Pyridooxazinone-Pyridone Compounds, Cardiotonic Compositions Including the Same, and Their Uses

This invention relates to substituted pyridooxazinone pyridones which are useful as cardiotonic agents for the treatment of congestive heart failure. This invention also relates to methods for increasing cardiac contractility using said compounds, and pharmaceutical compositions including said compounds.

Congestive heart failure is a life-threatening condition in which myocardial contractility is depressed so that the heart is unable to adequately pump the blood returning to it. Normal pathologic sequelae include decreased cardiac output, venous pooling, increased venous pressure, edema, increased heart size, increased myocardial wall tension, and eventually cessation of contractility.

Drugs which increase the tone of the heart muscle are described as having positive inotropic activity and are characterized as cardiotonic agents. Digitalis glycosides have long been used to increase myocardial contractility and reverse the detrimental changes seen in congestive heart failure. More recently, dopamine, dobutamine, and amrinone have been used to provide necessary inotropic support for the failing heart.

Cardiotonic agents which are described as having positive inotropic activity include the 5-pyridyl substituted pyridones disclosed in U.S. Pat. Nos.: 4,004,012; 4,072,746; 4,107,315; 4,137,233; 4,199,586; 4,271,168 and in GB No. 2070606A; and in PTC published Appl. No. PCT/CH81/00023. Other cardiotonic drugs include the diazacyclic substituted carbostyril compounds disclosed in U.S. Pat. Nos. 4,414,390 and 4,415,572, cardiotonic pyridyl substituted carbostyril compounds disclosed in EPO application Ser. No. 84308925.1 (EPO Pulbl. No. 0148623), and the 5-phenyl-thiazole compounds disclosed in U.S. Pat. No. 4,418,070.

Cardiotonic bicyclic heteroaryl-5-substituted pyridyl compounds are disclosed in PCT published application Ser. No. PCT/US83/01285; and, cardiotonic diazheterocyclic-5-substituted pyridyl compounds are disclosed in U.S. Pat. Nos. 4,432,979, 4,514,400 and 4,539,321. Each of the aforementioned is assigned to the same assignee as the present application.

The present invention relates to a method for increasing cardiac contractility in humans and other mammals comprising the administration of an effective inotropic amount of a pyridooxazinone-pyridone compound.

This invention comprises particularly the administration to a patient of an effective inotropic amount of pyridooazinone-pyridinone compounds within the scope of Formula I: ##STR1## where A is --C.dbd. or --N.dbd. and

B is --C.dbd.C--; --C.dbd.N-- or --N.dbd.C--; provided A+B together contain one nitrogen atom;

R is hydrogen,

alkyl,

alkoxyalkyl,

hydroxyalkyl,

nitro

halo,

cyano,

carbamoyl,

alkyl carbamoyl,

formyl,

aminoalkylene or,

amino;

X is --(CR.sub.4 R.sub.5).sub.a --O--(CR.sub.4 R.sub.5).sub.b --;

a and b are 0, 1 or 2 and a+b=0, 1 or 2;

R.sub.1, R.sub.2, R.sub.3, R.sub.4 and R.sub.5 are hydrogen, alkyl, or aralkyl;

R.sub.4 may also be aryl;

geminal R.sub.4 and R.sub.5 groups may together form a spiro substituent, --(CH.sub.2).sub.d --, where d is 2 to 5; or a pharmaceutically acceptable salt thereof.

Certain of the compounds encompassed within the present invention may exist in enolic or tautomeric forms, and all of these forms are considered to be included within the scope of this invention.

The compounds of this invention which have particular usefulness as cardiotonic agents are described by Formula I wherein the and pyridooxazinone portion of the molecule is described by one of Formulae IIa-IIc, IIIa-IIIc or IVa-IVc: ##STR2## wherein R.sub.3, R.sub.4 and R.sub.5 are as described above and x is 1 or 2.

A more preferred class of compounds within the present invention includes compounds of Formulae I-IV, wherein R is cyano, R.sub.2 is lower alkyl and R.sub.1, R.sub.3, R.sub.4 and R.sub.5 are hydrogen or lower alkyl.

Most preferred compounds are those disclosed by Formula I, wherein R is cyano, R.sub.1 is hydrogen, R.sub.2 is methyl and R.sub.3, R.sub.4 and R.sub.5 are hydrogen or methyl.

A special embodiment comprises compounds of Formula IIIc where x is 1.

