Benzopyran compound and its pharmaceutical use

Information

  • Patent Grant
  • 5143936
  • Patent Number
    5,143,936
  • Date Filed
    Thursday, March 21, 1991
    33 years ago
  • Date Issued
    Tuesday, September 1, 1992
    32 years ago
Abstract
A benzopyran compound of the general formula (I) ##STR1## wherein A represents --OR.sup.1 or --NH--COR.sup.2 (wherein R.sup.1 represents hydrogen, a lower alkyl, formyl, an alkanoyl, an aroyl or an aralkyl and R.sup.2 represents hydrogen, a lower alkyl, a lower alkoxy, amino, mono- or di-lower alkylamino, an amino-lower alkyl, a hydroxy-lower alkyl, a halo-lower alkyl, a lower alkoxy-lower alkyl, an acyloxy-lower alkyl, a lower alkoxycarbonyl-lower alkyl, an aryl or a heteroaryl); R.sup.3 represents hydrogen, a lower alkyl, a lower alkoxy, amino, a mono- or di-lower alkylamino, an amino-lower alkyl, a hydroxy-lower alkyl, a halo-lower alkyl, a lower alkoxy-lower alkyl, an acyloxy-lower alkyl, a lower alkoxycarbonyl-lower alkyl, an aryl or a heteroaryl, or R.sup.2 and R.sup.3 combinedly together form an alkylene having 1 to 2 carbon atoms; R.sup.4 and R.sup.5 are the same or different, and respectively represent hydrogen or a lower alkyl, or combinedly together form an alkylene having 2 to 5 carbon atoms; R.sup.6 represents hydroxyl group, formyloxy, an alkanoyloxy, a haloalkanoyloxy, a lower alkoxycarbonyloxy, an aroyloxy, a heteroaroyloxy, carbamoyloxy, a mono- or di-lower alkycarbamoyloxy and R.sup.7 represents hydrogen, or R.sup.6 and R.sup.7 combinedly together form a bond and X and Y are the same or different, and respectively represent hydrogen, halogen, nitro, cyano, a lower alkyl, a lower alkoxy, a halo-lower alkyl, carboxyl, formyl, an alkanoyl, an aroyl, a halo-alkanoyl, carbamoyl, a lower alkylsulfinyl, an arylsulfinyl, a lower alkylsulfonyl, an arylsulfonyl, sulfonamido or a mono- or di-lower alkylsulfonamido, or their pharmaceutically acceptable salts and its pharmaceutical use.The compounds of the present invention exhibit remarkable and long lasting antihypertensive actions and peripheral vascular relaxant actions and therefore are useful as therapeutic medicines for hypertensive. Since they also display selective coronary vasodilating actions and the duration of actions are very long, they are of use as therapeutic medicines for cardiovascular disturbances such as angina pectoris and cardiac insufficiency.
Description
Claims
  • 1. A benzopyran compound of the formula (I) ##STR8## wherein A represents --OR.sup.1 (wherein R.sup.1 represents hydrogen, formyl, an alkanoyl, benzoyl, naphthoyl, phenylakyl or naphthylalkyl having, as the alkyl moieties, straight- or branched-chain alkyls having 1 to 4 carbon atoms, or a phenylalkyl or a naphthylalkyl each substituted on the aromatic ring by at least one of halogen, lower alkyl, lower alkoxy, hydroxyl, trifluoromethyl, cyano, nitro and amino); R.sup.3 represents hydrogen, a lower alkyl, a lower alkoxy, amino, a mono- or di-lower alkylamino, an amino-lower alkyl, a hydroxy-lower alkyl, a halo-lower alkyl, a lower alkoxy-lower alkyl, a lower alkoxycarbonyl-lower alkyl, phenyl, naphthyl, or phenyl or naphthyl each substituted on the aromatic ring by at least one of halogen, lower alkyl, lower alkoxy, hydroxyl, trifluoromethyl, cyano, nitro and amino; R.sup.4 and R.sup.5 are the same or different, and respectively represent hydrogen or a lower alkyl, or taken together form an alkylene having 2 to 5 carbon atoms; R.sup.6 represents hydroxyl, formyloxy, an alkanoyloxy, a haloalkanoyloxy, a lower alkoxycarbonyloxy, benzoyloxy, naphthoyloxy, 2-furoyloxy, 3-furoyloxy, nicotinoyloxy, 4-pyridylcarbonyloxy, 2-thenoyloxy, 3-thenoyloxy, carbamoyloxy, a mono- or di-lower alkylcarbamoyloxy and R.sup.7 represents hydrogen, or R.sup.6 and R.sup.7 taken together form a bond and X and Y are the same or different, and respectively represent hydrogen, halogen, nitro, cyano, a lower alkyl, a lower alkoxy, a halo-lower alkyl, carboxyl, formyl, an alkanoyl, benzoyl, naphthoyl, a halo-alkanoyl, carbamoyl, a lower alkylsulfinyl, phenylsulfinyl, naphthylsulfinyl, or phenylsulfinyl or naphthylsulfinyl each substituted on the aromatic ring by at least one of halogen, lower alkyl, lower alkoxy, hydroxyl, trifluoromethyl, cyano, nitro and amino, a lower alkylsulfony, phenylsulfonyl, naphthylsulfonyl, or phenylsulfonyl or naphthysulfonyl each substituted on the aromatic ring by at least one of halogen, lower alkyl, lower alkoxy, hydroxyl, trifluoromethyl, cyano, nitro and amino, sulfonamido or a mono- or di-lower alkyl sulfonamido, or a pharmaceutically acceptable salt thereof.
