1,2-Dihydro-2-oxoquinol-4-ylacetic acid derivatives and pharmaceutical compositions

This invention relates to new quinolone alkanoic acid derivatives and in particular it relates to new quinolone alkanoic acid derivatives which have useful pharmaceutical properties.
According to the invention there is provided a quinolone alkanoic acid derivative of the formula: ##STR1## wherein A is a direct bond, or a C.sub.1-4 -alkylene or C.sub.2-4 -alkenylene radical; R.sup.1 is hydrogen or a halogen atom or a C.sub.1-4 -alkyl radical; R.sup.2 is hydrogen or a C.sub.1-4 -alkyl radical; R.sup.3 is a hydroxy, amino, hydroxylamino, C.sub.1-6 -alkoxy or a phenoxy radical which may optionally bear one or two substituents selected from halogen atoms, nitro, trifluoromethyl, C.sub.1-4 -alkyl and C.sub.1-4 -alkoxy radicals; and wherein the benzene ring X may optionally bear 1 or 2 substituents selected from halogen atoms, C.sub.1-6 -alkyl, C.sub.1-4 -alkoxy, C.sub.1-4 -alkylthio, trifluoromethyl, C.sub.1-3 -alkylenedioxy, nitro, amino, C.sub.1-4 -alkylamino, di-(C.sub.1-4 -alkyl)-amino and C.sub.2-4 -alkanoylamino radicals and from C.sub.7-10 -aralkoxy radicals optionally substituted by a halogen atom; and wherein the ring Y is a phenyl radical which may optionally bear 1,2 or 3 substituents selected from halogen atoms, C.sub.1-6 -alkyl, C.sub.1-4 -alkoxy, C.sub.1-4 -alkylthio, C.sub.1-4 -alkylsulphinyl, C.sub.1-4 -alkylsulphonyl, C.sub.1-4 -alkylamino, di-(C.sub.1-4 -alkyl)amino, nitro, cyano, trifluoromethyl and C.sub.2-8 -alkoxyalkyl radicals and from C.sub.6-10 -aryl radicals optionally substituted by 1 or 2 halogen atoms; or wherein the ring Y is a naphthyl or a monocyclic heterocyclic aromatic radical which may optionally bear 1 or 2 substituents selected from halogen atoms, C.sub.1-4 -alkyl and C.sub.1-4 -alkoxy radicals; or a pharmaceutically acceptable salt thereof.
It will be observed that those compounds of formula I wherein R.sup.2 is a C.sub.1-4 -alkyl radical contain an asymmetric carbon atom and that accordingly, such compounds can be isolated in a racemic form and two optically active forms. This specification is addressed to the racemic form of the compounds of formula I wherein R.sup.2 is a C.sub.1-4 -alkyl radical and to any optical isomer which shows any one or more of the useful pharmaceutical properties mentioned hereafter; it being a matter of general knowledge how to resolve the racemic form and to determine the biological properties of the optical isomers.
A particularly suitable value for A when it is a C.sub.1-4 -alkylene radical is, for example, a methylene or ethylene (--CH.sub.2.CH.sub.2 --) radical.
A particularly suitable value for A when it is a C.sub.1-4 -alkenylene radical is for example a propenylene (--CH.sub.2.CH.dbd.CH--) radical and preferably, a propenylene radical having the unsaturated bond in conjugation with the ring Y.
A particularly suitable value for R.sup.1 when it is a halogen atom is for example a fluorine, chlorine or bromine atom, and when it is a C.sub.1-4 -alkyl radical, a particularly suitable value is, for example a methyl or ethyl radical.
A particularly suitable value for R.sup.2 when it is a C.sub.1-4 -alkyl radical is, for example, a methyl or ethyl radical.
A particularly suitable value for R.sup.3 when it is a C.sub.1-6 -alkoxy radical is for example, a methoxy, ethoxy, n-butoxy or t-butoxy radical.
A particularly suitable value for a C.sub.1-4 -alkyl or C.sub.1-4 -alkoxy radical which may be present on a phenoxy radical when it is a value for R.sup.3 is, for example, a methyl or methoxy radical respectively.
A particularly suitable value for a halogen atom which may be present on a phenoxy radical when it is a value for R.sup.3 is, for example, a chlorine or bromine atom.
A particularly suitable value for a halogen atom when it is a substituent on ring X or Y is, for example, a fluorine, chlorine, bromine or iodine atom.
A particularly suitable value for a C.sub.1-6 -alkyl radical when it is a substituent on ring X or Y is, for example, a methyl, ethyl, n-propyl, i-propyl, n-butyl or t-butyl radical.
A particularly suitable value for a C.sub.1-4 -alkoxy radical when it is a substituent on ring X or Y is, for example, a methoxy or ethoxy radical.
A particularly suitable value for a C.sub.1-4 -alkylthio radical when it is a substituent on ring X or Y is, for example, a methylthio radical.
A particularly suitable value for a C.sub.1-4 -alkylsulphinyl radical when it is a substituent on ring Y is, for example a methylsuphinyl radical.
A particularly suitable value for a C.sub.1-4 -alkylsulphonyl radical when it is a substituent on ring Y is, for example, a methylsulphonyl radical.
A particularly suitable value for a C.sub.1-4 -alkylamino radical when it is a substituent on ring X or Y is, for example, a methylamino radical.
A particularly suitable value for a di-(C.sub.1-4 -alkyl)-amino radical when it is a substituent on ring X or Y is, for example, a dimethylamino radical.
A particularly suitable value for a C.sub.1-3 -alkylenedioxy radical when it is a substituent on ring X is, for example a methylenedioxy, ethylenedioxy or 2,2-propylenedioxy radical.
A particularly suitable value for a C.sub.2-4 -alkanoylamino radical when it is a substituent on ring X is, for example, an acetamido radical.
A particularly suitable value for a C.sub.7-10 -aralkoxy radical when it is a substituent on ring X is, for example, a benzyloxy radical.
A particularly suitable value for a C.sub.7-10 -aralkoxy radical optionally substituted by a halogen atom when that radical is a substituent on ring X is, for example, a chlorobenzyloxy radical, for example a 4-chlorobenzyloxy radical.
A particularly suitable value for a C.sub.2-8 -alkoxyalkyl radical when it is a substituent on ring Y is for example, an n-propoxymethyl radical.
A particularly suitable value for a C.sub.6-10 -aryl radical when it is a substituent on ring Y is for example a phenyl radical.
A particularly suitable value for a C.sub.6-10 -aryl radical optionally substituted by 1 or 2 halogen atoms when that radical is a substituent on ring Y is, for example, a chlorophenyl radical, for example, a 4-chlorophenyl radical.
It is to be understood that throughout this specification the numbering given to substituents in ring X relates to the actual position of attachment to the quinolone nucleus. Thus, for example, a 6-chloro substituent on ring X is to be interpreted as meaning a 6-chloro--quinoline derivative. Accordingly, specific particularly suitable arrangements of substituents on ring X are, for example, no substituents, or a 6-chloro, 6-bromo, 6-fluoro, 6-fluoro-7-ethoxy, 7-chloro, 7-fluoro, 6,7-difluoro, 6-methyl, 7-methyl, 6-n-butyl, 6,7-dimethyl, 6-methoxy, 7-methoxy, 8-methoxy, 7-ethoxy, 6,7-methylenedioxy, 6-benzyloxy, 6-(4-chlorobenzyloxy), 6-methylthio, 6-nitro, 6-amino, 6-acetamido, 6-dimethylamino, or a 6-methylamino substituent.
A particularly suitable value for ring Y when it is a naphthyl radical is, for example, a 2-naphthyl radical.
A particularly suitable value for ring Y when it is a monocyclic heterocyclic aromatic radical is for example such a radical having a 5- or 6-membered ring, for example, a furyl, thienyl or a pyridyl radical, for example, a fur-2-yl, thien-2-yl or a pyrid-2-yl radical.
A particularly suitable value for a C.sub.1-4 -alkyl or C.sub.1-4 -alkoxy radical which may be present as a substituent on a monocyclic heterocyclic aromatic radical when the latter radical is a value for ring Y is, for example, a methyl or methoxy radical, respectively.
A particularly suitable value for a halogen atom which may be present as a substituent on a monocyclic heterocyclic aromatic radical when the latter is a value for ring Y is, for example, a fluorine, chlorine or bromine atom.
Specific particularly suitable values for ring Y are, for example, a phenyl, 2-chloro-, 3-chloro-, 4-chloro-, 4-fluoro-, 4-bromo-, 4-iodo-, 2,4-dichloro-, 3,4-dichloro-, 3,4-difluoro-, 3,4-dibromo-, 3-chloro-4-bromo-, 4-chloro-2-methyl-, 4-chloro-3-trifluoromethyl-, 4-chloro-2-fluoro-, 2-chloro-4-fluoro-, 4-bromo-3-methyl-, 3,4,5-trichloro-, 3,4,5-tribromo-, 3,5-dichloro-4-bromo-, 2-methyl-, 4-methyl-, 4-ethyl-, 4-i-propyl-, 4-n-propyl-, 4-t-butyl-, 4-n-butyl-, 3,4-dimethyl-, 3,4,5-trimethyl-, 4-methoxy-, 4-n-propoxymethoxy-, 4-methylamino-, 4-dimethylamino-, 4-methylthio-, 4-methylsulphinyl-, 4-methylsulphonyl-, 4-nitro-, 4-cyano-, 4-p-chlorophenyl-, 3-trifluoromethyl-, or a 4-trifluoromethyl-phenyl; or a biphenyl, naphth-2-yl, pyrid-2-yl, pyrid-4-yl, 4,6-dimethylpyrid-2-yl, fur-2-yl, 5-methyl-fur-2-yl, 4,5-dibromo-fur-2-yl, thien-2-yl, 4,5-dimethylthien-2-yl or a 4,5-dichlorothien-2-yl radical.
Particularly suitable salts of a compound of formula I which is sufficiently basic, for example, a compound of formula I wherein ring X and/or ring Y bear at least one C.sub.1-4 -alkylamino or di-(C.sub.1-4 -alkyl-)amino group or wherein ring Y is a pyridyl radical, are pharmaceutically acceptable acid addition salts derived from an appropriate organic acid or an inorganic acid, for example hydrochloric acid. Particularly suitable salts of a compound of formula I which is sufficiently acidic, for example, a compound of formula I wherein R.sup.3 is a hydroxy radical, are pharmaceutically acceptable base-addition salts, for example, alkali metal or alkaline earth metal salts, for example, sodium, potassium, calcium or magnesium salts, aluminium salts, or salts or organic bases affording a pharmaceutically acceptable cation, for example, triethanolamine.
A particularly preferred group of compounds of the invention comprises those compounds of formula I wherein R.sup.3 is a hydroxy radical.
Specific compounds of formula I are set out in the Examples.
The compounds of the formula I may be made by any process applicable to the manufacture of chemically-analogous compounds. Such processes are exemplified by the following in which A, R.sup.1, R.sup.2, R.sup.3, ring X and ring Y have the meanings stated above unless specifically stated otherwise:
(a) For a compound of formula I wherein R.sup.3 is a hydroxy radical, hydrolysing and decarboxylating a malonate of the formula:- ##STR2## wherein R.sup.4 is a C.sub.1-4 -alkoxy radical, or an acid-addition salt thereof.
It is to be understood that in the above reaction the steps of hydrolysis and decarboxylation may be carried out together, for example, in the same vessel, for example, in the presence of acid, or separately for example, by akaline hydrolysis followed by decarboxylation in the presence of acid. Thus the hydrolysis and decarboxylation may be carried out together by reacting the malonate of formula II with an inorganic acid, for example sulphuric acid, in the presence of water at an elevated temperature, for example 50.degree. C. to 150.degree. C., and more particularly 80.degree. C. to 120.degree. C., for example under reflux. Alternatively, the hydrolysis and decarboxylation may be carried out separately by reacting the malonate with an inorganic base, for example an alkali metal hydroxide, for example sodium hydroxide, in the presence of water at an elevated temperature, for example as stated immediately above, and then acidifying the resulting salt of a substituted malonic acid so as to give the substituted malonic acid itself, and then decarboxylating the latter compound. The acidification may be carried out using an inorganic acid, for example sulphuric acid, and the decarboxylation may be carried out by heating the reaction mixture comprising the substituted malonic acid at an elevated temperature, for example as stated above.
The above hydrolysis and decarboxylation may optionally be carried out in the presence of an organic solvent, for example a C.sub.1-4 -alkanol, for example ethanol. In the case where the hydrolysis and decarboxylation is carried out by means of an inorganic acid, the organic solvent may be, for example, acetic acid.
The malonates of formula II which are used as starting materials in the above-mentioned process may be obtained by reacting a compound of the formula:- ##STR3## with a carbonate of the formula R.sup.4 COR.sup.4, wherein R.sup.4 has the meaning stated above, and sodium hydride or potassium hydride. The reaction may be carried out in an excess of the carbonate reactant, and/or it may be carried out in dimethylformamide. The reaction is conveniently carried out under reflux. The compounds of the formula III themselves can be obtained in an analogous manner to known processes for preparing 4-methyl-1-phenylcarbostyril and 1-benzyl-4-methylcarbostyril. It is to be noted that in a few cases a substituent in the ring X can be so reactive as to react with the carbonate reactant R.sup.4 COR.sup.4, or a decomposition product thereof, that displacement of the radical occurs so that the corresponding alkoxy derivative is obtained. This happens, for example, in the case of at least some 7-fluoro derivatives (see Examples 30 and 38), but the corresponding 7-fluoro end-products can be obtained by alternative procedures (see Examples 86 and 87).