Another special embodiment of the present invention comprises compounds of Formula I where R.sub.4 and R.sub.5 form a spiro ring system, an example of which is shown by Formula V: ##STR3##

As employed above and throughout the disclosure, the following terms, unless otherwise indicated, shall be understood to have the following meanings:

"Alkyl" means a saturated aliphatic hydrocarbon which may be either straight or branched-chained containing from about 1 to about 6 carbon atoms.

"Lower alkyl" means an alkyl group as above, having 1 to about 4 carbon atoms.

"Aralkyl" means an alkyl group substituted by an aryl radical. The preferred aralkyl groups are benzyl or phenethyl.

"Alkyl-carbamoyl" means a carbamoyl group substituted by one or two alkyl groups. Preferred groups are the lower alkyl carbamoyl groups.

"Hydroxyalkyl" means an alkyl group substituted by a hydroxy group. Hydroxy lower alkyl groups are preferred and include hydroxymethyl, 2-hydroxyethyl, 2-hydroxypropyl, and 3-hydroxypropyl.

"Alkoxy" means an alkyl-oxy group in which "alkyl" is as previously described. Lower alkoxy groups are preferred and include methoxy, ethoxy, n-propoxy, i-propoxy , n-butoxy among others.

"Alkoxyalkyl" means an alkyl group as previously described substituted by an alkoxy group as previously described.

"Aminoalkylene" means --(CH.sub.2).sub.n --NH.sub.2 where n is 1 to about 6. The preferred groups are the lower alkylene groups which mean amino groups substituted with alkylene groups of 1 to about 4 carbon atoms. The most preferred amino alkylene group is aminomethylene.

The compounds of this invention may be useful in the form of the free base, (if a basic group is present), in the form of salts and as a hydrate. All forms are within the scope of the invention. Acid addition salts may be formed and are simply a more convenient form for use; and in practice, use of the salt form inherently amounts to use of the base form. The acids which can be used to prepare the acid addition salts include preferably those which produce, when combined with the free base, pharmaceutically acceptable salts, that is, salts whose anions are non-toxic to the animal organism in pharmaceutical doses of the salts, so that the beneficial cardiotonic properties inherent in the free base are not vitiated by side effects ascribable to the anions. Although pharmaceutically acceptable salts of said basic compound are preferred, all acid addition salts are useful as sources of the free base form even if the particular salt per se is desired only as an intermediate product as, for example, when the salt is formed only for purposes of purification and identification, or when it is used as an intermediate in preparing a pharmaceutically acceptable salt by ion exchange procedures. Pharmaceutically acceptable salts within the scope of the invention are those derived from the following acids: mineral acids such as hydrochloric acid, sulfuric acid, phosphoric acid and sulfamic acid; and organic acids such as acetic acid, citric acid, lactic acid, tartaric acid, malonic acid, methanesulfonic acid, ethanesulfonic acid, benzenesulfonic acid, p-toluenesulfonic acid, cyclohexylsulfamic acid, quinic acid, and the like. The corresponding acid addition salts comprise the following: hydrochloride, sulfate, phosphate, sulfamate, acetate, citrate, lactate, tartarate, methanesulfonate, ethanesulfonate, benzenesulfonate, p-toluenesulfonate, cyclohexylsulfamate and quinate, respectively.

The acid addition salts of the compounds of this invention are prepared either by dissolving the free base in aqueous or aqueous-alcohol solution or other suitable solvents containing the appropriate acid and isolating the salt by evaporating the solution, or by reacting the free base and acid in an organic solvent, in which case the salt separates directly or can be obtained by concentration of the solution.

Compounds of this invention may be prepared by the following reaction sequences: ##STR4## where R.sub.3 is hydrogen or alkyl.

Bromination of a pyridooxazinone compound of Formula VI results in the corresponding brominated product VII. This can be carried out by brominating techniques such as with N-bromosuccinimide. Bromination occurs on the pyrido ring, para to the nitrogen of the oxazinone. Alkylation or aralkylation of the oxazinone nitrogen is then carried out in the usual way to obtain VIII. When this compound is treated in situ with tri-o-tolylphospine, palladium acetate, isopropenylacetate and tributyltin methoxide the resultant product is the 2'-oxypropyl compound IX. One such method is under sealed conditions. This is usually carried out in a non polar solvent such as benzene and at raised temperatures of 75.degree.-80.degree. C. When a mixture of IX is treated with N,N-dimethylformamide dimethylacetal and pyridine, the 1-N,N-dimethylamino-3-oxobuten- 2-yl product X is obtained. When the latter is heated at about 80.degree.-90.degree. C. with a solution of cyanoacetamide in the presence of sodium hydride, the pyridinone of Formula I is obtained. This reaction is usually carried out under inert conditions in a polar medium such as DMF.

