AU2002232182A1

AU2002232182A1 - 4-aminobenzopyran derivatives

Info

Publication number: AU2002232182A1
Application number: AU2002232182A
Authority: AU
Inventors: Yoshio Ohara; Kazuhiko Ohrai; Yukihiro Shigeta; Toru Tsukagoshi; Toru Yamashita; Kazufumi Yanagihara
Original assignee: Nissan Chemical Corp
Current assignee: Nissan Chemical Corp
Priority date: 2001-02-14
Filing date: 2002-02-14
Publication date: 2003-02-20
Anticipated expiration: 2022-02-14

Description

DESCRIPTION

4-A INOBENZOPYRAN DERIVATIVES

Technical Field

The present invention relates to benzopyran derivatives having a prolongation effect on the refractory period, which are used for treatments of arrhythmia in mammals including human being.

Background Art

As benzopyran derivatives, there have been known 4- acylaminobenzopyran derivatives exemplified by Cromakalim (Japanese Patent Application Laid-Open No. Sho 58-67683). These 4-acylaminobenzopyran derivatives exemplified by Cromakalim are known to open an ATP sensitive K⁺ channel and to be effective for treatments of hypertension and asthma, but there has not been any mention as to the treatment of arrhythmia based on a prolongation effect on the refractory period.

Now, conventional antiarrhythmic agents having a prolongation effect on the refractory period as a main function (such as Class I drugs of antiarrhythmic agent classification according to Vaughan Williams, or d-sotalol belonging to Class III) have highly dangerous arrhythmic inducing actions that can result in sudden death such as torsades de pointes based on extension of ventricular muscle action potential relating to the prolongation effect on the refractory period, which become the therapeutic problems. Thus, agents having less side effects are desired.

Disclosure of Invention

The inventors of the present invention have made an intensive search and study of compounds having a prolongation effect on the refractory period more selective for atrium muscle than for ventricular muscle, and found that the compound of the formula (I) has a prolongation effect on the refractory period selective for atrium muscle without any influence on the refractory period and action potential of ventricular muscle.

The inventors of the present invention have studied eagerly benzopyran derivatives, and surprisingly found that the compound of the formula (I) has a strong prolongation effect on the refractory period, and that it is useful as an antiarrhythmic agent. The present invention has been made based on this finding.

The present invention relates to a benzopyran derivative of the formula (I)

wherein,

R¹ and R² represent each independently a hydrogen atom or a C_halky! group in which said alkyl group may be optionally substituted with a halogen atom, a hydroxyl group or a C,_₆alkoxy group in which said alkoxy group may be optionally substituted with a fluorine atom,

R³ represents a hydroxyl group or a C,..₆alkylcarbonyloxy group,

R⁴ represents a hydrogen atom, or R³ and R⁴ together form a bond,

R⁶ represents a hydrogen atom,

R⁷ represents a hydrogen atom or a C,_₆alkyl group,

X is absent, or represents C=O or SO₂,

R⁸ represents a hydrogen atom or a C,_₆alkyl group in which said alkyl group may be optionally substituted with a hydroxyl group or a C_|_₆alkoxy group,

R⁹ represents a hydrogen atom or a nitro group, when R⁹ represents a hydrogen atom,

Y represents a C₃.₈alkylene group or -(CH₂)_m-CR¹¹R¹²-(CH₂)_n- in which m and n represent each independently 0, 1, 2, 3 or 4, and m+n is equal to or more than 2; when m represents 0, R¹¹ and R¹² represent each independently a C^alkyl group, and when m represents those other than 0, R¹¹ and R¹² represent each independently a C^alkyl group or a hydroxyl group, or R¹¹ and R¹² together form a oxygen atom,

R⁵ represents a fluorine atom, a trifluoromethyl group, an amino group, a C^alkylthio group, a C^alkylamino group, a di-C^_galkylamino group, a C,_₆ alkylcarbonylamino group, a group, an aminocarbonyl group, a C galkylaminocarbonyl group, a di-C-ι-₆alkylaminocarbonyl group, a C,_₆ alkylcarbonyl group, a C.,_₆alkoxycarbonyl group, a C^alkoxycarbonylamino group, an aminosulfonyl group, a C|_₆alkylsulfonyl group, a carboxyl group or a benzoyl group in which said benzoyl group may be optionally substituted with a C^alkyl group, a C.,.₆alkoxy group, a halogen atom, a nitro group or a cyano group, and when R⁹ represents a nitro group,

Y represents a C₄.₈alkylene group, -(CH₂)_m-CR¹¹R¹²-(CH₂)_n- in which m, n, R¹¹ and R¹² are same as the above or -(CH₂)₀-O-(CH₂)_P- in which o and p represent each independently 2, 3 or 4,

R⁵ represents a hydrogen atom, a fluorine atom, a trifluoromethyl group, a hydroxyl group, a formamide group, an amino group, a C,.₆alkoxy group, a C_3.8 cycloalkyl group, a group, a C.|_₆alkylcarbonylamino group, a C.,_₆alkylsulfonylamino group, an aminocarbonyl group, a group, a group, a group, a group, a C,_₆ alkoxycarbonylamino group, an aminosulfonyl group, a group, a carboxyl group or a benzoyl group in which said benzoyl group may be optionally substituted with a C,._βalkyl group, a C^alkoxy group, a halogen atom, a nitro group or a cyano group; or a pharmaceutically acceptable salt thereof.

