US 4,058,559 AGrant
4-Aroyl-Substituted Phenoxy Acetic Acids
Issue Date:1977-11-15
•14 Claims
Abstract
This invention provides 4-aroyl substituted phenoxy acetic acids and tetrazoles of the formula ##STR1## wherein R is a phenyl ring, a substituted phenyl ring, or naphthyl; R.sub.1 is --CH.sub.2 COOH or methyl tetrazole, and X.sub.1 and X.sub.2 are each a halogen or loweralkyl, or when taken together form with the two attached carbons a phenyl ring. These compounds are useful as antihypertensive agents, diuretics and uricosuric agents.
Metadata
Assignee
- Abbott Laboratories
Inventors
- Peter Hadley Jones
- Dilbagh Singh Bariana
- Anthony Kei Lun Fung
- Yvonne Connolly Martin
- Jaroslav Kyncl
- Amrit Lall
Application Information
Application Number:US 6162207
Filing Date:1975-09-24
Priority Date:1975-09-24
Art Unit:126
Classifications
IPC:
C07C 6333C07C 63337C07C 6514
Field of Search:
260520 C
Patent Drawings
This patent does not have any drawings.
Description
DESCRIPTION OF THE INVENTION
The present invention is related to the treatment of (1) all types of hypertension, (2) edema of all types (e.g., congestive heart failure, pulmonary edema, nephrosis, ascites, pre-menstrual tension, pregnancy, etc.), diminished kidney function, (3) hyperuricemia due to any cause, (4) an adjuvant to therapy with drugs which are lost due to rapid renal excretion, and (5) in the treatment of diabetes insipidus.
It may also be used to promote the excretion of excess fluids, electrolytes, toxic drugs and chemicals. This combination of effects represents a valuable new tool in the treatment of hypertension, edema, hyperuricemia, diabetes insipidus, fluid and electrolyte accumulation and poisoning with various toxic agents.
It is thus an object of this invention to provide a composition for treatment of hypertension in warm-blooded animals; to provide a composition for the treatment of hyperuricemia; to provide a composition for treatment of various forms of edema including congestive heart failure. In conjunction with these objects, it is an object of this invention to provide a diuretic composition in dosage unit form that virtually avoids all dangers of over-dosing with toxic side effects and diabetes insipidus.
These and other objects are accomplished by providing a medicinal composition consisting essentially of a 4-aroyl substituted phenoxy acetic acid or tetrazole represented by formula (I): ##STR2## wherein R is a phenyl ring, a substituted phenyl ring, or naphthyl; R.sub.1 is --CH.sub.2 COOH or methyl tetrazole; and X.sub.1 and X.sub.2 are each a halogen or loweralkyl, or when taken together form with the two attached carbons a phenyl ring.
As used herein, the term "halogen" means chlorine, bromine, fluorine or iodine.
The term "loweralkyl" means saturated, monovalent, aliphatic-radicals, including straight or branched chain radicals of from 1 to 6 carbon atoms, as illustrated by, but not limited to, methyl, ethyl, propyl, iso-propyl, sec-butyl, amyl, hexyl and the like.
As used herein, the term "substituted phenyl" means a phenyl nucleus ring which bears any number and kind of substituents including loweralkyl, halogen, loweralkoxy, nitro, hydroxy and the like.