Various R groups may be prepared from the nitrile which can be hydrolyzed to the acid which in turn can be esterified or converted to the amide. The ester may be changed by known methods to the formyl which in turn can be reduced to the alkyl or hydroxyalkyl substituent. The alkoxyalkyl may be formed from the hydroxyalkyl. Compound X may also be condensed with nitroacetamide. This would result in the compound of Formula I where R is NO.sub.2. The latter can also be reduced to the amino compound and the hydroxy and halo compounds can be formed. These methods and reaction conditions would vary, of course, depending on the desired substituent and the substituent present. The reaction conditions would be known to one skilled in the art.

The starting materials of this invention are either known or can be prepared by the following reaction sequences.

When 2-amino-3-hydroxypyridine is treated with sodium hydride followed by ring closure with a ? -haooacetate ester of the formula: ##STR5## the pyridooxazinones are formed. ##STR6##

When the seven membered ring is desired, the reaction is carried out using the halopropionate. ##STR7##

The five membered ring is prepared by reacting 2-amino-3-hydroxypyridine with either phosgene or N,N-carbonyldiimidazole. ##STR8##

Those compounds where the oxygen atom of the pridooxazinone ring is not directly on the pryidine ring can be prepared from the 2-aminonicotinic acid or ester, reducing the latter to the corresponding alcohol and ring closing as in the above synthesis. ##STR9##

When the starting pyridine is 3-amino-4-hydroxypyridine or 2-hydroxy-3-aminopoyridine then the corresponding pyridooxazinone is prepared. ##STR10##

When R.sub.3 substitution is deisred then corresponding R.sub.3 substituted amino-pyridine would be used.

The compounds of Formula I possess positive inotropic activity and are useful as cardiotonic agents in the treatment of humans and other mammals for cardiac disorders including congestive heart failure. The effectiveness of the compounds of this invention a inotropic agents may be determined by the following pharmacologic tests which evaluate the change in cardiac contractile force upon exposure to a dose of said compounds. The ganglionic-beta blocked anesthetized dog procedure is on such standard test procedure; the intotropic results of this procedure generally correlate with the inotropic activity found in human patients.

Adult mongrel dogs of either sex weighing 10 to 16 kg are fasted overnight, anesthetized with pentobarbital sodium 35 mg/kg, i.v. intubated, respired with room air using a Harvard respirator, and instrumented surgically to monitor myocardial contractile force, heart rate, arterial pressure, aortic flow and EKG limb lead II. The aforesaid measurements are recorded continuously on a strip chart recorder.

Myocardial contractile force is monitored by a Walton-Brodie strain gauge sutured to the left ventricular myocardium parallel to the left anterior descending coronary artery. Arterial pressure is measured using a fluid-filled catheter attached to a pressure transducer introduced via the right femoral artery and positioned in the thoracic aorta. Mean arterial pressure is determined by electronically clamping the pulsatile pressure signal. Aortic flow is monitored using a precalibrated, noncanulating electromagnetic flow probe positioned around the thoracic aorta. Heart rate is monitored using a cardiotachometer triggered by the QRS complex of the limb lead II EKG. The right femoral vein is cannulated for intravenous infusion of drugs. Body temperature is maintained at 37.degree. C.

Following a 30 min postsurgical stabilization period, control values are recorded. Myocardial depression is induced by ganglionic and beta receptor blockade. Initially, the responsiveness of the autonomic nervous system is assessed by performing a 30 sec bilateral carotid occlusion (BCO). Ten minutes later, a saline solution of isoproterenol 0.3 mg/kg, i.v. is administered to assess beta receptor integrity. Ten minutes after that, a saline solution of mecamylamine 2 mg/kg, i.v. is infused, followed by a saline solution of propranolol 1 mg/kg, i.v. plus 0.3 mg/kg/hr. Twenty minutes later, a second BCO is performed to demonstrate ganglionic blockade followed by a second injection of saline isoproterenol 0.3 mg/kg, i.v. to demonstrate beta blockade. Ten minutes later, the test compound or vehicle is administered intravenously in ascending doses at 30 min intervals at 1.5 ml/min in a total volume of 3.5 ml. On completion of the experiment, both BCO and isoproterenol challenges are repeated to verify ganglionic and beta blockade.