The compound according to the present invention has a strong prolongation effect on the refractory period and it can be used as a drug for treating arrhythmia.

Respective substituents for the compound (I) according to the present invention are illustrated concretely specifically as follows.

Herein, "n" means normal, "i" means iso, "s" means secondary, "t" means tertiary, "c" means cyclo, and "p" means para.

As C^alkyl groups, there may be mentioned methyl, ethyl, n-propyl, i- propyl and c-propyl, etc.

As C,_.6alkyl groups, there may be mentioned methyl, ethyl, n-propyl, i- propyl, c-propyl, n-butyl, i-butyl, s-butyl, t-butyl, c-butyl, 1-pentyl, 2-pentyl, 3-pentyl, i-pentyl, neopentyl, 2,2-dimethylpropyl, c-pentyl, 1-hexyl, 2-hexyl, 3-hexyl, 1- methyl-n-pentyl, 1 ,1 ,2-trimethyl-n-propyl, 1 ,2,2-trimethyl-n-propyl, 3,3-dimethyl-n- butyl and c-hexyl, etc. Preferably, there may be mentioned methyl, ethyl, n-propyl, i-propyl and n-butyl.

As halogen atoms, there may be mentioned a fluorine atom, a chlorine atom, a bromine atom and an iodine atom. Preferably, there may be mentioned a fluorine atom, a chlorine atom and a bromine atom.

As C|_₆alkoxy groups, there may be mentioned methoxy, ethoxy, n-propoxy, i-propoxy, n-butoxy, i-butoxy, s-butoxy, t-butoxy, 1-pentyloxy, 2-pentyloxy, 3- pentyloxy, i-pentyloxy, neopentyloxy, 2,2-dimethylpropoxy, 1-hexyloxy, 2-hexyloxy, 3-hexyloxy, 1 -methyl-n-pentyloxy, 1 ,1 ,2-trimethyl-n-propoxy, 1 ,2,2-trimethyl-n- propoxy and 3,3-dimethyl-n-butoxy, etc. Preferably, there may be mentioned methoxy, ethoxy, n-propoxy and i-propoxy.

As C₄.₈alkylene groups, there may be mentioned butylene, pentylene, hexylene, heptylene and octylene, etc. Preferably, there may be mentioned pentylene.

As C₃.₈alkylene groups, there may be mentioned propylene in addition to the aforementioned C₄.₈alkylene groups. Preferably, there may be mentioned pentylene.

As C^alkylcarbonyloxy groups, there may be mentioned methylcarbonyloxy, ethylcarbonyloxy, n-propylcarbonyloxy, i-propylcarbonyloxy, n- butylcarbonyloxy, i-butylcarbonyloxy, s-butylcarbonyloxy, t-butylcarbonyloxy, 1- pentylcarbonyloxy, 2-pentylcarbonyloxy, 3-pentylcarbonyloxy, i-pentylcarbonyloxy, neopentylcarbonyloxy, t-pentylcarbonyloxy, 1-hexylcarbonyloxy, 2- hexylcarbonyloxy, 3-hexylcarbonyloxy, 1-methyl-n-pentylcarbonyloxy, 1 ,1 ,2- trimethyl-n-propylcarbonyloxy, 1 ,2,2-trimethyl-n-propylcarbonyloxy and 3,3- dimethyl-n-butylcarbonyloxy, etc. Preferably, there may be mentioned methylcarbonyloxy, ethylcarbonyloxy, n-propylcarbonyloxy, i-propylcarbonyloxy, n- butylcarbonyloxy and t-butylcarbonyloxy.

As C₃.₈cycloalkyl groups, there may be mentioned c-propyl, c-butyl, c- pentyl, c-hexyl, c-heptyl and c-octyl, etc. Preferably, there mey be mentioned c- propyl, c-butyl and c-hexyl.

As C_|.₆aIkylthio groups, there may be mentioned metylthio, ethylthio, n- propylthio, i-propylthio, c-propylthio, n-butylthio, i-butylthio, s-butylthio, t-butylthio, c-butylthio, 1-pentylthio, 2-pentylthio, 3-pentylthio, i-pentylthio, neopentylthio, t- pentylthio, c-pentylthio, 1-hexylthio, 2-hexylthio, 3-hexylthio, c-hexylthio, 1-methyl- n-pentylthio, 1 ,1 ,2-trimethyl-n-propylthio, 1 ,2,2-trimethyl-n-propylthio and 3,3- dimethyl-n-butylthio, etc. Preferably, there may be mentioned methylthio, ethylthio, n-propylthio, i-propylthio and n-butylthio.