The compounds of this invention can generally be prepared as shown in the following scheme wherein R, X.sub.1 and X.sub.2 are as defined above: ##STR3##
In the above process scheme, the intermediate (A) is prepared by a Friedel-Crafts acylation of the disubstituted anisole by the appropriately substituted acid chloride. The diacyl ketone (A) can be demethylated by any of the usual methods. In the above process, a Lewis acid, aluminum chloride, was used. The anion of the phenol (B) is produced by any base in an appropriate solvent, e.g., Na.sub.2 CO.sub.3 in acetone or sodium methoxide in methanol, and alkylated by chloroethyl acetate. Hydrolysis of the ester (C) provides the desired acid. It should be understood that even though the route of from (A) to (B) to (C) to the product was used, the route of adding the acid directly to the phenol (D) could have also been used as shown in the following scheme wherein R, X.sub.1 and X.sub.2 are as defined above: ##STR4##
Some of the compounds produced by the general process scheme, illustrated above, which come within the scope of formula (I) are:
4-(4-fluorobenzoyl)-2,3-dichlorophenoxy acetic acid of the formula ##STR5##
4-(3-chlorobenzoyl)-2,3-dichlorophenoxy acetic acid of the formula ##STR6##
4-(3,4-dichlorobenzoyl)-2,3-dichlorophenoxy acetic acid of the formula ##STR7##
4-(3-methylbenzoyl)-2,3-dichlorophenoxy acetic acid of the formula ##STR8##
4-(4-methoxybenzoyl)-2,3-dichlorophenoxy acetic acid of the formula ##STR9##
4-(4-hydroxybenzoyl)-2,3-dichlorophenoxy acetic acid of the formula ##STR10##
4-(4-nitrobenzoyl)-2,3-dichlorophenoxy acetic acid of the formula ##STR11##
4-(3-fluorobenzoyl)-2,3-dichlorophenoxy acetic acid of the formula ##STR12##
4-(4-chlorobenzoyl)-2,3-dichlorophenoxy acetic acid of the formula ##STR13##
4-(2-fluorobenzoyl)-2,3-dichlorophenoxy acetic acid of the formula ##STR14##
4-(4-methylbenzoyl)-2,3-dichlorophenoxy acetic acid of the formula ##STR15##
4-(1-naphthoyl)-2,3-dichlorophenoxy acetic acid of the formula ##STR16##
4-(4-fluorobenzoyl)-2,3-dimethyl phenoxy acetic acid sodium salt of the formula ##STR17##
[4-(4-fluorobenzoyl)-1-naphthyloxy]acetic acid of the formula ##STR18##
5-[(4-fluorobenzoyl)-2,3-dichlorophenoxymethyl]tetrazole of the formula ##STR19##
5-[(4-benzoyl)-2,3-dichlorophenoxymethyl]tetrazole of the formula ##STR20##
5(4-fluorobenzoyl)-2,3-dimethyl phenoxy methyl tetrazole of the formula ##STR21##
The present compounds have particular activity as uricosuric-diuretic and antihypertensive agents. In contrast to the presently available antihypertensive diuretics, these compounds will produce potential diuretics and antihypertensive effects without the retention of uric acid. In fact, the compounds actually promote the excretion of uric acid which makes them superior to all other available drugs or compounds in this therapeutic category. These drug compounds may be used alone for the treatment of hypertension and edema due to any cause or may be used in conjunction with other diuretics and antihypertensives which have a propensity or activity for the retention of uric acid. The surprising characteristic of the present compounds is that they will reduce the blood pressure as well as increase the excretion of uric acid in warm-blooded animals. The present compound may be administered to warm-blooded animals orally or parenterally. It would be generally administered with a pharmaceutical carrier.
The term "pharmaceutical carrier" for the purpose of the present invention, is intended to refer to any medium that is suitable for the preparation of a dosage unit form and thus includes the tablet medium, pharmaceutically acceptable vehicle or solvent such as is ordinarilly used in the preparation of any intravenous or intramuscular solution.
A pharmaceutical composition containing the compound can be administered without danger to warm-blooded animals in parenteral or oral dosage form. For oral administration, amounts of from 0.01 to 200 mg./kg. per day per patient are extremely useful, with the total dose of about 3 grams per day being a suitable range for large animals including humans. The whole dosage range described increases the total uric acid excretion from about 1.5 to about 6.5 in most animals. From these figures it is apparent that the new uricosuric diuretic composition is particularly effective in increasing the excretion of uric acid from most animals.
For all dosage forms, the above illustrated compounds can be placed in capsules, formulated into pills, wafers or tablets in a usable fashion together with a pharmaceutical carrier well known in the art. Tablets may be prepared for immediate release of the active compounds or they may be made enteric, i.e., whereby the active ingredient is released slowly over a period of several hours from within the intestinal tract.
In order to further illustrate the manner in which the above compounds may be prepared and the properties and efficacy of the compounds, reference is made to the following examples, which however, are not meant to limit or restrict the scope of the invention in any respect.