In the case of compounds of formula III wherein R.sup.2 is hydrogen, reaction as described hereinbefore with sodium hydride or potassium hydride and a carbonate of the formula R.sup.4 COR.sup.4, results in the intermediate formation of a sodium or potassium salt respectively of the corresponding malonate of formula II wherein R.sup.2 is hydrogen. This sodium or potassium salt may either be acidified to yield the corresponding malonate of formula II wherein R.sup.2 is hydrogen or, more conveniently, may be reacted with a C.sub.1-4 -alkyl halide, for example a C.sub.1-4 -alkyl bromide or iodide, to give the corresponding malonate of formula II wherein R.sup.2 is a C.sub.1-4 -alkyl radical. The alkylation may be carried out in a suitable non-aqueous organic solvent, for example, dimethylformamide, and may conveniently be carried out at from 20.degree. C. to 160.degree. C., for example, under reflux.
(b) For a compound of formula I wherein R.sup.3 is a hydroxy radical, hydrolysing and decarboxylating a pyruvic acid derivative of the formula:- ##STR4## wherein R.sup.4 is a C.sub.1-4 -alkoxy radical as stated above.
The hydrolysis and decarboxylation may be carried out by reacting the pyruvic acid derivative of formula IV with a strong inorganic acid, for example, concentrated sulphuric acid or polyphosphoric acid, at an elevated temperature, for example at 50.degree. C. to 100.degree. C. Alternatively, it may be carried out by hydrolysing the pyruvic acid derivative of formula IV using aqueous inorganic acid or using base, for example, aqueous hydrochloric acid or sodium or potassium hydroxide, to obtain the corresponding pyruvic acid, followed by decarboxylation of this by reaction thereof with hydrogen peroxide in aqueous alkali metal hydroxide, for example, sodium hydroxide. The above mentioned hydrolysis is optionally carried out under the influence of heat, for example, at from 20.degree. C. to 100.degree. C., and conveniently in the presence of a C.sub.1-4 -alkanol, for example, ethanol. The above mentioned reaction with hydrogen peroxide is conveniently carried out, for example, in water at a temperature, for example, of from -10.degree. C. to 30.degree. C., preferably, at 0.degree. C.
The pyruvic acid derivative of formula IV which are used as starting materials in the above process may be obtained by reacting a compound of formula III with an oxalate of the formula (R.sup.4 CO).sub.2 wherein R.sup.4 is a C.sub.1-4 -alkoxy radical, with sodium or potassium or a hydride, amide or C.sub.1-4 -alkoxide thereof, at 0.degree. to 100.degree. C. The reaction may be carried out in an excess of the oxalate reactant, and/or in the presence of an inert organic solvent, for example ether, benzene, tetrahydrofuran or dimethylformamide. The compounds of the formula III themselves may be obtained in an analogous manner to known processes for preparing 4-methyl-1-phenylcarbostyril and 1-benzyl-4-methylcarbostyril.
(c) Reacting an alkali derivative of the formula:- ##STR5## wherein R.sup.4 is a C.sub.1-4 -alkoxy radical, and M is an alkali metal atom, with a C.sub.1-4 -alkyl halide.
A particularly suitable alkali metal atom is, for example a sodium or potassium atom. The starting material of formula V is conveniently obtained in situ by reacting the appropriate compound in which M is replaced by a hydrogen atom, that is a compound of formula I wherein R.sup.2 is hydrogen and R.sup.3 is a C.sub.1-4 -alkoxy radical, with for example, sodium or potassium or a hydride, amide or C.sub.1-4 -alkoxide thereof. A particularly suitable C.sub.1-4 -alkyl halide is for example a C.sub.1-4 -alkyl iodide or bromide, for example, methyl iodide or ethyl bromide. The reaction may be carried out in an inert organic solvent for example dimethylformamide and at a temperature of, for example, 20.degree. C. to 160.degree. C.
(d) For a compound of formula I wherein the benzene ring X bears at least one nitro group, nitrating the corresponding compound of formula I wherein the benzene ring X is either unsubstituted or bear 1-2 substituent(s) which are not nitro groups.
The nitration may be carried out by any standard method for the nitration of a benzene ring which is fused to a heterocyclic ring, for example by reacting the starting material with concentrated sulphuric acid and an alkali metal nitrate, for example, potassium nitrate, at about 0.degree. C.
(e) For a compound of formula I wherein the benzene ring X bears at least one amino radical, reducing the nitro group(s) in the corresponding compound of formula I wherein the benzene ring Y bears at least one nitro group.
The reduction may be carried out by any known suitable procedure, for example by reducing the nitro compound with iron powder in 50% v/v aqueous acetic acid at about 90.degree. C.
(f) For a compound of formula I wherein R.sup.3 is a hydroxy radical, reacting an alkali metal derivative of the formula: ##STR6## wherein W is a lithium, sodium or potassium atom, with dry carbon dioxide in a suitable dry organic solvent at approximately -30.degree. C. to -50.degree. C. and in an inert atmosphere, and then treating the product thereby obtained with water at ambient temperature approximately.
A particularly suitable organic solvent is an ether, for example tetrahydrofuran or diethyl ether, and a particularly suitable inert atmosphere is provided, for example, by the use of dry argon. The treatment of the intermediate product with water is preferably carried out at approximately pH 3-4, and at 10.degree. C. to 25.degree. C.
The starting materials of the formula VI may be obtained in a conventional manner, for example by reacting a compound of formula III with a metalating agent, for example n-butyl lithium. n-Butyl-lithium, is preferably used in the presence of triethylamine (which activates the n-butyllithium) in a suitable dry ether, for example tetrahydrofuran or diethyl ether, at approximately -30.degree. C. to -50.degree. C. and in an inert atmosphere, for example an atmosphere composed of dry argon. Alternatively the metalating agent may be, for example, phenyl-lithium, phenyl-sodium or potassium hydride. (g) Reacting a compound of the formula: ##STR7## wherein M is an alkali metal atom, with a compound of the formula: ##STR8## wherein A is a C.sub.1-4 -alkylene or C.sub.2-4 -alkenylene radical and Z is a bromine or iodine atom when A is a methylene radical, an iodine atom when A is an C.sub.2-4 -alkylene radical, and a bromine or iodine atom when A is a C.sub.2-4 -alkenylene radical.
The reaction of a compound of formula VII with that of formula VIII is conveniently carried out in the presence of a suitable organic solvent, for example, hexamethylphosphoramide, and at a temperature of for example from 10.degree. C. to 100.degree. C., conveniently at ambient temperature.
The starting materials of formula VI are conveniently obtained in situ by reacting the appropriate compound in which M is replaced by a hydrogen atom, that is a 1,2-dihydro-2-oxoquinoline derivative, with, for example, sodium hydroxide or potassium hydroxide at, for example, ambient temperature. The appropriate 1,2-dihydro-2-oxo-quinoline starting materials are themselves obtained by reacting an alkali metal derivative of the formula: ##STR9## wherein M is an alkali metal atom, with carbon dioxide using similar reaction conditions to those specified in connection with part (f) of the process above.
(h) For a compound of formula I wherein R.sup.3 is an amino, hydroxylamino, C.sub.1-4 -alkoxy or a phenoxy radical which may optionally bear one or two substituents selected from halogen atoms, nitro, trifluoromethyl, C.sub.1-4 -alkyl and C.sub.1-4 -alkoxy radicals, condensing a quinolone alkanoic acid of the formula: ##STR10## that is a compound of formula I wherein R.sup.3 is a hydroxy radical, or a reactive derivative thereof, with an active hydrogen compound of the formula HQ wherein Q is an amino, hydroxylamino, C.sub.1-4 -alkoxy or a phenoxy radical which may optionally bear one or two substituents selected from halogen atoms, nitro, trifluoromethyl, C.sub.1-4 -alkyl and C.sub.1-4 -alkoxy radicals.
A particularly suitable reactive derivative of a compound of formula X is, for example, an acid halide, for example an acid chloride or acid bromide, an acid azide, an acid anhydride or a mixed acid anhydride derived from the acid of formula X. When a reactive derivative is used the reaction is preferably carried out in the presence of base, for example pyridine or triethylamine and conveniently, in an inert solvent or diluent, for example, chloroform, methylene chloride, 1,2-dimethoxyethane or tetrahydrofuran, and at a temperature of, for example, from 0.degree. C. to 100.degree. C.
Alternatively the condensation may be carried out in the presence of a condensing agent for example dicyclohexyl-carbodiimide or a mixture of diethylazodicarboxylate and triphenylphosphine. When dicyclohexylcarbodiimide is used, the reaction is preferably carried out in an inert diluent or solvent, for example chloroform, methylene chloride, 1,2-dimethoxyethane or tetrahydrofuran, and conveniently at a temperature of, for example, from 10.degree. C. to 100.degree. C.; when a mixture of diethylazodicarboxylate and triphenylphosphine is used, the reaction is preferably carried out in an inert diluent or solvent, for example diethyl ether, and at a temperature of, for example, from 0.degree. C. to 80.degree. C. and, preferably, at 18.degree. C. to 25.degree. C.
The reactive derivative of a compound of formula X may in addition be a C.sub.1-4 -alkyl or phenyl ester thereof when the active hydrogen compound of the formula HQ is hydroxylamine or ammonia. In this particular case the condensation reaction is conveniently carried out in a suitable solvent, for example a C.sub.1-4 -alkanol, for example ethanol or methanol, and at a temperature of from 15.degree. C. to 100.degree. C., and it is preferable to use an excess of the hydroxylamine or ammonia reagent.
(i) For a compound of formula I wherein R.sup.3 is a hydroxy radical, oxidising a compound of the formula: ##STR11##
The oxidation is conveniently carried out using for example, an inorganic oxidising agent, for example, potassium permanganate or chromium trioxide, and is preferably carried out in the presence of a mineral acid, for example sulphuric acid. The oxidation is conveniently performed in a polar organic solvent or diluent, for example acetone, and at a temperature of, for example, from 0.degree. C. to 100.degree. C. and conveniently at from 20.degree. C. to 25.degree. C.
The starting materials of formula XI are obtained from the corresponding alkali metal derivative of the formula IX, for example the lithium derivative, with chloromethyl benzyl ether in a mixture of hexamethylphosphoramide and tetrahydrofuran at approximately -20.degree. C., to give the corresponding intermediate of the formula: ##STR12## The intermediates of formula XII are then metalated and reacted with the appropriate halide of formula VIII using analogous conditions to those described for the reaction of a compound of formula VII with that of formula VIII in part (g) of the above process, to give an intermediate of the formula: ##STR13## The intermediates of formula XIII are then debenzylated using standard conditions, for example hydrogenation over palladium-charcoal catalyst, to give the required starting materials of formula XI.
(j) For a compound of formula I wherein R.sup.3 is a hydroxy radical, hydrolysing a compound of the formula: ##STR14## wherein L is a cyano radical or a radical of the formula CO.R.sup.5 wherein R.sup.5 is a C.sub.1-6 -alkoxy, aryloxy, aralkoxy or amino radical. A particularly suitable value for R.sup.5 when it is a C.sub.1-6 -alkoxy radical is, for example, a n-butoxy, ethoxy or methoxy radical and, when it is an aryloxy or aralkoxy radical, is, for example, a phenoxy, p-chlorophenoxy or a benzyloxy radical.
The hydrolysis is preferably carried out under basic or acidic conditions. Particularly suitable basic conditions are provided by an alkali metal hydroxide, for example, sodium or potassium hydroxide. Particularly suitable acidic conditions are provided by a mineral acid, for example, hydrochloric or sulphuric acid. The hydrolysis is carried out in the presence of water, and an organic solvent, for example acetic acid or a C.sub.1-4 -alkanol, for example ethanol, may also be present. The reaction is conveniently carried out at, for example, 40.degree. C. to 150.degree. C., for example at reflux temperature.
Those of the starting materials of formula XIV wherein L is a cyano radical may be obtained from the corresponding pyruvic ester of formula IV by the following sequence of reactions using standard conditions for the preparation of analagous compounds:
(i) formation of the pyruvic ester oxime by reaction with hydroxylamine hydrochloride in a mixture of ethanol and pyridine under reflux;
(ii) basic hydrolysis of the pyruvic ester oxime to the pyruvic acid oxime followed by decarboxylation and dehydration to the required nitrile of formula XIV.
The above processes can be operated so that a quinoline alkanoic acid of formula I may be isolated as such, or as a pharmaceutically acceptable salt thereof. Such a pharmaceutically acceptable salt may be obtained by conventional procedures when the compound of formula I is sufficiently acidic or basic as hereinbefore defined.
Depending on its chemical structure a compound of the invention possesses analgesic or anti-inflammatory properties, or possesses the property of inhibiting the enzyme aldose reductase. It is to be understood that any particular compound of the invention may possess one or more, but not necessarily all, of the above properties. In addition, some of the compounds of the invention possess the property of inhibiting the enzyme prostaglandin synthetase.
In general, particularly good analgesic properties and/or good anti-inflammatory properties are possessed by those compounds of formula I wherein R.sup.2 is a C.sub.1-4 -alkyl radical, of which those wherein R.sup.2 is a methyl radical are preferred; good inhibition of the enzyme aldose reductase is in general shown by those compounds of formula I wherein R.sup.2 is hydrogen.
Compounds which possess analgesic and/or antiinflammatory properties have been used in the clinical treatment of the pain and/or inflammation associated with inflammatory diseases, for example rheumatoid or osteoarthritis or ankylosing spondylitis.
Those compounds of the invention which are inhibitors of aldose reductase are useful in the reduction or prevention of the development of the peripheral effects of diabetes, for example the effects of macular oedema, cataract. retinopathy or impaired neural conduction.