The results of the blocked dog test show that compounds of the present invention increase contractile force and heart rate, and aortic blood flow in a dose related manner while maintaining arterial pressure.

Additional test procedures which have been found to be an efficient means for ascertaining the inotropic activity of the compounds of this invention are described below.

Guinea pigs are stunned by a sudden blow to the head; their chests are opened and hearts excised and placed in Kreb's medium (concentrations, mM: NaCl, 118.39; KCl, 4.70; MgSO.sub.4, 1.18; KH.sub.2 PO.sub.4, 1.18; NaHCO.sub.3, 25.00; glucose, 11.66 and CaCl.sub.2, 1.25 gassed with a mixture of 95% O.sub.2. Left atria are removed and inserted into warmed (33.degree. C.) double jacketed tissue chambers containing oxygenated Kreb's medium (as above). The upper end of each tissue is attached to a Statham Universal Transducing Cell via a Statham Microscale Accessory. Resting tension on each tissue is set at 1 g and adjusted periodically.

Massive field stimulation is achieved via a pair of platinum or silver electrodes placed on opposite sides of the tissue. Electrodes are made from 2-gauge silver wire wound into a tight coil approximately 12-14 mm in diameter. Electrodes are connected to a Grass stimulator via Grass constant current unit. Tissues are driven at 90 pulses per minute with 5 msec duration at current levels 20% greater than threshold for continuous beat.

Cumulative concentrations of test drugs are added to the tissue bath at intervals sufficient to allow developed tension to peak at a new level.

The increase in developed tension in each tissue for each compound concentration is measured, and the results are averaged and used to construct cumulative concentration-response curves. Slopes for these regressions calculated via the method of Finney (1971) are compared using Student's t-test.

The following in vitro method is another means for measuring the inotropic potency of the present compounds. This method is a modification of the enzyme inhibition method reported by Thompson and Appleman (1970) and Thompson et al. (1974), and is believed to correlate to in vivo inotropic activity in humans.

The test compounds are included in media comprising a radioactivity labeled substrate (.sup.3 H-cyclic nucleotide) such as adenosine 3':5'-monophosphate (cyclic AMP) and quanine-3':5'-nucleotidease isoaated from a dog heart. The inhibition of the enzyme hydrolysis of the 5'-nucleotide product of the cNUC-PDEase to the corresponding nucleoside is measured by separating the charged, unhydrolyzed substrate from the uncharged hydrolysis product. Separation may be achieved either chromatographically from the uncharged nucleoside product of the assay with ionexchange resin so that it is not quantitated with the liquid scintillation counter.

Male mongrel dogs are anesthetized with pentobarbital (35 mg/kg, i.v.) and intubated. Femoral artery and veins are cannulated for measurement of blood pressure and injection of compounds, respectively. A catheter connected to a Statham transducer is inserted into the left ventricle via the right carotid artery for measurement of left ventricular pressure, left ventricular end diastolic pressure and dP/dt. Lead II ECG and heart rate are also monitored. All parameters are measured on a Beckman Dynagraph.

Two additional test procedures which have been found to be an efficient means for ascertaining the inotropic activity of the compounds of this invention are described below.

Female mongrel dogs (18.0-18.5 kg) are anesthetized with sodium pentobarbital (35 mg/kg, i.v., supplemented as necessary during surgery) intubated and connected to a Harvard respirator. The left side of the chest is opened at the fifth intercostal space, and a Konigsberg transducer inserted into the left ventricle through a puncture at the apex and secured. A fluid-filled polyethylene catheter is inserted into the left atrium through a puncture wound and secured for measurement of left atrial pressure. A second fluid-filled catheter is inserted into the aorta for measurement of blood pressure and heart rate and secured to the vessel wall. The two catheters and the Konigsberg transducer cable are passed out of the chest through the seventh intercostal space and advanced subcutaneously to the back of the neck and passed through the skin. The fluid-filled catheters are filled with haparinized 50% dextrose solution, and the chest is closed and evacuated.

The dogs are treated daily post-operatively with 600,000 units of penicillin-procaine i.m. for ten days and with chloramphenicol, 500 mg/kg, i.m., every other day for 10 days and allowed at least 7 days recovery before use.