As C,.₆alkylamino groups, there may be mentioned methylamino, ethylamino, n-propylamino, i-propylamino, c-propylamino, n-butylamino, i- butylamino, s-butylamino, t-butylamino, c-butylamino, 1-pentylamino, 2- pentylamino, 3-pentylamino, i-pentylamino, neopentylamino, t-pentylamino, c- pentylamino, 1-hexyIamino, 2-hexylamino, 3-hexylamino, c-hexylamino, 1-methyl- n-pentylamino, 1 ,1 ,2-trimethyl-n-propylamino, 1 ,2,2-trimethyl-n-propylamino and 3,3-dimethyl-n-butylamino, etc. Preferably, there may be mentioned methylamino, ethylamino, n-propylamino, i-propylamino and n-butylamino.

As di-C|_₆alkylamino groups, there may be mentioned dimethylamino, diethylamino, di-n-propylamino, di-i-propylamino, di-c-propylamino, di-n-butylamino, di-i-butylamino, di-s-butylamino, di-t-butylamino, di-c-butylamino, di-1-pentylamino, di-2-pentylamino, di-3-pentylamino, di-i-pentylamirio, di-neopentylamino, di-t- pentylamino, di-c-pentylamino, di-1-hexylamino, di-2-hexylamino, di-3-hexylamino, di-c-hexylamino, di-(1-methyl-n-pentyl)amino, di-(1 ,1 ,2-trimethyl-n-propyl)amino, di-(1 ,2,2-trimethyl-n-propyl)amino, di-(3,3-dimethyl-n~butyl)amino, methyl- (ethyl)amino, methyl(n-propyl)amino, methyl(i-propyl)amino, methyl(c-propyl)amino, methyl(n-butyl)amino, methyl(i-butyl)amino, methyl(s-butyl)amino, methyl(t- butyl)amino, methyl(c-butyl)amino, ethyl(n-propyl)amino, ethyl(i-propyl)amino, ethyl(c-propyl)amino, ethyl(n-butyl)amino, ethyl(i-butyl)amino, ethyl(s-butyl)amino, ethyl(t-butyl)amino, ethyl(c-butyl)amino, n-propyl(i-propyl)amino, n-propyl(c- propyl)amino, n-propyl(n-butyl)amino, n-propyl(i-butyl)amino, n-propyl(s- butyl)amino, n-propyl(t-butyl)amino, n-propyl(c-butyl)amino, i-propyl(c- propyl)amino, i-propyl(n-butyl)amino, i-propyl(i-butyl)amino, i-propyl(s-butyl)amino, i-propyl(t-butyl)amino, i-propyl(c-butyl)amino, c-propyl(n-butyl)amino, c-propyl(i- butyl)amino, c-propyl(s-butyl)amino, c-propyl(t-butyl)amino, c-propyl(c-butyl)amino, n-butyl(i-butyl)amino, n-butyl(s-butyl)amino, n-butyl(t-butyl)amino, n-butyl(c- butyl)amino, i-butyl(s-butyl)amino, i-butyI(t-butyl)amino, i-butyl(c-butyl)amino, s- butyl(t-butyl)amino, s-butyl(c-butyl)amino and t-butyl(c-butyl)amino, etc. Preferably, there may be mentioned dimethylamino, diethylamino, di-n-propylamino, di-i-propylamino and di-n-butylamino.

As C|.₆alkylcarbonylamino groups, there may be mentioned methylcarbonylamino, ethylcarbonylamino, n-propylcarbonylamino, i- propylcarbonylamino, n-butylcarbonylamino, i-butylcarbonylamino, s- butylcarbonylamino, ^• t-butylcarbonylamino, 1-pentylcarbonylamino, 2- pentylcarbonylamino, 3-penylcarbonylamino, i-pentylcarbonylamino, neopentylcarbonylamino, t-pentylcarbonylamino, 1-hexylcarbonylamino, 2- hexylcarbonylamino and 3-hexylcarbonylamino, etc. Preferably, there may be mentioned methylcarbonylamino, ethylcarbonylamino, n-propylcarbonylamino, i- propylcarbonylamino and n-butylcarbonylamino.

As C^alkylsulfonylamino groups, there may be mentioned methylsulfonylamino, ethylsulfonylamino, n-propylsulfonylamino, i-propyl- sulfonylamino, n-butylsulfonylamino, i-butylsulfonylamino, s-butylsulfonylamino, t- butylsulfonylamino, 1-pentylsulfonylamino, 2-pentylsulfonylamino, 3-pentylsulfonyl- amino, i-pentylsulfonylamino, neopentylsulfonylamino, t-pentylsulfonylamino, 1- hexylsulfonylamino, 2-hexylsulfonylamino and 3-hexylsulfonylamino, etc. Preferably, there may be mentioned methylsulfonylamino, ethylsulfonylamino, n- propylsulfonylamino, i-propylsulfonylamino and n-butylsulfonylamino.

As C,.₆alkylaminocarbonyl groups, there may be mentioned methylaminocarbonyl, ethylaminocarbonyl, n-propylaminocarbonyl, i-propyl- aminocarbonyl, n-butylaminocarbonyl, i-butylaminocarbonyl, s-butylaminocarbonyl, t-butylaminocarbonyl, 1-pentylaminocarbonyl, 2-pentyIaminocarbonyl, 3-pentyl- aminocarbonyl, i-pentylaminocarbonyl, neopentylaminocarbonyl, t-pentylamino- carbonyl, 1 -hexylaminocarbonyl, 2-hexylaminocarbonyI and 3-hexylaminocarbonyl, etc. Preferably, there may be mentioned methylaminocarbonyl, ethylaminocarbonyl, n-propylaminocarbonyl, i-propylaminocarbonyl and n-butylaminocarbonyl.