EXAMPLE 1
Preparation of 4(4-Fluorobenzoyl)-2,3-Dichlorophenoxy Acetic Acid
Step (A) 4(4-Fluorobenzoyl)-2,3-dichloroanisole ##STR22##
A mixture of 2,3-dichloroanisole (35.4 g.; 0.20 mole), 4-fluorobenzoyl chloride (34.8 g.; 0.22 mole) and methylene chloride (300 ml.) at 5.degree. C. was stirred vigorously and treated with finely powdered aluminum chloride (28.0 g.; 0.21 mole). The reaction mixture was slowly heated and refluxed for two hours. The reaction mixture was cooled to room temperature and decomposed with ice and hydrochloric acid (50 ml.). The aqueous solution was extracted twice with methylene chloride. The combined methylene chloride solution was washed with aqueous sodium bicarbonate solution and finally with water. The organic layer was dried (MgSO.sub.4) and filtered. The solvent was removed in vacuo, and the residue on triturating with pet. ether gave the product 32 g. (50%); m.p. 138.degree.-140.degree.. This product was used for Step B without further purification.
Step (B) 4-(4-Fluorobenzoyl)-2,3-dichlorophenol ##STR23##
A solution of 23.3 g. (0.078 mole) of 4(4-fluorobenzoyl)-2,3-dichloroanisole in 300 ml. of methylene chloride was treated slowly with 30.5 g. (0.23 mole) of AlCl.sub.3 and the dark mixture thus obtained was refluxed overnight. The reaction mixture was cooled to room temperature and decomposed with ice water. The aqueous phase was extracted with methylene chloride and the combined organic solution was extracted with a cold solution of 10% sodium hydroxide in water. The alkaline solution was acidified with concentrated hydrochloric acid and the resulting precipitate was dissolved in ethylacetate, dried (MgSO.sub.4) and vacuum evaporated. The residue was triturated with pet. ether and the product was collected by filtration and dried to yield 16.0 g. (72%); m.p. 157.degree.-159.degree.. This product was used in Step C without further purification.
Step (C) 4(4-Fluorobenzoyl)-2,3-dichlorophenoxy acetic acid ##STR24##
Into a solution of 1.4 g. (0.06 g. atom) of sodium in 200 ml. of absolute alcohol, 16.0 g. (0.056 mole) of 4(4-fluorobenzoyl)-2,3-dichlorophenol was added and the mixture was stirred for thirty minutes at room temperature. The excess of alcohol was vacuum removed and the residue was washed with ether to obtain the sodium salt. The sodium salt of 4(4-fluorobenzoyl)-2,3-dichlorophenol was dissolved in 200 ml. of ethanol and 10.5 g. (0.06 mole) of ethyl bromoacetate was added and the reaction mixture was refluxed for 16 hours, filtered and the solvent was removed in vacuo. The residue was triturated with pet. ether and filtered to obtain a solid product. The product obtained was dissolved in 150 ml. ethanol and 50 ml. of 20% NaOH aqueous solution was added. The reaction mixture was refluxed for 1/2 hour and the solvent was partially removed in vacuo. The residue was dissolved in hot water and filtered. The hot filtrate was acidified with concentrated hydrochloric acid at 60.degree. C. The resulting precipitate was collected by filtration and washed with water. Recrystallization from dichloroethane afforded 8.0 g. (47%) of the product; m.p. 174.degree.-176.degree..
Analysis Calcd. for C.sub.15 H.sub.9 Cl.sub.2 FO.sub.4: C, 52.48; H, 2.63; Cl, 20.70. Found: C, 52,68; H, 2.63; Cl, 20.78.
EXAMPLE 2
Preparation of 5-[(4-benzoyl)-2,3-dichlorophenoxymethyl]-tetrazole
Step (A) 4-Benzoyl-2,3-dichlorophenol ##STR25##
4-Benzoyl-2,3-dichlorophenol, m.p. 123.degree.-126.degree. was synthesized according to the method of Example 1 (steps A and B), using benzoyl chloride in place of 4-fluorobenzoyl chloride. This product was used for the next step without further purification.