Each dog is trained and acclimated to its environment and the presence of personnel during the experiment.

The dogs are fasted overnight before either intravenous or oral administration of the compound. On a test day, the dog is placed in a sling and connected to a recorder (Gould Instruments or Grass Instruments) for measurement of left ventricular pressure, left ventricular dP/dt.sub.max, blood pressure, heart rate (from the blood pressure signal), and the lead II electrocardiogram. The compound is administered both intravenously and orally (liquid and soft gelatin capsule forms) in different experiments and blood samples were taken for determination of blood levels of the compound.

The compounds of this invention can be normally administered orally or parenterally, in the treatment of cardiac disorders such as heart failure in humans or other mammals.

The compounds of this invention, preferably in the form of a salt, may be formulated for administration in any convenient way, and the invention includes within its scope pharmaceutical compositions containing at least one compound according to the invention adapted for use in human or veterinary medicine. Such compositions may be formulated in a conventional manner using one or more pharmaceutically acceptable carriers or excipients. Suitable carriers include diluents or fillers, sterile aqueous media and various non-toxic organic solvents. The compositions may be formulated in the form of tablets, capsules, lozenges, troches, hard candies, powders, aqueous suspensions, or solutions, injectable solutions, elixirs, syrups and the like and may contain one or more agents selected from the group including sweetening agents, flavoring agents, coloring agents and preserving agents, in order to provide a pharmaceutically acceptable preparation.

The particular carrier and the ratio of inotropic active compound to carrier are determined by the solubility and chemical properties of the compounds, the particular mode of administration and standard pharmaceutical practice. For example, excipients such as lactose, sodium citrate, calcium carbonate and dicalcium phosphate and various disintegratants such as starch, alginic acid and certain complex silicates, together with lubricating agents such as magnesium stearate, sodium lauryl; sodium lauryl sulphate and talc, can be used in producing tablets. For a capsule form, lactose and high molecular weight polyethylene glycols are among the preferred pharmaceutically acceptable carriers. Where aqueous suspensions for oral use are formulated, the carrier can be emulsifying or suspending agents. Diluents such as ethanol, propylene glycol, glycerin and chloroform and their combinations can be employed as well as other materials.

For parenteral administration, solutions or suspensions of these compounds in sesame or peanut oil or aqueous propylene glycol solutions, as well as sterile aqueous solutions of the soluble pharmaceutically acceptable salts described herein can be employed. Solutions of the salts of these compounds are especially suited for intramuscular and subcutaneous injection purposes. The acqueous solutions, including those of the salts dissolved in pure distilled water, are also useful for intravenous injection purposes, provided that their pH is properly adjusted, suitably buffered, made isotonic with sufficient saline or glucose and sterilized by heating or by microfiltration.

The dosage regimen in carrying out the methods of this invention is that which insures maximum therapeutic resonse until improvement is obtained and thereafter the minimum effective level which gives relief. Thus, in general, the dosages are-those that are therapeutically effective in increasing the contractile force of the heart or in the treatment of cardiac failure. In general, the oral dose may be between about 0.01 mg/kg and about 50 mg/kg (preferably in the range of 0.1 to 10 mg/kg), and the i.v. dose about 0.005 to about 30 mg/kg (preferably in the range of 0.01 to 3 mg/kg), bearing in mind, of course, that in selecting the appropriate dosage in any specific case, consideration must be given to the patient's weight, general health, age and other factors which may influence response to the drug. The drug may be administered as frequently as is necessary to achieve and sustain the desired therapeutic response. Some patients may respond quickly to a relatively large or small dose and require little or no maintenance dosage. On the other hand, other patients may require sustained dosing from about 1 to about 4 times a day depending on the physiological needs of the particular patient. Usually the drug may be administered orally 1 to 4 times per day. It is anticipated that many patients will require no more than about one to about two doses daily.

It is also anticipated that the present invention would be useful as an injectable dosage form which may be administered in an emergency to a patient suffering from acute cardiac failure. Such treatment may be followed by intravenous infusion of the active compound and the amount of compound infused into such a patient should be effective to achieve and maintain the desired therapeutic response.

Compounds of this invention may be prepared by the following examples.