As di-C^alkylaminocarbonyl groups, there may be mentioned dimethylaminocarbonyl, diethylaminocarbonyl, di-n-propylaminocarbonyl, di-i- propylaminocarbonyl, di-c-propylaminocarbonyl, di-n-butylaminocarbonyl, di-i- butylaminocarbonyl, di-s-butylaminocarbonyl, di-t-butylaminocarbonyl, di-c- butylaminocarbonyl, di-1-pentylaminocarbonyl, di-2-pentylaminocarbonyl, di-3- pentylaminocarbonyl, di-i-pentylaminocarbonyl, di-neopentylaminocarbonyl, di-t- pentylaminocarbonyl, di-c-pentylaminocarbonyl, di-1 -hexylaminocarbonyl, di-2- hexylaminocarbonyl and di-3-hexylaminocarbonyl, etc. Preferably, there may be mentioned dimethylaminocarbonyl, diethylaminocarbonyl, di-n-propylaminocarbonyl, di-i-propylaminocarbonyl, di-c-propylaminocarbonyl and di-n-butylaminocarbonyl.

As C,.₆alkylcarbonyl groups, there may be mentioned methylcarbonyl, ethylcarbonyl, n-propylcarbonyl, i-propylcarbonyl, n-butylcarbonyl, i-butylcarbonyl, s-butylcarbonyl, t-butylcarbonyl, 1-pentylcarbonyl, 2-pentylcarbonyl, 3- pentylcarbonyl, i-pentylcarbonyl, neopentylcarbonyl, t-pentylcarbonyl, 1- hexylcarbonyl, 2-hexylcarbonyl and 3-hexylcarbonyl. Preferably, there may be mentioned methylcarbonyl, ethylcarbonyl, n-propylcarbonyl, i-propylcarbonyl and n-butylcarbonyl.

As C^alkoxycarbonyl groups, there may be mentioned methoxycarbonyl, ethoxycarbonyl, n-propoxycarbonyl, i-propoxycarbonyl, n-butoxycarbonyl, i- butoxycarbonyl, s-butoxycarbonyl, t-butoxycarbonyl, 1-pentyloxycarbonyl, 2- pentyloxycarbonyl, 3-pentyloxycarbonyl, i-pentyloxycarbonyl, neopentyloxy- carbonyl, t-pentyloxycarbonyl, 1-hexyloxycarbonyl, 2-hexyloxycarbonyl and 3- hexyloxycarbonyl, etc. Preferably, there may be mentioned methoxycarbonyl, ethoxycarbonyl, n-propoxycarbonyl, i-propoxycarbonyl, n-butoxycarbonyl, i- butoxycarbonyl, s-butoxycarbonyl and t-butoxycarbonyl.

As C^alkoxycarbonylamino groups, there may be mentioned methoxycarbonylamino, ethoxycarbonylamino, n-propoxycarbonylamino, i- propoxycarbonylamino, n-butoxycarbonylamino, i-butoxycarbonylamino, s- butoxycarbonylamino, t-butoxycarbonylamino, 1-pentyloxycarbonylamino, 2- pentyloxycarbonylamino, 3-pentyloxycarbonylamino, i-pentyloxycarbonylamino, neopentyloxycarbonylamino, t-pentyloxycarbonylamino, 1-hexyloxycarbonylamino, 2-hexyloxycarbonylamino and 3-hexyloxycarbonylamino, etc. Preferably, there may be mentioned methoxycarbonylamino, ethoxycarbonylamino, n-propoxycarbonylamino, i-propoxycarbonylamino, n-butoxycarbonylamino, i-butoxycarbonylamino, s-butoxycarbonylamino and t-butoxycarbonylamino.

As C^alkylsulfonyl groups, there may be mentioned methanesulfonyl and ethanesulfonyl.

As preferable compounds used in the present invention, the following compounds may be mentioned.

(1) The benzopyran derivative of the formula (I) or pharmaceutically acceptable salt thereof, wherein R¹ and R² represent a methyl group, R³ represents a hydroxyl group and R⁴ represents a hydrogen atom.

(2) The benzopyran derivative or pharmaceutically acceptable salt thereof according to aforementioned (1), wherein X represents C=O, R⁷ represents a hydrogen atom, and R⁸ represents a methyl group.

(3) The benzopyran derivative or pharmaceutically acceptable salt thereof according to aforementioned (1), wherein X is absent, and R⁷ and R⁸ represent a hydrogen atom. (4) The benzopyran derivative or pharmaceutically acceptable salt thereof according to aforementioned (2), wherein R⁹ represents a hydrogen atom.

(5) The benzopyran derivative or pharmaceutically acceptable salt thereof according to aforementioned (2), wherein R⁹ represents a nitro group.

(6) The benzopyran derivative or pharmaceutically acceptable salt thereof according to aforementioned (3), wherein R⁹ represents a hydrogen atom.