  • 2. The benzopyran compound as claimed in claim 1 which is selected from the group consisting of trans-4-(N-acetyl-N-benzyloxy)amino-6-cyano-3,4-dihydro-2,2-dimethyl-2H-1-benzopyran-3-ol, trans-4-(N-acetyl-N-hydroxy)amino-6-cyano-3,4-dihydro-2,2-dimethyl-2H-1-benzopyran-3-ol, (-)-(3S,4R)-trans-4-(N-acetyl-N-hydroxy)amino-6-cyano-3,4-dihydro-2,2-dimethyl-2H-1-benzopyran-3-ol, or a pharmaceutically acceptable salt thereof.
  • 3. A pharmaceutical composition which contains, as the effective ingredient, the compound as claimed in claim 1.
  • 4. The benzopyran compound as claimed in claim 1 which is (+)-(3S,4R)-trans-4-(N-acetyl-N-benzyloxy)amino-6-cyano-3,4-dihydro-2,2-dimethyl-2H-1-benzopyran-3-ol or a pharmaceutically acceptable salt thereof.
  • 5. The benzopyran compound as claimed in claim 1 which is (-)-(3S,4R)-trans-4-(N-acetyl-N-hydroxy)amino-6-cyano-3,4-dihydro-2,2-dimethyl-2H-1-benzopyran-3-ol or a pharmaceutically acceptable salt thereof.
Priority Claims (3)
Number Date Country Kind
63-103222 Apr 1988 JPX
63-278142 Nov 1988 JPX
63-299190 Nov 1988 JPX
BACKGROUND ART

This is a Rule 60 Divisional of U.S. Ser. No. 07,340,271 filed Apr. 19, 1989, now U.S. Pat. No. 5,021,432. This invention relates to novel benzopyran compounds and their pharmaceutically acceptable salts which possess remarkable and durable antihypertensive actions, coronary vasodilating actions and relaxant actions on vascular smooth muscles and the other smooth muscles and pharmaceutical uses thereof. In U.S. Pat. No. 4,446,113, there is disclosed 6-cyano-3,4-dihydro-2,2-dimethyl-trans-4 (2-oxo-1-pyrrolidinyl)-2H-1-benzopyran-3-ol(BRL-34915). In European Patent Publication (Laid-open) Gazzette No. 273262/1988, British Patent Publication Gazzette No. 2204868/1988 and European Patent Publication (Laid-open) Gazzette No. 296975/1988, there are disclosed a group of 4-substituted benzopyran compounds having antihypertensive actions, smooth muscle-relaxant actions and the like. It was found that novel benzopyran compounds having a N-acyl-N-oxy-substituted amino group or hydrazine group at the 4-position possessed remarkable and durable hypotensive actions and coronary vasodilating actions, and also vascular smooth muscles- and the other smooth muscle-relaxant actions, which resulted in the accomplishment of the present invention. This invention relates to the benzopyran compounds of the general formula (I) ##STR2## wherein A represents --OR.sup.1 or --NH--COR.sup.2 (wherein R.sup.1 represents hydrogen, a lower alky, formyl, an alkanoyl, an aroyl or an aralkyl and R.sup.2 represents hydrogen, a lower alkyl, a lower alkoxy, amino, mono- or di-lower alkylamino, an amino-lower alkyl, a hydroxy-lower alkyl, a halo-lower alkyl, a lower alkoxy-lower alkyl, an acyloxy-lower alkyl, a lower alkoxy-carbonyl-lower alkyl, an aryl or a heteroaryl); R.sup.3 represents hydrogen, a lower alkyl, a lower alkoxy, amino, a mono- or di-lower alkylamino, an amino-lower alkyl, a hydroxy-lower alkyl, a halo-lower alkyl, a lower alkoxy lower alkyl, an acyloxy-lower alkyl, a lower alkoxycarbonyl-lower alkyl, an aryl or a heteroaryl, or R.sup.2 and R.sup.3 combinedly together form an alkylene having 1 to 2 carbon atoms; R.sup.4 and R.sup.5 are the same or different, and respectively represent hydrogen or a lower alkyl, or combinedly together form an alkylene having 2 to 5 carbon atoms; R.sup.6 represents hydroxyl group, formyloxy, an alkanoyloxy, a haloalkanoyloxy, a lower alkoxycarbonyloxy, an aroyloxy, a heteroaroyloxy, carbamoyloxy, a mono- or di-lower alkylcarbamoyloxy and R.sup.7 represents hydrogen, or R.sup.6 and R.sup.7 combinedly together form a bond and X and Y are the same or different, and respectively represent hydrogen, halogen, nitro, cyano, a lower alkyl, a lower alkoxy, a halo-lower alkyl, carboxyl, formyl, an alkanoyl, an aroly, a halo-alkanoyl, carbamoyl, a lower alkylsulfinyul, an arylsulfinyl, a lower alkylsulfonyl, an arylsulfonyl, sulfonamido or a mono- or di-lower alkylsulfonamido, or their pharmaceutically acceptable salts and their pharmaceutical use. In the above-mentioned definitions, halogens mean chlorine, bromine, fluorine