Step (B) 4-Benzoyl-2,3-dichlorophenoxyaceto nitrile ##STR26##
A mixture of 26.70 g. (0.10 mole) of 4-benzoyl-2,3-dichlorophenol, 7.40 g. (0.10 mole) of chloroaceto nitrile, 10.40 g. (0.15 mole) of anhydrous K.sub.2 CO.sub.3 and catalytic amount of KI in 200 ml. of acetone was refluxed overnight. The residue was triturated with ether and the product was collected by filtration and dried to yield 22.80 g. (75%); m.p. 110.degree.-112.degree.. This product was used in the next step without further purification.
Step (C) 5[(4-Benzoyl)-2,3-dichlorophenoxymethyl]-tetrazole ##STR27##
A mixture of 30.60 g. (0.1 mole) of 4-benzoyl-2,3-dichlorophenoxyacetonitrile, 7.80 g. (0.12 mole) of NaN.sub.3 and 15.96 g. (0.12 mole) of AlCl.sub.3 in 100 ml. of THF was refluxed for 24 hours. The reaction mixture was cooled and poured in dilute HCl. The solid obtained was filtered and recrystallized from benzene. Yield 26.80 g. (75%); m.p. 184.degree.-186.degree..
Analysis Calcd. for: C.sub.15 H.sub.10 Cl.sub.2 N.sub.4 O.sub.2 : C, 51.58; H, 2.87; N, 16.05. Found: C, 51.44; H, 2.82; N, 16.15.
EXAMPLE 3
4(3-Chlorobenzoyl)-2,3-Dichlorophenoxy Acetic Acid
4(3-Chlorobenzoyl)-2,3-dichlorophenoxy acetic acid, m.p. 155.degree.-156.degree., was prepared according to the method of Example 1, using 3-chlorobenzoyl chloride in place of 4-fluorobenzoyl chloride.
Analysis Calcd. for C.sub.15 H.sub.9 Cl.sub.3 O.sub.4 : C, 50.08; H, 2.50; Cl, 29.70. Found: C, 49.86; H, 2.46; Cl, 30.53.
EXAMPLE 4
4(3,4-Dichlorobenzoyl)-2,3-Dichlorophenoxy Acetic Acid
4(3,4-Dichlorobenzoyl)-2,3-dichlorophenoxy acetic acid, m.p. 165.degree.-167.degree., was prepared according to the method of Example 1, using 3,4-dichlorobenzoyl chloride in place of 4-fluorobenzoyl chloride.
Analysis Calcd. for C.sub.15 H.sub.8 Cl.sub.11 O.sub.4 : C, 45.70; H, 2.00; Cl, 36.05. Found: C, 45.67; H, 2.19; Cl, 34.06.
EXAMPLE 5
4(3-Methylbenzoyl)-2,3-Dichlorophenoxy Acetic Acid
4(3-Methylbenzoyl)-2,3-dichlorophenoxy acetic acid, m.p. 173.degree.-175.degree., was prepared according to the method of Example 1, using 3-methylbenzoyl chloride in place of 4-fluorobenzoyl chloride.
Analysis Calcd. for C.sub.16 H.sub.12 Cl.sub.2 O.sub.4 : C, 56.64; H, 3.54; Cl, 20.95. Found: C, 56.58; H, 3.52; Cl, 21.23.
EXAMPLE 6
4-(4-Methoxybenzoyl)-2,3-Dichlorophenoxy Acetic Acid
4-(4-Methoxybenzoyl)2,3-dichlorophenoxy acetic acid, m.p. 158.degree.-159.degree., was prepared according to the method of Example 1, using 4-methoxybenzoyl chloride in place of 4-fluorobenzoyl chloride.
Analysis Calcd. for C.sub.16 H.sub.12 Cl.sub.2 O.sub.5 : C, 54.09; H, 3.38; Cl, 20.00. Found: C, 52.70; H, 2.94; Cl, 20.76.
