{2-[2-(4-fluorophenyl)-5-isopropylpyrrol-1-yl]ethoxy}phenyl)-2-ethoxypropanoate;
• [0152] (+)Ethyl 3-(4-{2-[2-(4-fluorophenyl)-5-isopropylpyrrol-1-yl]ethoxy}phenyl)-
• [0153] (−)Ethyl 3-(4-{2-[2-(4-fluorophenyl)-5-isopropylpyrrol-1-yl]ethoxy}phenyl)-2-ethoxypropanoate;
• [0154] (±)Ethyl 3-(4-{2-[2-(4-fluorophenyl)-5-isopropyl-3-phenylpyrrol-1-yl]ethoxy}phenyl)-2-ethoxy propanoate;
• [0155] (+)Ethyl 3-(4-{2-[2-(4-fluorophenyl)-5-isopropyl-3-phenylpyrrol-1-yl]ethoxy}phenyl)-2-ethoxy propanoate;
• [0156] (−)Ethyl 3-(4-{2-[2-(4-fluorophenyl)-5-isopropyl-3-phenylpyrrol-1-yl]ethoxy}phenyl)-2-ethoxy propanoate;
• [0157] (±)Ethyl 3-(4-{2-[2-(4-fluorophenyl)-5-isopropyl-4-phenylcarbamoylpyrrol-1-yl]ethoxy}phenyl)-2-ethoxypropanoate;
• [0158] (+)Ethyl 3-(4-{2-[2-(4-fluorophenyl)-5-isopropyl-4-phenylcarbamoylpyrrol-1-yl]ethoxy}phenyl)-2-ethoxypropanoate;
• [0159] (−)Ethyl 3-(4-{2-[2-(4-fluorophenyl)-5-isopropyl-4-phenylcarbamoylpyrrol-1-yl]ethoxy}phenyl)-2-ethoxypropanoate;
• [0160] (±)Ethyl 3-(4-{2-[2-(4-fluorophenyl)-5-isopropyl-3-phenyl-4-phenylcarbamoylpyrrol-1yl]ethoxy}phenyl)-2-ethoxypropanoate;
• [0161] (+)Ethyl 3-(4-{2-[2-(4-fluorophenyl)-5-isopropyl-3-phenyl-4-phenylcarbamoylpyrrol-1-yl]ethoxy}phenyl)-2-ethoxypropanoate;
• [0162] (−)Ethyl 3-(4-{2-[2-(4-fluorophenyl)-5-isopropyl-3-phenyl-4-phenylcarbamoylpyrrol-1-yl]ethoxy}phenyl)-2-ethoxypropanoate;
• [0163] (±)Ethyl 3-(4-{3-[2-(4-fluorophenyl)-5-isopropyl-3-phenyl-4-phenylcarbamoylpyrrol-1-yl]propoxy}phenyl)-2-ethoxypropanoate;
• [0164] (+)Ethyl 3-(4-{3-[2-(4-fluorophenyl)-5-isopropyl-3-phenyl-4-phenylcarbamoylpyrrol-1-yl]propoxy}phenyl)-2-ethoxypropanoate;
• [0165] (−)Ethyl 3-(4-{3-[2-(4-fluorophenyl)-5-isopropyl-3-phenyl-4-phenylcarbamoylpyrrol-1-yl]propoxy}phenyl)-2-ethoxypropanoate;
• [0166] (+)Ethyl 3-(4-{2-[2-(4-fluorophenyl)-5-phenylpyrrol-1-yl]ethoxy}phenyl)-2-ethoxypropanoate;
• [0167] (+)Ethyl 3-(4-{2-[2-(4-fluorophenyl)-5-phenylpyrrol-1-yl]ethoxy}phenyl)-2-ethoxypropanoate;
• [0168] (−)Ethyl 3-(4-{2-[2-(4-fluorophenyl)-5-phenylpyrrol-1-yl]ethoxy}phenyl)-2-ethoxyropanoate;
• [0169] (±)Ethyl 3-[4-[2-[3-carboxy-5-phenyl-2-(4-fluorophenyl)pyrrol-1-yl)ethoxy]phenyl-2-ethoxy propanoate;
• [0170] (+)Ethyl 3-[4-[2-[3-carboxy-5-phenyl-2-(4-fluorophenyl)pyrrol-1-yl)ethoxy]phenyl-2-ethoxy propanoate;
• [0171] (−)Ethyl 3-[4-[2-[3-carboxy-5-phenyl-2-(4-fluorophenyl)pyrrol-1-yl)ethoxy]phenyl-2-ethoxy propanoate;
• [0172] (+)Ethyl 3-{4-[2-(2-methylthiopyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoate;
• [0173] (+)Ethyl 3-{4-[2-(2-methylthiopyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoate;
• [0174] (−)Ethyl 3-{4-[2-(2-methylthiopyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoate;
• [0175] Ethyl(E/Z)3-{4-[2-5-methyl-2-phenyl-pyrrol-1-yl)ethoxy]phenyl}-2-ethoxyprop-2enenoate;
• [0176] Ethyl(Z)3-{4-[2-(5-methyl-2-phenyl-pyrrol-1-yl)ethoxy]phenyl}-2-ethoxyprop-2-enenoate;
• [0177] Ethyl(E)3-{4-[2-(5-methyl-2-phenyl-pyrrol-1-yl)ethoxy]phenyl}-2-ethoxyprop-2-enenoate;
• [0178] [(2R)—N(1S)]-2-Ethoxy-3-{4-[2-(5-methyl-2-phenylpyrrol-1-yl)ethoxy]phenyl}-N-(2-hydroxy-1-phenylethyl)propanamide
• [0179] [(2S)—N(1S)]-2-Ethoxy-3-{4-[2-(5-methyl-2-phenylpyrrol-1-yl)ethoxy]phenyl}-N-(2-hydroxy-1-phenylethyl) propanamide
• [0180] (±)3-{4-[2-(pyrrol-1-yl)ethoxy]phenyl}-2ethoxypropanoic acid and its pharmaceutically acceptable salts;
• [0181] (±)3-{4-[2-(pyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoic acid and its pharmaceutically acceptable salts;
• [0182] (−)3-{4-[2-(pyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoic acid and its pharmaceutically acceptable salts;
• [0183] (±)3-{4-[2-(2,5-dimethylpyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoic acid and its pharmaceutically acceptable salts;
• [0184] (+)3-{4-[2-(2,5-dimethylpyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoic acid and its pharmaceutically acceptable salts;
• [0185] (−)3-{4-[2-(2,5-dimethylpyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoic acid and its pharmaceutically acceptable salts;
• [0186] (±)3-{4-[2-(2,4-dimethylpyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoic acid and its pharmaceutically acceptable salts;
• [0187] (+)3-{4-[2-(2,4-dimethylpyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoic acid and its pharmaceutically acceptable salts;
• [0188] (−)3-{4-[2-(2,4-dimethylpyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoic acid and its pharmaceutically acceptable salts;
• [0189] (±)3-{4-[2-(2-ethylpyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoic acid and its pharmaceutically acceptable salts;
• [0190] (+)3-{4-[2-(2-ethylpyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoic acid and its pharmaceutically acceptable salts;
• [0191] (−)3-{4-[2-(2-ethylpyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoic acid and its pharmaceutically acceptable salts;
• [0192] (±)3-{4-[2-(2-formylpyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoic acid and its pharmaceutically acceptable salts;
• [0193] (+)3-{4-[2-(2-formylpyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoic acid and its pharmaceutically acceptable salts;
• [0194] (−)3-{4-[2-(2-formylpyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoic acid and its pharmaceutically acceptable salts;
• [0195] (±)3-{4-[2-(2-acetylpyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoic acid and its pharmaceutically acceptable salts;
• [0196] (+)3-{4-[2-(2-acetylpyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoic acid and its pharmaceutically acceptable salts;
• [0197] (−)3-{4-[2-(2-acetylpyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoic acid and its pharmaceutically acceptable salts;
• [0198] (±)3-{4-[2-(2-ethyl-5-methylpyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoic acid and its pharmaceutically acceptable salts;
• [0199] (+)3-{4-[2-(2-ethyl-5-methylpyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoic acid and its pharmaceutically acceptable salts;
• [0200] (−)3-{4-[2-(2-ethyl-5-methylpyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoic acid and its pharmaceutically acceptable salts;
• [0201] (±)3-{4-[2-(5-methyl-2-propylpyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoic acid and its pharmaceutically acceptable salts;
• [0202] (+)3-{4-[2-(5-methyl-2-propylpyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoic acid and its pharmaceutically acceptable salts;
• [0203] (−)3-{4-[2-(5-methyl-2-propylpyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoic acid and its pharmaceutically acceptable salts;
• [0204] (±)3-{4-[2-(5-methyl-2-n-butylpyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoic acid and its pharmaceutically acceptable salts;
• [0205] (+)3-{4-[2-(5-methyl-2-n-butylpyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoic acid and its pharmaceutically acceptable salts;
• [0206] (−)3-{4-[2-(5-methyl-2-n-butylpyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoic acid and its pharmaceutically acceptable salts;
• [0207] (±)3-{4-[2-(5-methyl-2-phenylpyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoic acid and its pharmaceutically acceptable salts;
• [0208] (+)3-{4-[2-(5-methyl-2-phenylpyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoic acid and its pharmaceutically acceptable salts;
• [0209] (−)3-{4-[2-(5-methyl-2-phenylpyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoic acid and its pharmaceutically acceptable salts;
• [0210] (±)3-{4-[2-(5-methyl-2-phenylpyrrol-1-yl)ethoxy]phenyl}-2-methoxypropanoic acid and it pharmaceutically acceptable salts;
• [0211] (+)3-{4-[2-(5-methyl-2-phenylpyrrol-1-yl)ethoxy]phenyl}-2-methoxypropanoic acid and its pharmaceutically acceptable salts;
• [0212] (−)3-{4-[2-(5-methyl-2-phenylpyrrol-1-yl)ethoxy]phenyl}-2-methoxypropanoic acid and its pharmaceutically acceptable salts;
• [0213] (±)3-{4-[2-(5-methyl-2-(4-methylphenyl)pyrrol-1-yl)ethoxy]phenyl}-2-propoxypropanoic acid and its pharmaceutically acceptable salts;
• [0214] (+)3-{4-[2-(5-methyl-2-(4-methylphenyl)pyrrol-1-yl)ethoxy]phenyl}-2-propoxypropanoic acid and its pharmaceutically acceptable salts;
• [0215] (−)3-{4-[2-(5-methyl-2-(4-methylphenyl)pyrrol-1-yl)ethoxy]phenyl}-2-propoxypropanoic acid and its pharmaceutically acceptable salts;
• [0216] (±)3-{4-[2-(5-methyl-3-phenylpyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoic acid and its pharmaceutically acceptable salts;
• [0217] (+)3-{4-[2-(5-methyl-3-phenylpyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoic acid and it pharmaceutically acceptable salts;
• [0218] (−)3-{4-[2-(5-methyl-3-phenylpyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoic acid and its pharmaceutically acceptable salts;
• [0219] (±)3-{4-[2-(5-methyl-2-(4-methylphenyl)pyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoic acid and its pharmaceutically acceptable salts;
• [0220] (+)3-{4-[2-(5-methyl-2-(4-methylphenyl)pyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoic acid and its pharmaceutically acceptable salts;
• [0221] (−)3-{4-[2-(5-methyl-2-(4-methylphenyl)pyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoic acid and its pharmaceutically acceptable salts;
• [0222] (+)3-{4-[2-(5-methyl-2-(3-methylphenyl)pyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoic acid and its pharmaceutically acceptable salts;
• [0223] (+)3-{4-[2-(5-methyl-2-(3-methylphenyl)pyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoic acid and its pharmaceutically acceptable salts;
• [0224] (−)3-{4-[2-(5-methyl-2-(3-methylphenyl)pyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoic acid and its pharmaceutically acceptable salts;
• [0225] (±)3-{4-[2-(5-methyl-2-(2-methylphenyl)pyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoic acid and its pharmaceutically acceptable salts;
• [0226] (+)3-{4-[2-(5-methyl-2-(2-methylphenyl)pyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoic acid and its pharmaceutically acceptable salts;
• [0227] (−)3-{4-[2-(5-methyl-2-(2-methylphenyl)pyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoic acid and its pharmaceutically acceptable salts;
• [0228] (±)3-{4-[2-(5-methyl-2-(4-methoxyphenyl)pyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoic acid and its pharmaceutically acceptable salts;
• [0229] (+)3-{4-[2-(5-methyl-2-(4-methoxyphenyl)pyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoic acid and its pharmaceutically acceptable salts;
• [0230] (−)3-{4-[2-(5-methyl-2-(4-methoxyphenyl)pyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoic acid and its pharmaceutically acceptable salts;
• [0231] (±)3-{4-[2-(5-methyl-2-(4-bromophenyl)pyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoic acid and its pharmaceutically acceptable salts;
• [0232] (+)3-{4-[2-(5-methyl-2-(4-bromophenyl)pyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoic acid and its pharmaceutically acceptable salts;
• [0233] (−)3-{4-[2-(5-methyl-2-(4-bromophenyl)pyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoic acid and its pharmaceutically acceptable salts;
• [0234] (±)3-{4-[2-(5-methyl-2-(4-fluorophenyl)pyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoic acid and its pharmaceutically acceptable salts;
• [0235] (+)3-{4-[2-(5-methyl-2-(4-fluorophenyl)pyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoic acid and its pharmaceutically acceptable salts;
• [0236] (−)3-{4-[2-(5-methyl-2-(4-fluorophenyl)pyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoic acid and its pharmaceutically acceptable salts;
• [0237] (±)3-{4-[2-(5-methyl-2-(4-chlorophenyl)pyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoic acid and its pharmaceutically acceptable salts;
• [0238] (+)3-{4-[2-(5-methyl-2-(4-chlorophenyl)pyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoic acid and its pharmaceutically acceptable salts;
• [0239] (−)3-{4-[2-(5-methyl-2-(4-chlorophenyl)pyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoic acid and its pharmaceutically acceptable salts;
• [0240] (±)3-{4-[2-(4-methyl-2-phenylpyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoic acid and its pharmaceutically acceptable salts;
• [0241] (+)3-{4-[2-(4-methyl-2-phenylpyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoic acid and its pharmaceutically acceptable salts;
• [0242] (−)3-{4-[2-(4-methyl-2-phenylpyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoic acid and its pharmaceutically acceptable salts;
• [0243] (±)3-{4-[2-(5-methyl-2,3-diphenylpyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoic acid and its pharmaceutically acceptable salts;
• [0244] (+)3-{4-[2-(5-methyl-2,3-diphenylpyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoic acid and its pharmaceutically acceptable salts;
• [0245] (−)3-{4-[2-(5-methyl-2,3-diphenylpyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoic acid and its pharmaceutically acceptable salts;
• [0246] (±)3-{4-[2-(2-isopropyl-5-methylpyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoic acid and its pharmaceutically acceptable salts;
• [0247] (+)3-{4-[2-(2-isopropyl-5-methylpyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoic and its pharmaceutically acceptable salts;
• [0248] (−)3-{4-[2-(2-isopropyl-5-methylpyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoic and its pharmaceutically acceptable salts;
• [0249] (±)3-{4-[2-(2,5-diisopropylpyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoic acid and its pharmaceutically acceptable salts;
• [0250] (+)3-{4-[2-(2,5-diisopropylpyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoic acid and its pharmaceutically acceptable salts;
• [0251] (−)3-{4-[2-(2,5diisopropylpyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoic acid and its pharmaceutically acceptable salts;
• [0252] (±)3-{4-[2-(5-isopropyl-2-phenylpyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoic acid and its pharmaceutically acceptable salts;
• [0253] (+)3-{4-[2-(5-isopropyl-2-phenylpyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoic acid and its pharmaceutically acceptable salts;
• [0254] (−)3-{4-[2-(5-isopropyl-2-phenylpyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoic acid and its pharmaceutically acceptable salts;
• [0255] (±)3-{4-[2-(2,5-diisopropyl-3-phenylpyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoic acid and its pharmaceutically acceptable salts;
• [0256] (+)3-{4-[2-(2,5-diisopropyl-3-phenylpyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoic acid and its pharmaceutically acceptable salts;
• [0257] (−)3-{4-[2-(2,5-diisopropyl-3-phenylpyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoic acid and its pharmaceutically acceptable salts;
• [0258] (±)3-(4-{2-[5-isopropyl-2-(4-methoxyphenyl)pyrrol-1-yl]ethoxy}phenyl)-2-ethoxypropanoic acid and its pharmaceutically acceptable salts;
• [0259] (+)3-(4-{2-[5-isopropyl-2-(4-methoxyphenyl)pyrrol-1-yl]ethoxy}phenyl)-2-ethoxypropanoic acid and its pharmaceutically acceptable salts;
• [0260] (−)3-(4-{2-[5-isopropyl-2-(4-methoxyphenyl)pyrrol-1-yl]ethoxy}phenyl)-2-ethoxypropanoic acid and its pharmaceutically acceptable salts;
• [0261] (±)3-(4-{2-[2-(4-fluorophenyl)-5-isopropylpyrrol-1-yl]ethoxy}phenyl)-2-ethoxypropanoic acid and its pharmaceutically acceptable salts;
• [0262] (+)3-(4-{2-[2-(4-fluorophenyl)-5-isopropylpyrrol-1-yl]ethoxy}phenyl)-2-ethoxypropanoic acid and its pharmaceutically acceptable salts;
• [0263] (−)3-(4-{2-[2-(4-fluorophenyl)-5-isopropylpyrrol-1-yl]ethoxy}phenyl)-2-ethoxypropanoic acid and its pharmaceutically acceptable salts;
• [0264] (±)3-(4-(2-[2-(4-fluorophenyl)-5-isopropyl-3-phenylpyrrol-1-yl]ethoxy)phenyl)-2-ethoxypropanoic acid and its pharmaceutically acceptable salts;
• [0265] (+)3-(4-(2-[2-(4-fluorophenyl)-5-isopropyl-3-phenylpyrrol-1-yl]ethoxy)phenyl)-2-ethoxypropanoic acid and its pharmaceutically acceptable salts;
• [0266] (−)3-(4-(2-[2-(4-fluorophenyl)-5-isopropyl-3-phenylpyrrol-1-yl]ethoxy)phenyl)-2-ethoxypropanoic acid and its pharmaceutically acceptable salts;
• [0267] (±)3-(4-{2-[2-(4-fluorophenyl)-5-isopropyl-4-phenylcarbamoylpyrrol-1-yl]ethoxy}phenyl)-2-ethoxypropanoic acid and its pharmaceutically acceptable salts;
• [0268] (+)3-(4-{2-[2-(4-fluorophenyl)-5-isopropyl-4-phenylcarbamoylpyrrol-1-yl]ethoxy}phenyl)-2-ethoxypropanoic acid and its pharmaceutically acceptable salts;
• [0269] (−)3-(4-{2-[2-(4-fluorophenyl)-5-isopropyl-4-phenylcarbamoylpyrrol-1-yl]ethoxy}phenyl)-2-ethoxypropanoic acid and its pharmaceutically acceptable salts;
• [0270] (±)3-(4-{2-[2-(4-fluorophenyl)-5-isopropyl-3-phenyl-4-phenylcarbamoylpyrrol-1-yl]ethoxy}phenyl)-2-ethoxypropanoic acid its pharmaceutically acceptable salts;
• [0271] (+)3-(4-{2-[2-(4-fluorophenyl)-5-isopropyl-3-phenyl-4-phenylcarbamoylpyrrol-1-yl]ethoxy}phenyl)-2-ethoxypropanoic acid and its pharmaceutically acceptable salts;
• [0272] (−)3-(4-{2-[2-(4-fluorophenyl)-5-isopropyl-3-phenyl-4-phenylcarbamoylpyrrol-1-yl]ethoxy}phenyl)-2-ethoxypropanoic acid and its pharmaceutically acceptable salts;
• [0273] (±)3-(4-{3-[2-(4-fluorophenyl)-5-isopropyl-3-phenyl-4-phenylcarbamoylpyrrol-1-yl]propoxy}phenyl)-2-ethoxypropanoic acid and its pharmaceutically acceptable salts;
• [0274] (+)3-(4-{3-[2-(4-fluorophenyl)-5-isopropyl-3-phenyl-4-phenylcarbamoylpyrrol-1-yl]propoxy}phenyl)-2-ethoxypropanoic acid and its pharmaceutically acceptable salts;
• [0275] (−)3-(4-{3-[2-(4-fluorophenyl)-5-isopropyl-3-phenyl-4-phenylcarbamoylpyrrol-1-yl]propoxy}phenyl)-2-ethoxypropanoic acid and its pharmaceutically acceptable salts;
• [0276] (±)3-(4-(2-[2-(4-fluorophenyl)-5-phenylpyrrol-1-yl]ethoxy)phenyl)-2-ethoxypropanoic acid and its pharmaceutically acceptable salts;
• [0277] (+)3-(4-{2-[2-(4-fluorophenyl)-5-phenylpyrrol-1-yl]ethoxy}phenyl)-2-ethoxypropanoic acid and its pharmaceutically acceptable salts;
• [0278] (−)3-(4-{2-[2-(4-fluorophenyl)-5-phenylpyrrol-1-yl]ethoxy}phenyl)-2-ethoxypropanoic acid and its pharmaceutically acceptable salts;
• [0279] (±)3-[4-[2-(3-carboxy-5-phenyl-2-(4-fluorophenyl)pyrrol-1-yl)ethoxy]phenyl]-2-ethoxyropanoic acid and its pharmaceutically acceptable salts;
• [0280] (+)3-[4-[2-(3-carboxy-5-phenyl-2-(4-fluorophenyl)pyrrol-1-yl)ethoxy]phenyl]-2-ethoxypropanoic acid and its pharmaceutically acceptable salts;
• [0281] (−)3-[4-[2-(3-carboxy-5-phenyl-2-(4-fluorophenyl)pyrrol-1-yl)ethoxy]phenyl]-2-ethoxypropanoic acid and its pharmaceutically acceptable salts;
• [0282] (±)3-{4-[2-(2-methylthiopyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoic acid and its pharmaceutically acceptable salts;
• [0283] (+)3-{4-[2-(2-methylthiopyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoic acid and its pharmaceutically acceptable salts;
• [0284] (−)3-{4-[2-(2-methylthiopyrrol-1-yl)ethoxy]phenyl}-2-ethoxypropanoic acid and its pharmaceutically acceptable salts;
• [0285] (E/Z)3-{4-[2-(5-methyl-2-phenylpyrrol-1-yl)ethoxy]phenyl}-2-ethoxyprop-2-enoic acid and its pharmaceutically acceptable salts;
• [0286] (E)3-{4-[2-(5-methyl-2-phenylpyrrol-1-yl)ethoxy]phenyl}-2-ethoxyprop-2-enoic acid and its pharmaceutically acceptable salts; and
• [0287] (Z)3-{4-[2-(5-methyl-2-phenylpyrrol-1-yl)ethoxy]phenyl}-2-ethoxyprop-2-enoic acid and its pharmaceutically acceptable salts.