and iodine; lower alkyls mean straight- or branched-chain alkyls having 1 to 6 carbon atoms, which are exemplified by methyl, ethyl, propyl, isopropyl, butyl, isobutyl, tert-butyl, pentyl, isopentyl, hexyl and the like; amino-lower alkyls mean straight- or branched-chain aminoalkyls having 1 to 6 carbon atoms, which are examplified by aminomethyl, 2-aminoethyl, 3-aminopropyl, 1-aminomethylethyl, 4-aminobutyl, 5-aminopentyl, 6-aminohexyl and the like; hydroxy-lower alkyls mean straight- or branched-chain hydroxyalkyl having 1 to 6 carbon atoms, which are exemplified by hydroxymethyl, 2-hydroxyethyl, 3-hydroxypropyl, 1-hydroxymethylethyl, 4-hydroxybutyl, 5-hydroxypentyl, 6-hydroxyhexyl and the like; halo-lower alkyls mean straight- or branched-chain halogenated alkyls having 1 to 4 carbon atoms, which are exemplified by chloromethyl, bromomethyl, fluoromethyl, iodomethyl, dichloromethyl, dibromomethyl, difluoromethyl, diiodomethyl, trifluoromethyl, chloroethyl, bromoethyl, fluoroethyl, iodoethyl, difluoroethyl, trifluoroethyl, chloropropyl, bromopropyl, fluoropropyl, iodopropyl, difluoropropyl, trifluoropropyl, chlorobutyl, bromobutyl, fluorobutyl, iodobutyl, difluorobutyl, trifluorobutyl and the like; lower alkoxys mean straight- or branched-chain alkoxys having 1 to 6 carbon atoms, which are exemplified by methoxy, ethoxy, propoxy, isopropoxy, butoxy, isobutoxy, tert-butoxy, pentyloxy, hexyloxy and the like; lower alkoxy-lower alkyls mean alkoxyalkyls having, as the alkoxy moieties and the alkyl moieties, respectively straight- or branched-chain ones having 1 to 4 carbon atoms, which are exemplified by methoxymethyl, 2-methoxyethyl, 3-methoxypropyl, 4-methoxybutyl, ethoxymethyl, propoxymethyl, butoxymethyl and the like; lower alkoxycarbonyl-lower alkyls mean alkoxycarbonylalkyls having, as the alkoxy moieties and the alkyl moieties, respectively straight- or branched-chain ones having 1 to 4 carbon atoms, which are exemplified by methoxycarbonylmethyl, 2-methoxycarbonylethyl, 3-methoxycarbonylpropyl, 4-methoxycarbonylbutyl, ethoxycarbonylmethyl, propoxycarbonylmethyl, butoxycarbonylmethyl, and the like; aralkyls mean aralkyls having, as the alkyl moieties, straight- or branched-chain alkyls having 1 to 4 carbon atoms, which are exemplified by benzyl, 2-phenylethyl, 3-phenylpropyl, 4 -phenylbutyl, naphthylmethyl, 2-naphthylethyl, 3-naphthylpropyl, 4-naphthylbutyl, and benzyls, 2-phenylethyls, 3-phenylpropyls, 4-phenylbutyls, naphthylmethyls, 2-naphthylethyls, 3-naphthylpropyls and 4-naphthylbutyls each of which has on the aromatic ring at least one substituent selected from among halogens, lower alkyls, lower alkoxys, hydroxyl group, trifluoromethyl, cyano, nitro, amino, and the like; aryls mean phenyl naphthyl, and phenyls and naphthyls each of which has on the aromatic ring at least one substituent selected from among halogens (chlorine, bromine, iodine, fluorine), lower alkyls, lower alkoxys (straight- or branched-chain alkoxys having 1 to 4 carbon atoms, exemplified by methoxy, ethoxy, propoxy, isopropoxy, butoxy, isobutoxy and tert-butoxy), hydroxyl group, trifluoromethyl, cyano, nitro and amino; heteroaryls include, for example, furyl (2-furyl, 3-furyl), pyridyl (2-pyridyl, 3-pyridyl, 4-pyridyl) and thienyl (2-thienyl, 3-thienyl), and furyls, pyridyls and thienyls each of which has on the heteroring at least one substituent selected from among halogens, lower alkyls, lower alkoxys, hydroxyl group, trifluoromethyl, cyano, nitro and amino; alkanoyls mean straight- or branched-chain alkyanoyls having 2 to 5 carbon atoms, optionally substituted by phenyl, which are exemplified by acetyl, propionyl, butyryl, valeryl, pivaloyl, phenylacetyl, phenylpropionyl, phenylbutyryl; aroyls mean benzoyl, naphthoyl and the like; mono- or di-lower alkylaminos mean mono- or dialkylaminos having, as the alkyl moieties, straight- or branched-chain alkyls having 1 to 6 carbon atoms, which are exemplified by methylamino, ethylamino, propylamino, isopropylamino, butylamino, isobutylamino, tert-butylamino, pentylamino, hexylamino, dimethylamino, diethylamino, dipropylamino, diisopropylamino, dibutylamino, diisobutylamino, di-tert-butylamino, dipentylamino, dihexylamino