To a solution of 5.6 g 2H-pyrido[3,2-b]-1,4-oxazin-3(4H)-one dissolved in 85 ml of DMF under nitrogen is added 7.96 g NBS in 50 ml of DMF. This is allowed to stir at room temperature overnight. To this is added 35 ml of water and chilled. The solid material which separates is filtered and washed with 3.times.100 ml H.sub.2 O. This is then dried in a vac oven at 70.degree. C. and then used directly in the next step.

To a suspension of 5 g of 7-bromo-2H-pyrido[3,2-b]-1,4-oxazin-3(4H)-one (0.022 mole) in 90 ml of THF is added 24 ml of LiN(TMS)2 (0.024 mole) in THF. The homogenous solution is maintained under nitrogen at room temperature for 20 min., 3.03 g (0.024 mole) of dimethylsulfate is added and the reaction mixture allowed to stir overnight. The reaction mixture is then quenched with 20 ml of sat. ammonium chloride and extracted with 3.times.80 ml ethyl acetate. The ethyl acetate is then washed with 3.times.30 ml sat. ammonium chloride, dried over sodium sulfate and concentrated to obtain off white product which is used directly in the next step.

4-Methyl-7-bromo-2H-pyrido[3,2-b]-1,4-oxazin-3(4H)-one (3 g) (0.012 mole) in 80 ml of benzene is treated with 365 mg tri-o-tolylphosphine, 138 mg palladium acetate, 1.87 g (0.018 mole) of isopropenyl acetate and 5.9 g (0.18 mole) of tributyltin methoxide. The mixture is heated to 70.degree. C. for 25 hours. The reaction mixture is then quenched with 20 ml sat. ammonium chloride and diluted with 50 ml ethyl acetate. The organic phase separates, dried over sodium sulfate and concentrated to dryness. The residue is dissolved in methylene chloride, washed with sat. KF solution, filtered through a cotton plug, dried over sodium sulfate and concentrated to dryness to obtain crude product. This is chromatographed using 200.times.60 mm SiO.sub.2, EtOAc (100%) as eluent. The desired product is identified by NMR and used directly in the next step.

To 1.05 g (0.0047 mole) of 4-methyl-7-(2'-oxopropyl)2H-pyrido[3,2-b]-1,4-oxazin-3(4H)-one suspended in 10 ml of dimethylformamide dimethylacetal is added 1 ml of pyridine. This is then heated under nitrogen at 70.degree. C. for 5 hours. The reaction mixture is then concentrated in vacuo to leave an dark oily solid. Trituration with methylene chloride gives a pale yellow solid which is filtered off and identified to be desired product by NMR. This is then used directly in the next step.

Sodium hydride (87 mg/oil) is washed with pet. ether and suspended in 4 ml of DMF under nitrogen. To this is added 166 mg of cyanoacetamide in 3 ml of DMF and the mixture stirred for about 5 min. A solution of 500 mg of 4-methyl-7-[1'-N,N-dimethylamino-3'-oxobuten-2'-yl]-2H-pyrido[3,2-b]-1,4-o xazin-3(4H)-one in 4 ml of DMF is added to the mixture and heated under nitrogen at 80.degree. C. for 4.5 hours. This is then diluted with 15 ml of sat. ammonium chloride and extracted with 4.times.40 ml of ethyl acetate, dried over sodium sulfate and concentrated in vacuo. (M.P.>350.degree. C.).

Calc'd. C, 59.36; H, 4.25; N, 18.46; Found C, 59.44; H, 4.32; N, 18.56.

When 2H-pyrid [3,2-b]-1,4-oxazin-3-(4H)-one of Example 1, Step 1 is replaced with the compounds of Table I below, then the corresponding product is obtained.