Particularly preferred compounds of the invention are:
(a) as inhibitors of aldose reductase:
1-(3,4-dichlorobenzyl)-6-fluoro-1,2-dihydro-2-oxoquinol-4-ylacetic acid, 1-(4-bromobenzyl)-6-fluoro-1,2-dihydro-2-oxoquinol-4-ylacetic acid, 1-(3,4-dichlorobenzyl)-1,2-dihydro-2-oxoquinol-4-ylacetic acid, 6-fluoro-1-(4-iodobenzyl)-1,2-dihydro-2-oxoquinol-4-ylacetic acid, 1-(3,4-dichlorobenzyl)-3-methyl-1,2-dihydro-2-oxoquinol-4-ylacetic acid, 1-(4-bromo-3-chlorobenzyl)-6-fluoro-1,2-dihydro-2-oxoquinol-4-ylacetic acid, 1-(3,4-dibromobenzyl)-6-fluoro-1,2-dihydro-2-oxoquinol-4-ylacetic acid, 1-(3,4-dichlorobenzyl)-6-fluoro-3-methyl-1,2-dihydro-2-oxoquinol-4-ylacetic acid, 1-(3,4-dichlorobenzyl)-6,7-difluoro-1,2-dihydro-2-oxoquinol-4-ylacetic acid, 1-(3-chloro-4-bromobenzyl)-3-methyl-1,2-dihydro-2-oxoquinol-4-ylacetic acid, and 1-(3,5-dichloro-4-bromobenzyl)-3-methyl-1,2-dihydro-2-oxoquinol-4-ylacetic acid;
(b) as anti-inflammatory agents:
.alpha.-[1-(4-chlorobenzyl)-6-methyl-1,2-dihydro-2-oxoquinol-4-yl]propionic acid, and .alpha.(1-benzyl-6-methyl-1,2-dihydro-2-oxoquinol-4-yl)propionic acid;
(c) as analgesic agents:
.alpha.-(1-benzyl-1,2-dihydro-2-oxoquinol-4-yl)propionic acid, .alpha.-[1-(4-methylbenzyl)-1,2-dihydro-2-oxoquinol-4-yl]-propionic acid, .alpha.-(1-benzyl-6-methyl-1,2-dihydro-2-oxoquinol-4-yl]propionic acid, .alpha.-[1-(4-methylbenzyl)-6-methyl-1,2-dihydro-2-oxoquinol-4-yl]propionic acid, .alpha.-[1-(4-chlorobenzyl)-6-methyl-1,2-dihydro-2-oxoquinol-4-yl]propionic acid, .alpha.[1-(4-ethylbenzyl)-1,2-dihydro-2-oxoquinol-4-yl]propionic acid, .alpha.-[1-(4-trifluoromethylbenzyl)-1,2-dihydro-2-oxoquinol-4-yl]propionic acid, .alpha.-(1-benzyl-7-methyl-1,2-dihydro-2-oxoquinol-4-yl)-propionic acid, and .alpha.-[1-(4-trifluoromethylbenzyl)-6-methyl-1,2-dihydro-2-oxoquinol-4-yl]propionic acid;
(d) as inhibitors of prostaglandin synthetase:
.alpha.-[1-(4-methylbenzyl)-6-methyl-1,2-dihydro-2-oxo-quinol-4-yl]propionic acid and .alpha.-[1-(4-methylbenzyl-1,2-dihydro-2-oxoquinol-4-yl]propionic acid; and pharmaceutically acceptable salts thereof.
The biological properties of any particular compound of the invention may be demonstated by their behaviour in the following standard tests:
(a) Aldose reductase inhibition
Inhibition of the enzyme aldose reductase may be demonstrated either in vitro or in vivo.
Thus, in the in vitro test, purified aldose reductase is isolated in known manner from bovine lenses. The percentage inhibition of this enzyme's ability in vitro to reduce aldoses to polyhydric alcohols, and particularly to reduce glucose to sorbitol, caused by a test compound is then determined using standard spectrophotometric methods.
In the in vivo test, rats are made diabetic by dosing with streptozotocin and are then dosed daily with the test compound for 4 days. The animals are then killed and the eye lenses and sciatic nerves are removed. After a standard work-up procedure the residual sorbitol levels in each tissue are determined by gas liquid chromatography after conversion to the poly trimethylsilyl derivatives. Inhibition of aldose reductase in vivo is then assessed by comparing the residual sorbitol levels in tissues from the dosed diabetic group of rats with those of an undosed group of diabetic rats and an undosed, normal group of rats. Active compounds in this test reduce the residual sorbitol levels to levels which are similar to those of normal, undosed rats.
(b) Anti-inflammatory activity
This activity is demonstrated in either of the standard tests of adjuvant induced arthritis or carrageenin induced oedema, both of which tests are in rats.
(c) Analgesic acitivity
This activity is demonstrated in a standard analgesic test which involves the induction of writhing in mice following intraperitoneal injection of acetylcholine.
(d) Prostaglandin Synthetase Inhibition
This activity is demonstrated in a standard in vitro test, which involves the use of prostaglandin synthetase isolated from the ram.
The potency of any particular compound depends upon its chemical structure, but in general, depending upon the particular test involved, an active compound is active at a dose or molar concentration in the range:
(a) (aldose reductase inhibition-in vitro test): 10.sup.-8 to 10.sup.-5 M; (aldose reductase inhibition-in vivo test): 10-200 mg./kg.;
(b) (anti-inflammatory activity - adjuvant arthritis test): 1-100 mg./kg.; (anti-inflammatory activity - carrageenin oedema test): 5-200 mg./kg.
(c) (analgesic activity): 1-200 mg./kg.;
(d) (inhibition of prostaglandin synthetase): 10.sup.-6 to 10.sup.-4 M.
The particularly preferred compounds mentioned hereinbefore show activity in one or more of the above tests at a minimum dose or molar concentration in the range:
(a) (aldose reductase inhibition - in vitro test): 10.sup.-8 to 10.sup.-7 M; (aldose reductase inhibition - in vivo test): 10-100 mg./kg.
(b) (anti-inflammatory activity -adjuvant arthritis test): 1-50 mg./kg. (anti-inflammatory activity - carrageenin oedema test): 5-50 mg./kg.
(c) (analgesic activity) - 1-25 mg./kg.;
(d) (prostaglandin synthetase inhibition): 10.sup.-6 to 10.sup.-5 M.
No overt toxic or other undesirable effects have been detected with the compounds of the invention at doses at which activity is detected in one or more of the above-mentioned tests.
When a compound of the invention is used to produce an effect in warm-blooded animals, it may be administered orally at the following daily doses:
(a) to inhibit the enzyme aldose reductase: a daily dose of 5 to 100 mg./kg.; in man this is equivalent to a total daily dose of 50 to 1200 mg. per 70 kg. man;
(b) to obtain an anti-inflammatory effect: a daily dose of 5 to 150 mg./kg.; in man this is equivalent to a total daily dose of 50 to 1500 mg. per 70 kg. man.
(c) to obtain an analgesic effect: a daily dose of 5 to 150 mg./kg.; in man this is equivalent to a total daily dose of 50 to 1500 mg. per 70 kg. man; the daily doses may conveniently be given in divided form.
When 1-(3,4-dichlorobenzyl)-3-methyl-1,2-dihydro-2-oxoquinol-4-ylacetic acid is used to obtain an effect in warm-blooded animals as mentioned in (a) immediately above, a daily oral dose of 20 to 50 mg./kg. is administered; in man this is equivalent to a total daily dose of 200 to 600 mg. per 70 kg. man.
When .alpha.-(1-benzyl-1,2-dihydro-2-oxoquinol-4-yl)-propionic acid is used to obtain an effect in warm-blooded animals as mentioned in (b) and/or (c) immediately above, a daily oral dose of 5 to 20 mg./kg. is administered; in man this equivalent to a total daily dose of 50 to 250 mg. per 70 kg. man.
The compounds of the invention may be administered in the form of pharmaceutical compositions and according to a further feature of the invention there is provided a pharmaceutical composition which comprises a compound of formula I or a pharmaceutically acceptable salt thereof in pharmaceutically accpetable form.
By "pharmaceutically acceptable form" is meant either a pharmaceutical preparation in which the compound is associated with a pharmaceutically acceptable diluent or carrier, or a pharmaceutical preparation, for example a capsule, in which the compound is confined in a unit dosage form without necessarily being associated with a diluent or carrier.
Especially preferred pharmaceutically acceptable forms are those suitable for oral administration, for example tablets, capsules, suspensions or solutions, which may be obtained by conventional methods and, if desired, may incorporate conventional diluents, carriers or other excipients. Other preferred pharmaceutically acceptable forms are those suitable for parenteral administration, for example sterile injectable aqueous or non-aqueous solutions or suspensions, and for rectal administration, for example suppositories. Dosage forms should contain from 50 mg. to 500 mg. of a compound of formula I per dosage unit.
Compositions intended for use in the treatment of the peripheral effects of diabetes, may also contain other agents which may have a beneficial effect on the disease or on associated conditions, for example a known hypoglycaemic agent, for example tolbutamide.
Compositions intended for use in the treatment of the pain and/or the inflammation of inflammatory diseases may also contain other known agents having analgesic and/or anti-inflammatory properties, for example paracetamol, codeine, acetyl salicylic acid, chloroquine, phenylbutazone, D-penicillamine, indomethacin, ibuprofen, naproxen, ketoprofen, or an anti-inflammatory steroid, for example prednisolone, or a uricosuric agent, for example probenecid.
A particular group of compounds of the invention having analgesic and, in some cases, in addition anti-inflammatory properties comprises those compounds of formula I wherein A is a methylene, ethylene or propenylene; R.sup.1 is hydrogen; R.sup.2 is methyl; R.sup.3 is hydroxy, amino, hydroxylamino, C.sub.1-6 -alkoxy or phenoxy; and wherein the benzene ring X is unsubstituted or bears either a single substituent selected from the group consisting of halogen, methyl, methoxy, nitro and amino, or two methyl substituents; and wherein ring Y is phenyl which may optionally bear a single substituent selected from the group consisting of halogen, methyl, methoxy, methylthio and trifluoromethyl; and the pharmaceutically-acceptable salts thereof.
A preferred group of compounds of the invention having analgesic properties comprises those compounds of formula I wherein A is methylene or ethylene; R.sup.1 is hydrogen; R.sup.2 is methyl; R.sup.3 is hydroxy or C.sub.1-6 -alkoxy; benzene ring X optionally bears a methyl substituent; and ring Y is phenyl which may optionally bear a substituent selected from the group consisting of halogen, methyl or trifluoromethyl; and the pharmaceutically-acceptable salts thereof.

The invention is illustrated, but not limited by the following Examples:
EXAMPLE 1
A solution of 1-(4-chlorobenzyl)-1,2-dihydro-4-methyl-2-oxoquinoline (18.0 g.) in diethyl carbonate (80 ml.) was added to a stirred suspension of sodium hydride (15.4 g.; weighed as a 60% w/w dispersion in oil, but subsequently washed by decantation with light petroleum, b.p. 40.degree.-60.degree. C., to remove the oil) in diethyl carbonate (20 ml.). The mixture was stirred under reflux for 11/2 hours, and formed a thick suspension. This was cooled and treated with a small amount of methanol to destroy any remaining sodium hydride. Dilution with ether (400 ml.) gave a suspension from which the solid was filtered. This was suspended in ethanol (180 ml.) and brought to pH 3 by addition of hydrochloric acid. Water (600 ml.) was added, and the suspension was stirred for 30 minutes before the solid was collected by filtration, washed with water, and well drained. This solid [which comprised diethyl 1-(4-chlorobenzyl)-1,2-dihydro-2-oxoquinol-4-ylmalonate] was dissolved in ethanol (180 ml.), to which was added aqueous 40% w/v sodium hydroxide (20 ml.), and the mixture was heated under reflux for 4 hours. The cooled mixture was added to water (600 ml.) to give a solution which was brought to pH 3 by addition of concentrated hydrochloric acid. The resultant precipitate was collected by filtration, washed with water, drained, and crystallised from ethanol to give 1-(4-chlorobenzyl)-1,2-dihydro-2-oxoquinol-4-ylacetic acid, m.p. 208.degree.-209.degree. C., in 51% overall yield.