[0288] The present invention also provides methods for the preparation of novel compounds described in the general formula (I), their tautomeric forms, their derivatives, their analogs, their stereoisomers, their polymorphs, their pharmaceutically acceptable salts and their pharmaceutically acceptable solvates, wherein R¹, R², R³, R⁴, R⁵, R⁶, R⁷, R⁸, W, X, Y, Z, Ar and n are as defined earlier. These methods are described below, comprising:

Route 1:

[0289]

[0290] The reaction of a compound of general formula (1a), wherein all symbols are as defined earlier with a compound of formula (1b) which may be optically active or racemic, wherein all symbols are as defined earlier to yield a compound of general formula (I) may be carried out using Paal-Knorr cyclization (Paal C. Ber., 1885, 18, 367; Knorr, L., Ber., 1885, 18, 299). The reaction may be carried out neat or in the presence of a solvent or a mixture thereof such as tetrahydrofuran, hexane, toluene, methanol, ethanol, heptane, petroleum ether, xylene, benzene, ethyl acetate, tert-butyl acetate, 1,2-dichloroethane, iso-propanol, dioxane, cyclohexane, acetonitrile and the like. The reaction temperature may range from 0° C. to the reflux temperature of the solvent(s) used. The water produced may be removed by using a Dean Stark water separator or by water scavengers such as molecular sieves. The reaction may be carried out in the absence or presence of an inert atmosphere such as N₂, He or Ar. The reaction may be carried out under acidic condition provided by acids like acetic acid, propanoic acid, butyric acid, isobutyric acid, pivalic acid, p-toluenesulfonic acid, camphorsulfonic acid, benzenesulfonic acid, trifluoroacetic acid, chloroacetic acid, chloropropanoic acid, phenylacetic acid, phenylpropanoic acid, malonic acid, succinic acid, benzoic acid, halogenated benzoic acid, toluic acid and the like. Mineral acids such as HCl or HBr may also be used. The reaction time may range from 5 minutes to 72 hours, preferably from 1 to 48 hours.

Route 2:

[0291]

[0292] The reaction of compound of formula (1c), where all symbols are as defined earlier and L¹ represents a leaving group such as halogen atom, p-toluenesulfonate, methanesulfonate, trifluoromethanesulfonate and the like with a compound of formula (1d) which may be optically active or racemic, where W is either O or S and all other symbols are as defined earlier, to produce a compound of general formula (I). This reaction may be carried out in the presence of solvents, such as acetone, tetrahydrofuran, dimethylsulfoxide, dioxane, acetonitrile, dimethyl formamide, DME, benzene, toluene, pet. ether, heptane, hexane, 2-butanone, xylene, alcohols such as methanol, ethanol, propanol, butanol, iso-butanol, tert-butanol, pentanol and the like or a mixture thereof Base such as alkali metal carbonate such as K₂CO₃, Na₂CO₃, CsCO₃, and the like; or alkali metal hydroxide such as NaOH, KOH and the like, may be used during this reaction. Alkali metal hydrides such as NaH, KH can be used whenever solvent employed does not contain protic or containing carbonyl group. The reaction may be carried out at a temperature in the range 0° C. to reflux temperature of the solvent(s) used and the reaction time may range from 1 to 48 hours.

Route 3:

[0293]

[0294] The reaction of compound of general formula (1e) where all symbols are as defined earlier and W represents oxygen atom, with a compound of general formula (1d) which may be optically active or racemic, where W is O or S and all other symbols are as defined earlier may be carried out using coupling agents such as DCC, EDC, triaryl phosphine/dialkyl azadicarboxylate such as PPh₃/DEAD or PPh₃/DIAD and the like. Inert atmosphere may be maintained using N₂, Ar or He. Solvents such as tetrahydrofuran, dioxane, DME, toluene, dichloromethane, chloroform, carbon tetrachloride, acetonitrile and the like may be used. Compounds such as DMAP, HOBT may be used in the range of 0.05 to 2 equivalents. The reaction temperature in the range of 0° C. to reflux temperature of the solvent may be used, preferably, 20° C. to 80° C. The duration of the reaction may range from 0.5 to 24 h, preferably 0.5 to 12 hours.

Route 4:

[0295]

[0296] The reaction of a compound of formula (1f) where all symbols are as defined earlier with an alcohol of formula (1g) where R⁷ is as defined earlier, to produce a compound of formula (I) where all symbols are as defined earlier, may be carried out in the presence of rhodium salts such as rhodium (II) acetate. Solvents such as benzene, toluene, ether, THF, dioxane and the like may be used. R⁷XH may also be used as solvent to enhance the rate of the reaction. Inert atmosphere may be maintained using N₂, Ar or He. The reaction time may range from 0.25 to 48 hours, preferably 0.25 h to 8 h.

Route 5:

[0297]

[0298] The reaction of a compound of general formula (1h) wherein all the symbols are as defined earlier, with a compound of formula (1i), where all the symbols are as defined earlier and R represents (C₁-C₈) alkyl to afford a compound of formula (I) where R⁵ and R⁶ represent a bond and all other symbols are as defined earlier, may be carried out under Wittig Horner reaction conditions in the presence of a base such as alkali metal hydrides, like NaH or KH, alkali metal alkoxides such as NaOMe, NaOEt, K⁺ t-BuO⁻ or mixture thereof, organolithiums like CH₃Li, BuLi, sec-BuLi, LDA and the like. Aprotic solvents such as THF, dioxane, DMF, DMSO, DME and the like or mixture thereof may be employed. HMPA favours the progression of the reaction but not essential. The reaction may be carried out at a temperature ranging from −80° C. to 100° C., preferably from 0° C. to 30° C. The reaction proceeds more effectively under anhydrous and inert conditions.

[0299] The compound of formula. (I) where R⁵ and R⁶ represent a bond may be reduced to a compound of general formula (I) where R⁵ and R⁶ each represent hydrogen atom by reacting with hydrogen gas in the presence of a catalyst such as 5-10% Pd/C, Rh/C, Pt/C Raney Ni and the like, 5-100% w/w of the catalyst may be employed or the mixture thereof. The pressure of hydrogen gas may be one atmosphere to 80 psi. Suitable solvents are alcohols such as ethanol, methanol and the like, ethyl acetate, THF, dioxane, acetic acid and the like. Temperature may be in the range of 20° C. to 80° C., may be used for this reduction process. Metal-solvent such as magnesium in alcohol or sodium amalgam in alcohol may also be used, for this reduction process.

[0300] According to a feature of the present invention, there is provided an intermediate of formula (1h),

[0301]
wherein one or more groups R¹, R², R³, R⁴ may be same or different and represent hydrogen, halogen, perhaloalkyl, hydroxy, thio, amino, nitro, cyano, formyl, amidino, guanidino, substituted or unsubstituted groups selected from linear or branched (C₁-C₁₂)alkyl, linear or branched (C₂-C₁₂)alkenyl, (C₃-C₇)cycloalkyl, (C₃-C₇)cycloalkenyl, bicycloalkyl, bicycloalkenyl, (C₁-C₁₂)alkoxy, cyclo(C₃-C₇)alkoxy, aryl, aryloxy, aralkyl, aralkoxy, heterocyclyl, heteroaryl, heterocyclyl(C₁-C₁₂)alkyl, heteroaralkyl, heteroaryloxy, heteroaralkoxy, heterocyclyloxy, heterocyclylalkyloxy, acyl, acyloxy, acylamino, monoalkylamino, dialkylamino, arylamino, aralkylamino, alkoxycarbonyl, aryloxycarbonyl, aralkoxycarbonyl, heterocyclylalkoxycarbonyl, heteroaryloxycarbonyl, heteroaralkoxycarbonyl, heterocyclyloxycarbonyl, hydroxyalkyl, aminoalkyl, monoalkylaminoalkyl, dialkylaminoalkyl, alkoxyalkyl, aryloxyalkyl, aralkoxyalkyl, alkylthio, thioalkyl, arylthio, alkoxycarbonylamino, aryloxycarbonylamino, aralkyloxycarbonylamino, aminocarbonylamino, alkylaminocarbonylamino, alkylamidino, alkylguanidino, dialkylguanidino, hydrazino, alkyl hydrazino, alkoxyamino, hydroxylamino, derivatives of sulfenyl and sulfonyl groups, carboxylic acid and its derivatives, sulfonic acid and its derivatives, phosphonic acid and its derivatives; or the adjacent groups R² and R³ together may form a five or a six membered ring, optionally containing one or more double bonds and optionally containing one or more heteroatoms selected from O, N, or S; n is an integer ranging from 1 to 8; W represents O, S or NR⁹ where R⁹ represents hydrogen, alkyl or aryl; Ar represents a substituted or unsubstituted divalent single or fused aromatic, heteroaromatic or heterocyclic group.