2H-pyrido[3,2-b]-1,4-oxazin-3(4H)-one

2H-pyrido[4,3-b]-1,4-oxazin-3(4H)-one

2H-pyrido[2,3-b]-1,4-oxazin-3(4H)-one

4H-pyrido[2,3-d][1,3]oxazin-2(1H)-one

4H-pyrido[3,4-d][1,3]oxazin-2(1H)-one

4H-pyrido[3,2-d][1,3]oxazin-2(1H)-one

oxazolo[4,5-b]pyridin-2(3H)-one

oxazolo[4,5-c]pyridin-2(3H)-one

oxazolo[5,4-b]pyridin-2(3H)-one

2,3-dihydropyrido[3,2-b][1,4]oxazepin-4(5H)-one

2,3-dihydropyrido[4,3-b][1,4]oxazepin-4(5H)-one

2,3-dihydropyrido[2,3-b][1,4]oxazepin-4(5H)-one

3,5-dihydropyrido[2,3-e]-1,4-oxazepin-2-(1H)-one

3,5-dihydropyrido[3,4-e]-1,4-oxazepin-2-(1H)-one

3,5-dihydropyrido[3,2-e]-1,4-oxazepin-2-(1H)-one

4,5-dihydropyrido[2,3-d]-1,3-oxazepin-2(1H)-one

4,5-dihydropyrido[3,4-d]-1,3-oxazepin-2(1H)-one

4,5-dihydropyrido[3,2-d]-1,3-oxazepin-2(1H)-one

To a solution of 5.07 g oxazolo[4,5-b]pyridin-2(3H)-one dissolved in 85 ml of DMF under nitrogen is added 7.46 g NBS in 50 ml of DMF. This is allowed to stir at room temperature overnight. To this is added 35 ml of water and chilled. The solid material which separates is filtered and washed with 3.times.100 ml H.sub.2 O. This is then dried in a vac oven at 70.degree. C. and then used directly in the next step.

To a suspension of 4.7 g of 6-bromo-oxazolo[4,5-b]-pyridin-2(3H)-one (0.022 mole) in 90 ml of THF is added 24 ml of LiN(TMS).sub.2 (0.024 mole) in THF. The homogenous solution is maintained under nitrogen at room temperature for 20 min., 3.03 g (0.024 mole) of dimethylsulfate is added and the reaction mixture allowed to stir overnight. The reaction mixture is then quenched with 20 ml of sat. ammonium chloride and extracted with 3.times.80 ml ethyl acetate.

The ethyl acetate is then washed with 3.times.30 ml sat. ammonium chloride, dried over sodium sulfate and concentrated to obtain off white product which is used directly in the next step.

3-Methyl-6-bromo-oxazolo[4,5-b]pyridin-2(3H)-one (2.58 g) (0.012 mole) in 80 ml of benzene is treated with 365 mg tri-o-tolylphosphine, 138 mg palladium acetate, 1.87 g (0.018 mole) of isopropenyl acetate and 5.9 g (0.18 mole) of tributyltin methoxide. This is sealed in a high pressure tube and heated to 70.degree. C. for 25 hours. The reaction mixture is then quenched with 20 ml sat. ammonium chloride and diluted with 50 ml ethyl acetate. The organic phase separates, dried over sodium sulfate and concentrated to dryness. The residue is dissolved in methylene chloride, washed with sat. KF solution, filtered through a cotton plug, dried over sodium sulfate and concentrated to dryness to obtain crude product. This is chromatographed using 200.times.60 mm SiO.sub.2, EtOAc (100%) as eluent. The desired product is identified by NMR and used directly in the next step.

To 1.47 g (0.007 mole) of 3-methyl-6-(2'-oxopropyl)-oxazolo[4,5-b]pyridin-2(3H)-one suspended in 15 ml of dimethylformamide dimethylacetal is added 1.5 ml of pyridine. This is then heated under nitrogen at 70.degree. C. for 5 hours. The reaction mixture is then concentrated in vacuo to leave a dark oily solid. Trituration with methylene chloride gives a solid which is filtered off and identified to be desired product by NMR. This is then used directly in the next step.

Sodium hydride (174 mg/oil) is dashed with pet. ether and suspended in 10 ml of DMF under nitrogen. To this is added 330 mg of nitroacetamide in 6 ml of DMF and the mixture stirred for about 5 min. A solution of 940 mg of 3-methyl-6-[1'-N,N-dimethylamino-3'-oxobuten-2'-yl]-oxazolo[4,5-b]pyridin- 2(3H)-one in 10 ml of DMF is added to the mixture and heated under nitrogen at 80.degree. C. for 4.5 hours. This is then diluted with 30 ml of sat. ammonium chloride and extracted with 4.times.75 ml of ethyl acetate, dried over sodium sulfate and concentrated in vacuo.

When nitroacetamide is replaced in Example 3, Step 5 by cyanoacetamide then the product prepared is 6-[3'-cyano-6'-methyl-2'-oxo-(1H)pyridin-5'-yl]-3-methyl-oxazolo[4,5-b]-py ridin-2(3H)-one.

When dimethylsulfate is replaced in Examples 1 and 3, Step 2, with benzylbromide, then the corresponding 4-benzyl-7-bromo-2H-pyrido[3,2-b]-1,4-oxazin-3(4H)-one and 3-benzyl-6-bromo-oxazolo[4,5-b]pyridin-2(3H)-one is prepared.