(7) The benzopyran derivative or pharmaceutically acceptable salt thereof according to aforementioned (3), wherein R⁹ represents a nitro group.

Concrete examples of the compounds that can be used in the present invention are shown as follows, but the present invention is not limited thereto. Herein, "Me" means a methyl group, "Et" means an ethyl group, "Pr" means a propyl group, "Bu" means a butyl group, "Pen" means a pentyl group, "Hex" means a hexyl group, "Ac" means an acetyl group (COCH₃), "Ph" means a phenyl group, "n" means normal, "i" means iso, "t" means tertiary, and "c" means cyclo, respectively.

Y R⁵

(CH₂)₄ H

(CH₂)₄ NH₂

(CH₂)₄ NHSO₂Me

(CH₂)₄ NMe₂

(CH₂)₄ CONH₂

(CH₂)₄ CO₂Et

(CH₂)₄ CONMe₂

(CH₂)₄ NHCOMe

(CH₂)₅ H

(CH₂)₅ NHSO₂Me

(CH₂)₅ NHMe

(CH₂)₅ CO₂Et

(CH₂)₅ c-Hex

(CH₂)₅ CONHMe

(CH₂)₅ CONMe₂

(CH₂)₅ NHCOMe

(CH₂)₆ H

(CH₂)₆ COPh

(CH₂)₆ NHMe

(CH₂)₆ NMe₂

(CH₂)₆ CONH₂

(CH₂)2O(CH₂)2 H

(CH₂)₃O(CH₂)2 H

(CH₂)₄O(CH₂)₂ H

(CH₂)₃OCH₂ H

(CH₂)₄C=OCH₂ H

CHOHCH₂ H

CH₂CHMeCH₂ H

CH₂CMe₂CH₂ H

The compound according to the present invention has asymmetric carbon atoms at 3-position and 4-positon, thus optical isomers thereof based on the asymmetric carbon atoms are present, which can be used in the application of the present invention similar to racemate. Further, a cis- and trans isomer based on configuration at 3-position and 4-position may be included, but the trans isomer is preferable.

Further, when the compounds can form their salts, the pharmaceutically acceptable salts thereof can be also used as active ingredients.

As pharmaceutically acceptable salts, there may be mentioned hydrochlorides, hydrobromides, sulfates, methanesulfonates, acetates, benzoates, tartrates, phosphates, lactates, maleates, fumarates, malates, gluconates and salicylates, etc. Preferably, there may be mentioned hydrochlorides, methanesulfonates and maleates.

Then, the preparation method of the compound according to the present invention is illustrated.

Of the compounds of the general formula (I), those wherein R⁴ represents a hydrogen atom and R³ represents a hydroxyl group, which are the compounds of formula (l-a), can be obtained by reacting a compound of the general formula (2) with a compound (3) in an inert solvent, as shown in the following reaction scheme.

The compound of the general formula (2) can be synthesized according to known methods (methods described in J. M. Evans et al., J. Med. Chem. 1984, 27, 1127; J. Med. Chem. 1986, 29, 2194; J. T. North et al., J. Org. Chem. 1995, 60, 3397; as well as Japanese Patent Application Laid-Open No. Sho 56-57785, Japanese Patent Application Laid-Open No. Sho 56-57786, Japanese Patent Application Laid-Open No. Sho 58-188880, Japanese Patent Application Laid- Open No. Hei 2-141 , Japanese Patent Application Laid-Open No. Hei 10-87650 and Japanese Patent Application Laid-Open No. Hei 11-209366, etc.).

( 2 ) ( l-a )

As the solvents used in the reaction of the compound of the general formula (2) with the compound (3), the following may be mentioned.

There may be mentioned sulfoxide type solvents exemplified by dimethylsulfoxide; amide type solvents exemplified by dimethylformamide and dimethylacetamide; ether type solvents exemplified by ethylether, dimethoxyethane and tetrahydrofuran; halogen type solvents exemplified by dichloromethane, chloroform and dichloroethane; nitrile type solvents exemplified by acetonitrile and propionitrile; aromatic hydrocarbon type solvents exemplified by benzene and toluene; hydrocarbon type solvents exemplified by hexane and heptane; and ester type solvents exemplified by ethyl acetate. Further, the reaction can be carried out in the absence of a solvent. Preferably, ether type solvents and nitrile type solvents may be mentioned.

The reaction temperature is generally from -80°C to the reflux temperature of the reaction solvent, preferably from -10°C to 100°C.

The molar ratio of the reaction materials is within the range of 0.5-20.0, preferably 1.0-10.0, for the compound (3)/the compound (2).

An acid catalyst may be used in the reaction.

As the acid catalysts used, there may be mentioned inorganic acids exemplified by hydrochloric acid and sulfuric acid, and Lewis acids exemplified by aluminum chloride, titanium tetrachloride, boron trifluoride diethyl ether complex, perchloric acid, lithium perchlorate, lithium bromide and ytterbium trifluoromethanesulfonate, etc. Preferably, there may be mentioned lithium bromide, perchloric acid and lithium perchlorate.