EXAMPLE 7
Preparation of 4-(4-Hydroxybenzoyl)-2,3-Dichlorophenoxy Acetic Acid
A mixture of 4-(4-methoxybenzoyl)-2,3-dichlorophenoxy acetic acid (3.55 g., 0.01 mole) and hydriodic acid (7.5 ml.) was refluxed at 180.degree.-190.degree. C. for 4 hours. The reaction mixture was concentrated and the solid residue was stirred with water for one hour and filtered. The solid obtained was dissolved in ether and dried (MgSO.sub.4). The solvent was removed in vacuo and the residue was recrystallized from ether - pet. ether mixture to give 2 g. (60%) of the product; m.p. 218.degree.-219.degree. C.
Analysis Calcd. for C.sub.15 H.sub.10 Cl.sub.2 O.sub.5 : C, 52.78; H, 2.93; O, 23.46. Found: C, 52.61; H, 3.18; O, 23.12.
EXAMPLE 8
4(4-Chlorobenzoyl)-2,3-Dichlorophenoxy Acetic Acid
4(4-Chlorobenzoyl)-2,3-dichlorophenoxy acetic acid, m.p. 196.degree.-198.degree., was prepared according to the method of Example 1, using 4-chlorobenzoyl chloride in place of 4-fluorobenzoyl chloride.
Analysis Calcd. for C.sub.15 H.sub.9 Cl.sub.3 O.sub.4 : C, 50.08; H, 2.50; O, 17.80. Found: C, 49.86; H, 2.44; O, 16.95.
EXAMPLE 9
4(2-Fluorobenzoyl)-2,3-Dichlorophenoxy Acetic Acid
4(2-Fluorobenzoyl)-2,3-dichlorophenoxy acetic acid, m.p. 161.degree.-162.degree., was prepared according to the method of Example 1, using 2-fluorobenzoyl chloride in place of 4-fluorobenzoyl chloride.
Analysis Calcd. for C.sub.15 H.sub.9 FCl.sub.2 O.sub.4 : C, 52.48; H, 2.63. Found: C, 52.48; H, 2.60.
EXAMPLE 10
4-(3-Fluorobenzoyl)-2,3-Dichlorophenoxy Acetic Acid
4-(3-Fluorobenzoyl)-2,3-dichlorophenoxy acetic acid, m.p. 166.degree.-168.degree. was prepared according to the method of Example 1, using 3-fluorobenzoyl chloride in place of 4-fluorobenzoyl chloride.
Analysis Calcd. for C.sub.15 H.sub.9 Cl.sub.2 FO.sub.4 : C, 52.48; H, 2.63. Found: C, 52.48; H, 2.60.
EXAMPLE 11
4-(4-Nitrobenzoyl)-2,3-Dichlorophenoxy Acetic Acid
4(4-Nitrobenzoyl)-2,3-dichlorophenoxy acetic acid, m.p. 172.degree.-175.degree., was prepared according to the method of Example 1, using 4-nitrobenzoyl chloride in place of 4-fluorobenzoyl chloride.
Analysis Calcd. for C.sub.15 H.sub.9 Cl.sub.2 NO.sub.6 : C, 48.60; H, 2.44; N, 3.78. Found: C, 48.33; H, 2.44; N, 3.67.
EXAMPLE 12
4(4-Methylbenzoyl)-2,3-Dichlorophenoxy Acetic Acid
4(4-Methylbenzoyl)-2,3-dichlorophenoxy acetic acid, m.p. 176.degree.-177.degree., was prepared according to the method of Example 1, using 4-methylbenzoyl chloride in place of 4-fluorobenzoyl chloride.
Analysis Calcd. for C.sub.16 H.sub.12 Cl.sub.2 O.sub.4 : C, 56.61; H, 3.54; Cl, 20.94. Found: C, 56.75; H, 3.57; Cl, 20.88.
EXAMPLE 13
4-(1-Naphthoyl)-2,3-Dichlorophenoxy Acetic Acid
4-(1-Naphthoyl)-2,3-dichlorophenoxy acetic acid, m.p. 173.degree.-175.degree., was prepared according to the method of Example 1, using 1-naphthoyl chloride in place of 4-fluorobenzoyl chloride.
Analysis Calcd. for C.sub.19 H.sub.12 Cl.sub.2 O.sub.4 : Cl, 18.93. Found: Cl, 19.00.