[0302] According to another feature of the present invention, there is provided a process for the preparation of intermediate of the general formula (1h) as defined earlier which comprises reacting a compound of general formula (1c),

[0303]
HW—Ar—CHO  (1j)
wherein, R¹—R⁴, n are as defined earlier and L¹ is a halogen atom such as chlorine, bromine or iodine or a leaving group such as methanesulfonate, trifluoromethanesulfonate, p-toluenesulfonate and the like with the compound of the formula (1j), where Ar and W are as defined earlier. The reaction of the compound of formula (1c) with the compound of formula (1j) to produce a compound of formula (1h) may be carried out in the presence of solvents such as acetone, THF, DMSO, dioxane, 2-butanone, acetonitrile, DMF, DME, benzene, toluene, xylene, alcohols such as methanol, ethanol, propanol, butanol, iso-butanol, tert-butanol, pentanol and the like or a mixture thereof Bases such as alkali metal carbonates such as K₂CO₃, Na₂CO₃, CsCO₃ and the like may be used; alkali metal hydroxides like NaOK KOH and the like; or mixtures thereof may, be used. Alkali metal hydrides such as NaH, KH and the like, may be used incases when the solvent used not protic and does not contain carbonyl group. The reaction temperature may range from 20° C. to reflux temperature of the solvent(s) used and the reaction time may range from 1 to 48 hours. The inert atmosphere may be maintained by using inert gases such as N₂, Ar or He.

[0304] Alternatively, the intermediate of the general formula (1h), can also be prepared by the reaction of compound of general formula (1e),

[0305]
L²-Ar—CHO  (1k)
wherein R¹—R⁴, n and W are as defined earlier and with a compound of the formula (1k), where Ar is as defined earlier and L² is a halogen atom such as fluorine, chlorine, bromine or iodine. The reaction of the compound of formula (1e) with the compound of formula (1k) to produce a compound of formula (1h) may be carried out in the presence of solvents such as THF, DMF, DMSO, DME and the like. Mixture of solvents may be used. The inert atmosphere may be maintained by using inert gases such as N₂, Ar or He. The reaction may be effected in the presence of a base such as K₂CO₃, Na₂CO₃, NaH or mixtures thereof. The reaction temperature may range from 20° C. to 150° C., preferably at a temperature in the range from 30° C. to 100° C. The duration of reaction may range from 1 to 24 hours, preferably from 2 to 6 hours.

[0306] The reaction of compound of general formula (1e) wherein W represents O and all other symbols are as defined earlier with the compound of formula (1j) may be carried out using suitable coupling agents such as dicyclohexyl urea, triarylphosphine/dialkylazadicarboxylate such as PPh₃/DEAD and the like. The reaction may be carried out in the presence of solvents such as THF, DME, CH₂Cl₂, CHCl₃, toluene, acetonitrile, carbontetrachloride and the like. The inert atmosphere may be maintained by using inert gases such as N₂, Ar or He. The reaction may be effected in the presence of DMAP, HOBT and they must be used in the range of 0.05 to 2 equivalents, preferably 0.25 to 1 equivalents. The reaction temperature may range from 0° C. to 100° C., preferably at a temperature in the range from 20° C. to 80° C. the duration of reaction of the reaction may range from 0.5 to 24 hours, preferably from 6 to 12 hours.

[0307] In another embodiment of this invention, there is provided a process for the preparation of a compound of the general formula (1c), which comprises reacting the compound of general formula (1a) wherein R¹—R⁴ are as defined earlier,

[0308]
with either substituted amino compound (1m), where all symbols are is as defined earlier, to yield the intermediate of the general formula (1c).

[0309] In yet another embodiment of this invention, there is provided a process for the preparation of a compound of the general formula (1e), which comprises reacting the compound of general formula (1a) wherein R¹—R⁴ are as defined earlier,

[0310]
with either substituted amino compound (1l), where all symbols are is as defined earlier, to yield the intermediate of the general formula (1e).

[0311] The reactions of a compound of general formula (1a) with a compound of general formula (1l) or a compound of general formula (1m) may be carried out neat or in presence of solvents or a mixture thereof such as tetrahydrofuran, hexane, toluene, methanol, ethanol, heptane, petroleum ether, xylene, benzene, ethyl acetate, tert-butyl acetate, 1,2-dichloroethane, iso-propanol, tert-butanol, dioxane, cyclohexane, acetonitrile and the like. The reaction temperature may range from 0° C. to the reflux temperature of the solvent(s) used. The water produced may be removed by using a Dean Stark water separator or by water scavengers such as molecular sieves. The reaction may be carried out in the presence of an inert atmosphere such as N₂, He or Ar. The reaction may be carried out in the presence of an acid, such as acetic acid, propanoic acid, butyric acid, isobutyric acid, pivalic acid, p-toluenesulfonic acid, camphorsulfonic acid, benzenesulfonic acid, trifluoroacetic acid, chloroacetic acid, chloropropanoic acid, phenylacetic acid, phenylpropanoic acid, malonic acid, succinic acid, benzoic acid, halogenated benzoic acid, toluic acid and the like.

[0312] Yet another embodiment of this invention, there is provided an alternate process for the preparation of a compound of the general formula (1c), which comprises reacting the compound of general formula (1n) wherein R¹—R⁴ are as defined earlier,

[0313]
with the compound of formula (1o) where L₁ and L₂ may be same or different and represent leaving groups such as halogen atom as Cl, Br, or I, methanesulfonate, p-toluenesulfonate and the like; and n as defined earlier.

[0314] In yet another embodiment of this invention, there is provided an alternate process for the preparation of a compound of the general formula (1e), which comprises reacting the compound of general formula (1n) where R¹—R⁴ are as defined earlier,

[0315]
with the compound of formula (1p) where L₂ represent leaving groups such as halogen atom as Cl, Br, or 1, methanesulfonate, p-toluenesulfonate and the like; and n as defined earlier.

[0316] The reaction of compound of general formula (1n), with either (1o) or (1p) may be carried out in solvents such as alcohol like methanol, ethanol, iso-propanol and the like; THF, dioxane, DMSO, DMF, acetonitrile, heptane, benzene, toluene, xylene and the like. The reaction may be carried out in presence of bases such as NaH, KH, Na₂CO₃, K₂CO₃, NaOH, KOK LiNH₂, NaNH₂ and the like. Phase transfer catalyst such as tetrabutyl ammonium halide, tetrabutyl ammonium hydroxide (TBAH) and the like may be used. The reaction temperature may range from 0° C. to the reflux temperature of the solvent employed. The reaction may be carried out in the presence of an inert atmosphere such as N₂, He or Ar.

[0317] In another embodiment of this invention, there is provided a process for the preparation of a compound of the general formula (1e), wherein R¹—R⁴ and n are as defined earlier and W represents O, which comprises reducing the corresponding acid

[0318]

[0319] The reduction of compound of general formula (1q) may be carried out in presence of solvents or a mixture thereof such as tetrahydrofuran, dioxane, ether and the like. The reaction temperature may range from 0° C. to the reflux temperature of the solvent(s) used. The reaction may be carried out in the presence of an inert atmosphere such as N₂, He or Ar. Suitable reducing agent such as sodium borohydride/iodine, diborane and its derivative, LiAlH₄ and the like may be used.

[0320] The compound of general formula (1q) may be prepared by the reaction of compound of general formula (1n) with a compound of L₁(CH₂)_n-1COOR, where L₁ and R are as defined earlier, followed by hydrolysis of the ester group to acid using methods commonly used.

[0321] Another feature of the present invention, is to provide an intermediate of formula (1f) wherein R¹, R², R³, R⁴, R⁵, R⁸, W, Z, n and Ar are as defined earlier.

[0322]
wherein one or more groups R¹, R², R³, R⁴ may be same or different and represent hydrogen, halogen, perhaloalkyl, hydroxy, thio, amino, nitro, cyano, formyl, amidino, guanidino, substituted or unsubstituted groups selected from linear or branched (C₁-C₁₂)alkyl, linear or branched (C₂-C₁₂)alkenyl, (C₃-C₇)cycloalkyl, (C₃-C₇)cycloalkenyl, bicycloalkyl, bicycloalkenyl, (C₁-C₁₂)alkoxy, cyclo(C₃-C₇)alkox aryl, aryloxy, aralkyl, ar(C₁-C₁₂)alkoxy, heterocyclyl, heteroaryl, heterocyclyl(C₃-C₇)alkyl, heteroar(C₁-C₁₂)alkyl, heteroaryloxy, heteroar(C₁-C₁₂)alkoxy, heterocyclyloxy, heterocyclylalkyloxy, acyl, acyloxy, acylamino, monoalkylamino, dialkylamino, arylamino, aralkylamino, alkoxycarbonyl, aryloxycarbonyl, aralkoxycarbonyl, heterocyclylalkoxycarbonyl, heteroaryloxycarbonyl, heteroaralkoxycarbonyl, heterocyclyloxycarbonyl, hydroxyalkyl, aminoalkyl, monoalkylaminoalkyl, dialkylaminoalkyl, alkoxyalkyl, aryloxyalkyl, aralkoxyalkyl, (C₁-C₁₂)alkylthio, thio(C₁-C₁₂)alkyl, arylthio, (C₁-C₁₂)alkoxycarbonylamino, aryloxycarbonylamino, aralkyloxycarbonylamino, aminocarbonylamino, alkylaminocarbonylamino, alkylamidino, alkylguanidino, dialkylguanidino, hydrazino, alkyl hydrazino, alkoxyamino, hydroxylamino, derivatives of sulfenyl and sulfonyl groups, carboxylic acid and its derivatives, sulfonic acid and its derivatives, phosphonic acid and its derivatives; or the adjacent groups R² and R³ together may form a five or a six membered ring, optionally containing one or more double bonds and optionally containing one or more heteroatoms selected from O, N, or S; n is an integer ranging from 1 to 8; W represents O, S or NR⁹ where R⁹ represents hydrogen, (C₁-C₁₂)alkyl or aryl; Ar represents a substituted or unsubstituted divalent single or fused aromatic, heteroaromatic or heterocyclic group; R⁵ represent hydrogen or a hydroxy, (C₁-C₁₂)alkyl, (C₁-C₁₂)alkoxy, halogen, acyl, substituted or unsubstituted aralkyl group; Y represents O or S; Z represents oxygen, sulfur or NR¹⁰, where R¹⁰ represents hydrogen or substituted or unsubstituted groups selected from (C₁-C₁₂)alkyl, aryl, ar(C₁-C₁₂)alkyl, hydroxy(C₁-C₁₂)alkyl, amino(C₁-C₁₂)alkyl, heteroaryl, heteroar(C₁-C₁₂)alkyl groups; R⁸ represents hydrogen, substituted or unsubstituted groups selected from (C₁-C₁₂)alkyl, aryl, ar(C₁-C₁₂)alkyl, heteroaryl, heteroar(C₁-C₁₂)alkyl, heterocyclyl, heterocyclylalkyl, hydroxyalkyl, alkoxyalkyl, alkylaminoalkyl groups; R¹⁰ and R⁸ together may form a 5 or 6 membered substituted or unsubstituted cyclic ring structure containing carbon atoms or containing one or more heteroatoms selected from O, N and S, and a process for its preparation and its use in the preparation of β-aryl-α-substituted alkanoic acid derivatives.

[0323] The compound of formula (1f) where all the symbols are as defined earlier may be prepared by reacting a compound of formula (1r)

[0324]
where R⁶ is hydrogen atom and all other symbols are as defined earlier, with an appropriate diazotizing agent.

[0325] The diazotization reaction may be under conventional conditions. A suitable diazotizing agent is an alkyl nitrile such as iso-amyl nitrile, amyl nitrite and the like. The reaction may be carried out in presence of solvents such as THF, dioxane, DMSO, DMF, acetonitrile, heptane, benzene, toluene, xylene and the like or the combination thereof. The reaction temperature may carried out in an inert atmosphere which may be maintained by using inert gases such as N₂, He or Ar. Temperature is in the range of −50° C. to 60° C. the duration of the reaction may range from 1 to 24 hr, preferably 1 to 12 hr.

[0326] The compound of formula (1r) where all the symbols are as defined earlier may also be prepared by reaction between (1c) where all symbols are as defined earlier and a compound of formula (1s),

[0327]
where R⁶ is hydrogen atom and all other symbols are as defined earlier.

[0328] The reaction of compound of general formula (1c), with (1s) may be carried out in solvents such as alcohol like methanol, ethanol, iso-propanol and the like; THF, dioxane, DMSO, DMF, acetonitrile, heptane, benzene, toluene, xylene and the like. The reaction may be carried out in presence of bases such as NaOH, KOH, K₂CO₃, Na₂CO₃, LiNH₂, NaNH₂, NaH,KH, CsCO₃ and the like. Acetone may be used as a solvent when K₂CO₃ or Na₂CO₃ is used as a base. The reaction temperature may range from 10° C. to the reflux temperature of the solvent employed. The duration of the reaction may be from 1 to 24 hrs, preferably from 3 to 12 hrs. The reaction may be carried out in the presence of an inert atmosphere such as N₂, He or Ar.

[0329] The compounds of the present invention may have asymmetric centers and occur either as racemates or racemic mixtures as well as individual diastereomers of any of the possible isomers, including optical isomers, being included in the present invention The stereoisomers of the compounds of the present invention may be prepared by one or more ways presented below:

• • [0330] i. One or more of the reagents may be used in their single isomeric form. For example, compound (1b) or (1d) may be pure stereoisomers.
  • [0331] ii. Optically pure catalysts or chiral ligands along with metal catalysts may be employed in the reduction process. The metal catalyst may be Rhodium, Ruthenium, Indium and the like. The chiral ligands may preferably be chiral phosphines. (Principles of Asymmetric synthesis J E Baldwin Ed. Tetrahedron series, Volume 14, Page no. 311-316)
  • [0332] iii. Mixture of stereoisomers may be resolved by conventional methods such as microbial resolution, resolving the diastereomeric salts formed with chiral acids or chiral bases. Chiral acids may be tataric acid, mandelic acid, lactic acid, camphorsulfonic acid, amino acids and the like. Chiral bases may be cinchona alkaloids, (+) or (−) brucine, α-methyl benzylamine, (+) or (−) phenyl glycinol, ephedrine, amino sugars such as glucosamines or a basic amino acid such as lysine, arginine and the like.
  • [0333] iv. Resolution of the mixture of stereoisomers may also be effected by chemical methods by derivatization of the compound with a chiral compound such as chiral amines, chiral acids, chiral amino alcohols, amino acids into a 1:1 mixture of diastereomers and the diastereomers may be separated by conventional methods of fractional crystallization, chromatography and the like followed by cleaving the derivative (Jaques et al. “Enantiomers, Racemates and Resolution”, Wiley Interscience, 1981; R. A. Sheldon, in “Chirotechnology”, Marcel Dekker, Inc. NY, Basel, 1993, 173-204 and references therein; A. N. Collins, G. N. Sheldrack and J Crosby, in “Chirality in Industry II”, John Wiley & Sons, Inc, 1997, 81-98 and references therein; E. L. Eliel and S. H. Wilen, in “Stereochemistry of Organic Compound”, John Wiley & Sons, Inc, 1999, 297-464 and references therein.)

[0334] It will be appreciated that in any of the above mentioned reactions any reactive group in the substrate molecule may be protected, according to conventional chemical practice. Suitable protecting groups in any of the above mentioned reactions are those used conventionally in the art. The methods of formation and removal in such protecting groups are those conventional methods appropriate to the molecule being protected. T. W. Greene and P. G. M. Wuts “Protective groups in Organic Synthesis”, John Wiley & Sons, Inc, 1999, 3^rd Ed., 201-245 along with references therein.

[0335] It will be appreciated that the above-mentioned preparation of the compounds of Formula (I), or a pharmaceutically acceptable salt thereof, and/or pharmaceutically acceptable solvate thereof is a stereoselective procedure and that the compound of formula (I) is a single stereoisomer. Favorably, a compound of formula (I) is present in admixture with less than 50% w/w of its racemic isomer, suitably 80-100% and preferably 90-100% pure, such as 90-95%, most preferably 95-100%, for e 95%, 96%, 97%, 98%, 99% and 99.99% optically pure.

[0336] Preferably the compounds of Formula (I), or a pharmaceutically acceptable salt thereof, and/or pharmaceutically acceptable solvate thereof is in optically pure form.

[0337] The absolute stereochemistry of the compounds may be determined using conventional methods, such as X-ray crystallography.