Of the compounds of the general formula (I), those other than the compounds of the formula (l-a) (the compounds wherein R³ and R⁴ together form a bond and the compounds wherein R⁴ represents a hydrogen atom and R³ represents a C.,_₆ alkylcarbonyloxy group) can be prepared by the methods similar to those described in Japanese Patent Application Laid-Open No. Sho 52-91866 and Japanese Patent Application Laid-Open No. Hei 10-87650, etc.

Syntheses of optically active compounds of the compounds of the general formula (I) can be attained by utilizing optical r -Sόlution methods (Japanese Patent Application Laid-Open No. Hei 3-141286, U.S. Patent No. 5,097,037 and European Patent No. 409,165). Further, syntheses of optically active compounds of the general formula (2) can be attained by utilizing asymmetric synthesis methods (Japanese National Publication No. Hei 5-507645, Japanese Patent Application Laid-Open No. Hei 5-301878, Japanese Patent Application Laid-Open No. Hei 7- 285983, European Patent Application Laid-open No.535,377 and U.S. Patent No. 5,420,314).

As described above, the inventors of the present invention found that the compound of the formula (I) has a strong prolongation effect on the refractory period. The prolongation effect on the refractory period is one of the functions of antiarrhythmic action and an important indicator that can be extrapolated to efficiency for clinical arrhythmia. Conventional antiarrhythmic agents having a prolongation effect on the refractory period as the main function (such as d-sotalol belonging to Class III of the antiarrhythmic agent classification according to Vaughan Williams) have highly dangerous arrhythmic inducing actions that can result in sudden death such as torsades de pointes based on extension of ventricular muscle action potential relating to the prolongation effect on the refractory period, which become the therapeutic problems for arrhythmia based on atrium (such as supraventricular tachycardia, atrial flutter and atrial fibrillation). In order to solve the problems, the inventors of the present invention carried out searching and studying of compounds having the prolongation effect on the refractory period more selective for atrium muscle than for ventricular muscle, and found that the compound of the formula (I) has the prolongation effect on the refractory period selective for atrium muscle without any influence on the refractory period and action potential of ventricular muscle. The difference between the findings by the inventors of the present invention and the known techniques is to provide the prolongation effect on the refractory period selective for atrium muscle to these compound group, which is shown by the following facts; there is no influence on the action potential sustaining period of removed ventricular muscle, and there is no influence on the electrocardiogram QT of anesthetized animal. From the above, the compounds of the present invention have no arrhythmic inducing action in ventricular muscle, thus they can provide possibilities of a contribution to more safe uses for arrhythmia based on atrium muscle than known techniques. This technique is useful for therapeutic or preventive uses as anti- atrial fibrillation agents, anti-atrial flutter agents and anti-atrial tachycardia agents relating to paroxysmal, chronic, preoperative, intraoperative or postoperative atrial arrhythmia, prevention of proceeding to embolus based on atrial arrhythmia, prevention of proceeding to ventricular arrhythmia or tachycardia originated from atrial arrhythmia or tachycardia, and prevention of the life prognosis worsening based on the preventive action for atrial arrhythmia or tachycardia which can be proceeded to ventricular arrhythmia or tachycardia.

The present invention provides a pharmaceutical composition or veterinary pharmaceutical composition containing a compound of the generally formula (I) in an effective amount for these treatments.

As administering forms of the compound according to the present invention, there may be mentioned parenteral administrations by means of injections (subcutaneous, intravenous, intramuscular and intraperitoneal injections), ointments, suppositories and aerosol, and oral administrations by means of tablets, capsules, granules, pills, syrups, solutions, emulsions and suspensions, etc.

The aforementioned pharmaceutical or veterinary pharmaceutical composition contains the compound according to the present invention in an amount of about 0.01-99.5%, preferably about 0.1-30%, of the total composition weight. In addition to the compound according to the present invention or the composition containing the compound, other pharmaceutically or veterinary pharmaceutically active compounds may be contained. Further, these compositions may contain the plurality of compounds according to the present invention.

A clinical administration amount of the compound of the present invention varies depending on age, weight and sensitivity of the patient, extent of condition, etc. and an effective administration amount is generally about 0.003-1.5g, preferably 0.01 -0.6g, per day for adult. If necessary, however, the amount outside of the aforementioned range may be used.

The compound according to the present invention is formulated for administration by conventional pharmaceutical means.

That is, tablets, capsules, granules and pills for oral administration are prepared by using excipients such as sucrose, lactose, glucose, starch and mannitol; binders such as hydroxypropyl cellulose, syrup, gum arabic, gelatin, sorbitol, tragacanth, methyl cellulose and polyvinyl pyrrolidone; disintegrators such as starch, carboxymethyl cellulose or its calcium salt, microcrystalline cellulose and polyethylene glycol; lubricants such as talc, magnesium or calcium stearate, and silica; lubricaing agents such as sodium laurate and glycerol, etc.