EXAMPLE 14
4(4-Fluorobenzoyl)-2,3-dimethylphenoxy acetic acid sodium salt
4(4-Fluorobenzoyl)-2,3-dimethyl phenoxy acetic acid sodium salt, m.p. 203.degree.-205.degree., was prepared according to the method of Example 1, using 2,3-dimethyl anisole in place of 2,3-dichloro anisole.
EXAMPLE 15
[4-(4-Fluorobenzoyl)-1-naphthyloxy]acetic acid
4-(4-Fluorobenzoyl)-1-naphthyloxy acetic acid, m.p. 105.degree.-108.degree., was prepared according to the method of Example 1, using 1-methoxynaphthalene in place of 2,3-dichloroanisole.
EXAMPLE 16
Several tests have been made to determine the antihypertensive, diuretic and uricosuric activities of the present alkanonic acid compounds, and to compare such activity with that of known compounds. The tests have been made with the following compounds:
(I) 4-(4-Fluorobenzoyl)-2,3-dichlorophenoxy acetic acid
(II) 4-(2-Thienylketo)-2,3-dichlorophenoxy acetic acid ##STR28## (III) 4(4-Nitrobenzoyl)-2,3-dichlorophenoxy acetic acid (IV) 4-Benzoyl-2,3-dichlorophenoxy acetic acid
(V) 4-(4-Methoxybenzoyl)-2,3-dichlorophenoxy acetic acid
(VI) 4-(4-Chlorobenzoyl)-2,3-dichlorophenoxy acetic acid
(VII) 4-(4-Hydroxybenzoyl)-2,3-dichlorophenoxy acetic acid
Compound (II), as described in U.S. Pat. No. 3,758,506, is a known diuretic.
TEST 1
Antihypertensive Activity in Genetically Hypertensive (SH) Rats
In this test, adult male SH rats of the Okamoto strain were trained to be restrained in a wire mesh cylinder for measurement of blood pressure. One half hour prior to blood pressure measurement, the rats were placed in a warm chamber maintained at a constant temperature of 36.degree. C. An occluding cuff, attached to a programmed sphygmomanometer, was placed near the base of the tail of each rat and the pressure in the cuff was increased automatically from 0 to 250 mm Hg at a rate of 10 mm Hg per second. The cuff was then deflated at the same rate. The total time required for each cycle of inflation and deflation of the cuff was 50 seconds and the interval between successive cycles was one minute. A photocell was placed distal to the cuff to sense the arterial pulse wave. As the pressure in the cuff increased, the pulse wave completely disappeared when the cuff pressure just exceeded the systolic arterial blood pressure. During deflation, the pulse wave reappeared at approximately the same pressure. Five interference-free signals obtained during deflation were recorded for each rat. Only those rats with a systolic blood pressure of 180 mm Hg or more during the control period were used in this study. A model 7 Grass polygraph was used to record the cuff pressure and the arterial pulse wave. The heart rate of the rat was computed from the record of the arterial pulse wave.
The compounds tested were administered orally to the rats, repeatedly for four consecutive days as recorded below in Table I.
As shown in Table I, compound (I) exhibited a statistically significant antihypertensive activity at both tested doses of 30 and 100 mg./kg. With the dose of 30 mg./kg. of Compound (I), the blood pressure of the hypertensive rats fell significantly at the third day of administration. No statistically significant antihypertensive effect was observed in rats receiving this dosage of compound (II).
With the dose of 100 mg./kg., the effect of compound (I) on the blood pressure was apparent already at the interval of three hours after the first administration. No statistically significant antihypertensive effect was observed in rats given the same dosage of Compound (II).
In view of the results shown in Table I, Compound (I) clearly exhibited antihypertensive effects in SH rats at doses where compound (II) was inactive.