By an analogous procedure, but starting from the appropriately sustituted 1,2-dihydro-4-methyl-2-oxo-quinolines, the following compounds were prepared in 15-65% yield
__________________________________________________________________________ ##STR15## XV Substituent(s) Substituent(s) Recrystallisation M.p. (.degree.C.)Example on ring X on ring Y solvent (decomposition)__________________________________________________________________________ 2 -- -- EtOH 194-5 3 -- 4-OMe MeOH 182-3 4 6-Cl -- EtOH 221-2 5 6-Cl 4-OMe Pr.sup.n OH 188-9 6 6-OMe -- EtOH 196-7 7 6-OMe 4-Cl * 205-6 8 6-OMe 4-OMe EtOH 191-2 9 -- 2,4-Cl.sub.2 MeOH 202-310 -- 3-CF.sub.3 EtOH 20311 -- 4-isoPr MeOH 186-7 dimethyl formamide12 6,7-OCH.sub.2 O 3,4-Cl.sub.2 ("DMF") 213 DMFH.sub.2 O13 6,7-OCH.sub.2 O 4-Cl (3/1 v/v) 208 DMFH.sub.2 O14 6-Br 4-Cl (3/1 v/v) 20715 -- 4-Cl, 3-CF.sub.3 * 20316 -- 2-Me, 4-Cl * 20717 6-n-Bu 4-Cl MeOH 19918 6-F 4-Cl MeOH 20519 -- 2-Cl MeOH 201-3 DMFMeOH20 6-OMe 2-Cl (1/1 v/v) 21921 -- 4-F MeOH 19322 8-OMe 4-Cl EtOH 192-323 7-OMe 4-Cl * 20324 6-Me 4-Cl DMF 33025 -- 3-Cl * 182-526 -- 4-Br * 193 DMFH.sub.2 O27 6-p-Clbenzyloxy 4-Cl (3/1 v/v) 185 MeOHH.sub.2 O28 6-F 4-n-Pr (4/1 v/v) 176-729 -- 4-n-PrOCH.sub.2 MeOH 178-930 6-F-7-OEt.sup.1 3,4-Cl.sub.2 MeCN 188 isoPrOHH.sub.2 O31 6-F 4-Br (4/1 v/v) 194-632 6-F 4-Me * 19533 -- 4-Me.sub.2 N EtOH 19734 6-MeCONH 4-Cl * 21035 -- 4-Me EtOH 193 DMFH.sub.2 O36 6-MeS 3,4-Cl.sub.2 (3/1 v/v) 20937 6-F -- MeOH 189-9038 7-OEt.sup.2 3,4-Cl.sub.2 MeCO.sub.2 H 195-639 6-F 4-I MeOH 193-440 7-Me 3,4-Cl.sub.2 * 20941 6-F 3-Cl, 4-Br CH.sub.3 CN 189-91 MeOHH.sub.2 O42 6-F 3,4-Br.sub.2 (4/1 v/v) 18843 -- 2-F, 4-Cl MeOH 19944 -- 2-Cl, 4-F * 196-745 6,7-OCMe.sub.2 O 3,4-Cl.sub.2 EtOH 22746 6-Cl 4-Cl * 19247 7-Cl 3,4-Cl.sub.2 EtOH 222-348 6-F 4-F EtOH 188 EtOAc-cyclohexane49 6-F 4-t-Bu (1/1 v/v) 18250 6-F 3,4,5-Me.sub.3 * 187-851 6-F 4-CN * 19652 6-F 3-Me, 4-Br EtOH 19753 6-F 3,4-F.sub.2 EtOH 189-90 DMFMeOH54 6,7-O(CH.sub.2).sub.2 O (1/1 v/v) 19955 --.sup.3 3,4-Cl.sub.2 MeOH 217-8__________________________________________________________________________ *Purified by dissolution in 2Naqueous ammonia and reprecipitation with 2Nhydrochloric acid. 1. This compound was obtained from the corresponding 6,7difluoro compound i.e. under the described reaction conditions the 7fluoro substituent was replaced by a 7ethoxy substituent. End products containing a 7fluoro substituent can be obtained by alternative processes, see Examples 86 and 87. 2. Essentially as with the compound mentioned in footnote 1, this compoun was obtained from the corresponding 7fluoro compound. 3. This compound also contained a methyl substituent at the 3position of the quinolone nucleus.
The N-aralkylquinoline derivatives used as starting materials in these preparations were usually obtained by forming the anions of the parent quinolines with sodium hydride in dimethylformamide, and then treating them with the appropriate aralkyl chlorides at temperatures up to 100.degree. C. Complications arising from O-aralkylation were sometimes encountered, but these could be avoided by first preparing the N-aralkylanilines and converting these into the quinolines by known procedures. These procedures are described in Example 74.
The following new intermediates were prepared by such methods:
______________________________________ ##STR16## XVISubstituent Substituent(s) Recrystallisationon ring X on ring Y solvent M.p. (.degree.C.)______________________________________-- 4-Cl MeOH 126-7-- 4-OMe MeOH/H.sub.2 O 160-26-Cl -- (washed with 102-4 light petroleum)6-Cl 4-Cl MeOH 165-86-Cl 4-OMe C.sub.6 H.sub.6 /C.sub.6 H.sub.12 157.5-96-OMe -- C.sub.6 H.sub.12 117-86-OMe 4-Cl C.sub.6 H.sub.6 /C.sub.6 H.sub.12 170-26-OMe 4-OMe MeOH 155-6-- 2-Cl C.sub.6 H.sub.12 165-76-OMe 2-Cl MeOH 177-9-- 3,4-Cl MeOH 130-1-- 3-CF.sub.3 EtOH 146-7-- 3-IsoPr petroleum ether 88-90 b.p. 60.degree.-80.degree. C.6,7-OCH.sub.2 O 3,4-Cl.sub.2 MeOH 199-2026,7-OCH.sub.2 O 4-Cl MeOH 197-2006-Br 4-Cl EtOH ---- 4-Cl-3-CF.sub.3 MeOH 165- 7-- 2-Me-4-Cl EtOH 197-96-n-Bu 4-Cl MeOH 113-46-F 4-Cl MeOH 154-6-- 2-Cl MeOH 180-36-OMe 2-Cl MeOH 177-9-- 4-F MeOHH.sub.2 O 193 (4/1 v/v)8-OMe 4-Cl MeOH 1047-OMe 4-Cl EtOH 193-56-Me 4-Cl MeOH 156-8-- 3-Cl EtOH 115-6-- 4-Br EtOH 137-96-F 4-Et petroleum ether 114-6 b.p. 60.degree.-80.degree. C.6-F 4-n-Pr petroleum ether 110-2 b.p. 60.degree.-80.degree. C.6-F 4-Br cyclohexane 153-46-F -- cyclohexane 144-67-F 3,4-Cl.sub.2 cyclohexane 175-76-F 3,4-Br.sub.2 toluene 180-16-F 3,4,5-Br.sub.3 DMFMeOH 217-9 (1/1 v/v)6-F 3-Cl, 4-Br toluene 170-26-F 4-t-Bu petroleum ether 78 b.p. 60.degree.-80.degree. C.6-F 4-Me EtOH 140-16-F 3,4-Me.sub.2 petroleum ether 128-30 b.p. 60.degree.-80.degree. C.-- 4-Me petroleum ether 93-4 b.p. 80.degree.-100.degree. C.6-F 4-I cyclohexane 1617-Cl 3,4-Cl.sub.2 petroleum ether 166-7 b.p. 60.degree.-80.degree. C.7-Me 3,4-Cl.sub.2 MeOH 175-66-F 3-Me, 4-Br cyclohexane 1516-F 3,4-F.sub.2 EtOH 150-26-F 4-CN toluene 158-606,7-F.sub.2 3,4-Cl.sub.2 EtOAc 206-86-F 3,4,5-Me.sub.3 EtOH 135-66-p-Cl-benzyloxy 4-Cl chloroform 169-70--* 3,4-Cl.sub.2 petroleum ether 128 b.p. 80.degree.-100.degree. C.______________________________________ *This compound contained a methyl substituent at the 3position of the quinolone nucleus.
EXAMPLE 56
Diethyl 1,2-dihydro-2-oxo-1-phenylquinol-4-ylmalonate (2.7 g.) was dissolved in ethanol (50 ml.), and a solution of sodium hydroxide (2.85 g.) in water (3 ml.) was added. The mixture was heated under reflux for 1 hour, and then cooled and poured into water (200 ml.) to give a solution which was treated with decolourising carbon, filtered, and adjusted to pH 3 by addition of hydrochloric acid. The precipitate was collected by filtration, washed with water, drained, and crystallised from methanol to give 1,2-dihydro-2-oxo-1-phenylquinol-4-ylacetic acid, m.p. 185.5.degree.-186.degree. C. (decomposition), in 51% yield.
The malonate used as starting material was obtained as follows:
A mixture of 1,2-dihydro-4-methyl-2-oxo-1-phenylquinoline (4.7 g.), sodium hydride (4.8 g., 60% w/w dispersion in oil, washed as in Example 1) and diethyl carbonate (50 ml.) was stirred under reflux for 2 hours. Any excess of sodium hydride was then destroyed by addition of methanol to the cooled suspension, and the mixture was then poured into ether (1 l.). The yellow precipitate was collected by filtration, and washed with ether (200 ml.). It was suspended in ethanol (50 ml.), concentrated hydrochloric acid was added to give a pH of 3, and the resultant solution was poured into water (200 ml.). The precipitate was extracted into ether, and the combined extracts were washed with water, dried over magnesium sulphate, and evaporated in vacuo. A sample of the residual solid was recrystallised from a mixture of benzene and cyclohexane to give diethyl, 1,2-dihydro-2-oxo-1-phenylquinol-4-ylmalonate, m.p. 101.degree.-103.degree. C.
EXAMPLE 57
6-Chloro-1-(4-chlorobenzyl)-1,2-dihydro-4-methyl-2-oxoquinoline (7.9 g.) was added to a suspension of sodium hydride (6.0 g., 60% w/w dispersion in oil, washed as in Example 1) in diethyl carbonate (100 ml.). The mixture was then stirred and heated under reflux for 3 hours. A small quantity of methanol was added to the cooled suspension to destroy any remaining sodium hydride, and the mixture was then poured into ether (1 l.) to give a solid which was collected and washed well with ether. This solid (16 g.) was suspended in dimethylformamide (40 ml.), and methyl iodide (30.0 g.) was added. The mixture was stirred at room temperature for 1 hour and then heated under reflux on the steam-bath for 1 hour. The mixture was cooled and poured into water (200 ml.) to give an oil which was extracted into ethyl acetate, washed three times with water, and, after drying over magnesium sulphate, was recovered by evaporation under reduced pressure. The residual oil (4.8 g.), which comprised diethyl .alpha.-[6-chloro-1-(4-chlorobenzyl)-1,2-dihydro-2-oxoquinol-4-yl]-.alpha.-methylmalonate, was dissolved in a mixture of ethanol (50 ml.) and aqueous 40% w/v sodium hydroxide (4 ml.), and heated under reflux for 2 hours. The resultant suspension was poured into water (200 ml.) to give a solution which was adjusted to pH 3 by addition of concentrated hydrochloric acid. The precipitate was collected by filtration, washed with water, drained well, and recrystallised from aqeous ethanol to give .alpha.-[6-chloro-1-(4-chlorobenzyl)-1,2-dihydro-2-oxoquinol-4-yl]propionic acid, m.p. 192.5.degree.-193.5.degree. C., (decomposition) in 43% yield.
In analogous manner, but starting from the appropriately substituted 1-benzyl-1,2-dihydro-4-methyl-2-oxo-quinolines and using the requisite alkyl iodides, the following compounds were prepared in yields of 30-62%.
__________________________________________________________________________ ##STR17## XVII Substituent Substituent(s) Recrystallisation M.p. (.degree.C.)Example on ring X on ring Y R.sup.2 solvent (decomposition)__________________________________________________________________________58 -- -- Me * 179-18059 -- 4-Cl Me MeCN 186-6.560 -- 4-OMe Me C.sub.6 H.sub.6 166.761 6-Cl 4-OMe Me AcOH/H.sub.2 O 203.5-4 (4/1 v/v)62 6-OMe 4-Cl Me MeCN 185-663 -- 2-Cl Me EtOH 201-264 -- -- Et MeCN 194-4.565 6-OMe 2-Cl Me MeOH 187-866 6-Cl -- Me Toluene-cyclohexane 172-3 (1/1 v/v)67 6-OMe -- Me EtOH 179-8068 6-OMe 4-OMe Me * 182-369 -- 2,4-Cl.sub.2 Me MeOH 187-970 -- 4-F Me MeOH 19371 6,7-OCH.sub.2 O 4-Cl Me EtOH 199-20072 6-F 3,4-Cl.sub.2 Me DMF-MeOH 195-6 (1/1 v/v)__________________________________________________________________________ *Purified by dissolution in 2Naqueous ammonia and reprecipitation with 2Nhydrochloric acid
The required appropriately substituted 1-benzyl-1,2-dihydro-4-methyl-2-oxo-quinolines are described in Examples 1-55. The following additional starting materials were obtained in a similar manner to that described for the starting materials in Example 1-55:
1-(2,4-dichlorobenzyl)-1,2-dihydro-4-methyl-2-oxoquinoline, m.p. 137.degree.-8.degree. C.;
1-(3,4-dichlorobenzyl)-1,2-dihydro-6-fluoro-4-methyl-2-oxoquinoline, m.p. 182.degree.-3.degree. C.
EXAMPLE 73
Ethyl 1-(4-chlorobenzyl)-1,2-dihydro-2-oxoquinol-4-ylpyruvate (25 g.) was dissolved in concentrated sulphuric acid (100 ml.) and heated at 80.degree. C. until a test sample no longer gave a positive colour reaction with aqueous ferric chloride solution (2 to 3 hours). The mixture was then cooled, poured into ice-water (1 l.), the resulting mixture filtered, and the solid residue washed with water, drained and crystallised from ethanol to give 1-(4-chlorobenzyl)-1,2-dihydro-2-oxoquinol-4-ylacetic acid, m.p. 208.degree.-209.degree. C., in 48% yield.
The starting material was obtained as follows:
Sodium hydride (18 g.; 60% w/w dispersion in oil, washed as described in Example 1) was stirred in dry dimethylformamide (300 ml.), and 1-(4-chlorobenzyl)-1,2-dihydro-4-methyl-2-oxoquinoline (64.7 g.) was added, followed by diethyl oxalate (55 g.). The mixture was stirred at room temperature for 2.5 hours with occasional external cooling to keep the temperature below 25.degree. C. Ether (2 l.) was added, and the mixture was filtered. The solid residue was washed with ether (500 ml.), and then suspended in dimethylformamide (200 ml.) and acidified to pH 2 by the addition of concentrated hydrochloric acid. The resultant mixture was added to water (3 l.), and the mixture filtered, and the solid residue washed with water (2 l.), drained well, and crystallised from ethanol to give ethyl 1-(4-chlorobenzyl)-1,2-dihydro-2-oxoquinol-4-ylpyruvate, m.p. 180.degree.-182.degree. C.