and the like; alkylenens having one to two carbon atoms include methylene, ethylene and the like and alkylenes having 2 to 5 carbon atoms include ethylene, trimethylene, propylene, tetramethylene, pentamethylene and the like; alkanoyloxies mean alkanoyloxies having, as the alkanoyl moieties, straight- or branched-chain alkanoyls having 2 to 5 carbon atoms optionally substitued by phenyl, which are exemplified by acetyloxy, propionyloxy, butyryloxy, valeryloxy, pivaloyloxy, phenylacetyloxy, phenylpropionyloxy, phenylbutyryloxy and the like; haloalkanoyloxies mean those having halogenated alkanoyls having, as the alkanoyl moieties, straight- or branched-chain alkanoyls having 2 to 5 carbon atoms, which are exemplified by chloroacetyloxy bromoacetyloxy, fluoroacetyloxy, iodoacetyloxy, dichloroacetyloxy, dibromoacetyloxy, difluoroacetyloxy, diiodoacetyloxy, trifluoroacetyloxy, chloropropionyloxy, bromopropionyloxy, fluoropropionyloxy, iodopropionyloxy, difluoropropionyloxy, trifluoropropionyloxy, chlorobutyryloxy, bromobutyryloxy, fluorobutyryloxy, iodobutyryloxy, difluorobutyryloxy, trifluorobutyryloxy, fluorovaleryloxy, fluoropivaloyloxy and the like; lower alkoxy carbonyloxys mean alkoxycarbonyloxys having, as the alkoxy moieties, straight- or branched-chain alkoxys having 1 to 6 carbon atoms, which are exemplified by methoxycarbonyloxy, ethoxycarbonyloxy, propoxycarbonyloxy, isopropoxycarbonyloxy, butoxycarbonyloxy, isobutoxycarbonyloxy, tert-butoxycarbonyloxy, pentyloxycarbonyloxy, hexyloxycarbonyloxy and the like; aroyloxys include benzoyloxy, naphthoyloxy and the like; heteroaroyloxys include 2-furoyloxy, 3-furoyloxy, nicotinoyloxy, 4-pyridylcarbonyloxy, 2-thenoyloxy, 3-thenoyloxy and the like; mono-or di-lower alkylcarbamoyloxys mean mono- or dialkylcarbamoyloxys having, as the alkyl moieties, straight- or branched-chain alkyls having 1 to 6 carbon atoms, which are exemplified by methylcarbamoyloxy, ethylcarbamoyloxy, propylcarbamoyloxy, isopropylcarbamoyloxy, butylcarbamoyloxy, isobutylcarbamoyloxy, tert-butylcarbamoyloxy, pentylcarbamoyloxy, hexylcarbamoyloxy, dimethylcarbamoyloxy, diethylcarbamoyloxy, dipropylcarbamoyloxy, diisopropylcarbamoyloxy, dibutylcarbamoyloxy, diisobutylcarbamoyloxy, di-tert-butylcarbamoyloxy, dipentylcarbamoyloxy, dihexylcarbamoyloxy and the like; lower alkylsulfinyls include alkylsulfinyls having, as the alkyl moieties, straight- or branched-chain alkyls having 1 to 6 carbon atoms, which are exemplified by methylsulfinyl, ethylsulfinyl, propylsulfinyl, isopropylsulfinyl, butylsulfinyl, isobutylsulfinyl, tert-butylsulfinyl, pentylsulfinyl, hexylsulfinyl and the like; arylsulfinyls include, for example, phenylsulfinyl, naphthylsulfinyl and phenylsulfinyls and naphthylsulfinyls each of which has on the aromatic ring at least one substituent selected from among halogens (chlorine, bromine, iodine, fluorine), lower alkyls, lower alkoxys, hydroxy group, trifluoromethyl, cyano, nitro, and amino; lower alkylsulfonyls include alkylsulfonyls having, as the alkyl moieties, straight- or branched-chain alkyls having 1 to 6 carbon atoms, which are exemplified by methylsulfonyl, ethylsulfonyl, propionylsulfonyl, isopropylsulfonyl, butylsulfonyl, isobutylsulfonyl, tert-butylsulfonyl, pentylsulfonyl, hexylsulfonyl and the like; arylsulfonyls include, for example, phenylsulfonyl, naphthylsulfonyl and phenylsulfonyls and naphthylsulfonyls each of which has on the aromatic ring at least one substituent selected from among halogens (chlorine, bromine, iodine, fluorine), lower alkyls, lower alkoxys, hydroxyl group, trifluoromethyl, cyano, nitro and amino and mono- or di-lower alkylsulfonamidos mean mono- or di-alkylsulfonamidos having, as the alkyl moieties, straight- or branched-chain alkyls having 1 to 6 carbon atoms, which are exemplified by methylsulfonamido, ethylsulfonamido, propylsulfonamido, isopropylsulfonamido, butylsulfonamido, isobutylsulfonamido, tert-butylsulfonamido, pentylsulfonamido, hexylsulfonamido, dimethylsulfonamido, diethylsulfonamido, dipropylsulfonamido, diisopropylsulfonamido, dibutylsulfonamido, diisobutylsulfonamido, di-tert-butylsulfonamido, dipentylsulfonamido, dihexylsulfonamido and the like. The compounds of the present invention can be prepared by, for example, the per se known methods. The compound of the formula (I) wherein A is --OR.sup.1 can be prepared by the following method. ##STR3## [in the above reaction formulae, R.sup.1 represents a protective group for hydroxyl group (lower alkyls, lower alkoxy-lower alkyls, benzyl, substituted benzyls, diphenylmethyl, trityl, and the like) and the other symbols are as defined above.] The reaction of process 1 is usually conducted at 10.degree.