Following the procedures of Examples 1-5, the following compounds may be prepared:

7-[3'-cyano-6'-methyl-2'-oxo-(1H)pyridin-5'-yl]-4-methyl-2H-pyrido[4,3-b]-1 ,4-oxazin-3(4H)-one.

7-[3'-cyano-6'-methyl-2'-oxo-(1H)pyridin-5'-yl]-4-methyl-2H-pyrido[2,3-b]-1 ,4-oxazin-3(4H)-one.

6-[3'-cyano-6'-methyl-2'-oxo-(1H)pyridin-5'-yl]-3-methyloxazolo[4,5-b]pyrid in-2(3H)-one.

6-[3'-cyano-6'-methyl-2'-oxo-(1H)pyridin-5'-yl]-3-methyloxazolo[4,5-c]pyrid in-2(3H)-one.

6-[3'-cyano-6'-methyl-2'-oxo-(1H)pyridin-5'-yl]-3-methyloxazolo[5,4-c]pyrid in-2(3H)-one.

6-[3'-cyano-6'-methyl-2'-oxo-(1H)pyridin-5'-yl]-1-methyl-4H-pyrido[2,3-d][1 ,3]oxazin-2(1H)-one.

8-[3'-cyano-6'-methyl-2'-oxo-(1H)pyridin-5'-yl]-5-methyl-2,3-dihydropyrido[ 3,2-b][1,4]oxazepin-4(5H)-one.

8-[3'-cyano-6'-methyl-2'-oxo-(1H)pyridin-5'-yl]-5-methyl-2,3-dihydropyrido[ 4,3-b][1,4]oxazepin-4(5H)-one.

7-[3'-cyano-6'-methyl-2'-oxo-(1H)pyridin-5'-yl]-1-methyl-3,5-dihydropyridin [2,3-e]-1,4-oxazepin-4(1H)-one.

7-[3'-amino-6'-methyl-2'-oxo-(1H)pyridin-5'-yl]-4-methyl-2H-pyrido[3,2-b]-1 ,4-oxazin-3(4H)-one.

7-[3'-chloro-6'-methyl-2'-oxo-(1H)pyridin-5'-yl]-4-methyl-2H-pyrido[3,2-b]- 1,4-oxazin-3(4H)-one.

7-[3'-methoxymethyl-6'-methyl-2'-oxo-(1H)pyridin-5'yl]-4-methyl-2H-pyrido[3 ,2-b]-1,4-oxazin-3(4H)-one.

7-[3',6'-dimethyl-2'-oxo-(1H)pyridin-5'-yl]-4-methyl-H-pyrido[3,2-b]-1,4-ox azin-3(4H)-one.

6-[3'-ethoxy-6'-methyl-2'-oxo-(1H)pyridin-5'-yl]-3-methyloxazolo[4,5-b]pyri din-2(3H)-one.

7-[3'-cyano-6'-methyl-2'-oxo-(1H)pyridin-5'-yl]-4-benzyl-2H-pyrido[3,2-b]-1 ,4-oxazin-3(4H)-one.

7-[3'-cyano-6'-methyl-2'-oxo-(1H)pyridin-5'-yl]-4-ethyl-2H-pyrido[3,2-b]-1, 4-oxazin-3(4H)-one.

7-[3'-cyano-6'-methyl-2'-oxo-(1H)pyridin-5'-yl]-2H-pyrido[3,2-b]-1,4-oxazin -3(4H)-one.

7-[3'-cyano-6'-methyl-2'-oxo-(1H)pyridin-5'yl]-2,2,4-trimethyl-2H-pyrido[3, 2-b]-1,4-oxazin-3(4H)-one.

7-[3'-cyano-6'-methyl-2'-oxo-(1H)pyridin-5'yl]-2-methyl-2H-pyrido[3,2-b]-1, 4-oxazin-3(4H)-one.

7-[3'-cyano-6'-methyl-2'-oxo-(1H)pyridin-5'yl]-2,4-dimethyl-2H-pyrido[3,2-b ]-1,4-oxazin-3(4H)-one.

7-[3'-cyano-6'-methyl-2'-oxo-(1H)pyridin-5'yl]-2-phenyl-2H-pyrido[3,2-b]-1, 4-oxazin-3(4H)-one.