EXAMPLE 74
A mixture of 1-o-chlorobenzyl-4-methyl-6-methoxy-2-oxo-1,2-dihydroquinoline (2.5 g.), oil-free sodium hydride (obtained from 2.5 g. of a 50% w/w suspension as described in Example 1) and diethyl carbonate (50 ml.) was heated over 1 hour to reflux and the reflux maintained for 3 hours. The mixture was cooled and treated with methanol (2 ml.) to destroy excess sodium hydride. Ether (200 ml.) was added and the yellow precipitate was filtered off, washed with ether (50 ml.), and dried, and was then suspended in dimethylformamide (100 ml.) containing methyl iodide (4 ml.). After 24 hours standing at room temperature, the mixture was diluted with water (200 ml.) and the aqueous mixture extracted with ether (3.times.100 ml.). The combined ethereal extracts were washed with water (2.times.100 ml.), and dried with magnesium sulphate, and the ether was evaporated. The residue, which comprised diethyl .alpha.-(1-o-chlorobenzyl-6-methoxy-2-oxo-1,2-dihydroquinol-4-yl)-.alpha.-methylmalonate, was dissolved in a solution of potassium hydroxide (3.6 g.) in water (4 ml.) and ethanol (100 ml.). The mixture was refluxed for 1 hour, cooled, and diluted with N-hydrochloric acid (100 ml.). The resulting mixture was filtered, and the solid residue washed with water and crystallised from methanol (100 ml.) to give .alpha.-(1-o-chlorobenzyl-6-methoxy-2-oxo-1,2-dihydroquinol-4-yl)propionic acid, m.p. 187.degree.-188.degree. C. in 48% yield.
The o-chlorobenzyl derivative used as starting material was obtained as follows:
A solution of 2-chlorobenzaldehyde (70 g.) and 4-methoxyaniline (61.5 g.) in toluene (750 ml.) was refluxed under a Dean and Stark separator until no more water collected (ca. 1 hour). The toluene was evaporated in vacuo, and the residue was dissolved in methanol (1.5 l.). The methanolic solution was treated at room temperature with sodium borohydride (60 g.) added portionwise so that, with gentle cooling, the temperature was maintained at 40.degree.-50.degree. C. The solution was then refluxed for 15 minutes, diluted with water (1.5 l.), and the aqueous mixture extracted with ether (3.times.200 ml.). The combined ethereal extracts were washed with water (2.times.100 ml.), dried (K.sub.2 CO.sub.3), and evaporated to give N-(4-methoxyphenyl)-2-chlorobenzylamine as a brown oil, Infra Red .nu. max 3400, 1618 cm..sup.-1, which was used directly in the next stage.
The above-mentioned benzylamine derivative (42.6 g.) was dissolved in glacial acetic acid (400 ml.) containing mercuric acetate (5.5 g.), and to the solution was added diketen (17.4 g.) at room temperature. The mixture was stirred and warmed to 40.degree. C. and, when the exotherm had subsided, the mixture was heated at 70.degree. C. for 15 minutes. The mixture was then cooled and diluted with water (700 ml.), and the aqueous mixture was extracted with ether (1.times.300 ml., 2.times.200 ml.). The combined ethereal extracts were successively washed with saturated aqueous sodium bicarbonate and water, and then dried (K.sub.2 CO.sub.3) and evaporated to give a brown oil, .nu. max 1710, 1650 cm..sup.-1. The oil was added dropwise to stirred concentrated sulphuric acid (100 ml.) at 70.degree. C. The stirred mixture was kept at 20.degree. C. for 10 minutes after the addition was complete, and then poured into ice-water (500 g.). The aqueous mixture was extracted with chloroform (1.times.500 ml., 2.times.200 ml.) and the combined chloroform extracts were washed with water, dried (MgSO.sub.4) and evaporated. The residue was crystallised from methanol (120 ml.) to give 1-o-chlorobenzyl-4-methyl-6-methoxy-2-oxo-1,2-dihydroquinoline, m.p. 177.degree.-179.degree. C.
EXAMPLE 75
In similar manner to that described in Example 74, 1-p-chlorophenyl-6-methoxy-4-methyl-2-oxo-1,2-dihydroquinoline gave .alpha.-(1-p-chlorophenyl-6-methoxy-2-oxo-1,2-dihydroquinol-4-yl)propionic acid, m.p. 177.degree.-178.degree. C., in 50% yield.
The p-chlorophenyl derivative used as starting material was obtained as follows:-
A solution of 4-methoxyacetanilide (30 g.) and 1-chloro-4-iodobenzene (69 g.) in nitrobenzene (250 ml.) containing potassium carbonate (14 g.) and copper bronze (0.8 g.) was refluxed for 32 hours. The nitrobenzene was removed by steam distillation and the steam-involatile residue was extracted into ether (3.times.200 ml.). The ethereal solution was washed with water, dried (MgSO.sub.4) and evaporated. A solution of the residue (36.2 g.) in 2 N-ethanolic potassium hydroxide solution (250 ml.) was refluxed overnight, and then cooled and diluted with water (1200 ml.). The aqueous mixture was extracted with chloroform (2.times.250 ml.) and the combined extracts were washed with water (2.times.250 ml.), dried (MgSO.sub.4) and evaporated to give a dark red solid (26.6 g.) which, on crystallisation from petroleum ether (b.p. 40.degree.-60.degree. C.), gave 4-chloro-4'-methoxydiphenylamine (10 g.), m.p. 52.degree.-53.degree. C. A solution of the residue (from the evaporated mother liquors) in a mixture of ether (25% v/v) and petroleum ether (b.p. 40.degree.-60.degree. C.) was passed down a silica gel column (250 g.), and from the eluate a further quantity of product was obtained. Mercuric sulphate (43.2 g.) was added to a solution of 4-chloro-4'-methoxydiphenylamine (17 g.) in glacial acetic acid (250 ml.) at ambient temperiature. Diketen (2 ml.) was added to the stirred mixture and the mixture was warmed (to ca. 40.degree. C.) to initiate the reaction. Diketen (10 ml.) was added dropwise so as to maintain a temperature of 40.degree.-50.degree. C. The mixture was then stirred at room temperature for 1 hour, and then poured into water (1.2 l.). The aqueous mixture was extracted with ether (3.times.200 ml.) and the combined extracts were washed with saturated, aqueous sodium bicarbonate solution. The acid-free ethereal extract was washed with water (2.times.200 ml.), dried (MgSO.sub.4) and evaporated to give N-acetoacetyl-4-chloro-4'-methoxydiphenylamine as a red oil, .nu. max 1665, 1720 cm..sup.-1, which was used directly in the next stage.
The above-mentioned acetoacetyl derivative (12 g.) was added portionwise to stirred concentrated sulphuric acid (12 ml.) at room temperature. The mixture was slowly warmed and then kept at 60.degree. C. for 3 hours. The mixture was cooled and poured into water (500 ml.), and the aqueous mixture was extracted with chloroform (3.times.100 ml.). The combined extracts were washed with water (100 ml.), dried (MgSO.sub.4), and evaporated to give an orange oil which crystallised on treatment with ethanol to give, on filtration, 1-p-chlorophenyl-4-methyl-6-methoxy-2-oxo-1,2-dihydroquinoline, m.p. 234.degree.-235.degree. C.
EXAMPLE 76
1-(4-Chlorobenzyl)-1,2-dihydro-2-oxoquinol-4-ylacetic acid (33 g.) was added to concentrated sulphuric acid (210 ml.) at 0.degree. C. The mixture was stirred at 0.degree. C. and potassium nitrate (11 g.) was added in small portions over 8 minutes. The mixture was then stirred at 0.degree. C. for a further 10 minutes and then for 2 hours at room temperature. The mixture was poured into an ice-water mixture (2.5 l.), and the precipitated solid was filtered off. The dried solid was crystallised from 3/1 v/v dimethylformamide-ethanol to give 1-(4-chlorobenzyl)-1,2-dihydro-6-nitro-2-oxoquinol-4-ylacetic acid, m.p. 217.degree.-9.degree. C., in 85% yield.
EXAMPLE 77
Iron powder (18 g.) was added over 40 minutes to a stirred solution of 1-(4-chlorobenzyl)-1,2-dihydro-6-nitro-2-oxoquinol-4-ylacetic acid (13 g.) in 50% v/v aqueous acetic acid (200 ml.) at 90.degree. C. When the addition was completed, the mixture was stirred a further 70 minutes at 90.degree. C. and then poured into an ice-water mixture (700 ml.). The mixture was adjusted to pH 1 with hydrochloric acid, and then filtered. The filtrate was adjusted to pH 6 with ammonium hydroxide solution, and the resulting mixture filtered. The solid residue (13 g.) was dissolved as far as possible in 2 N-sodium hydroxide solution, and the mixture was filtered. The filtrate was adjusted to pH 6 with glacial acetic acid, and the precipitated solid was filtered off, stirred with hot water (85.degree. C., 200 ml.) and filtered while hot to give 6-amino-1-(4-chlorobenzyl)-1,2-dihydro-2-oxoquinol-4-ylacetic acid, m.p. 196.degree.-9.degree. C., (decomposition) in 52% yield.
EXAMPLES 78-85
The process described in Example 1 was repeated, but using the appropriate 1-benzyl-1,2-dihydro-4-methyl-2-oxoquinoline derivative as starting material, and there were thus obtained the following compounds of formula XV in yields of 25-60%:-
______________________________________ Re- crys- talli- Substituent Substituent(s) sation M.p. (.degree.C.)Example on ring X on ring Y solvent (decomposition)______________________________________78 6-F 3,4-Cl.sub.2 MeOH 196-779 -- 4-Et * 182-380 6-F 4-Et MeOH 197-881 6-Br 3,4-Cl.sub.2 EtOH 19782 -- 2-Me * 20783 -- 4-NO.sub.2 * 208-21084 -- 4-n-Bu MeOH 174-585 -- 4-p-ClPh * 182-4______________________________________ *Purification by dissolution in 2N aqueous ammonia and reprecipitation with 2N hydrochloric acid.
The starting materials of formula XVI used in preparing the above compounds were obtained as described hereinbefore and had the following melting points:-
______________________________________Substituent Substituent(s) Recrystallisationon ring X on ring Y solvent M.p. (.degree.C.)______________________________________6-F 3,4-Cl.sub.2 MeOH 182-3-- 4-Et * 76-76-F 4-Et MeOH 114-66-Br 3,4-Cl.sub.2 washed with EtOH 183-5-- 2-Me washed with EtOH 172-4-- 4-NO.sub.2 EtOH 149-150-- 4-n-Bu * 58-60-- 4-p-ClPh EtOH 156-8______________________________________ *Purified by chromatography on a column of silica gel;; elution with diethyl ether.
EXAMPLE 86
1-(3,4-Dichlorobenzyl)-1,2-dihydro-7-fluoro-4-methyl-2-oxoquinoline (7 g.) was added portionwise to a solution of n-butyl-lithium (9.8 ml. of a 2.32 N-solution in hexane) and triethylamine (1.15 g.) in dry tetrahydrofuran (150 ml.) maintained at -40.degree. C. The mixture was stirred at -30.degree. C. to -40.degree. C. for one hour under an atmosphere of dry argon, and then added to a saturated solution of dry carbon dioxide in dry tetrahydrofuran (200 ml.). The mixture was stirred at -30.degree. C. for 2 hours and then allowed to reach ambient temperature overnight. Water (400 ml.) was added and the concentrated hydrochloric acid to bring the pH of the mixture to 3-4. The crude acid was filtered off and recrystallised from methanol to give 1-(3,4-dichlorobenzyl)-1,2-dihydro-7-fluoro-2-oxoquinol-4-ylacetic acid, m.p. 205.degree.-207.degree. C. (dec.), in 66% yield.
EXAMPLE 87
A solution of 1-(3,4-dichlorobenzyl)-6,7-difluoro-1,2-dihydro-4-methyl-2-oxoquinoline (5 g.) in benzene (15 ml.) was added with stirring at ambient temperature to a mixture of diethyl oxalate (2.3 g.), benzene (2 ml.) and a 6 N-solution of potassium ethoxide in ethanol (6 ml.). The mixture was allowed to stand overnight at ambient temperature under dry nitrogen. The yellow solid was filtered off, washed with benzene (5 ml.) and dried by suction on the filter. The dried solid (5.7 g.) was mixed with 2.77 N-aqueous sodium hydroxide (21 ml.) at 0.degree. C. and kept at 0.degree. C. overnight. Ice (11.5 g.) and then 100 vol. hydrogen peroxide (4.04 ml.) were added to the mixture and it was again kept overnight at 0.degree. C. A further quantity of 100 vol. hydrogen peroxide (1.7 ml.) was added and the mixture kept at 0.degree. C. for 72 hours. The mixture was then treated with manganese dioxide (1 g.). When the effervescence had ceased the mixture was warmed to 50.degree. C. and filtered. The filter cake was washed with warm 2.77 N-aqueous sodium hydroxide (20 ml.) and the total filtrate acidified with concentrated hydrochloric acid. The precipitate was collected and recrystallised first from a mixture (1/2 v/v) of ethyl acetate and cyclohexane, and then from ethanol to give 1-(3,4-dichlorobenzyl)-6,7-difluoro-1,2-dihydro-2-oxoquinol-4-ylacetic acid m.p. 185.degree.-7.degree. C. (dec.), in 10% yield.