[0338] The pharmaceutically acceptable salts forming a part of this invention may be prepared by treating the compound of formula (I) with 1-6 equivalents of a base such as sodium hydride, sodium methoxide, sodium ethoxide, sodium hydroxide, potassium tert-butoxide, calcium hydroxide, calcium acetate, calcium chloride, magnesium hydroxide, magnesium chloride, magnesium alkoxide and the like. Solvents such as water, acetone, ether, THF, methanol, ethanol, t-butanol, 2-butanone, dioxane, propanol, butanol, isopropanol, diisopropyl ether, tert-butyl ether or mixtures thereof may be used. Organic bases such as lysine, arginine, methyl benzylamine, ethanolamine, diethanolamine, tromethamine, choline, guanidine and their derivatives may be used. Acid addition salts, wherever applicable may be prepared by treatment with acids such as tartaric acid, mandelic acid, fumaric acid, malic acid, lactic acid, maleic acid, salicyhc acid, citric acid, ascorbic acid, benzene sulfonic acid, p-toluene sulfonic acid, hydroxynaphthoic acid, methane sulfonic acid, acetic acid, benzoic acid, succinic acid, palmitic acid, hydrochloric acid, hydrobromic acid, sulfuric acid, nitric acid and the like in solvents such as water, alcohols, ethers, ethyl acetate, dioxane, THF, acetonitrile, DMF or a lower alkyl ketone such as acetone, or mixtures thereof.

[0339] Different polymorphs may by prepared by crystallization of compound of formula (I) under different conditions such as different solvents or solvent mixtures in varying proportions for recrystallization, various ways of crystallization such as slow cooling, fast cooling or a very fast cooling or a gradual cooling during crystallization. Different polymorphs may also be obtained by heating the compound, melting the compound and solidification by gradual or fast cooling, heating or melting under vacuum or under inert atmosphere, and cooling under either vacuum or inert atmosphere. The various polymorphs may be identified by differential scanning calorimeter, powder X-ray diffraction, IR spectroscopy or solid probe ¹³C NMR spectroscopy.

[0340] Another aspect of the present invention comprises a pharmaceutical composition, containing at least one of the compounds of the general formula (I), their derivatives, their analogs, their tautomeric forms, their stereoisomers, their polymorphs, their pharmaceutically acceptable salts, their pharmaceutically acceptable solvates thereof as an active ingredient, together with pharmaceutically employed carriers diluents and the like.

[0341] Pharmaceutical compositions containing a compound of the present invention may be prepared by conventional techniques, e.g. as described in Remington: the Science and Practice of Pharmacy, 19^th Ed., 1995. The compositions may be in the conventional forms, such as capsules, tablets, powders, solutions, suspensions, syrups, aerosols or topical applications. They may contain suitable solid or liquid carriers or in suitable sterile media to form injectable solutions or suspensions. The compositions may contain 0.5 to 20%, preferably 0.5 to 10% by weight of the active compound, the remaining being pharmaceutically acceptable carriers, excipients, diluents, solvents and the like.

[0342] Typical compositions containing a compound of formula (I) or a pharmaceutically acceptable acid addition salt thereof, associated with a pharmaceutically acceptable excipients which may be a carrier or a diluent or be diluted by a carrier, or enclosed within a carrier which can be in the form of a capsule, sachet, paper or other container. When the carrier serves as a diluent, it may be a solid, semi-solid, or liquid material, which acts as a vehicle, excipients or medium for the active compound. The active compound can be absorbed on a granular solid container for example in a sachet. Some of suitable carriers are water, salt solutions, alcohols, polyethylene glycols, polyhydroxyethoxylated castor oil, peanut oil, olive oil, gelatin, lactose, terra alba, sucrose, cyclodextrin, amylose, magnesium sterate, talc, gelatin, agar, pectin, acacia, stearic acid or lower alkyl ethers of cellulose, silicic acid, fatty acids, fatty acid amines, fatty acids monoglycerides and diglycerides, pentaerythritol fatty acids esters, polyoxyethylene, hydroxymethylcellulose and polyvinylpyrrolidone. Similarly, the carrier or diluent may include any sustained release material known in the art, such as glyceryl monostearate or glyceiyl distearate, alone or mixed with a wax. The formulations may also include wetting agents, emulsifying and suspending agents, preservatives, sweetening agents or flavoring agents. The formulations of the invention may be formulated so as to provide quick, sustained, or delayed release of the active ingredient after administration to the patient by employing procedures well known in the art.

[0343] The pharmaceutical compositions can be sterilized and mixed, if desired, with auxiliary agents, emulsifiers, buffers and/or coloring substances and the like, which do not deleteriously react with the active compounds.

[0344] The route of administration may be any route, which effectively transports the active drug to the appropriate or desired site of action effectively, such as oral, nasal, transdermal, pulmonary or parental e.g. rectal, depot, subcutaneous, intravenous, intraurethral, intramuscular, intranasal, ophthalmic solution or an ointment, preferably through oral route.

[0345] If a solid carrier is used for oral administration, the preparation may be tabletted, placed in a hard gelatin capsule in powder or pellet form or it can be in the form of a troche or lozenge. If a liquid carrier is used, the preparation may be in the form of a syrup, emulsion, soft gelatin capsule or sterile injectable liquid such as an aqueous or non-aqueous liquid suspension or solution.

[0346] For nasal administration, the preparation may contain a compound of formula (I) dissolved or suspended in a liquid carrier, in particular an aqueous carrier, for aerosol application. The carrier may contain additives such as solubilizing agent, e.g. propylene glycol, surfactants, absorption enhancers such as lecithin (phosphatidylcholine) or cyclodexirin, or preservatives such as parabens.

[0347] For parental application, particularly suitable are injectable solutions or suspensions, preferably aqueous solutions with the active compound dissolved in polyhydroxylated castor oil.

[0348] Tablet, dragees or capsules having talc and/or a carbohydrate carrier or binder or the like are particularly suitable for oral application. Preferably, carriers for tablets, dragees or capsules include lactose, corn starch and/or potato starch. A syrup or elixir can be used in cases where a sweetened vehicle can be employed.

[0349] A typical tablet which may be prepared by conventional tabletting techniques may contain:

[0350] Core:

[0351]

	Active compound (as free compound or salt thereof)	5.0 mg
	Colloidal silicon dioxide (Aerosil)	1.5 mg
	Cellulose, misrocrytalline (Avicel)	70.0 mg
	Modified cellulose gum (Ac-Di-Sol)	7.5 mg
	Magnesium sterate	ad.
	Coating:
	HPMC approx	9.0 mg
	*Mywacett 9-40 T approx.	0.9 mg
	*Acylated monoglyceride used as plasticizer for film coating.

[0352] The compounds of general formula (I) or the compositions thereof are useful for the treatment and/or prophylaxis of disease caused by metabolic disorders such as hyperlipidemia, insulin resistance, Leptin resistance, hyperglycemia, obesity, or inflammation.

[0353] These compounds are useful for the treatment of hypercholesteremia, familial hypercholesteremia, hypertriglyceridemia, type 2 diabetes, dyslipidemia, disorders related to syndrome X such as hypertension, obesity, insulin resistance, coronary heart disease, atherosclerosis, xanthoma, stroke, peripheral vascular diseases and related disorders, diabetic complications, certain renal diseases such as glomerulonephritis, glomerulosclerosis, nephrotic syndrome, hypertensive nephrosclerosis, retinopathy, nephropathy, psoriasis, polycystic ovarian syndrome, osteoporosis, inflammatory bowel diseases, myotonic dystrophy, arteriosclerosis, Xanthoma, pancreatitis and for the treatment of cancer.

[0354] The compounds of the invention may be administered to a mammal, especially, a human in need of such treatment, prevention, elimination, alleviation or amelioration of diseases mentioned above.

[0355] The compounds of the present invention are effective over a wide dosage range, however, the exact dosage, mode of administration and form of composition depends upon the subject to be treated and is determined by the physician or veterinarian responsible for treating the subject. Generally, dosages from about 0.025 to about 200 mg preferably from about 0.1 to about 100 mg, per day may be used. Generally, the unit dosage form comprises about 0.01 to 100 mg of the compound of formula (I), as an active ingredient together with a pharmaceutically acceptable carrier. Usually suitable dosage forms for nasal, oral, transdermal or pulmonary administration comprises from about 0.001 mg to about 100 mg, preferably from 0.01 mg to about 50 mg of the active ingredient mixed with a pharmaceutically acceptable carrier or diluent.

[0356] In another aspect of the present invention, method of treatment and/or prevention of the diseases mentioned above are provided.

[0357] In a further aspect of the present invention, use of one or more compounds of the general formula (I) or pharmaceutically acceptable salts, for the preparation of a medicament thereof for the treatment and/or prevention of diseases mentioned in this document is provided.

[0358] In still further aspect of the present invention use of the compounds of the present invention alone or in combination with statins, glitazones, biguanides, angiotensin II inhibitors, aspirin, insulin secretagogue, β-sitosterol inhibitor, sulfonylureas, insulin, fibric acid derivatives, nicotinic acid, cholestyramine, cholestipol or probucol, α-glycosidase inhibitors or antioxidants, which may be administered together or within such a period as to act synergistically together.

[0359] The invention is explained in detail by the examples given below, which are provided by way of illustration only and therefore should not be construed to limit the scope of the invention.

[0360]

[0361] A mixture of hexan-2,5-dione (5 g), ethanol amine (26.7 g) and pivalic acid (23.26 g) in a solvent mixture containing n-heptane: tetrahydrofliran: toluene (4:1:1, 50 mL) was refluxed with stirring at 110-120° C. Water formed during the reaction was removed azeotropically during 3 to 4 hrs. The reaction mixture was cooled and the solvent was removed. The residue obtained was dissolved in dichloromethane (30 mL), washed with saturated sodium bicarbonate solution (30 mL), water (30 mL), and then with brine (30 mL), dried (Na₂SO₄) and the solvent was evaporated. The crude compound obtained as an oily mass, was purified by column chromatography (silica gel 100-200), using ethyl acetate:hexane (2:8) as an eluent to obtain the title compound.

[0362] In the like manner to that described in Preparation 1, the following compounds of general formula (1e) were prepared from the appropriately substituted diketones as mentioned in Table 1. The latter can be synthesized by using various routes found in literature.

[0363]

TABLE 1
	Mol.	Yield
Comp.	Substituents on the pyrrole ring in (1e)		Wt.	(%	1H NMR
No.	R1	R2	R3	R4	n =	(mp° C.)	w/w)	(300 MHz, δ, CDCl3)
1.	CH3	H	H	CH3	2	139	65	2.21 (6H, s);
								3.70-3.72 (2H, m);
								3.89 (2H, t, J=5.8Hz);
								5.76 (2H, s).
2.	CH3	H	H	CH2CH3	2	153	53	1.26 (3H, t, J=74Hz);
								2.22 (3H, s);
								2.56 (2H, q, J=7.4Hz);
								3.71 (2H, t, J=5.86Hz)
								3.88 (2H, t, J=5.89Hz);
								5.79-5.81 (2H, m).
3.	CH3	H	H	(CH2)2CH3	2	167	36	1.02 (3H, t, J=7Hz);
								1.65 (2H, m);
								2.25 (3H, s);
								2.5 (2H, t, J=7.7Hz);
								4.1 (2H, t, J=5.9Hz);
								4.35 (2H, t, J=5.9Hz);
								5.8-5.82 (2H, m).
4.	CH3	H	H	(CH2)3CH3	2	181	58	0.94 (3H, t, J=7.2Hz)
								1.36-1.4 (2H, m);
								1.58-1.67 (2H, m);
								2.22 (3H, s);
								2.53 (2H, t, J=7.7Hz);
								3.7 (2H, t, J=5.8Hz)
								3.89 (2H, t, J=5.8Hz);
								5.7-5.8 (2H, m).
5.	CH3	H	H		2	201	62	2.33 (3H, s);3.5-3.6 (2H, t, J=5.9Hz);4.05-4.09 (2H, t, J=6.0Hz);5.95 (1H, d, J=3.3Hz);6.09 (1H, d, J=3.3Hz);7.25-7.29 (1H, m);7.30-7.38 (4H, m).
6.	CH3	H	H		2	215	55	2.32 (3H, s);2.37 (3H, s);3.59 (2H, t, J=6.9Hz);4.10 (2H, t, J=6.9Hz);5.94 (1H, d, J=3.36Hz);6.0 (1H, d, J=3.36Hz);7.2 (2H, d, J=8.5Hz);7.25 (2H, d, J=8.5Hz).
7.	CH3	H	H		2	215	60	2.32 (3H, s);2.36 (3H, s);3.57 (2H, t, J=6Hz);4.08 (2H, t, J=6.06Hz);5.94 (1H, d, J=2.28Hz);6.1 (1H, d, J=3.39Hz);7.09-7.3 (4H, m).
8.	CH3	H	H		2	215	60	2.32 (3H, s);2.36 (3H, s);3.58 (2H, t, J=6Hz);4.07 (2H, t, J=6.06Hz);5.94 (1H, d, J=2.28Hz);6.07 (1H, d, J=3.39Hz);7.09-7.15 (2H, m);7.24-7.29 (2H, m).
9.	CH3	H	H		2	231	45	2.3 (1H, s);3.53 (2H, t, J=6.9Hz)3.84 (3H, s);4.0 (2H, t, J=6.9Hz);5.9 (1H, d, J=3.36Hz);6.0 (1H, d, J=3.36Hz);6.95 (2H, d, J=6.78Hz);7.2 (2H, d, J=6.78Hz).
10.	CH3	H	H		2	280	55	2.32 (3H, s);3.61-3.63 (2H, m)4.05 (3H, t, J=6.2Hz);5.95 (1H, dd);6.1 (1H, d, J=3.4Hz);7.25-7.3 (2H, m);7.47-7.52 (2H, m).
11.	CH3	H	H		2	219	32	2.3 (3H, s);3.6 (2H, t, J=6.0Hz);4.05 (2H, t, J=6.0Hz);5.9 (1H, d, J=2.8);6.0 (1H, d, J=3.3Hz);7.04-7.1 (2H, m);7.26-7.37 (2H, m).
12.	CH3	H	H		2	235.5	61	2.3 (3H, s);3.6 (2H, t, J=5.9Hz);4.12 (2H, t, J=5.9Hz);5.97 (1H, d, J=3.2Hz);6.10 (1H, d, J=3.2Hz);7.09-7.37 (4H, m).
13.	CH3	H			2	277	90	2.37 (3H, s);3.5 (2H, t, J=6Hz);3.95 (2H, t, J=6.0Hz);6.2 (1H, d, J=2.8);7.1-7.4(10H, m).
14.	i-Pr	H	H	CH3	2	167	68	1.2 (6H, d, J=8Hz);2.2 (3H, s);2.94 (1H, septet);3.77 (2H, t, J=6.9Hz);3.97 (2H, t, J=6.9Hz)
15.	i-Pr	H	H	i-Pr	2	195	93	1.21-1.24 (12H, d, J=6.7Hz);
								2.91-2.98 (2H m);
								3.77 (1H, t, J=6.2Hz);
								4.01 (2H, t, J=6.2Hz);
								5.8 (2H, s).
16.	i-Pr	H	H		2	229	86	1.29 (6H, d, J=6.78Hz);3.0-3.05 (1H, m);3.51 (2H, t, J=6.21Hz);4.12 (2H, t, J=6.25Hz);6.0 (1H, d, J=3.54Hz);6.125 (1H, d, J=3.54Hz);7.27-7.31 (3H, m)7.37 (2H, m)
17.	i-Pr		H	i-Pr	2	271	42	1.25 (12 H, d, J=6.5Hz);2.97 (1H, sep, J=6.7Hz);3.24 (1H, sep. J=6.7Hz);3.85 (2H, m);4.1 (2H, t, J=7Hz);5.87 (1H, s);7.19-7.32 (5H, m)
18.	i-Pr	H	H		2	259	84	1.27 (6H, d, J=6.5Hz);2.99-3.04 (1H, m);3.53 (2H, t, J=6.15Hz)3.82 (3H, s);4.09 (2H, t, J=6.2Hz);5.96 (1H, d, J=3.5Hz);6.67 (1H, d, J=3.48Hz);6.91 (2H, d, J=8.9Hz);7.29 (2H, d, J=8.6Hz)
19.	i-Pr	H	H		2	247	22	1.27 (6H, d, J=6.0Hz);2.97-3.06 (1H, m);3.53 (2H, t, J=6.0Hz);4.08 (2H, t, J=6.0Hz);5.99 (1H, d, J=3.60Hz);6.10 (1H, d, J=3.3Hz);7.05-7.1 (2H, t, J=8.8Hz);7.34-7.37 (2H, m)
20.	i-Pr	H			2	323.2(109° C.)	55	1.34 (6H, d, J=7Hz);3.09 (1H, sep, J=7Hz);3.57 (2H, t, J=4.5Hz);4.02 (2H, t, J=4.5Hz);7.03-7.30 (9H, m)
21.	i-Pr		H		2	366	45	1.43-1.45 (6H, d, J=7.2Hz);3.3-3.4 (1H, m);409-4.1 (2H, m);3.80-3.85 (2H, m);6.85 (1H, s);7.0-7.5 (9H, m).
22.	i-Pr				2	442(175-178° C.)	52	1.47 (6H, d, J=7.2Hz);3.5-3.6 (1H, m);3.59 (2H, t, J=6.2Hz);3.99 (2H, t, J=6.6Hz);6.79 (1H, s);6.91-7.0 (3H, m)7.08-7.19 (10H, m).
23.	i-Pr				3	456(58-62° C.)	50	—
24.		—H	H		2	281	79	1.55 (1H, s);3.3 (2H, dd, J=6.0Hz);4.2 (2H, J=6.0Hz);6.25 (2H, dd, J=3.6Hz);7.1 (2H, t, J=7.0Hz);7.4 (1H, m, J=9.0Hz);7.42-7.47 (6H, m)
25.		—COOEt	H		2	353	55	1.10 (3H, t, J=7.0Hz);1.60 (1H, s);3.35 (2H, t, J=6.0Hz);4.00 (2H, t, J=6.0Hz);4.10 (2H, t, J=Hz);6.69 (1H, s);7.10 (2H, t, J=9.9Hz);7.39-7.46 (7H, m)