-100.degree. C. in a solvent such as an alcohol having 1 to 4 carbon atoms, particularly methanol, ethanol, propanol and the like. The reaction proceeds particularly smoothly when conducted under reflux in said solvent. In the reaction of process 2, in the case where the compound of the general formula (III) is a free carboxylic acid, the reaction is conducted under cooling, at room temperature or under heating in an inert solvent in the presence of a condensing agent such as dicyclohexylcarbodiimide, titanium tetrachloride, a phosphorus halogenide (phosphorus trichloride, phosphorus oxychloride etc.), diethylchlcrophosphite, o-phenylenechlorophosphite, ethyldichlorophosphite and the like. The reaction can be carried out by allowing a phosphorus halogenide in advance to act on the compound (II) in an inert solvent, followed by the condensation reaction with the compound (III). For example, in the case where the phosphorus halogenide is phosphorus trichloride, about 1/2 mol phosphorus trichloride is allowed to act on the compound (II) in an inert solvent in the presence of a tertiary base such as triethylamine, pyridine, N,N-dimethylaniline or the like under cooling or at room temperature, followed by the reaction with the compound (III) in an inert solvent at room temperature or under heating, preferably while heating under reflux. In the case where an acid halide such as an acid chloride, or an acid bromide, as a reactive derivative of the carboxylic acid of the compound (III), is used, the reaction can be conducted in an inert solvent in the presence of a tertiary base such as triethylamine, pyridine or N,N-dimethylaniline under cooling or at room temperature, or in water in the presence of an alkali such as sodium hydroxide or potassium hydroxide under cooling or at room temperature. In the case where a mixed acid anhydride such as an alkyl carbonate mixed acid anhydride, an alkyl phosphate mixed acid anhydride, an alkyl phosphite mixed acid anhydride or a mixed acid anhydride with sulfuric acid, as a reactive derivative of the compound (III), is used, the reaction can be conducted in an inert solvent in the presence of tertiary base such as triethylamine, pyridine or N,N-dimethylaniline under cooling, at room temperature or under heating. In the case where an active amide such as acid imidazolide, acid pyrrolidide or 2,4-dimethylpyrazolide, as a reactive derivative of the compound (III), is used, the reaction can be conducted in an inert solvent at room temperature or under heating. In the case where an active ester such as methyl ester, ethyl ester, p-nitrophenyl ester or p-chlorophenyl ester, as a reactive derivative of the compound (III), is used, the reaction can be conducted in an inert solvent at room temperature or while heating, preferably while heating under reflux. As the inert solvents, mention may be made of benzene, toluene, xylene, methanol, ethanol, isopropylalcohol, ethyl ether, dioxane, tetrahydrofuran, chloroform, dichloromethane, dichloroethane, hexamethylphosphoric triamide, diethylene glycol, dimethylformamide and the like or their mixed solvents. When the compound (III) is a reactive derivative, the solvent is appropriately selected depending upon the species of the reactive derivative. The deprotection of the protected hydroxyl group can be conducted by conducting hydrogenolysis under ordinary pressure with the use of palladium-carbon in a suitable solvent (ethanol, methanol, dimethylformamide, dioxane etc.), or by allowing hydrobromic acid-acetic