EXAMPLE 88
.alpha.-(1,2-Dihydro-2-oxoquinol-4-yl)propionic acid (217 mg.) was dissolved in a mixture of hexamethylphosphoramide (2 ml.) and 2 N-sodium hydroxide (2 ml.). A solution of benzyl bromide (0.528 ml.) in hexamethylphosphoramide (2 ml.) was added dropwise to the stirred solution during 2 hours. The mixture was then poured into water (10 ml.), and the resulting mixture washed with chloroform (3.times.5 ml.). The aqueous solution was acidified to pH 1 with concentrated hydrochloric acid, and the resulting mixture was filtered and the white solid residue washed with water and dried in vacuo over phosphorus pentoxide. The solid was crystallised from ethanol to give .alpha.-(1-benzyl-1,2-dihydro-2-oxoquinol-4-yl)propionic acid, m.p. 178.degree.-180.degree. C. (decomposition), in 39% yield.
The propionic acid derivative used as starting material was obtained as follows:
1,2-Dihydro-4-methyl-2-oxoquinoline (79.5 g.) was dissolved in a mixture of dry hexamethylphosphoramide (530 ml.) and tetrahydrofuran (530 ml.), and the solution was cooled to -10.degree. C. under a nitrogen atmosphere. n-Butyl-lithium (1.54 M solution in hexane; 770 ml.) was added to the stirred solution at such a rate as to keep the temperature below 0.degree. C. When the addition was completed, the deep red solution was cooled to -50.degree. C. and methyl iodide (50 ml.) was rapidly added. The resulting pale yellow solution was immediately poured into water (2000 ml.) and acidified to pH 1 with concentrated hydrochloric acid. The resulting mixture was filtered and the solid residue washed with water and then dried in vacuo over phosphorus pentoxide. Crystallisation from ethanol gave 4-ethyl-1,2-dihydro-2-oxoquinoline, m.p. 197.degree. C.
4-Ethyl-1,2-dihydro-2-oxoquinoline (50 g.) was dissolved in a mixture of dry hexamethylphosphoramide (280 ml.) and dry tetrahydrofuran (280 ml.), and the solution cooled to -10.degree. C. under a nitrogen atmosphere. n-Butyl-lithium (1.54 M solution in hexane; 435 ml.) was added at such a rate as to keep the temperature below 0.degree. C. The resulting deep red solution was added to a stirred saturated solution of carbon dioxide in tetrahydrofuran (750 ml.) at -70.degree. C. and under a nitrogen atmosphere. The resulting pale yellow suspension was poured into water (800 ml.), and the mixture was washed with chloroform (3.times.300 ml.). The aqueous solution was acidified to pH 1 with concentrated hydrochloric acid, the resulting mixture filtered, and the solid residue washed with water and dried in vacuo over phosphorus pentoxide. There was thus obtained .alpha.-(1,2-dihydro-2-oxoquinol-4-yl)propionic acid, m.p. 196.degree.-8.degree. C. (decomposition).
EXAMPLES 89-91
In a similar manner to that described in Example 88 the following compounds were obtained from the appropriate starting materials, in yields of 32-68%:
__________________________________________________________________________ ##STR18## XVIII Substituent Substituent RecrystallisationExample on ring X on ring Y R.sup.2 A solvent m.p. (.degree.C.)__________________________________________________________________________89 -- -- H CH.sub.2 EtOH 194-590 -- -- Me CH.sub.2 CHCH* EtOH 170 (trans)91 -- 4-Me Me CH.sub.2 Et.sub.2 O 172 (precipitated)__________________________________________________________________________ *note: the ring Y is attached to the double bond.
The starting materials were obtained in analogous manner to that described in Example 88.
EXAMPLE 92
A mixture of .alpha.-(1-benzyl-1,2-dihydro-2-oxoquinol-4-yl)propionic acid (0.5 g.), methanol (5 ml.) and concentrated sulphuric acid (4 drops) was heated under reflux for six hours. The mixture was then poured into water (10 ml.), and the resulting mixture was neutralised with sodium bicarbonate solution. The mixture was extracted with ethyl acetate (3.times.5 ml.) and the combined extracts were washed successively with sodium bicarbonate solution (5 ml.) and water (5 ml.), and then dried with sodium sulphate. The solvent was evaporated in vacuo and the residue crystallised from cyclohexane to give methyl .alpha.-(1-benzyl-1,2-dihydro-2-oxoquinol-4-yl)propionate m.p. 90.degree.-92.5.degree. C., in 74% yield.
EXAMPLES 93-97
The following compounds of formula X (wherein R.sup.1 is hydrogen) were prepared in a similar manner to that described in Example 57 from the appropriate starting materials, in yields of 30-62%.
__________________________________________________________________________ Substituent Substituent RecrystallisationExample on ring X on ring Y R.sup.2 A solvent m.p. (.degree.C.)__________________________________________________________________________93 6-Me 4-Cl Me CH.sub.2 EtOH 20694 6-Me 4-F Me CH.sub.2 EtOH 19295 6-Me -- Me CH.sub.2 EtOH 186-796 -- -- Me CH.sub.2 CH.sub.2 Water 176-897 6-Me 4-Me Me CH.sub.2 Ethanol 194__________________________________________________________________________
The required starting materials of formula III (wherein R.sup.1 and R.sup.2 are hydrogen) were obtained in analogous manner to that described in Example 1, and had the following melting points:
______________________________________ Substituent on Substituent on m.p.A ring X phenyl ring Y .degree.C.______________________________________CH.sub.2 6-Me 4-Cl 156-158CH.sub.2 6-Me 4-F 165-6CH.sub.2 6-Me -- 141-2CH.sub.2 CH.sub.2 -- -- 122-4CH.sub.2 6-Me 4-Me 134-6______________________________________
EXAMPLES 98-105
The following compounds were prepared in a similar manner to that described in Example 1 from the appropriate starting materials, in yields of 11-57%.
__________________________________________________________________________ ##STR19## XIX Substituent Substituent Recrystallisation m.p.(.degree.C.)Example on ring X on ring Y R.sup.1 solvent (decomposition)__________________________________________________________________________ 98 6-Me -- H EtOH 201 99 6-F 3,4-Cl.sub.2 Me MeOH 219-222100 -- 3,4-Cl.sub.2 Et MeOH 231-2101 -- 3,4-Cl.sub.2 Cl MeOH 197-8102 6-F 4-CF.sub.3 H EtOH 285 dimethyl-103 6,7-Me.sub.2 3,4-Cl.sub.2 H formamide/ 197 MeOH, 1:1 v/v EtOAc/104 6,7-F.sub.2 3,4-Cl.sub.2 H cyclohexane, 182-5 1:1 v/v105 6-F 3,4,5-Cl.sub.3 H MeOH 280-2__________________________________________________________________________
The corresponding 1-benzyl-1,2-dihydro-4-methyl-2-oxo-quinoline starting materials of the formula ##STR20## were obtained by an analogous method to that described in Example 1 and had the following melting points:
______________________________________ Substituent on Substituent on m.p.R.sup.1 ring X ring Y .degree.C.______________________________________H 6-Me -- 141-2Me 6-F 3,4-Cl.sub.2 148-50Et -- 3,4-Cl.sub.2 116-8Cl -- 3,4-Cl.sub.2 128-9H 6-F 4-CF.sub.3 154-5H 6,7-Me.sub.2 3,4-Cl.sub.2 182-3H 6,7-F.sub.2 3,4-Cl.sub.2 206-8H 6-F 3,4,5-Cl.sub.3 208-9______________________________________
EXAMPLES 106-107
The following compounds were prepared in a similar manner to that described in Example 1 from the appropriate starting materials:
6-fluoro-1-(naphth-2-ylmethyl)-1,2-dihydro-2-oxoquinol-3-ylacetic acid, m.p. 195.degree. C., (19% yield) crystallised from toluene (Example 106); and
1-(pyrid-2-ylmethyl)-1,2-dihydro-2-oxoquinol-4-ylacetic acid hydrochloride, m.p. 210.degree.-2.degree. C., (15% yield) after washing with ethanol (Example 107).
The starting materials were obtained by an analogous method to that described in Example 1, and had the following melting points:
6-fluoro-1-(naphth-2-ylmethyl)-4-methyl-1,2-dihydro-2-oxo-quinoline, m.p. 146.degree.-7.degree. C.
1-(pyrid-2-ylmethyl)-4-methyl-1,2-dihydro-2-oxoquinoline, m.p. 129.degree.-30.degree. C.
EXAMPLE 108
Using an analogous procedure to that described in Example 86, 3-methyl-1-(naphth-2-ylmethyl)-1,2-dihydro-2-oxo-quinol-4-ylacetic acid, m.p. 186.degree. C. (recrystallised from ethanol) was obtained in 18% yield from 3,4-dimethyl-1-(naphth-2-ylmethyl)-1,2-dihydro-2-oxo-quinolone, m.p. 124.degree.-5.degree. C.
EXAMPLE 109
A stirred solution of 4-(2-hydroxyethyl)-6-fluoro-1-(3,4,5-tribromobenzyl)-1,2-dihydro-2-oxoquinoline (1.8 g.) in acetone (700 ml.) at 25.degree. C. was treated with Jones reagent (CrO.sub.3 (267 g.) in concentrated sulphuric acid (23 ml.) diluted with water to 100 ml. 2.5 ml.). After 30 minutes, isopropanol (0.5 ml.) was added to the mixture which was then filtered through kieselguhr. The filtrate was diluted to 1.8 l. with water. Acetone was then distilled out until the solution was faintly hazy. The cooled solution yielded crystals on cooling which were filtered off and recrystallised from ethyl acetate. There was thus obtained 6-fluoro-1-(3,4,5-tribromobenzyl)-1,2-dihydro-2-oxoquinol-4-ylacetic acid, m.p. 207.degree. C. (decomposition), in 71% yield.
The required starting material, 4-(2-hydroxyethyl)-6-fluoro-1-(3,4,5-tribromobenzyl)-1,2-dihydro-2-oxoquinoline, was obtained as follows:
6-Fluoro-4-methyl-1,2-dihydro-2-oxoquinoline (10 g.) was suspended in a mixture of dry hexamethylphosphoramide (68 ml.) and dry tetrahydrofuran (68 ml.) and the suspension was cooled to -20.degree. C. under an argon atmosphere. n-Butyl lithium (1.6 M. solution in n-hexane; 78 ml.) was added at such a rate that the temperature was maintained below 0.degree. C. To the resulting deep red solution, there was added at -20.degree. C. chloromethyl benzyl ether (8.5 g.), as rapidly as possible. The mixture was stirred at -20.degree. C. for one hour and then diluted with water (200 ml.). The mixture was partially evaporated in vacuo to remove the tetrahydrofuran and then extracted with ethyl acetate (3.times.150 ml.). The combined organic extracts were washed with water (2.times.100 ml.), dried (MgSO.sub.4) and evaporated. The residue was recrystallised from isopropanol and there was thus obtained 4-(2-benzyloxyethyl)-6-fluoro-1,2-dihydro-2-oxo-quinoline, m.p. 135.degree.-140.degree. C.
To a suspension of sodium hydride (0.675 g. of 80% w/w suspension; freed of mineral oil as in Example 1) in dimethylformamide (100 ml.) under a nitrogen atmosphere was added 4-(2-benzyloxyethyl)-6-fluoro-1,2-dihydro-2-oxoquinoline (6.0 g.). The mixture was stirred at 40.degree. C. for one hour and then treated at this temperature with 3,4,5-tribromobenzylbromide (9.1 g.). The mixture was stirred overnight at ambient temperature and then diluted with water (200 ml.) and the product extracted with ethyl acetate (3.times.150 ml.). The combined organic extracts were washed with water (2.times.100 ml.), dried (MgSO.sub.4), and evaporated. The residue was a mixture of O- and N-substituted products. Chromatography of this residue on silica gel using a 50:50 v/v mixture of ether and petroleum ether (b.p. 40.degree.-60.degree. C.) as eluant gave 4-(2-benzyloxyethyl)-6-fluoro-1-(3,4,5-tribromobenzyl)-1,2-dihydro-2-oxoquinoline, as an oil, Infra-Red Spectral Absorption .nu. max. 1665 cm..sup.-1.
A solution of 4-(2-benzyloxyethyl)-6-fluoro-1-(3,4,5-tribromobenzyl)-1,2-dihydro-2-oxoquinoline (6.0 g.) in a mixture of dioxan (50 ml.), ethanol (50 ml.), and concentrated hydrochloric acid (2 ml.) was hydrogenated at atmospheric pressure over 5% palladium on carbon (1 g.). The theoretical quantity of hydrogen (390 ml. at N.T.P.) was absorbed in four minutes. The hydrogenation was stopped and the mixture filtered. Evaporation of the filtrate gave the crude product which was recrystallised twice from methanol to give 4-(2-hydroxyethyl)-6-fluoro-1-(3,4,5-tribromobenzyl)-1,2-dihydro-2-oxoquinoline, m.p. 199.degree.-201.degree. C., in 71% yield.
EXAMPLES 110-111
In a similar manner to that described in Example 109 there was obtained, from 4-(2-hydroxyethyl)-3-methyl-1-(3-chloro-4-bromobenzyl)-1,2-dihydro-2-oxoquinoline, m.p. 142.degree.-143.degree. C., 3-methyl-1-(3-chloro-4-bromobenzyl)-1,2-dihydro-2-oxoquinol-4-ylacetic acid (Example 110), m.p. 219.degree.-221.degree. C. (decomposition) recrystallised from ethyl acetate in 73% yield, and from 4-(2-hydroxyethyl)-3-methyl-(3,5-dichloro-4-bromobenzyl)-1,2-dihydro-2-oxoquinoline, m.p. 132.degree.-135.degree. C., 3-methyl-1-(3,5-dichloro-4-bromobenzyl)-1,2-dihydro-2-oxoquinol-4-ylacetic acid (Example 111), m.p. 250.degree.-252.degree. C. (decomposition) (recrystallised from 2-ethoxyethanol), in 60% yield.