Injections, solutions, emulsions, suspensions, syrups and aerosols are prepared by using solvents for the active components such as water, ethyl alcohol, isopropyl alcohol, propylene glycol, 1 ,3-butylene glycol and polyethylene glycol; surfactants such as sorbitan fatty acid ester, polyoxyethylene sorbitan fatty acid ester, polyoxyethylene fatty acid ester, polyoxyethylene ether of hydrogenated castor oil and lecithin; suspending agents such as carboxymethyl sodium salt, cellulose derivatives such as methyl cellulose, tragacanth, and natural rubbers such as gum arabic; and preserves such as p-hydroxybenzoic acid esters, benzalkonium chloride and sorbic acid salts, etc.

For ointments that are transdermally adsorptive pharmaceutics, for example, white vaseline, liquid paraffin, higher alcohols, Macrogol ointments, hydrophilic ointments and aqueous gel-type bases, etc are used.

Suppositories are prepared by using, for example, cocoa fats, polyethylene glycol, lanolin, fatty acid triglyceride, coconut oil and Polysorbate etc.

Best Mode for Carrying Out the Invention

The present invention is illustrated in detail by the Examples as follows, but the present invention is not limited to these Examples.

Herein, in following formulae, "Boc" means a t-butoxycarbonyl group.

[Synthesis Examples]

Synthesis Example 1

(3R^*, 4S^*)-6-acetylamino-3,4-dihydro-2,2-dimethyl-7-nitro-4-n-pentylamino-2H-1- benzopyran-3-ol

To a solution of 1.0g (3.59mmol) of (+)-(3R* 4R*)-6-acetamide-3,4-epoxy- 3,4-dihydro-2,2-dimethyl-7-nitro-2H-1 -benzopyran (above 99%ee) and lithium perchlorate (1.53g, 14.36mmol) in acetonitrile (10 mL), n-pentylamine (0.942mL, 7.18mmol) was added at the room temperature and stirred at 65"C for 3 hours. After an addition of an aqueous saturated sodium bicarbonate solution and an extraction with ethyl acetate, it was washed with an aqueous saturated sodium chloride solution and dried over anhydrous magnesium sulfate. A purification by silica gel column chromatography (Hex/AcOEt = 1/2) was conducted to obtain the intended substance at 60% yield. Yellow amorphous substance.

¹H-NMR (CDCI₃) δ : 0.89 (t, J = 7.0Hz, 3H), 1.22 (s, 3H), 1.30-1.36 (m, 4H), 1.52 (s, 3H), 1.48-1.56 (m, 2H), 2.55-2.71 (m, 2H), 3.57 (d, J = 10.1 Hz, 1H), 3.70 (d, J = 10.1Hz, 1H), 7.62 (s, 1H), 8.68 (s, 1H), 10.02 (s, 1H). MS (El) m / z; 365 [M]⁺, 308, 293 (bp).

The following compounds were obtained by the similar manner (Synthesis Examples 2-7).

Synthesis Example No. R

.NHBoc

Synthesis Example 2

56 % yield.

Yellow amorphous substance.

¹H-NMR (CDCI₃) <5 : 1.21 (s, 3H), 1.52 (s, 3H), 1.70 (s, 2H), 1.79 (quint, J = 6.1 Hz,

2H), 2.26 (s, 3H), 2.70-2.85 (m, 2H), 3.36 (s, 3H), 3.54 (t, J = 5.8Hz, 2H), 3.58 (d, J

= 10.3Hz, 1H), 3.71 (d, J = 10.3Hz, 1H), 7.62 (s, 1H), 8.68 (s, 1H), 10.00 (s, 1H).

MS (El) m / z; 367 [M]\ 297 (bp).

Synthesis Example 3 23 % yield.

Yellow oil substance.

¹H-NMR (CDCI₃) δ : 1.22 (s, 3H), 1.53 (s, 3H), 1.62 (s, 2H), 1.83 (quint, J = 6.8Hz,

2H), 2.10 (s, 3H), 2.26 (s, 3H), 2.63 (t, J= 7.0Hz, 2H), 2.68-2.86 (m, 2H), 3.60 (d, J

= 10.2Hz, 1H), 3.72 (d, J= 10.2Hz, 1H), 7.63 (s, 1H), 8.70 (s, 1H), 10.01 (s, 1H).

MS (El) m / z; 383 [M]⁺, 220 (bp).

Synthesis Example 4

93 % yield.

Red oil substance.

¹H-NMR (CDCI₃) δ : 0.92 (t, J = 7.2Hz, 3H), 1.21 (s, 3H), 1.33-1.60 (m, 4H), 1.52 (s,

3H), 2.27 (s, 3H), 2.56-2.72 (m, 2H), 3.56 (d, J= 10.2Hz, 1H), 3.71 (d, J= 10.2Hz,

1H), 7.63 (s, 1H), 8.68 (s, 1H), 10.03 (s, 1H).

MS (El) m / z; 353 [M]⁺, 263, 222 (bp).

Synthesis Example 5

96 % yield.

Red amorphous substance.

¹H-NMR (CDCI₃) c : 0.89 (s, 9H), 1.21 (s, 3H), 1.46 (t, J = 8.1 Hz, 2H), 1.53 (s, 3H),

2.27 (s, 3H), 2.53-2.72 (m,2H), 3.69 (d,J= 10.2Hz, 1H), 3.71 (d, J= 10.2Hz, 1H),

7.63 (s, 1H), 8.68 (s, 1H), 10.02 (s, 1H).