TEST 2
Diuretic and Saluretic Activity in Genetically Hypertensive (SH) Rats
In this test, male genetically hypertensive (SH) rats, weighing 250-350 grams, were used. The rats were loaded with 0.9% sodium chloride solution, the volume of the load being five percent of their body weight. At the same time, the rats were dosed with the drugs to be tested and placed individually in stainless steel metabolism cages. No food or water was given to the animals during the test. Urine was collected at hourly intervals during the first eight hours and at the 24-hour interval following drug administration. The volume of excreted urine was accurately measured at each time interval. Pooled urine samples at time intervals of 2, 8 and 24 hours were analyzed for sodium, potassium, and chloride ions and for uric acid. Sodium and potassium were estimated using a Digital Readout Flame Photometer (Instrumentation Labs.). Chloride was estimated by the method of Shales and Shales (J. Biol. Chem., 140:879, 1941). Uric acid was determined by a colorimetric-uricase method adapted according to an American Monitor Corporation procedure using Beckman's DSA-560 colorimeter.
Compounds (I) and (II) were orally administered in various comparable doses. Each dose was tested in at least eight rats. Controls received vehicle (0.5% methylcellulose), orally administered in the same volume of 2 ml./kg. Statistical analysis of the data was done by student's t-test.
The results of the tests are recorded below in Tables 2 and 3.
As shown above in Tables 2 and 3, Compound (I) exhibited a significant diuretic, natriuretic, and chloruretic activity in spontaneously hypertensive rats at oral dose as low as 30 mg./kg. At the higher dose of 300 mg./kg., these effects were further increased. Compound (I) also caused a significant excretion of uric acid. Compound (II) was much less potent diuretic and saluretic agent in this animals model, even though its profile was similar to that of Compound (I).
As indicated in the results recorded in Tables 2 and 3, Compound I is a potent diuretic, saluretic and uricosuric agent in spontaneously hypertensive rats, and is a much more potent agent than Compound (II).
TEST 3
Diuretic And Saluretic Activity In Spontaneously Hypertensive Rats
This test was performed by a method similar to that of Test 2, above. In this test, Compounds (I), (III), (IV), (V), (VI) and (VII) were administered with a saline load (5% of body weight) to the rats. The results of the test (i.e., excretion of urine, Na, K, Cl and Uric Acid measured over a period of 2 hours) are provided below in Table 4.
TEST 4
Uricosuric And Diuretic Activity In Anesthetized Cebus Monkeys (Cebus Capucinus)
In this test, female Cebus monkeys weighing 1.3-1.8 kg. were immobilized with phenylcyclidine hydrochloride, 1 mg./kg. intramuscularly, and anesthetized with sodium pentobarbital, 15 mg./kg. intravenously. The trachea was incised just caudal to the larynx and was cannulated. One femoral artery was cannulated to record arterial blood pressure and the other to collect blood samples. One femoral vein was cannulated for infusion of solutions and the other was used for drug administration. The urinary bladder was catheterized through the urethral opening for collection of urine samples. Lead II electrocardiogram was recorded to monitor the heart rate.
On completion of surgical preparation of the monkey, a priming dose of inulin, 50 mg./kg. (20 mg./ml. solution) was administered intravenously. It was followed by an infusion of inulin in a concentration suitable to deliver 4 mg./min. The infusion rate was adjusted to deliver 0.38 ml./min. The infusion solution also included, in addition to inulin, uric acid in a concentration suitable to deliver 0.6 mg./kg./min., 0.15% lithium carbonate and 5% mannitol. The test drug was dissolved or suspended in the same solution that contained the priming dose of inulin (that is, a single dose of the given drug was injected at the beginning of the experiment).
The bladder was emptied and the urine was discarded at the time of priming with inulin. Urine samples were collected every 30 minutes thereafter. The last sample was collected at 270 minutes. The volume of each urine sample was measured and recorded. Two ml. blood samples were collected at the midpoint of the interval between collection of two urine samples and the blood samples were centrifuged to obtain plasma. Analysis of the plasma and urine was done to determine osmolality and the concentration of sodium, potassium, chloride, inulin and uric acid.
Compounds (I) and (II) were administered intravenously in comparable doses, whereas Compound (III), (IV), (V), (VI) and (VII) were administered in a dose of 50 mg./kg.
The results of the test are provided below in Tables 5 and 6.
As shown in Table 5, Compound (I) exhibited significant uricosuric and diuretic effects, when given intravenously to the anesthetized Cebus monkey. In both activities, i.e., uricosuric and diuretic, Compound (I) is clearly more potent than Compound (II).