The following new intermediates necessary for the preparation of Example 110 and Example 111 were obtained using similar procedures to those described in Example 109 and had the following characteristic properties:
4-(2-benzyloxyethyl)-3-methyl-1,2-dihydro-2-oxoquinoline, m.p. 157.degree.-160.degree. C.; 4-(2-benzyloxyethyl)-3-methyl-1-(3-chloro-4-bromobenzyl)-1,2-dihydro-2-oxoquinolone, oil, Infra-red Spectral Absorption, .nu. max. 1660 cm..sup.-1 ; 4-(2-benzyloxyethyl)-3-methyl-1-(3,5-dichloro-4-bromobenzyl)-1,2-dihydro-2-oxoquinoline, 143.degree.-4.degree. C.
EXAMPLE 112
In a similar manner to that described in Example 109 there was obtained in 51% yield, 6-fluoro-1(3,4-dichlorobenzyl)-1,2-dihydro-2-oxoquinol-4-ylacetic acid, m.p. 198.degree.-199.degree. C. (decomposition), from 4-(2-hydroxyethyl)-6-fluoro-1-(3,4-dichlorobenzyl)-1,2-dihydro-2-oxoquinoline, m.p. 191.degree.-2.degree. C., which starting material was itself obtained in a similar manner to that described in Example 109 from 4-(2-benzyloxyethyl)-6-fluoro-1-(3,4-dichlorobenzyl)-1,2-dihydro-2-oxoquinoline, m.p. 122.degree.-4.degree. C.
EXAMPLES 113-115
In a similar manner to that described in Example 88 there were obtained in yields of 32-68% the following compounds of formula XVII but from the corresponding starting .alpha.-(1,2-dihydro-2-oxoquinol-4-yl)propionic acid and the appropriate benzyl halide:
______________________________________ Re- Crys- m.p. talli- .degree.C. Substituent Substituent sation (decompo-Example R.sup.2 on ring X on ring Y Solvent sition)______________________________________113 Me 6-NO.sub.2 -- EtOH 204-5114 Me -- 4-Et EtOAc 201-3115 Me -- 4-CF.sub.3 EtOAc 190-2______________________________________
The .alpha.-(6-nitro-1,2-dihydro-2-oxo-quinol-4-yl)-propionic acid starting material for the above Example 113 was obtained as follows:
.alpha.-(1,2-Dihydro-2-oxo-quinol-4-yl)propionic acid (15 g.) was added in portions to stirred fuming nitric acid cooled to 5.degree. C. The rate of addition was such that the reaction temperature remained between 5.degree. and 10.degree. C. After the addition was complete, the mixture was stirred at ambient temperature for 40 minutes and was then poured into water (1.2 l.). The resultant solid was separated by filtration, washed with water and dried in vacuo to give .alpha.-(6-nitro-1,2-dihydro-2-oxo-quinol-4-yl)propionic acid as a white solid (90% yield), with m.p. 276.degree.-278.degree. C. (decomposition).
EXAMPLE 116
.alpha.-(1-Benzyl-1,2-dihydro-6-nitro-2-oxo-quinol-4-yl)-propionic acid (352 mg.) was dissolved in a mixture of 2 N sodium hydroxide solution (0.5 ml.) and water (4.5 ml.). Palladium on charcoal catalyst (33% Pd) (0.2 g.) was then added and the resulting mixture was hydrogenated with shaking, at atmospheric pressure and at 20.degree. C. during 3 hours. The catalyst was separated by filtration of the mixture through kieselguhr and the filtrate was acidified to pH 4 using glacial acetic acid. The resultant precipitate was collected by filtration and recrystallised from ethyl acetate. There was thus obtained .alpha.-(1-benzyl-1,2-dihydro-6-amino-2-oxo-quinol-4-yl)propionic acid in 50% yield, m.p. 140.degree.-2.degree. C. (decomposition).
EXAMPLE 117
A solution of methyl .alpha.-(1-benzyl-1,2-dihydro-2-oxo-quinol-4-yl)propionate (250 mg.) in methanol (3 ml.) was mixed with a solution containing an excess of 9 molar equivalents of hydroxylamine in methanol (3 ml.) and the mixture was left at 20.degree. C. for 18 hours. The mixture was then poured into water (5 ml.) and neutral material (largely unreacted methyl ester) was removed by extraction with ethyl acetate (3.times.5 ml.). The aqueous phase was separated and acidified to pH 1 by addition of hydrochloric acid. The resultant precipitate was recrystallised from ethanol to give N-[.alpha.-(1-benzyl-1,2-dihydro-2-oxo-quinol-4-yl)propionyl]hydroxamic acid in 40% yield, m.p. 211.degree.-3.degree. C. (decomposition).
EXAMPLES 118-122
The following compounds of formula I (wherein R.sup.3 is a hydroxy radical) were prepared in yields of 27-65%, in a similar manner to that used in Example 1, but from the appropriate starting materials:
__________________________________________________________________________ Substituent m.p. .degree.C. Recrystallisa-Example A R.sup.1 R.sup.2 on ring X Ring Y (decomposition) tion Solvent__________________________________________________________________________118 CH.sub.2 CH.sub.2 H H -- Ph 196-7 MeOH119 (direct) H H 7-MeO Ph 205-7 EtOH bond)120 CH.sub.2 Me H 6-ME 3,4-Cl.sub.2 -Ph 261-2 MeOH/D.M.F. (2:1 v/v)121 CH.sub.2 Me H -- 3,4-Me.sub.2 -Ph 204-5 EtOH122 CH.sub.2 Me H 6-Cl 3,4-Cl.sub.2 -Ph 229-231 EtOH__________________________________________________________________________
The 1-benzyl-1,2-dihydro-4-methyl-2-oxo-quinolines of formula III (wherein R.sup.2 is hydrogen), required as starting materials for the above Examples, were obtained as described hereinbefore and had the following melting points:
______________________________________ Substituent on Substituent onA R.sup.1 ring X phenyl ring Y m.p..degree.C.______________________________________CH.sub.2 CH.sub.2 H -- -- 127-8--(direct bond) H 7-MeO -- 122CH.sub.2 Me 6-Me 3,4-Cl.sub.2 138-9CH.sub.2 Me -- 3,4-Me.sub.2 107-8CH.sub.2 Me 6-Cl 3,4-Cl.sub.2 154-6______________________________________
EXAMPLES 123-127
The following compounds of formula XVIII were obtained in a similar manner to that described in Example 57 but from methyl iodide and the appropriately substituted 1-benzyl-1,2-dihydro-4-methyl-2-oxoquinolines, in yields of 20-62%:
__________________________________________________________________________ Substituent Substituent m.p. .degree.C. RecrystallisationExample A R.sup.2 on ring X on ring Y (decomposition) solvent__________________________________________________________________________123 CH.sub.2 Me -- 2-Me 248 EtOH124 CH.sub.2 Me 7-Me -- 207-8 EtOH125 CH.sub.2 Me 7-Me 4-Cl 175-7 EtOH126 CH.sub.2 CH.sub.2 Me 6-Me -- 185 EtOH127 CH.sub.2 Me 6,7-Me.sub.2 3,4-Cl.sub.2 201 EtOH__________________________________________________________________________
The corresponding, new substituted 1-benzyl-1,2-dihydro-4-methyl-2-oxo-quinolines of formula III (wherein R.sup.1 and R.sup.2 are hydrogen), used as starting materials in the above Examples were obtained as described hereinbefore and had the following melting points:
______________________________________ Recrystal- Substituent Substituent lisation m.p.A on ring X phenyl ring Y Solvent .degree.C.______________________________________CH.sub.2 -- 2-Me Ethanol 172-4CH.sub.2 7-Me -- Cyclohexane 152CH.sub.2 7-Me 4-Cl " 154CH.sub.2 CH.sub.2 6-Me -- " 110-2______________________________________
EXAMPLE 128
1-(4-Nitrobenzyl)-1,2-dihydro-2-oxoquinol-4-ylacetonitrile (0.5 g.) was added to a solution of sodium hydroxide (0.2 g.) in ethanol (50 ml.) and the mixture was heated under reflux for 5 hours. The ethanol was evaporated under reduced pressure and the residue was treated with 2 N hydrochloric acid (100 ml.). The precipitate thus formed was separated off and recrystallised from ethanol to give 1-(4-nitrobenzyl)-1,2-dihydro-2-oxoquinol-4-ylacetic acid (0.42 g.) m.p. 208.degree.-210.degree. C., (decomposition).
The starting material was obtained as follows:
Ethyl 1-(4-nitrobenzyl)-1,2-dihydro-2-oxoquinol-4-yl-pyruvate (19 g.; obtained by the method described for the starting material in Example 73) and hydroxylamine hydrochloride (13.6 g.) were added to a mixture of pyridine (150 ml.) and ethanol (150 ml.). The resulting solution was heated under reflux for 3 hours and the solvents were then evaporated under reduced pressure. The residue was triturated with water (65 ml.) and the solid filtered off. Trituration of this solid with ethanol (100 ml.) and filtration gave ethyl 3-[1-(4-nitrobenzyl)-1,2-dihydro-2-oxoquinol-4-yl]-2-oximinopyruvate (18.7 g.) m.p. 267.degree. C. (decomposition) which was sufficiently pure for use in the next stage of the reaction.
Ethyl 3-[1-(4-nitrobenzyl)-1,2-dihydro-2-oxoquinol-4-yl]-2-oximino-pyruvate (8.7 g.) was dissolved in a solution of sodium hydroxide (2.6 g.) in aqueous methanol [100 ml., MeOH:H.sub.2 O(2:1 v/v)] and the mixture was heated under reflux for 1.5 hours. The cooled solution was acidified to pH 3 with glacial acetic acid. The precipitate was filtered off, washed with water and dried in vacuo over phosphorus pentoxide. This dried solid (5.8 g.) was suspended in acetic anhydride (50 ml.) and the mixture was heated on a steam bath until gas evolution ceased and all the solid had dissolved. The solution was cooled to 0.degree. C. and the solid was separated by filtration. A further crop of product was obtained by evaporating the filtrate to dryness and triturating the residue with ethanol. The combined solids were recrystallised from methanol to give 1-(4-nitrobenzyl)-1,2-dihydro-2-oxoquinol-4-ylacetonitrile (2.9 g.), m.p. 190-93.
EXAMPLE 129
In a similar manner to that described in Example 88 there was obtained in 30% yield .alpha.-[6-methyl-1-(4-trifluoromethylbenzyl)-1,2-dihydro-2-oxoquinol-4-yl]propionic acid, m.p. 201.degree.-3.degree. C. (decomposition) (after recrystallisation from ethyl acetate), from .alpha.-(6-methyl-1,2-dihydro-2-oxoquinol-4-yl)propionic acid, m.p. 197.degree. C. (decomposition), which was itself obtained in a similar manner to that described for the starting material in Example 88, but starting from 4,6-dimethyl-1,2-dihydro-2-oxoquinolone.
EXAMPLE 130
1-(3,4-Dichlorobenzyl)-3-methyl-1,2-dihydro-2-oxoquinol-4-ylacetic acid (200 g.) is throughly mixed with lactose (400 g.) and 10% w/v gelatin solution (9 g.). The mixture is granulated and the granules are mixed with maize starch (35 g.) followed by magnesium stearate (6 g.). The mixture is then compressed into tablets containing 50, 100 or 250 mg. of active ingredient.
The 1-(3,4-dichlorobenzyl)-3-methyl-1,2-dihydro-2-oxoquinol-4-ylacetic acid active ingredient may be replaced by a salt thereof or any one of the compounds of formula I described in any of the Examples 1-129.
EXAMPLES 131-135
Using an analogous procedure to that described in Example 57, there were obtained in 20-45% yields, from the corresponding 1-substituted-4-methyl-2-oxo-quinolines of formula III, the following quinoline 4-alkanoic acids of formula I wherein R.sup.1 is hydrogen and R.sup.3 is a hydroxy radical:
__________________________________________________________________________ m.p. Substituent(s) Recrystallisation (.degree.C.)Example on ring X AY.circle. R.sup.2 solvent (decomposition)__________________________________________________________________________131 6-F ##STR21## H MeOH 205-207132 -- ##STR22## H MeOH 190-192133 6,7-Me.sub.2 ##STR23## Me EtOH 191-192134 6-Me ##STR24## Me EtOH 177-179135 -- ##STR25## Me EtOH 181-183__________________________________________________________________________
The necessary starting materials of formula III, wherein R.sup.1 is hydrogen, were obtained in a similar manner to that described for the preparation of 1-o-chlorobenzyl-4-methyl-6-methoxy-2-oxo-1,2-dihydroquinoline in Example 74, and had the following properties:
__________________________________________________________________________Substituent(s) Recrystallisation m.p.on ring X AY.circle. R.sup.2 solvent(s) (.degree.C.)__________________________________________________________________________6-F ##STR26## H EtoAc-petrol 182-184-- ##STR27## H cyclohexane 1086,7-Me.sub.2 ##STR28## Me EtoAc-petrol 164-1666-Me ##STR29## Me EtOH 106-108-- ##STR30## Me EtOH 104-106__________________________________________________________________________
EXAMPLES 136-140
In a similar manner to that described in Example 88, there were obtained in 21-55% yields from the appropriate .alpha.(1,2-dihydro-2-oxo-quinol-4-yl)propionic acids of formula VII, wherein M and R.sup.1 are hydrogen, R.sup.2 is a methyl radical and R.sup.3 is a hydroxyl radical, the following quinoline 4-propionic acids of formula XVIII wherein, R.sup.2 is a methyl radical and A is a methylene radical:
__________________________________________________________________________ Substituent(s) m.p. Substituent(s) on phenyl ring Recrystallisation (.degree.C.)Example on ring X Y solvents (decomposition)__________________________________________________________________________136 6-Me 4-CF.sub.3 EtOH-EtOAc 201-203137 -- 4-SMe EtoAc 169-170138 -- 4-Cl EtOH 180-181139 7-Me 4-Me EtOH 185-186140 7-Me 4-CF.sub.3 EtOH 191-192__________________________________________________________________________
The starting propionic acids of formula VII as defined above are described in Example 88 and 129. The additional starting material, .alpha.-(7-methyl-1,2-dihydro-2-oxoquinol-4-yl)propionic acid, was obtained, as a solid, m.p. 209.degree.-210.degree. C., in a similar manner to that described in Example 88, from 4,7-dimethyl-1,2-dihydro-2-oxoquinoline, m.p. 225.degree.-226.degree. C.