[0364] Alternatively, compound no. 22 as described in the table 1, can be prepared by using the corresponding aldehyde in better yields. The process is given below:

[0365] A mixture containing suitably substituted aldehyde (2 g) and sodium borohydride (0.167 g) was dissolved in absolute alcohol (20 mL). It was stirred at 0° C.-5° C. for about 2 hr. A solid product was obtained, which was diluted with ice-cold water (40 mL), stirred for 15 min, filtered and washed with DM water (2×10 mL). The compound was dried in a vacuum desiccator over phosphorous pentoxide (2 g, 100%).

[0366]

[0367] A mixture containing 2-bromoethyl-2-acetyl-1H-pyrrole (8.2 g), ethylene glycol (45 mL), 85% potassium hydroxide pellets (8.91 g) and 80% hydrazine hydrate (6.76 mL) was stirred at 200° C. for about 1.5 hr along with simultaneous distillation of volatile materials. The product obtained was extracted with ethyl acetate (2×100 mL). The ethyl acetate layer was washed with water (100 mL), dried over sodium sulfate, filtered and evaporated. The crude product obtained was purified by column chromatography (silica gel 100-200), using ethyl acetate:pet. ether (8:2) as an eluent to obtain 2.2 g of the title compound.

[0368]

	TABLE 2
	Substituents on the		Mol.
Comp.	pyrrole ring in (1e)		Wt.	Yield	1H NMR
No.	R1	R2	R3	R4	N =	(mp° C.)	(% w/w)	(300MHz, δ, CDCl3)
26.	C2H5	H	H	H	2	139	42	1.26(3H, t, J=6.0Hz);
								2.59(2H, q, J1=7.62Hz,
								J2=7.44Hz);
								3.84(2H, t, J=5.4Hz);
								3.98(2H, t, J=5.35Hz);
								5.92-5.93(1H, m);
								6.11(1H, t, J=3.12Hz);
								6.65(1H, t, J=2.22Hz).

[0369]

[0370] A mixture of 2-formylpyrrole (1 g), potassium hydroxide (2.3 g) and dry DMSO (20 mL) was stirred under nitrogen atmosphere. 1,2-dibromoethane (7.9 g) was added dropwise at 20-25° C. and stirred till the reaction is complete. Water (50 mL) was added and the reaction mixture was extracted with diethyl ether (3×50 mL). The combined organic layer was washed with water (30 mL), followed by brine (30 mL) and was dried over Na₂SO₄. The solvent was evaporated and the compound obtained was purified by column chromatography (silica gel 100-200) using ethyl acetate:hexane (2:8) as an eluent to obtain the title compound.

[0371] In like manner to that described in Preparation 4, following compounds of the formula (1c) (Given in Table 3) were prepared from the appropriately substituted pyrrole derivatives. The latter can be synthesized by using various routes found in literature.

[0372]

TABLE 3
	Mol.	Yield
Comp.	Substituents on the pyrrole ring in (1c)		Wt.	(%	1H NMR
No.	R1	R2	R3	R4	n =	(mp° C.)	w/w)	(300 MHz, δ, CDCl3)
27.	CHO	H	H	H	2	202	47	3.65 (2H, t, J=6Hz)
								4.65 (2H, t, J=6Hz)
								6.33 (1H, m);
								6.95-7.05 (2H, m);
								9.5 (1H, m).
28.	COCH3	H	H	H	2	216	32	2.44 (3H, s);
								3.67 (2H, t, J=6Hz);
								4.65 (2H, t, J=6Hz);
								6.16-6.18 (1H, m);
								6.94 (1H, t, J=6Hz);
								7.01-7.03 (1H, m).

[0373]

[0374] To a mixture of potassium hydroxide (16.7 g) and dry DMSO (150 mL), pyrrole (5 g) was added dropwise at 20-25° C., with stirring under nitrogen atmosphere. Stirring was continued for 1 hr at 20-25° C. Ethyl bromoacetate (24.5 g) was added dropwise at 20-25° C. and stirring was continued for 2 hr. In the reaction mixture (150 mL) DM water was added and pH was made acidic (pH=3) with 20% HCI (50 mL). The reaction mixture was extracted with diethyl ether (2×100 mL). The combined organic extract was washed with DM water (100 mL), saturated brine (100 mL) and dried over Na₂SO₄. The solvent was evaporated to obtain pyrrol-1-yl-acetic acid.

[0375] To a suspension of sodium borohydride (3.6 g) in tetrahydrofuran (70 mL), pyrrol-1-yl-acetic acid (6 g) dissolved in THF (70 mL) was added dropwise at 20° C.-25° C. within 10-15 min under nitrogen atmosphere. When the evolution of hydrogen gas ceases, the reaction mixture was cooled to 5-10° C. and iodine (5.9 g) dissolved in THF was added dropwise at 5° C.-10° C. and was stirred further for 2 hrs at 20° C.-25° C. The reaction mixture poured in mixture of ice-cold KOH solution (10 mL) and DM water (50 mL). The solution was with ethyl acetate (2×50 mL). The organic extract was washed with water (30 mL), brine (30 mL) and dried over Na₂SO₄. The solvent was evaporated under reduced pressure, to obtain the title compound.

[0376] In like manner to that described in Preparation 5, following compounds of the formula (1e) (Given in Table 4) were prepared from the appropriately substituted pyrrole. The latter can be synthesized by using various routes found in literature.

[0377]

TABLE 4
	Mol.	Yield
Comp.	Substituents on the pyrrole ring in (1e)		Wt.	(%	1H NMR
No.	R1	R2	R3	R4	n =	(mp° C.)	w/w)	(300 MHz, δ, CDCl3)
29.	H	H	H	H	2	111	98	—
30.	CH3	H	CH3	H	2	139	40.4	2.02 (3H, s); 2.19 (3H, s);
								3.7-3.9 (4H, m);
								5.73 (1H, s); 6.38 (1H, s).
31.		H	CH3	H	2	201	13	2.05 (3H, s);3.75 (2H, t, J=6Hz);4.03 (2H, t, J=5.5Hz);6.07 (1H, s);6.62 (1H, s);7.27-7.42 (5H, m).
32.	CH3	H		H	2	201	57	2.24 (3H, s);3.82-4.01 (4H, m);6.19 (1H, s);6.9 (1H, s);7.1-7.4 (5H, m).
33.	SCH3	H	H	H	2	157	90	2.2 (3H, s);3.85 (2H, t, J=6.0Hz);4.1 (2H, t, J=5.5Hz);6.14 (1H, dd);6.38 (1H, dd);6.85 (1H, dd)

[0378]

[0379] To a solution of compound 1 (3.0 g in 20 mL dichloromethane) obtained in preparation 1, triethylamine (11 mL) was added followed by addition of methanesulfonyl chloride (5 g) at 0° C. The reaction mixture was stirred at 0° C. for 1 h under nitrogen atmosphere. The mixture was warmed to temperature of about 20 to 25° C. and was stirred at that temperature for about 2 h (TLC). After the completion of the reaction, water (30 mL) was added and the organic layer was separated. The mixture was washed with saturated sodium bicarbonate solution (20 mL), water (20 mL) and then with brine (20 mL) and dried over Na₂SO₄. The organic layer was concentrated under reduced pressure. The crude substance was used in the next step without purification.

[0380] In like manner to that described in Preparation 6 following compounds of the formula (1c) (given in Table 5) were prepared from the appropriately substituted pyrrole derivatives (1e) described earlier.

[0381]

TABLE 5
	Mol.	Yield
Comp.	Substituents on the pyrrole ring in (1c)		Wt.	(%	1H NMR
No.	R1	R2	R3	R4	n =	(mp° C.)	w/w)	(300 MHz, δ, CDCl3)
34.	H	H	H	H	2	189	26	2.7 (3H, s);
								4.43 (2H, t, J=5.2Hz);
								6.17 (2H, t, J=21Hz);
								6.7 (2H, t, J=2.1Hz);
35.	CH3	H	H	CH3	2	217	64	2.23 (6H, s);
								2.68 (3H, s);
								4.08 (2H, t, J=5.8Hz);
								4.34(2H, t, J=5.8Hz),
								5.78 (2H, s)
36.	CH3	H	CH3	H	2	217	98	—
37.	C2H5	H	H	H	2	217	90	1.29 (3H, t, J=2.64Hz);
								2.58 (2H, q, J=7.32Hz);
								2.71 (3H, s);
								4.15 (2H, t, J=5.52Hz);
								4.41 (2H, t, J=5.5Hz);
								5.92 (1H, m);
								6.11 (1H, t, J=3.16Hz);
								6.63 (1H, t, J=2.26Hz).
38.	CH3	H	H	CH2CH3	2	231	56	1.26 (3H, t, J=7.4Hz);
								2.25 (3H, m)
								2.57 (2H, q, J=7.42Hz);
								2.69 (3H, s);
								4.12 (2H, t, J=5.9Hz);
								4.34 (2H, t, J=5.9Hz);
								5.8-5.83 (2H, m).
39.	CH3	H	H	(CH2)2CH3	2	246	45	1.02 (3H, t, J=7Hz);
								1.65 (2H, m);
								2.25 (3h, s);
								2.5 (2H, t, J=7.7Hz);
								2.69 (3H, s);
								4.1 (2H, t, J=5.9Hz);
								4.35 (2H, t, J=5.9Hz);
								5.8-5.83 (2H, m).
40.	CH3	H	H	(CH2)3CH3	2	259	72	0.95 (3H, t, J=7.2Hz);
								1.44-1.46 (2H, m);
								1.58-1.62 (2H, m);
								2.25 (3H, s);
								2.5 (2H, t, J=5.9Hz;)
								2.7 (3H, s);
								4.1 (2H, t, J=5.9Hz);
								4.39 (2H, t, J=5.9Hz),
								5.8 (2H, s).
41.	CH3	H	H		2	279	98	2.34 (3H, s), 283 (3H, s);4.11 (2H, t, J=5.7Hz);4.27 (2H, t, J=5.7Hz),5.96 (1H, d, J=3.4Hz);6.10 (1H, d, J=3.4Hz);7.27-7.43 (5H, m).
42.	CH3	H		H	2	279	86	2.28 (3H, s), 2.73 (3H, m),4.16 (2H, d, J=5.4Hz);4.4 (2H, d, J=5.4Hz),6.2 (1H s);6.9 (1H s);7.17 (1H, d, J=6.75Hz);7.3 (2H, d, J=7.0Hz),7.46 (2H, d, J=7.0Hz).
43.	CH3	H	H		2	293	68	2.33 (3H, s), 238 (3H, s),2.65 (3H, s);4.12 (2H, t, J=6.3Hz),4.25 (2H t, J=6.3Hz);5.95 (1H d, J=3.4Hz);6.10 (1H d, J=3.4Hz);7.19-7.25 (4H, m).
44.	CH3	H	H		2	293	95	2.33 (3H, s); 238 (3H, s);2.66 (3H, s);4.12 (2H t, J=5.8Hz);4.27 (2H t, J=5.7Hz);5.95 (1H, d, J=3.37Hz);6.09 (1H d, J=3.42Hz);7.12-7.16 (2H, m);7.25-7.31 (2H m).
45.	CH3	H	H		2	293	55	2.34 (3H s); 2.38 (3H s);2.67 (3H s);4.13 (2H, t, J=5.8Hz);4.27 (2H t, J=5.7Hz);5.96 (1H, d, J=3.36Hz);6.1 (1H d, J=3.39Hz);7.13-7.29 (4H, m).
46.	CH3	H	H		2	309	62	2.3 (3H, s); 2.67 (3H, s);3.8 (3H s);4.12 (2H, t, J=5.45Hz);4.24 (2H, t, J=5.45Hz);5.9 (1H, d, J=3.39Hz);6.0 (1H d, J=3.39Hz);6.95 (2H d, J=6.78Hz);7.26 (2H d, J=6.78Hz).
47.	CH3	H	H		2	358	70	2.33 (3H, s); 2.7 (3H, s);4.13-4.15 (2H, m);4.2-4.25 (2H, m);5.97 (1H, d, J=3.4Hz);6.12 (1H, 3.4Hz);7.21-7.26 (2H, m);7.52-7.55 (2H, m).
48.	CH3	H	H		2	297	90	2.3 (3H, s);2.7 (3H, s);3.6 (2H, t, J=6.0Hz);4.1 (2H, d, J=5.6Hz);4.22 (2H, d, J=5.4Hz);5.9 (1H, d, J=3.4Hz);6.0 (1H, d, J=3.4Hz),7.04-7.1 (2H, m);7.2-7.3 (2H, m).
49.	CH3	H	H		2	313.5	82	2.3 (3H, s);2.69 (3H, s);4.15 (2H, d, J=6.3Hz);4.25 (2H, d, J=6.3Hz);5.96-5.97 (1H, dd);6.1 (1H, d, J=3.4Hz);7.27-7.4 (4H, m).
50.		H	CH3	H	2	279	90	2.13 (3H, s);2.73 (3H, m);4.2-4.28 (4H, m);6.05 (1H, s);6.59 (1H, s);7.29-7.43 (5H, m).
51.	CH3	H			2	355	90	2.73 (3H, s);4.09-4.14 (4H, m);6.2 (1H, s);7.0-7.4 (10H, m).
52.	i-Pr	H	H	CH3	2	245	97.1	1.28 (6h, d, J=7.7Hz);2.25 (3H, s);2.83-2.92 (1H, m);4.14 (2H, t, J=6.9Hz);4.34 (2H, t, J=6.9Hz);5.83 (2H, s).
53.	i-Pr	H	H	i-Pr	2	272	37	1.23-1.25 (12H, d, J=6.7
								Hz);
								2.76 (3H, s);
								2.82-2.99 (2H, m);
								4.18 (2H, m);
								4.33 (2H, m);
								5.86 (2H, s).
54.	i-Pr	H	H		2	307	100	1.30 (6H, t, J=6.78Hz);2.65 (3H, m);2.96-3.00 (1H, m);4.04 (2H, t, J=6Hz);4.32 (2H, t, J=6Hz);6.0 (1H, d, J=3.54Hz);6.12 (1H, d, J=3.54Hz);7.32-7.43 (5H, m).
55.	i-Pr		H	i-Pr	2	349	97	—
56.	i-Pr	H	H		2	337	99	—
57.	i-Pr	H	H		2	325	72	1.29 (6H, d, J=6.0Hz);2.69 (3H, s);2.92-2.99 (1H, m);4.05 (2H, t, J=6.0Hz);4.27 (2H, t, J=6.0Hz);6.00 (1H, d, 3.4Hz);6.1 (1H, d, J=3.4Hz);7.07-7.1 (2H, t, J=6.0Hz);7.30-7.35 (2H, m)
58.	i-Pr	H			2	369	61	1.35 (6H, d, J=7Hz);2.76 (3H, s);3.0-3.05 (1H, m);4.05 (2H, t, J=62Hz);4.15 (2H, t, J=6Hz);6.22 (1H, s);7.07-7.30 (9H, m)
59.	i-Pr		H		2	444	15	1.5-1.52 (6H, d, J=7.1Hz); 2.84 (3H, s);3.44-3.52 (1H, m);4.12-4.15 (2H, t, J=6.4Hz); 4.34-34 (2H, t, J=6.4Hz); 6.32 (1H, s);7.12-7.18 (3H, t, J=8.5Hz); 7.3-7.4 (4H, m);7.56-7.59 (2H, d, J=7.6Hz).
60.	i-Pr				2	520(160-162)	85	—
61.	i-Pr				3	534	100	—
62.		H/ H		2	359	98	—
63.		—COOEt	H		2	431	98.3	—
64.	SCH3	H	H	H	2	235	95	2.29 (3H, s); 2.77 (3H, s);4.35-4.48 (4H, m);6.17 (1H, dd);6.4 (1H, dd);6.85 (1H, dd).