Compounds (III), (IV), (V), (VI) and (VII), as shown in Table 6, all have substantially uricosuric and diuretic activity, when given intravenously to the anesthetized Cebus monkeys.
EXAMPLE 17
Antidiuretic and Antidipsogenic Effect Of 4-(4-Fluorobenzoyl)-2,3-Dichlorophenoxy Acetic Acid In Rats With Hereditary Hypothalamic Diabetes Insipidus
In this experiment, the antidiuretic and antidipsogenic effect of Compound (I) of Example 16, 4-(4-Fluorobenzoyl)-2,3-dichlorophenoxy acetic acid, in rats with diabetes insipidus was determined.
Eleven rats were used in this experiment, including males and females suffering from hereditary hypothalamic diabetes insipidus (Brattleborro Strain) with the average body weight of the rats being 242 .+-. 16 grams. The rats were placed individually in metal metabolic cages and their water intake and urine output were measured daily. The effect of 4-(4-fluorobenzoyl)-2,3-dichlorophenoxy acetic acid (Compound I) on the fluid turnover in these animals was tested according to the following experimental schedule:
Day:
1 -- control period
2 -- control period
3 -- Compound (I), 30 mg./kg.
4 -- Compound (I), 100 mg./kg.
5 -- Compound (I), 300 mg./kg.
8 -- control period
9 -- control period
The values of the fluid turnover, measured on two consecutive days before and after the testing of Compound (I) were averaged. Compound (I) was administered orally, suspended in 0.5% methylcellulose in a total volume less than 1cc.
The results of the experiment are summarized below, in Table 7. The results indicate that Compound (I) exhibited a significant, dose-dependent antidiuretic effect in rats with hereditary hypothalamic diabetes insipidus. The drug dependent decrease of the excessive urine output is accompanied by a corresponding dose-dependent decrease in the spontaneous drinking in these animals.
As shown by the results in Table 7, above, the compound 4-(4-fluorobenzoyl)-2,3-dichlorophenoxy acetic acid demonstrated good efficacy in the treatment of the diabetes insipidus in rats. From the results it can therefore be expected to be effective in the treatment of diabetes insipidus in man.
Claims
We claim:
1. A compound of the formula ##STR29## wherein R is a phenyl ring, naphthyl or a substituted phenyl ring where the substituents are loweralkyl, halogen, loweralkoxy, nitro or hydroxy; R.sub.1 is --CH.sub.2 COOH; and X.sub.1 and X.sub.2 are each a halogen, or when taken together form with the two attached carbons a phenyl ring.
2. A compound according to claim 1, 4(4-fluorobenzoyl)-2,3-dichlorophenoxy acetic acid.
3. A compound according to claim 1, 4(3-chlorobenzoyl)-2,3-dichlorophenoxy acetic acid.
4. A compound according to claim 1, 4(3,4-dichlorobenzoyl)-2,3-dichlorophenoxy acetic acid.
5. A compound according to claim 1, 4(3-methylbenzoyl)-2,3-dichlorophenoxy acetic acid.
6. A compound according to claim 1, 4-(4-methoxybenzoyl)-2,3-dichlorophenoxy acetic acid.
7. A compound according to claim 1, 4-(4-hydroxybenzoyl)-2,3-dichlorophenoxy acetic acid.
8. A compound according to claim 1, 4-(4-nitrobenzoyl)-2,3-dichlorophenoxy acetic acid.
9. A compound according to claim 1, 4-(3-fluorobenzoyl)-2,3-dichlorophenoxy acetic acid.
10. A compound according to claim 1, 4-(4-chlorobenzoyl)-2,3-dichlorophenoxy acetic acid.
11. A compound according to claim 1, 4-(2-fluorobenzoyl)-2,3-dichlorophenoxy acetic acid.
12. A compound according to claim 1, 4-(4-methylbenzoyl)-2,3-dichlorophenoxy acetic acid.
13. A compound according to claim 1, 4-(1-naphthoyl)-2,3-dichlorophenoxy acetic acid.
14. A compound according to claim 1, 4-benzoyl-2,3-dichlorophenoxy acetic acid.
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