EXAMPLES 141-147
In a similar manner to that described in Example 109, there were obtained in yields of 45-65%, from the appropriate starting materials of formula XI, the following quinoline
4-alkanoic acids of formula I, wherein in both formula XI and I, ring X is unsubstituted, R.sup.2 is hydrogen, R.sup.3 is a hydroxy radical and A is a methylene radical:
______________________________________ m.p. (.degree.C.)Ex- Recrystallisation (decom-ample R.sup.1 Ring Y solvent(s) position)______________________________________141 Me ##STR31## EtoAc 165-167142 Me ##STR32## EtOH 198-200143 Me ##STR33## MeOH 190144 Me ##STR34## i-PrOH:petrol 208-210145 Me ##STR35## EtOH 213146 Me ##STR36## EtOH 209147 i-Pr ##STR37## DMF:MeOH 251-253______________________________________
The required starting materials of formula XI as defined above were obtained in an analogous manner to that described in 109, and had the following properties:
______________________________________ m.p. Recrystallisation (.degree.C.)R.sup.1 Ring Y solvent(s) (decomposition)______________________________________Me ##STR38## Toluene 101-103Me ##STR39## EtOH:Et.sub.2 O 191-194 (hydrochloride)Me ##STR40## EtOAc 130Me ##STR41## EtoAc 194-196Me ##STR42## EtoAc 115Me ##STR43## EtOH 228i-Pr ##STR44## EtoAc 165______________________________________
EXAMPLE 148-149
Using a similar procedure to that described in Example 92, there were obtained, from the appropriate quinoline 4-alkanoic acid of formula XVIII, the following esters in yields of 68-79%:
n-propyl .alpha.-[1-(4-chlorobenzyl)-6-methyl-1,2-dihydro-2-oxoquinol-4-yl]propionate, (Example 148), m.p. 116.degree.-117.degree. C., and ethyl .alpha.-[1-(4-methylbenzyl)-6-methyl-1,2-dihydro-2-oxoquinol-4-yl]propionate, (Example 149), m.p. 92.degree.-93.degree. C.
EXAMPLE 150
Thionyl chloride (0.109 ml.) was added by syringe to a suspension of .alpha.-[1-(4-methylbenzyl)-6-methyl-1,2-dihydro-2-oxoquinol-4-yl]propionic acid (0.335 g.) in toluene (3.5 ml.) (dried over sodium wire). The mixture was heated under reflux until evolution of gas ceased, and was then evaporated in vacuo. The residue was mixed with further dry toluene (5 ml.) and then evaporated in vacuo, and dried at ambient temperature under high vacuum, to give .alpha.-[1-(4-methylbenzyl)-6-methyl-1,2-dihydro-2-oxoquinol-4-yl]propionyl chloride, which was dissolved without purification in dry toluene (2.5 ml.). The solution thus obtained was added by syringe to a solution of phenol (0.052 g.) in pyridine (0.044 ml.). The mixture was then stirred at ambient temperature for 45 minutes and then at 80.degree. C. for 30 minutes. After being left at ambient temperature overnight, the reaction solution was mixed with ethyl acetate (20 ml.). The solution was then washed successively with 2 N-hydrochloric acid (20 ml.), water (20 ml.), 2 N-sodium hydroxide solution (2.times.20 l ml.), water (20 ml.) and then saturated sodium chloride solution (20 ml.). The organic phase was separated, dried (MgSO.sub.4) and evaporated in vacuo. The residue was recrystallised from cyclohexane to give phenyl .alpha.-[1-(4-methylbenzyl)-6-methyl-1,2-dihydro-2-oxoquinol-4-yl]propionate, m.p. 111.degree.-113.degree. C., in 58% yield.
EXAMPLES 151-160
In a similar manner to that described in Example 150, there were obtained from the corresponding quinoline 4-alkanoic acids, the following esters of formula I, wherein A is a methylene radical, in yields of 55-80%:
__________________________________________________________________________ Substituent(s) Substituent on phenyl m.p.Example R.sup.1 R.sup.2 R.sup.3 on ring X radical Y (.degree.C.)__________________________________________________________________________151 Me H OPh -- 3,4-Cl.sub.2 174-175152 Me H OCHMe.sub.2 -- 3,4-Cl.sub.2 139-140153 Me H OMe -- 3,4-Cl.sub.2 152-153154 H H OEt 6-F 3,4-Cl.sub.2 154-155155 H H OEt -- 2-Cl, 4-F 167-168156 H H OEt -- 2-F, 4-Cl 156-157157 H Me OEt 6-Me 4-Me 92-93158 H Me OPr-n 6-Me 4-Cl 116-117159 H Me OMe -- -- 90-92__________________________________________________________________________
Methyl 1-(pyrid-2-ylmethyl)-3-methyl-1,2-dihydro-2-oxoquinol-4-ylacetate, (Example 160), m.p. 156.degree.-157.degree. C., was obtained in 75% yield by a similar esterification of the corresponding acetic acid.
EXAMPLE 161
A solution of ethyl .alpha.-[1-(4-methylbenzyl)-6-methyl-1,2-dihydro-2-oxoquinol-4-yl]propionate (0.1 g.) in ethanol (2.0 ml.), containing potassium hydroxide (0.07 g.) and water (0.2 ml.), was heated under reflux for 2 hours. The ethanol was then removed in vacuo and the residue was dissolved in water (10 ml.). The solution obtained was acidified, by addition of 5 N-hydrochloric acid, to give a creamy solid, which was separated by filtration, washed with water and air dried to give .alpha.-[1-(4-methylbenzyl)-6-methyl-1,2-dihydro-2-oxoquinol-4-yl]propionic acid, 0.08 g., m.p. 188.degree.-190.degree. C., (m.p. 193.degree.-194.degree. C., after recrystallisation from ethanol).
In a similar manner, the following quinoline 4-alkanoic acids of formula I wherein R.sup.3 is a hydroxy radical and A is a methylene radical, were obtained in 70-85% yields by analogous hydrolysis of the corresponding esters:
__________________________________________________________________________Quinoline 4-alkanoic acid obtained Substituent Recrystallisation m.p.* EsterR.sup.1 R.sup.2 on ring X Y.circle. solvent(s) (.degree.C.) hydrolysed__________________________________________________________________________H Me 6-Me ##STR45## EtOH 188-190 PhenylH Me 6-Me ##STR46## EtOH 204-206 n-PropylH Me -- ##STR47## EtOH 178-180 MethylH H -- ##STR48## Not recrystallised 196-197 EthylH H -- ##STR49## MeOH 199-200 EthylMe H -- ##STR50## MeOH 217-218 i-Propyl or MethylH H 6-F ##STR51## MeOH 196-197 EthylMe H -- ##STR52## EtOH:Et.sub.2 O 191-194** Methyl__________________________________________________________________________ *decomposition **isolated as hydrochloride
EXAMPLE 162
In a similar manner to that described in Example 117, there was obtained from methyl 1-(3,4-dichlorobenzyl)-3-methyl-1,2-dihydro-2-oxoquinol-4-ylacetate, N-[1-(3,4-dichlorobenzyl)-3-methyl-1,2-dihydro-2-oxoquinol-4-ylacetyl]hydroxamic acid in 45% yield, m.p. 229.degree.-230.degree. C. (decomposition), after recrystallisation from methanol.
EXAMPLES 163-164
In a similar manner to that described in Example 92, except that dry hydrogen chloride was used instead of sulphuric acid, the following esters were obtained in yields of 70-85% from the corresponding acids:
(Example 163): ethyl 1-(3,4-dichlorobenzyl)-6-fluoro, 1,2-dihydro-2-oxoquinol-4-ylacetate, m.p. 153.degree.-154.degree. C., (recrystallised from ethanol);
(Example 164): methyl 1-(pyrid-2-ylmethyl)-3-methyl-1,2-dihydro-2-oxoquinol-4-ylacetate, m.p. 156.degree.-157.degree. C., [recrystallised from ethyl acetate and petrol (b.p. 60.degree.-80.degree. C.)].
EXAMPLE 165
An aqueous solution (1.63 ml.) of 1 M-sodium hydrogen carbonate was added to a stirred suspension of powdered .alpha.-(1-benzyl-1,2-dihydro-2-oxoquinol-4-yl)propionic acid (0.50 g.) in distilled water (3.37 ml.), and the mixture was stirred overnight, at ambient temperature. The solid which had formed was separated and dried in vacuo over phosphorus pentoxide to give sodium .alpha.-(1-benzyl-1,2-dihydro-2-oxoquinol-4-yl)-propionate (0.52 g.) as its monohydrate (m.p., indefinite;
C.sub.19 H.sub.16 NO.sub.3.H.sub.2 O requires: C, 65.5; H, 4.9; N, 3.8; found: C, 65.7; H, 5.2; N, 4.0).
EXAMPLE 166
Triethanolamine (0.243 g.) was added to a stirred suspension of finely powdered .alpha.-(1-benzyl-1,2-dihydro-2-oxoquinol-4-yl)propionic acid (0.50 g.) in distilled water (5.0 ml.), and the mixture was stirred overnight at ambient temperature. The solid which had formed was separated and dried in vacuo over phosphorus pentoxide to give triethanolamine .alpha.-(1-benzyl-1,2-dihydro-2-oxoquinol-4-yl)propionate (0.7 g.), m.p. 163.degree.-165.degree. C. (decomposition).
EXAMPLE 167
A solution of diethyl .alpha.-(1-benzyl-1,2-dihydro-2-oxoquinol-4-yl)-.alpha.-methylmalonate (3.0 g.) in ethanol (20 ml.) containing sodium hydroxide (3.0 g.) and water (3.0 ml.) was heated under reflux for 1 hour. The solution was then cooled and poured into water (200 ml.). The resultant solution was acidified to pH 3 by addition of concentrated hydrochloric acid to give .alpha.-(1-benzyl-1,2-dihydro-2-oxoquinol-4-yl)propionic acid 1.5 g., m.p. 179.degree.-180.degree. C.
The starting malonate was obtained as follows:
4-Methylquinol-2-one (24.0 g.) was added in portions to a stirred suspension of sodium hydride [6.5 g.; weighed as a 60% w/w dispersion in oil, but subsequently washed by decantation with petroleum ether (b.p. 40.degree.-60.degree. C.)] in dimethylformamide (150 ml.), at 20.degree.-25.degree. C. After the addition was complete the mixture was stirred at 20.degree.-25.degree. C. for a further 1 hour. Benzyl chloride (23.0 g.) was then added and the subsequent mixture was heated at 95.degree.-100.degree. C. for 20 hours. The mixture, which contained some solid, was then added to water (1 liter) and the resultant mixture was stirred for 1 hour. The solid which formed was separated by filtration, washed with water, and then was resuspended in a mixture of water (300 ml.) and 2 N hydrochloric acid (50 ml.). This mixture was stirred for 15 minutes and then the solid separated by filtration to give 1-benzyl-4-methylquinol-2-one, as a white crystalline solid, 20.0 g., m.p. 109.degree.-111.degree. C. after recrystallisation from cyclohexane.
1-Benzyl-4-methylquinol-2-one (5.0 g.) was added to a suspension of sodium hydride (4.8 g.; 60% w/w dispersion in oil, washed as described above) in diethyl carbonate (100 ml.). The mixture was then stirred and heated under reflux for 3 hours. A small quantity of methanol was added to the cooled suspension to destroy any remaining sodium hydride and the mixture was then poured into ether (300 ml.) to give a pale yellow precipitate which was collected by filtration and washed well with ether. This solid (8.6 g.) was suspended in dimethylformamide (70 ml.) and methyl iodide (16.8 g.) was added. The mixture was stirred at 20.degree.-25.degree. C. for 24 hours and then added to water (250 ml.) to give an oil which was extracted with ether. The extracts were washed with water, dried over magnesium sulphate, and then evaporated to give diethyl .alpha.-(1-benzyl-2-oxoquinol-4-yl)-.alpha.-methylmalonate as a crystalline solid, 3.0 g., m.p. 130.degree.-131.degree. C. after recrystallisation from cyclohexane.

Number	Date	Country	Kind
11644/75	Mar 1975	GBX
4204375	Oct 1975	GBX

1,2-Dihydro-2-oxoquinol-4-ylacetic acid derivatives and pharmaceutical compositions

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