[0382]

[0383] To a suspension of potassium carbonate (16.43 g) in dimethyl formamide (50 mL), 4-hydroxy benzaldehyde (4.37 g) was added and warmed to 90° C. to 95° C. To the solution, methyl 1-[5-methyl phenyl-1H-pyrrol-1yl]ethane sulfonate (10 g) (compound no. 41) dissolved in dimethyl formamide (50 mL) was added within 30 min and the reaction was continued for further 4 hours. The reaction mixture was diluted with water (100 mL) and was extracted with ethyl acetate (3×100 mL), washed with water (3×100 mL), brine (200 mL), and was dried over sodium sulfate. The solvent was evaporated under reduced pressure, to yield the title compound.

[0384]

TABLE 6
	Mol.	Yield
Comp.	Substituents on the pyrrole ring in (1p)	Wt.	(%	1H NMR
No.	R1	R2	R3	R4	(mp° C.)	w/w)	(300 MHz, δ, CDCl3)
65.	CH3	H	H	Phenyl	306	99	2.39 (3H, s);
							4.0 (2H, t, J=6.3Hz);
							4.35 (2H, t, J=6.3Hz);
							5.98 (1H, d, J=3.4Hz);
							6.12 (1H, t, J=3.4Hz);
							6.74 (2H, d, J=8.7);
							7.38-7.42 (5H, m);
							7.73-7.75 (2H, d, J=8.8Hz);
							9.85 (1H, s).

[0385]

[0386] A mixture (S)-ethyl 3-(4-hydroxyphenyl)-2-ethoxypropanoate (1.12 g), and potassium carbonate (2.37 g) in dimethyl formamide (20 mL) was stirred at 70° C.-80° C. for 10 min. The respective mesylate (Compound. No. 35) (2.3 g) dissolved in dimethyl formamide (10 mL) was added and stirred at 70° C. to 80° C. for 24 h and was allowed to stand overnight at 70° C.-80° C. (ca.16 h). The reaction mixture was diluted with water (40 mL). The product was extracted with ethyl acetate (2×50 mL), washed with water (2×40 mL), brine (50 mL) and was dried over sodium sulfate. Ethyl acetate was evaporated under reduced pressure to obtain an oily product. The crude (3 g) product was chromatographed over silica gel using ethyl acetate:petroleum ether (60-80) (1:9) as an eluent to afford the pure titled compound (2.6 g, 57%).

[0387] A mixture of (S)-ethyl 3-(4-hydroxyphenyl)-2-ethoxypropionate (1.12 g) and dry potassium carbonate (2.37 g) in dimethyl formamide (20 mL) was stirred at 80° C. for 30 min. 1-(2-bromoethyl)2-carbaldehyde pyrrole (1.0 g, Compound. No. 27) was added at 40° C. and stirring was continued at 80° C. for 24 h. The reaction mixture was cooled to 20° C.-25° C. and 20 mL water was added. The reaction mixture was extracted with ethyl acetate (2×25 mL), washed with water (2×20 mL), brine (25 mL) and was dried over sodium sulfate. The organic layer was evaporated under reduced pressure to obtain an oily product. The crude oily product was chromatographed over silica gel (100-200 mesh) using ethyl acetate:petroleum ether (1:9) as an eluent to afford the title compound as a yellow oil (0.4 g, 22%).

[0388] A mixture of (S)-ethyl 3-(4-hydroxyphenyl)-2-ethoxypropionate (1.09 g), and dry potassium carbonate (2.37 g) in toluene (15 mL) was heated to reflux for 45 min with continuous removal of water using a Dean-Stark water separation. The mixture was cooled to 50° C. and mesylate compound No. 8 (1.2 g) was added. The reaction mixture was continued to reflux for 24 hrs. Later it was cooled to 20° C.-25° C. and toluene was distilled at reduced pressure. To the residue, DM water (20 mL) was added and the crude product was extracted with ethyl acetate (2×25 mL), washed with water (2×20 mL), brine (25 mL) and was dried over sodium sulfate. The solvent was evaporated under reduced pressure to obtain an oily product. The crude oily product was chromatographed over silica gel using ethyl acetate:petroleum ether (60-80) (1:9) as an eluent to afford the title product as a yellow oil (63%).

[0389] In like manner to that described in preparation 8-10, the following compounds of the formula (I) (given in Table 7) were prepared from appropriately substituted pyrrole derivatives described in either Table 5 or obtained from other methods described herein.

[0390]

TABLE 7
	Mol.	Yield
Ex.	Substituents on the pyrrole ring in (I)		Wt.	(%	1H NMR
No.	R1	R2	R3	R4	n =	(mp° C.)	w/w)	(300 MHz, δ, CDCl3)
1.	H	H	H	H	2	331	37	1.15 (3H, t, J=6.9Hz);
								1.22 (3H, t, J=6.9Hz);
								2.94 (2H, dd);
								3.33-3.38 (1H, m);
								3.54-3.65 (1H, m);
								3.95 (1H, dd);
								4.12-4.26 (6H, m);
								6.16 (2H, t, J=2.1Hz);
								6.7 (2H, t, J=2.1Hz);
								6.8 (2H, d, J=8.5Hz);
								7.15 (2H, d, J=8.5Hz).
2.	CH3	H	H	CH3	2	359	57	1.15 (3H, t, J=6.9Hz);
								1.25 (3H, t, J=6.9Hz);
								2.27 (6H, s);
								2.91-2.94 (2H, m);
								3.32-3.60 (2H, m);
								3.97-4.2 (7H, m);
								5.78 (2H, s);
								6.78 (2H, d, J=8.5Hz);
								7.15 (2H, d, J=8.5Hz).
3.	CH3	H	CH3	H	2	359	18	1.15 (3H, t, J=7Hz);
								1.26 (3H, t, J=7Hz);
								2.04 (3H, s); 2.23 (3H, s);
								2.91-2.94 (2H, m);
								3.3-3.39 (1H, m);
								3.5-3.62 (1H, m);
								3.92 (1H, dd, J=6.0 Hz);
								4.12-4.2 (6H, m);
								5.7 (1H, s); 6.4 (1H, s);
								6.77 (2H, d, J=8.6Hz);
								7.15 (2H, d, J=8.6Hz).
4.	C2H5	H	H	H	2	359	18	1.15 (3H, t, J=7.02Hz);
								1.22 (3H, t, J=5.74Hz);
								1.26 (3H, t, J=6.03Hz);
								2.62 (2H, q);
								2.93 (2H, d, J=5.7Hz);
								3.94 (2H, t, J=?? Hz);
								4.12-4.20 (5H, m);
								5.91 (1H, m);
								6.10 (1H, t, J=3.12Hz);
								6.69-6.75 (1H, m);
								6.76 (2H, d, J=6.7Hz);
								7.13 (2H, d, J=8.61Hz).
5.	CHO	H	H	H	2	359	22	1.1 (3H, t, J=69Hz);
								1.26 (3H, t, J=6.9Hz)
								2.94-4.08 (5H, m);
								4.22 (2H, t, J=4.9Hz);
								4.7 (2H, t, J=4.9Hz);
								6.23 (1H, dd);
								6.7 (2H, dd, J=8.5Hz);
								6.97 (1H, dd);
								7.1 (1H, dd);
								9.5 (1H, s).
6.	COCH3	H	H	H	2	137	10	1.15 (3H, t, J=3.48Hz);
								1.2 (3H, t, J=5.1Hz);
								2.44 (3H, s);
								2.93 (2H, dd, J=5.55Hz);
								3.0-3.35 (2H, m);
								3.94 (2H, t, J=3.58Hz);
								4.16 (2H, q, J1=1.44Hz,
								J2=1.41Hz);
								4.21 (1H, t, J=5.04Hz);
								4.69 (2H, t, J=4.99Hz),
								6.14-6.15 (1H, m);
								6.75 (2H, d, J=8.37Hz),
								6.99-7.01 (2H, m)
								7.11 (2H, d, J=8.64Hz).
7.	CH3	H	H	CH2CH3	2	373	45	1.15 (3H, t, J=7Hz);
								1.22 (3H, t, J=7Hz);
								1.27 (3H, t, J=7Hz);
								2.28 (3H, m);
								2.63 (2H, q, J=7.4Hz);
								2.9-2.96 (2H, m);
								3.3-3.6 (2H, m);
								3.92-4.19 (7H, m);
								5.8-5.83 (2H, m);
								6.75 (2H, d, J=6.78Hz);
								7.14 (2H, d, J=6.78Hz).
8.	CH3	H	H	(CH2)2CH3	2	389	41	1.02 (3H, t, J=6.9Hz);
								1.15 (3H, t, J=6.9Hz);
								1.23 (3H, t, J=7.14Hz);
								1.65-1.7 (2H, m);
								2.28 (3H, s);
								2.5 (2H, t, J=7.75Hz);
								2.9-2.92 (2H, m);
								3.25-3.5 (2H, m);
								3.94 (1H, t, J=3.66Hz);
								4.0-4.2 (6H, m)
								5.8-5.83 (2H, m);
								6.75 (2H, d, J=8.5Hz);
								7.15 (2H, d, J=8.5Hz).
9.	CH3	H	H	(CH2)3CH3	2	401	46	0.95 (3H, t, J=7.2Hz);
								1.15 (3H, t, J=7Hz);
								1.23 (3H, t, J=7Hz);
								1.4-1.47 (2H, m);
								1.6-1.7 (2H, m);
								2.28 (3H, s);
								2.5 (2H, t, J=7.7Hz),
								2.9-2.97 (2H, m);
								3.3-3.39 (1H, m);
								3.55-3.63 (1H, m);
								4.04-4.22 (6H, m)
								5.8-5.83 (2H, m);
								6.7 (2H, d, J=8.5Hz);
								7.15 (2H, d, 8.5Hz).
10.	CH3	H	H		2	421	85	1.15 (3H, t, J=6.9Hz);1.22 (3H, t, J=7.1Hz);2.37 (3H, s);2.9-2.92 (2H, dd);3.32-3.35 (1H, m);3.5-3.58 (1H, m);3.9-3.92 (3H, m);4.12-4.19 (2H, q);4.28 (2H, t, J=6.5Hz);5.96-5.97 (1H, d, J=3.1Hz);6.1-6.11 (1H, d, J=3.11Hz);6.6 (2H, d, J=8.5Hz);7.06-7.09 (2H, d, J=8.5Hz);7.3-7.4 (5H, m).
11.	CH3	H		H	2	421	63	1.15 (3H, t, J=6.9Hz);1.22 (3H, t, J=7.1Hz);2.37 (6H, s);2.9-2.92 (2H, m);3.3-3.4 (1H, m);3.53-3.62 (1H, m);3.9 (3H, t, J=6.6Hz);4.1-4.22 (6H, m);6.2 (1H, s);6.8 (2H, d, J=8.5Hz);6.98 (1H, s);7.15 (2H, d, J=8.5Hz);7.23-7.33 (3H, m)7.4 (2H, t, J=7.1Hz).
12.	CH3	H	H		2	435	34	1.16 (3H, t, J=6.9Hz);1.22 (3H, t, J=6.9Hz);2.37 (3H, s); 2.39 (3H, s);2.9-2.92 (2H, m);3.3-3.37 (1H, m);3.56-3.62 (1H, m);3.91-4.2 (5H, m);4.27 (2H, m);5.95 (1H, d, J=3.36Hz);6.10 (1H, d, J=3.36Hz);6.6 (2H, d, J=8.5Hz);7.0 (2H, d, J=6.78Hz);7.19 (2H, d, J=8.5Hz);7.28 (2H, d, J=6.78Hz).
13.	CH3	H	H		2	435	37	1.15 (3H, t, J=6.9Hz);1.22 (3H, t, J=7.13Hz);2.37 (6H, s);2.91 (2H, d, J=5.94Hz);3.89-3.95 (5H, m);4.15 (2H, q, J1=7.11Hz, J2=7.11Hz);4.28 (2H, t, J=6.63Hz);5.95 (1H, d, J=3.39Hz);6.07 (1H, d, J=3.39Hz);6.59 (2H, d, J=7.62Hz);7.07 (2H, d, J=8.64Hz);7.15-7.28 (4H, m).
14.	CH3	H	H		2	435	53	1.15 (3H, t, J=6.9Hz);1.22 (3H, t, J=7.13Hz);2.37 (6H, s);2.9-2.92 (2H, m);3.3-3.58 (2H, m);3.89-3.95 (3H, m);4.15 (2H, t, J=6Hz);4.28 (2H, t, J=6Hz);5.95 (1H, d, J=3.2Hz);6.0 (1H, d, J=3.2Hz);6.6 (2H, d, J=7.62Hz);7.0 (2H, d, J=8.64Hz);7.12-7.28 (4H, m).
15.	CH3	H	H		2	451	41	1.1 (3H, t, J=7Hz);1.22 (3H, t, J=7Hz);2.36 (3H, s);2.9-2.92 (2H, dd);3.3-3.32 (1H, m);3.52-3.62 (1H, m);3.84 (3H, m);3.9-3.94 (3H, m);4.14 (2H, t, J= 6.68Hz);4.22 (2H, t, J=6.68Hz);5.9 (1H, d, J=3.36Hz);6.0 (1H, d, J=3.36Hz);6.64 (2H, d, J=8.58Hz);6.95 (2H, d, J=6.78Hz);7.10 (2H, d, J=8.5Hz);7.31 (2H, d, J=6.78Hz).
16.	CH3	H	H		2	500	40	1.16 (3H, t, J=7Hz);1.2 (3H, t, J=7Hz);2.37 (3H, s);2.95 (2H, dd);3.29-3.38 (1H, m);3.55-3.63 (1H, m);3.9-3.95 (3H, m);4.17 (2H, t, J=6.3Hz);4.28 (2H, t, J=6.3Hz);5.9 (1H, d, J=3.42Hz);6.1 (1H, d, J=3.42Hz),6.6 (2H, d, J=8.5Hz);7.21 (2H, d, J=8.5Hz);7.29 (2H, d, J=8.5Hz);7.5 (2H, d, J=8.5Hz).
17.	CH3	H	H		2	439	30	1.15 (3H, t, J=6.99Hz);1.23 (3H, t , J=6.99Hz);1.58 (3H, s);2.9-2.93 (2H, dd);3.55-3.65 (1H, m);3.85-4.0 (3H, m);4.1-4.2 (2H, m);4.24 (2H, t, J=6.4Hz)5.9 (1H, d, J=3.3);6.0 (1H, d, J=3.4Hz);6.6 ( 2H, t, J=8.6Hz)7.0-7.1 (4H, m);7.26-7.38 (2H, m).
18.	CH3	H	H		2	455.5	62	1.15 (3H, t, J=7Hz);1.23 (3H, t, J=7Hz);2.36 (3H, s);2.9-2.95 (2H, dd);3.33-3.4 (1H, m);3.53-3.62 (1H, m);3.9-4.13 (3H, m);4.18 (2H, d, J=6.3Hz);4.26 (2H, t, J=6.3Hz);5.97 (1H, d, J=3.27Hz);6.1 (1H, d, J=3.4Hz);6.6 (2H, d, J=8.4Hz);7.1 (2H, d, J=8.4Hz);7.25-7.38 (2H, m).
19.		H	CH3	H	2	421	13	1.15 (3H, t, J=6.9Hz);1.23 (3H, t, J=7.2Hz);2.13 (3H, s); 2.92 (2H, d);3.33 (1H, m); 3.59 (1H, m);3.94 (3H, m);4.07-4.26 (4H, m);6.05 (1H, s);6.67-6.72 (3H, m);7.12 (2H, m);7.3-7.43 (5H, m).
20.	CH3	H			2	497	32	1.153 (3H, t, J=7.0Hz);1.24 (3H, t, J=7Hz);2.4 (3H, s);2.9-2.92 (2H, m);3.33-3.36 (1H, m);3.53-3.63 (1H m);3.85-3.95 (3H, m);4.1-4.2 (4H, m);6.2 (1H, s);6.5-7.4(14H, m).
21.	i-Pr	H	H	CH3	2	387	32.4	1.15 (3H, t, J=6.9Hz);
								1.2 (3H, 6.9Hz);
								1.25 (6H, d, J 32 6.7Hz);
								2.27 (3H, s);
								2.9-3.0 (3H, m);
								3.3-3.63 (2H, m);
								3.96 (1H, dd, );
								4.06 (2H, t, J=6.9Hz);
								4.14-4.24 (4H, m);
								5.83 (2H, s);
								6.73 (2H d, J=8.5Hz);
								7.15 (2H, d, J=8.5Hz).
22.	i-Pr	H	H	i-Pr	2	415	36	1.15 (3H, t, J=6.9Hz);
								1.23 (3H, t, J=?? Hz);
								1.24-1.26 (12H, , J=6.7Hz);
								2.9 (4H, m); 3.35 1(H);
								3.6 (1H, m);
								3.95 (1H, dd, J=?? Hz);
								4.05 (2H, t);
								4.1-4.2 (2H, q, J1=6.8Hz,
								J2=7.1Hz);
								4.23 (2H, t, J=6.6Hz);
								5.87 (2H, s);
								6.75-6.76 (2H, d, J=8.6 H);
								7.12-7.15 (2H, d, J=8.6Hz)
23.	i-Pr	H	H		2	449	31	1.14 (3H, t, J=6.99Hz);1.21 (3H, t, J=5.55Hz);(6H, d, J=6.15Hz);2.90 (2H, d, J=6.15Hz);3.32-3.57 (2H, m);3.84 (2H, t, J=6.75Hz);3.91 (1H, t, J=3.55Hz);4.12-4.19 (2H, q, J1=7.14Hz, J2=7.14Hz);4.33 (2H, t, J=6.8Hz);6.00 (1H, d, J=3.51Hz);6.12 (1H, d, J=3.51Hz);6.53 (2H, d, J=8.64Hz);6.93 (2H, d, J=8.7Hz)7.05 (2H, d, J=8.61Hz);7.31-7.40 (5H, m).
24.	i-Pr		H	i-Pr	2	491	35	1.15 (3H, t, J=6.9Hz);1.22 (3H, t, J=7.1Hz);1.31 (6H, d, J=6Hz);2.90 (2H, dd);3.33-3.35 (1H, m);3.84 (2H, t, J=6.6Hz);3.33-3.58 (2H, m);3.91-3.95 (1H, dd);4.12-4.19 (2H, q, J=7.0Hz);4.29 (2H, t, J=6.6Hz);6.55 (2H, d, J=8.6Hz);6.10 (1H, d, J=3.5Hz);5.98 (1H, d, J=3.4Hz);7.0-7.1 (4H, m);7.3-7.38 (2H, m)
25.	i-Pr	H	H		2	479	33	1.1 (3H, t, J=7Hz);1.2 (3H, t, J=7Hz);1.31 (6H, d, J=6Hz);3.0-3.1 (1H, m);2.90 (2H, dd); 3.33 (2H, m);3.8 (3H, s); 3.85 (2H, t);3.92 (1H, t);4.12-4.16 (2H, q, J=7.14Hz);4.28 (2H, t, J=6.8Hz);5.98 (1H, J=3.4Hz);6.07 (1H, d, J=3.5Hz);6.56 (2H, d, J=8.6Hz);6.93 (2H, d, J=8.7Hz)7.32 (2H, d, J=8.5Hz);7.05 (2H, d, J=8.5Hz);
26.	i-Pr	H	H		2	467	51	1.15 ( 3H, t, J=6.9Hz);1.22 (3H, t, J=7.1Hz);1.31 (6H, d, J=6Hz);2.90 (2H, dd);3.33-3.35 (1H, m);3.84 (2H, t, J=6.6Hz);3.33-3.58 (2H, m);3.91-3.95 (1H, dd);4.12-4.19 (2H, q, J=7.0Hz);4.29 (2H, t, J=6.6Hz);6.55 (2H, d, J=8.6Hz);6.10 (1H, d, J=3.5Hz);5.98 (1H, d, J=3.4Hz);7.0-7.1 (4H, m);7.3-7.38 (2H, m)
27	i-Pr	H			2	543	48	1.1 (3H, t, J=6.99Hz);1.2 (3H, t, J=7.1Hz);1.36 (6H, d, J=7Hz);2.9 (2H, d, J=6.29Hz);3.0-3.1 (1H, m);3.3-3.58 (2H, m);3.8 (2H, t, J=6.8Hz);3.9 (2H, t, J=7Hz);4.1-4.2 (4H, m);6.2 (1H, s);6.5-7.3 (13H, m).
28.	i-Pr		H		2	586	20	1.15 (3H, t, J=6.9Hz);1.23 (3H, t, J=7.1Hz);1.51-1.53 (6H, d, J=7.1Hz);2.92 (2H, dd, J=?? Hz);3.33-3.4 (1H, m);3.5-3.6 (2H, Complex);3.9-4.0 (3H, m);4.1-4.2 (2H, q, J=?? Hz);4.3-4.4 (2H, t, J=6.3Hz);6.31 (1H, s);6.58-6.61 (2H, d, J=8.5Hz);7.0-7.2 (4H, m); 7.3-7.4 (4H, m);7.5 (1H, s); 7.6 (2H, d, J=7.6Hz)
29.	i-Pr				2	662	44	1.08 (3H, t, J=7.0Hz);1.16 (3H, t, J=7.0Hz);1.49 (6H d, J=7Hz);2.85 (2H, dd)3.26 (1H, m); 3.5 (2H, m)4.09 (2H, q); 4.19 (2H, t);6.53 (2H, d, J=8.5Hz)6.79 (1H, s);6.90-7.18 (16H, m)
30.	i-Pr				3	676	89	1.14 (2H, t, , J=6.9Hz)1.22 (3H, t, J=7Hz);1.53 (6H, d, J=7Hz);1.97 (2H, m); 2.91 (2H, dd)3.32 (1H, m); 3.56 (2H, m);3.76 (2H, t); 3.93 (1H, t);4.07 (2H, t);4.15 (2H, q, J=7Hz);6.62-6.65 (2H, d);6.84 (1H, s);6.9-6.98 (3H, m);7.03-7.05 (2H, d);7.09-7.18 (10H, m).
31		H	H		2	501	15	1.12 (3H, t, J=7.0Hz);1.21 (3H, t, J=7.0Hz);2.88 (2H, d, J=6.0Hz);3.3 (1H, m); 3.6 (1H, m); 3.614.1 (2H, t, J=7.9Hz);4.37 (2H, t, J=6.0Hz);6.26 (2H, dd, J=3.3Hz);6.9 (2H, d, J=9.0Hz);7.1 (2H, m);7.41-7.49 (9H, m).
32.		—COOEt	H		2	573	13.5	1.1-1.25 (9H, m);2.8 (2H, d, J=63Hz);3.3 (1H, m); 3.6 (1H, m); 3.614.1-4.21 (6H, m);6.3 (1H, s);6.9 (2H, d, J=9.0Hz);7.1 (2H, m);7.42-7.47 (9H, m)
33.	SCH3	H	H	H	2	377	20	1.14 (3H, t, J=7.0Hz);
								1.24 (3H, J=7.0Hz);
								2.29 (3H, s);
								2.90-2.94 (2H, m);
								3.30-3.40 (1H, m);
								3.54-3.62 (1H, m);
								3.95 (1H, t, J=3.6Hz);
								4.13-4.22 (4H, m);
								4.40 (2H, t, 5.6Hz);
								6.15 (2H, d, J=3.2Hz);
								6.37 (1H, dd);
								6.80 (2H, d, J=8.5Hz);
								6.94 (1H, m);
								7.15 (2H, d, J=8.5Hz).