acid, aluminium chloride, methionine-methanesulfonic acid, a lower alkyl disulfide-aluminium chloride or the like to act thereon. The reaction can be conducted in a suitable solvent (acetic acid, methylene chloride, chloroform, dichloroethane, methansulfonic acid etc.) at room temperature to under reflux of the solvent. The reaction usually proceeds for 1 to 24 hours. Further, the thus obtained compound of the formula (IV) is subjected, if necessary, to deprotection under appropriate conditions to give the corresponding compound (I) wherein R.sup.1 is hydrogen. The compound of the general formula (I) wherein R.sup.1 is a group as defined above other than hydrogen can be produced by reacting the compound of the formula (I) wherein R.sup.1 is hydrogen with the compound of the general formula. The reaction usually proceeds in an inert solvent (water, methanol, ethanol, dimethylformamide, or their mixed solvent, preferably aqueous ethanol) in the presence of a base (sodium hydroxide, potassium hydroxide, sodium hydride, potassium hydride, sodium methoxide, sodium ethoxide, sodium carbonate, potassium carbonate, metal sodium, triethylamine, pyridine etc.) at a temperature ranging from about 0.degree. C. to the boiling point of the used solvent, preferably at 20.degree.-80.degree. C., for about 10 minutes to 24 hours, preferably 30 minutes to 3 hours. The compound of the general formula (I), wherein A is --NH--COR.sup.2 can be prepared by the following method. ##STR4## (in the reaction formulae, R.sup.2' and R.sup.3' represent respectively a defined above other than an alkylene having 1 to 2 carbon atoms which is combinedly together formed thereby and other symbols are all as defined above.) This method is usable for the production of the compound of the general formula (I) wherein R.sup.2 and R.sup.3 are respectively a group as defined above other than an alkylene having 1 to 2 carbon atoms which is combinedly together formed thereby. The reaction of process 1 can be conducted in an alcohol such as methanol or ethanol, if necessary, in the presence of triethylamine, pyridine or the like at room temperature or while heating, preferably while heating under reflux. In the reaction of process 2, in the case where the compound of the general formula (IX) is a free carboxylic acid, the reaction can be conducted in an inert solvent in the presence of a condensing agent such as cyclohexylcarbodiimide, titanium tetrachloride, phosphorus halogenides (phosphorus trichloride, phosphorus oxychloride etc.), diethylchlorophosphite, o-phenylenechlorophosphite, ethyldichlorophosphite or the like under cooling, at room temperature or under heating. The reaction can be conducted by allowing a phosphorus halogenide in advance to act on the compound (VIII) in an inert solvent, followed by condensation with the compound (IX). For example, in the case where the phosphorus halogenide is phosphorus trichloride, about 1/2 mol phosphorus trichloride is in advance allowed to act on the compound (VIII) in an inert solvent in the presence of a tertiary base such as triethylamine, pyridine, N,N-dimethylaniline or the like under cooling or at room temperature, followed by the reaction with the compound (IX) at room temperature or while heating, preferably while heating under reflux. In the case where an acid halide such as acid chloride or acid bromide, as a reactive derivative of the carboxylic acid of the general formula (IX), is used, the reaction can be conducted in an inert solvent in the presence of a tetiary base such as triethylamine, pyridine, N,N-dimethylaniline or the like under cooling or at room temperature, or in water in the presence of an alkali such as sodium hydroxide or potassium hydroxide under cooling or at room temperature. In the case where an acid anhydride or a mixed acid anhydride such as an alkyl carbonate mixed acid anhydride, an alkyl phosphate mixed acid anhydride, an alkyl phosphite mixed acid anhydride, a mixed acid anhydride with sulfuric acid, as a reactive derivative of the compound (IX), is used, the reaction can be conducted in an inert solvent in the presence of a tertiary base such as