[0391]

[0392] Using a similar procedure to that described in preparation 8, (S)-methyl 3-(4-hydroxyphenyl)-2-methoxypropanoate (3.3 g), and mesylate (Compound. No. 41, 4.38 g), gave the titled compound (1.2 g, 20%).

[0393] In the like manner to that described in above example, the corresponding propoxy derivative (Example no. 35) was prepared using (S)-Propyl 3-(4-hydroxyphenyl)-2-propoxy propionate and mesylate (given in the Table 8).

[0394]

TABLE 8
	Mol.	Yield
Ex.	Substituents on the pyrrole ring in (I)		Wt.	(%	1H NMR
No.	R1	R2	R3	R4	R =	(mp° C.)	w/w)	(300 MHz, δ, CDCl3)
34.	CH3	H	H		CH3	393	20	2.37 (3H, s);3.33 (3H, m);3.71 (3H, m);3.92 (3H, t, J=6.96Hz);4.29 (3H, t, J=6.6Hz);5.97 (1H, d, J=3.36Hz);6.11 (1H, d, J=3.39Hz);6.6 (2H, d, J=8.67Hz);7.05 (2H, d, J=8.64Hz);7.30-7.40 (5H, m).
35.	CH3	H	H		C3H7	449	20	0.83 (3H, t, J=7.4Hz);0.89 (3H, t, J=7.4Hz);1.53-1.63 (4H, m);2.37 (3H, s)2.91 (2H, d, J=5.54Hz);3.20-3.48 (2H, m);3.92 (6H, t, 6.59Hz);4.06 (2H, t, J=6.67Hz);4.28 (2H, t, J=7.4Hz);5.97 (1H, J=3.39Hz);6.11 (1H, d, J=3.4Hz);6.59 (2H, d, J=8.64Hz);7.07 (2H, d, J=8.63Hz);7.25-7.4 (5H, m).

[0395]

[0396] To a solution of triethyl 2-ethoxyphosphonoacetate (12.5 g) in dry THF (60 mL) was added slowly to a well-stirred ice-cold suspension of NaH (1.8 g, 60% dispersion in oil) in dry THF (60 mL) under N₂ atmosphere. The reaction mixture was stirred at 0° C. for 30 min. and 4-[2-(5-methyl-2-phenylpyrrol-1-yl) ethoxy]benzaldehyde (compound no. 65) (10.8 g) in dry THF (80 mL) was added. The mixture was allowed to warm up to 20° C. to 25° C. and stirred for 3.5 hrs. The solvent was evaporated and the residue was diluted with water (150 mL) further the product was extracted with ethyl acetate (2×150 mL). The combined extract was washed with water (150 mL), brine (50 mL), and was dried over sodium sulfate. The solvent was evaporated under reduced pressure to afford crude product. The crude product was chromatographed over silica gel using pet. ether:ether (9:1) as an eluent to afford E and Z isomers, which were isolated by removing the of solvents.

[0397]

	TABLE 9
	Substituents on
Ex.	the pyrrole ring	Mol. Wt.	Yield	1H NMR
No.	R1	R2	R3	R4	(mp° C.)	(% w/w)	(300MHz, δ, CDCl3)
36.	CH3	H	H	Phenyl	419	40	E/Z-isomer
37.	CH3	H	H	Phenyl	419	15	E-isomer
							1.13(3H, t, J=7.14Hz);
							1.4(3H, t, J=6.9Hz);
							2.3(3H, s);
							3.86-3.95(4H, m);
							4.13(2H, q, J=7.1Hz);
							4.27-4.31(2H, t, J=6.6Hz);
							5.96(1H, d, J=3.3Hz);
							6.03(1H, s);
							6.11(1H, d, J=3.3Hz);
							6.5-6.6(2H, d, J=8.7Hz);
							7.03-7.06(2H, d, J=8.5Hz)
							7.32-7.34(1H, m);
							7.35-7.41(4H, m).
38.	CH3	H	H	Phenyl	419	15	Z-isomer
							1.33-1.38(6H, t, J=7.0Hz);
							2.38(3H, s);
							3.92-3.99(4H, m);
							4.24-4.33(4H, m);
							5.98(1H, d, J=3.3Hz);
							6.11(1H, d, J=3.3Hz);
							6.63-6.6(1H, d, J=8.9Hz);
							6.92(1H, s); 7.33(1H, m);
							7.36-7.41(4H, m);
							7.64-7.67(2H, d, J=8.8Hz).

[0398]

[0399] Mixture of E/Z compounds (Example no. 36 and 37) obtained in preparation 12 (7.1 g, 0.016 mole) and magnesium turnings (7.3 g, 0.3 mole) in dry methanol (70 mL) was stirred at 25° C. for 3.5 hrs. H₂O (150 mL) was added and pH of the reaction mixture was adjusted to 2-3 with 35% hydrochloric acid. The product was extracted in ethyl acetate (2×100 mL) combined extract was washed with H₂O (2×100 mL) brine (100 mL) and dried over Na₂SO₄. The extract was concentrated under reduced pressure. The crude product was chromatographed over silica gel using pet. ether:ether (9:1) as an eluent. The product obtained was racemic mixture.

[0400] Alternatively, the E and Z compound mixture is hydrogenated in the presence of 10% Pd/C catalyst at 60 psi pressure to obtain the title compound.

[0401]

	TABLE 10
	Substituents on
Ex.	the pyrrole ring	Mol. Wt.	Yield	1H NMR
No.	R1	R2	R3	R4	(mp° C.)	(% w/w)	(300MHz, δ, CDCl3)
39.	CH3	H	H	Phenyl	407	50	1.15(6H, t, J=7.0Hz);
							2.37(3H, s); 2.90-2.92(2H,
							dd); 3.32-3.35(1H, m);
							3.55-3.57(1H, m);
							3.69(3H, s);
							3.90-3.97(3H, m);
							4.29(2H, t, J=6.9Hz);
							5.9(1H, d, J=3.4Hz);
							6.1(1H, d, J=3.4Hz);
							6.59(2H, d, J=8.6Hz);
							7.05(2H, d, J=8.5Hz);
							7.26-7.41(5H, m).

[0402]

[0403] A mixture of substituted ester (prepared in example 2) (1.38 g), sodium hydroxide (3.0%, 15 mL) in methanol (20 mL) was stirred at 20° C. to 25° C. for 10 h. Methanol was evaporated under reduced pressure. The residue was diluted with water (20 mL) and was acidified with dilute hydrochloric acid. The product was extracted with ethyl acetate (3×20 mL) and washed with water (2×80 mL), brine (80 mL) and was dried over sodium sulfate to obtain an oily product (1.2 g, 94%). The crude product (3 g) was separated by column chromatography using silica gel using hexane:ethyl acetate (9:1) as an eluent to afford the pure title compound (0.75 g, 59%).