triethylamine, pyridine, N,N-dimethylaniline or the like under cooling, at room temperature or under heating. In the case where an active amide such as acid imidazolide, acid pyrrolidide or 2,4-dimethylpyrazolide, as a reactive derivative of the compound (IX), is used, the reaction can be conducted in an inert solvent at room temperature or under heating. In the case where an active ester such as methyl ester, ethyl ester, p-nitrophenyl ester, p-chlorophenyl ester or the like, as a reactive derivative of the compound (IX), is used, the reaction can be conducted in an inert solvent at room temperature or while heating, preferably while heating under reflux. As the inert solvents to be used in the above-mentioned condensation reactions, mention may be made of benzene, toluene, xylene, methanol, ethanol, isopropyl alcohol, ethyl ether, dioxane, tetrahydrofuran, chloroform, dichloromethane, dichloroethane, hexamethylphosphoricamide, diethylene glycol, dimethylformamide and the like and their mixed solvents. When the compound (IX) is a reactive derivative, the solvent can be suitably selected depending upon the species of the reaction derivative. In general, preferably, the compound (IX) is an acid chloride, and the reaction is conducted in a solvent such as chloroform, methylenechloride or benzene in the presence of an organic base such as pyridine or triethylamine at 0.degree.-50.degree. C. In this case, the compound of the general formual (I) wherein R.sup.6 is a group as defined above other than hydroxyl group can be obtained by adjusting the amount ratio of the compound (IX) or the reactive derivative to be used and the reaction conditions. ##STR5## [in the above reaction formulae, R.sup.8 represents an amino-protective group (benzyloxycarbonyl), tert-butoxycarbonyl, formyl, trityl, tosyl, etc.) and the other symbols are as defined above.] This method is usable for the production of the compound of the general formula (I) wherein R.sup.2 and R.sup.3 are respectively a group as defined above other than an alkylene having 1 to 2 carbon atoms which is combinedly together formed thereby. The reaction of process 1 can be conducted under the same conditions as those of process 1 of Method 2 mentioned above and the reactions of process 2 and process 4 can be conducted under the same conditions as those of process 2 of Method 2 mentioned above. The deprotection reaction of process 3 can be conducted by conducting hydrogenolysis under ordinary pressure in ethanol or methanol with the use of palladium-carbon when R.sup.8 is benzyloxycarbonyl and by allowing trifluoroacetic acid, hydrochloric acid-ethyl acetate or the like to act thereon when R.sup.8 is a tert-butoxycarbonyl. ##STR6## (in the above reaction formulae, each of the symbols is as defined above.) This method is usable for the production of the compound of the general formula (I) wherein R.sup.2 and R.sup.3 are the same and as defined above except an alkylene which is combinedly together formed thereby. The N-amination reaction of process 1 can be conducted in water at 0.degree.-100.degree. C., preferably in the presence of a small amount of gelatin when chloramine as a N-amination reagent is used and in an aqueous solution of potassium hydroxide or sodium hydroxide at room temperature to 100.degree. C. when hydroxylamine-o-sulfonic acid as a N-amination reagent is used. In the method with cyclohexanespiro-3'-oxazilidine, in accordance with Synthesis pp. 529-533 (1988), N-amination reaction can be conducted by reacting in toluene at 80.degree.