[0404] In like manner to that described in Preparation 14 above following compounds of the formula (I) (given in Table 11) were prepared from the appropriately substituted pyrrole derivatives described elsewhere:

[0405]

TABLE 11
	Mol.	Yield
Ex.	Substituents on the pyrrole ring in (I)		Wt.	(%	1H NMR
No.	R1	R2	R3	R4	N =	(mp° C.)	w/w)	(300 MHz, δ, CDCl3)
40.	H	H	H	H	2	303	79	1.16 (3H, t, J=6.9Hz);
								2.97 (1H, dd);
								3.0 (1h, dd);
								3.36-3.6 (2H, m);
								4.01 (1H, dd);
								4.17-4.28 (4H, m)
								6.16 (2H, t, J=2.1Hz);
								6.75-6.80 (4H, m);
								6.7 (2H, t, J=2.1Hz);
								6.8 (2H, d, J=8.5Hz);
								7.15 (2H, d, J=8.5Hz).
41.	CH3	H	H	CH3	2	331.2	59	1.18 (3H, t, J=7Hz);
						(102)		2.28 (6H, s);
								2.93-3.08 (2H, m);
								3.45-3.59 (2H, m);
								4.03-4.18 (5H, m);
								5.79 (1H, s);
								6.78 (2H, d, J=8.5Hz);
								7.15 (2H, d, J=8.5Hz).
42.	CH3	H	CH3	H	2	331	88	0.96 (3H, t, J=6.76Hz);
								1.9 (3H, s); 2.13 (3H, s);
								2.78 (2H, m);
								3.3-3.6 (2H, m);
								4.05 (5H, m);
								5.53 (1H, s);
								6.43 (1H, s
								6.75 (2H, d, 9.0Hz);
								7.07 (2H, d, J=9.0Hz).
43.	C2H5	H	H	H	2	331	10	1.16 (3H, t, J=6.9Hz);
								1.27 (3H, t, J=3.51Hz);
								2.62 (2H, q);
								3.44-3.46 (2H, m);
								4.03 (1H, dd, J1=4.23Hz,
								J24.5Hz);
								4.13 (2H, t, J=5.2Hz);
								4.18 (2H, t, J=3.76Hz);
								5.91-5.92 (1H, m)
								6.10 (1H, t, J=3.12Hz);
								6.70 (1H, d, J=2.01Hz);
								6.77 (2H, d, J=8.7Hz);
								7.135 (2H, d, J=8.64Hz).
44.	CHO	H	H	H	2	331	75	1.10 (2H, t, J=7Hz);
								2.8-3.8 (5H, m);
								4.16 (2H, t, J=4.9Hz);
								4.65 (2H, t, J=4.9Hz);
								6.22 (1H, dd)
								6.7 (2H, d, J=8.5Hz);
								7.1 (2H, d, 1=8.5Hz);
								9.49 (1H, s).
45.	COCH3	H	H	H	2	345	10	0.87 (3H, t, J=6.87Hz);
								2.39 (3H, s);
								2.66 (2H, dd, J=11.55Hz);
								2.95-3.06 (2H, m);
								3.73 (1H, t, J=4.5Hz);
								4.09 (3H, t, J=4.74Hz);
								4.60 (2H, t, J=4.89Hz);
								6.08 (1H, dd, J1=2.64Hz,
								J2=2.64Hz);
								6.58 (2H, d, J=8.37Hz);
								6.92-6.99 (2H, m);
								7.00 (2H, d, J=8.34Hz).
46.	CH3	H	H	CH2CH3	2	345	54	1.16 (3H, t , J=7Hz);
								1.28 (3H, t, J=7Hz);
								2.28 (3H, m);
								2.55 (2H, t, J=7.4Hz);
								3.06 (2H, dd);
								3.4-3.62 (2H, m);
								4.0-4.16 (5H, m);
								5.8-5.84 (2H, m);
								6.75 (2H, d, J=6.78Hz);
								7.14 (2H, d, J=6.78Hz).
47.	CH3	H	H	(CH2)2CH3	2	423	66	1.02 (3H, t, J=6.9Hz);
								1.17 (3H, t, J=6.9Hz);
								1.7 (2H, sextet);
								2.28 (3H, s);
								2.55 (2H, t, J=7.7Hz);
								2.94 (1H, dd);
								3.4 (1H, dd);
								3.4-3.62 (2H, m);
								4.0-4.2 (5H, m);
								5.8-5.84 (2H, m);
								6.75 (2H, d, J=8.5Hz);
								7.14 (2H, d, J=8.5Hz).
48.	CH3	H	H	(CH2)3CH3	2	373	76	0.95 (3H, t, J=7.2Hz);
								1.17 (3H, t, J=7.0Hz);
								1.4-1.5 (2H, m);
								2.28 (3H, s);
								2.57 (2H, t, J=7.7Hz);
								2.95 (1H, dd);
								3.07 (1H, dd);
								3.4-3.5 (1H, m);
								3.53-3.62 (1H, m);
								4.0-4.2 (5H, m);
								5.8-5.83 (2H, m);
								6.77 (2H, d, J=8.5Hz);
								7.15 (2H, d, J=8.5Hz).
49.	CH3	H	H		2	393	96	1.16 (3H, t, J=6.9Hz);2.37 (3H, s);2.92-3.02 (2H, dd, J1=7Hz,J2=4.2Hz);3.41-3.58 (2H, m);3.92 (2H, t);3.98-4.01 (1H, m);4.1-4.3 (2H, t, J=6.5Hz);5.96 (1H, d, J=3.3Hz);6.1 (1H, d, J=3.3Hz);6.6 (2H, d, J=8.5Hz);7.0 (2H, d, J=8.5Hz);7.06-7.09 (2H, d, J=8.6Hz);7.2-7.4 (5H, m).
50.	CH3	H		H	2	393	96	1.16 (3H, J=6.9Hz);2.37 (3H, s);2.92-3.02 (2H, dd, J1=7Hz,J2=4.2Hz);3.41-3.58 (2H, m);3.92 (2H, t);3.98-4.01 (1H, m);4.1-4.3 (2H, t, J=6.5Hz);5.96 (1H, d, J=3.3Hz);6.1 (1H, d, J=3.3Hz);6.6 (2H, d, J=8.5Hz);7.0 (2H, d, J=8.5Hz);7.06-7.09 (2H, d, J=8.6Hz);7.2-7.4 (5H, m).
51.	CH3	H	H		2	407	75	1.02 (3H, t, J=6.9Hz);2.34 (3H, s); 2.36 (3H, s);2.74 (1H, dd);3.0 (1H, dd);3.19-3.22 (1H, m);3.4-3.45 (1H, m);3.78-3.79 (1H, m);3.8 (2H, t, J=6.4Hz);4.25 (2H, t, J=6.4Hz);5.96 (1H, d, J=3.36Hz);6.1 (1H, d, J=8.5Hz);6.6 (2H, d, J=8.5Hz);7.19 (2H, d, J=8.5Hz);7.28 (2H, d, J=8.5Hz).
52.	CH3	H	H		2	407	100	1.25 (3H, t, J=7.15Hz);2.37 (3H, s);3.0 (1H, m);3.41-3.58 (2H, dd);3.91 (2H, t, J=6.58Hz);4.00 (1H, dd, J=4.29Hz);6.07 (1H, d, J=3.42Hz);6.6 (2H, d, J=8.6Hz);7.07 (2H, d, J=8.58Hz);7.14-7.28 4H, m).
53	CH3	H	H		2	407	20	—
54.	CH3	H	H		2	423	62	1.077 (3H, t, J=7Hz);2.368 (3H, s); 2.93 (3H, s);2.94 (1H, m);3.35-3.5 (2H, m);3.78 (1H, t, J=7.1Hz);3.8 (3H, m),3.9 (2H, t, J=7Hz),4.25 (2H, t, J=7Hz);5.9 (1H, d, J=3.36Hz);6.0 (1H, d, J=3.36Hz),6.64 (2H, d, J=8.5Hz);7.1 (2H, d, J=8.5Hz);7.31 (2H, d, J=6.78Hz).
55.	CH3	H	H		2	472	84	1.02 (3H, t, J=6.9Hz);2.353 (3H, s);2.74 (1H, dd);2.95 (1H, dd);3.19-3.28 (1H, m);3.4-3.45 (1H, m);3.8 (1H, dd);3.9 (2H, t, J=6.21Hz);4.26 (2H, t, J=6.2Hz);5.9 (1H, d, J=3Hz);6.1 (2H, d, J=3.4Hz);6.6 (2H, d, J=8.5Hz);7.1 (2H, d, J=8.5Hz);7.29 (2H, d, J=8.5Hz).
56.	CH3	H	H		2	419	77	1.02 (3H, t, J=6.9Hz);2.3 (3H, s);2.7-2.8 (1H, m);2.96 (1H, m);3.1-3.2 (1H, m);3.4-3.5 (1H, m);3.86-3.91 (2H, t, J=6.3Hz);4.2-4.24 (2H, t, J=6.3Hz);5.9 (1H, d, J=3.3Hz);6.05 (1H, d, J=3.3Hz);6.56-6.59 (2H, d, J=8.6Hz);7.05-7.09 (4H, m);7.28-7.37 (2H, m).
57.	CH3	H	H		2	427.5	37	—
58.		H	CH3	H	2	393	41	—
59.	CH3	H			2	469	83	1.16 (3H, t, J=7Hz);2.41 (3H, s);2.9 (1H, dd);3.05 (1H, dd);3.4-3.6 (2H, m);3.9 (2H, t, J=6.5Hz);4.03 (1H, dd);4.16 (2H, t, J=6.5Hz);6.2 (2H, s);6.5-7.4 (14H, m).
60.	i-Pr	H	H	CH3	2	359	20	1.17 (3H, t, J=6.9Hz)
								1.26 (6H, d, J=6.7Hz);
								2.27 (3H, s);
								2.9-3.0 (1H, m);
								3.07 (1H, dd);
								3.42-3.58 (2H, m);
								4.02-4.08 (3H, m);
								4.2 (2H, t, J=6.3Hz);
								5.83 (2H, s);
								6.7 (2H, d, J=8Hz);
								7.15 (2H, d, J=8Hz).
61.	i-Pr	H	H	i-Pr	2	387	50	1.19 (3H, t, J=6.8Hz);
								1.24-1.26 (12H, d, J=6.7Hz);
								2.92-2.99 (4H, complex);
								3.40 (1H, m); 3.6 (1H, m);
								4.03 (3H, complex);
								4.24 (2H, t, J=Hz);
								5.87 (2H, s);
								6.75-6.76 (2H, d, J=?? Hz);
								7.13-7.15 (6H, d, J=8.6Hz).
62.	i-Pr	H	H		2	443	87	0.94 (3H, t, J=7.29Hz);1.22 (6H, d, J=7.29Hz);2.49-2.51 (2H, dd, J=6.75Hz);3.03-3.08 (1H, m);3.45-3.53 (1H, t, J=4.5Hz);3.82 (2H, t, J=5.91Hz);4.29 (2H, t, J=5.92Hz);5.85 (1H, d, J=3.51Hz),5.95 (1H, d, J=3Hz),6.52 (2H, d, J=8.58Hz),7.01 (2H, d, J=8.52Hz)7.29-7.40 (5H, m).
63.	i-Pr		H	i-Pr	2	463	48	1.12 (3H, t, J=6.9Hz);2.96-3.76 (7H, m);4.03-4.05 (2H, m);4.30 (2H, t, J=6.9Hz);5.89 (1H, s);6.80 (2H, d, J=8.5Hz);7.15 (2H, d, J=8.5Hz);7.2-7.33 (5H, m).
64.	i-Pr	H	H		2	451	84	1.2 (3H, t, J=7Hz);1.29 (6H, d, J=6Hz);2.90 (2H, dd);3.04-3.06 (1H, m);3.33-3.59 (2H, m);3.8 (3H, s); 4.0 (1H, t);3.84 (2H, t, J=6Hz);4.28 (2H, t, J=6.7Hz);5.98 (1H, d, J=3.4Hz);6.56 (2H, d, J=8.6Hz);6.08 (1H, d, J=3.5Hz);6.93 (2H, d, J=8.7Hz);7.03 (2H, t, J=8.5Hz);7.32 (2H, d, J=8.5Hz).
65.	i-Pr	H	H		2	439	36	1.17 (3H, t, J=6.9Hz);1.31 (6H, d, J=6.9Hz);2.93 (2H, dd);3.03-3.1 (1H, m);3.33-3.58 (2H, m);3.84 (2H, t, J=6.5Hz);4.0 (1H, m);4.29 (2H, t, J=6.6Hz);6.56 (2H, d, J=8.6Hz);6.10 (1H, d, J=3.5Hz);6.00 (1H, d, J=3.5Hz);7.0-7.1 (4H, m);7.3-7.38 (2H m).
66.	i-Pr	H			2	515(127-128)	53	1.19 (3H, t, J=6.9Hz);1.36 (6H d, J=7Hz);2.95 (2H, dd, J=7.1Hz);3.0-3.1 (1H, m);3.45-3.57 (2H, m);3.83 (2H, t, J=6.5Hz);4.0-4.04 (1H, m);4.2 (2H, t, J=6.7Hz);6.2 (1H, s);6.5-7.28 (13H, m).
67.	i-Pr		H		2	558	50	1.18 (3H, t, J=6.9Hz);1.51-1.53 (6H, d, J=7Hz);2.9-3.1 (2H, dd, J=?? Hz);3.5-3.6 (3H, Complex);3.92 (2H, t, J=6.2Hz);4.05 (1H, dd, J=?? Hz);4.3 (2H, t, J=6.2Hz);6.31 (1H, s);6.58-6.60 (2H, d, J=6.7Hz);7.1 (4H, m); 7.30-7.38 (4H, m);7.5 (1H, s); 7.58-7.59 (2H, d)
68.	i-Pr				2	634(112-114)	61	0.91 (3H, t, J=6.7Hz);1.45 (6H, d, J=6.8Hz);2.91 (2H, dd);3.13 (1H, m);3.32-3.49 (2H, m);3.80 (3H, m)4.15 (2H, t, J=6.5Hz);6.46 (2H, d); 6.78 (1H, s);6.86-7.18 (16H, m).
69.	i-Pr				3	648(114-116)	24	1.1 (3H, t, J=7Hz);1.47 (6H, d, J=7Hz);1.91 (2H, m); 3.01 (2H, dd);3.41 (1H, m); 3.98 (1H, t);3.71 (2H, t, J=6Hz);4.02 (2H, t, J=7.2Hz);6.59 (1H, t); 6.78 (1H, s);6.9 (2H, m); 7.1 (10H, m).
70.		—H	H		2	473	60.3	0.9 (3H, t); 2.6 (1H, t);2.9 (2H, d); 3.2 (1H, m);3.5 (2H, t); 3.6 (1H, m);6.21 (2H, dd, J=3Hz);6.9 (2H, d);7.0 (2H, t, J=9.0Hz);7.31-7.6 (9H, m).
71.		—COOEt	H		2	545	83	0.9 (3H, t); 2.6 (1H, t);2.9 (2H, d); 3.2 (1H, m);3.5 (2H, t); 3.6 (1H, m);6.7 (1H, s); 6.9 (2H, d);7.1 (2H, t);7.29-7.6 (9H, m).
72.	SCH3	H	H	H	2	349	93	1.18 (2H, t, J=7Hz);
								2.29 (3H, s);
								2.9-3.1 (2H, m);
								3.4-3.6 (2H, m);
								4.0-4.04 (1H, m);
								4.2 (2H, t, J=5.6Hz);
								4.42 (2H, t, J=5.6Hz);
								6.1 (1H, t, J=3.2Hz);
								6.38 (1H, dd);
								6.8 (2H, d, J=8.5Hz);
								6.95 (1H, dd);
								7.15 (2H, d, J=8.5Hz).

[0406] In a like manner to the procedure given in Preparation 14, the esters described in examples 36, 37 and 38 can be converted to a corresponding acid.

[0407]