-90.degree. C. for 2-6 hours. The reaction of process 2 can be conducted under the same conditions as those of process 2 of Method 2 as mentioned above. ##STR7## (in the above reaction formulae, R.sup.9 represents a lower alkyl, n represents 1 or 2, and the other symbols are as defined above.) This method is usable for the production of the compound of the general formula (I) wherein R.sup.2 and R.sup.3 combinedly together form an alkylene having 1 to 2 carbon atoms. The reaction of process 1 can be conducted under the same conditions as those of process 2 of Method 2 as mentioned above and the reaction of process 2 can be conducted under the same conditions as those of process 3 of Method 3 as mentioned above. The cyclization reaction of process 3 can be conducted by eliminating the alcohol (R.sup.9 OH) at pH higher than neutral range, if necessary, in the presence of an organic base such as pyridine, triethylamine or the like in ethanol, toluene, benzene or xylene while heating under reflux for 1-30 hours. The compound of the general formula (I) wherein R.sup.6 and R.sup.7 combinedly together form a bond can be produced by treating the compound of the general formula (I) wherein R.sup.6 is hydroxyl group and R.sup.7 is hydrogen with a dehydrating agent (e.g. sulfuric acid, potassium sulfate, zinc chloride, phosphorus pentaoxide, phosphoric acid, metaphosphoric acid, boric anhydride, oxalic acid.) The reaction can be conducted in the presence of a base (a hydroxide, a hydride or an amide of an alkali metal or an alkaline earth metal such as sodium hydroxide, potassium hydroxide, calcium hydroxide, sodium hydride, potassium hydride, calcium hydride, sodium amide or potasium amide, or an organic base such as triethylamine or pyridine) in a suitable inert solvent (e.g. alcohols such as methanol, ethanol, isopropanol, n-butanol and tert-butanol; ethers such as diethyl ether, diisopropyl ether, tetrahydrofuran and dioxane; glycol ethers such as ethylene glycol monomethyl ether, ethylene glycol monoethyl ether (methyl glycol or ethyl glycol) or ethylene glycol dimethyl ether (diglyme), ketons such as acetone or butanone; acetonitrile; nitro-compounds such as nitromethane and nitrobenzene; esters such as ethyl acetate; amides such as dimethylformamide (DMF), dimethylacetamide, and hexamethyl phosphoramide; sulfoxides such as dimethylsulfoxide (DMSO); halogenated hydrocarbons such as methylene dichloride, chloroform, trichloroethylene, 1,2-dichloroethane and carbon tetrachloride; hydrocarbons such as benzene, toluene and xylene and their mixed solvents). For example, the reaction can be carried out by allowing sodium hydride to act thereon in dimethylsulfoxide at a temperature in the range from 0.degree. C. to 150.degree. C. The compound of the general formula (I) wherein R.sup.6 is a group other than hydroxyl group as defined above, can be produced by converting the corresponding compound of the general formula (I) wherein R.sup.6 is hydroxyl group by the per se known acylation method. Since the compounds of the present invention have at least one asymmetric carbon atom, there exist the optical isomers and stereoisomers due to the asymmetric carbon atom, which are encompassed in the present invention. The thus obtained compounds of the general formula (I) can be separated from the reaction mixture and purified by a per se known method such as recrystallization or chromatography. The compounds of the general formula (I) can be converted into their pharmaceutically acceptable salts by treating them with an inorganic acid (hydrochloric acid, hydrobrcmic acid, sulfuric acid, phosphoric acid, nitric acid etc.), or an organic acid (acetic acid, propionic acid, succinic acid, glycolic acid, lactic acid, malic acid, tartaric acid, citric acid, maleic acid, fumaric acid, methanesulfonic acid, p-toluenesulfonic acid, ascorbic acid etc.). Furthermore, they can be converted into their hydrates or various solvates. Among the compounds of the present invention, the compounds having a chiral carbon atom as mentioned above are usually obtained as racemic bodies. Racemic bodies can be resolved into the optical isomers by the conventional methods. These optical isomers can also be produced by employing the optically active starting compounds. Individual diastereomers can be purified by fractional recrystallization or chromatography. The antihypertensive actions of the compounds of the present invention are detailedly described by the following Pharmacological Experimental Examples.

US Referenced Citations (1)
Number Name Date Kind
4446113 Evans May 1984
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Entry
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Divisions (1)
Number Date Country
Parent 340271 Apr 1989