MS (El) m / z; 379 [M]⁺, 260, 146 (bp).

Synthesis Example 6

89 % yield.

Yellow crystal. m.p.210.0-212.0°C H-NMR (CDCLJS: 0.85-1.90 (m, 13H), 1.18 (s, 3H), 1.54 (s, 3H), 2.25 (s, 3H),

2.76-2.85 (m, 1H), 3.08-3.18 (m, 1H), 4.05 (d, J = 8.8Hz, 1H), 4.59 (d, J = 8.8Hz,

1H), 7.68 (s, 1H), 8.78 (s, 1H), 9.77 (s, 1H).

MS (El) m / z; 405 [M]⁺, 335, 292 (bp).

Synthesis Example 7

98 % yield.

Red oil substance. ¹H-NMR (CDCI₃) c5 : 1.21 (s, 3H), 1.44 (s, 9H), 1.52 (s, 3H), 1.52-1.61 (m, 2H), 1.63-1.74 (m, 2H), 2.27 (s, 3H), 2.58-2.71 (m, 2H), 3.07-3.16 (m, 2H), 3.60 (d, J = 10.1 Hz, 1H), 3.73 (d, J = 10.1Hz, 1H), 7.63 (s, 1H), 8.68 (s, 1H), 10.00 (s, 1H). MS (El) m / z; 466 [M]⁺, 394, 277, 70 (bp).

Synthesis Example 8

To the compound of Synthesis Example 7 (500mg, 1.18mmol), a hydrogen chloride - dioxane (4mol/L) solution (1.18mL, 4.72mmol) was added under an ice cooling, stirred for 30 minutes, then heated to room temperature, and stirred for another 30 minutes. An aqueous sodium hydroxide (1mol/L) was added thereto, an extraction was conducted with chloroform, an organic phase was washed once with an aqueous saturated sodium chloride solution and dried over anhydrous magnesium sulfate. A solvent was distilled off to obtain the intended substance at 100% yield. Yellow solid.

¹H-NMR (CDCI₃) S : 1.19 (s, 3H), 1.50 (s, 3H), 1.55-1.67 (m, 4H), 2.26 (s, 3H), 2.58-2.70 (m, 2H), 3.14 (brs, 4H), 3.64 (d, J = 10.2Hz, 1H), 3.75 (d, J= 10.2Hz, 1H), 7.61 (s, 1 H), 8.65 (s, 1 H), 10.02 (s, 1H). MS (El) m / z; 394 [M]⁺, 350 (bp).

Synthesis Example 9

Trans-6-amino-3,4-dihydro-2,2-dimethyl-7-nitro-4-n-pentylamino-2H-1- benzopyran-3-ol

To the ethanol solution (11mL) of compound of Synthesis Example 1 (550mg, 1.51 mmol), a 35% hydrochloric acid (1.1 mL) was added at room temperature, and refluxed for 12 hours. An aqueous saturated sodium bicarbonate solution was added thereto, an extraction was conducted with ethyl acetate, an organic phase was washed once with an aqueous saturated sodium chloride solution and dried over anhydrous magnesium sulfate. After distilling off the solvent, the residue was purified by silica gel column chromatography (Hex/AcOEt = 1/1) to obtain the intended substance at 75% yield. Red amorphous substance.

¹H-NMR (CDCI₃) δ : 0.91 (t, J = 8.1 Hz, 3H), 1.19 (s, 3H), 1.25-1.35 (m, 4H), 1.34 (s, 3H), 1.50-1.80 (m, 4H), 2.48-2.75 (m, 2H), 3.58-3.65 (m, 2H), 5.70 (s, 2H), 6.81 (s, 1 H), 7.59 (s, 1 H). MS (El) m / z; 323 [M]⁺, 252 (bp).

[Preparation Examples] Preparation Example 1 Tablet:

a compound according to the invention 10g lactose 260g microcrystailine cellulose 600g corn starch 350g hydroxypropyl cellulose 100g

CMC-Ca 150g magnesium stearate 30g total 1 ,500g

The aforementioned ingredients were mixed by a conventional method and thereafter 10,000 sugar-coated tablets each containing 1 mg of the active ingredient per a tablet were prepared. Preparation Example 2 Capsule:

a compound according to the invention 10g lactose 440g microcrystalline cellulose 1 ,000g magnesium stearate 50g total 1 ,500g

The aforementioned ingredients were mixed by a conventional method and thereafter filled in gelatin capsules to prepare 10,000 capsules each containing 1 mg of the active ingredient per a capsule.

Preparation Example 3 Soft capsule:

a compound according to the invention 10g

PEG 400 479g saturated fatty acid triglyceride 1 ,500g peppermint oil 1g

Polysorbate 80 10g total 2,000g

The aforementioned ingredients were mixed by a conventional method and thereafter filled in No.3 soft gelatin capsules to prepare 10,000 soft capsules each containing 1 mg of the active ingredient per a capsule.

Preparation Example 4

Ointment:

a compound according to the invention 1.0g liquid paraffin 10. Og cetanol 20.0g white vaseline 68.4g ethylparaben 0.1g

1 -menthol 0.5g total 100.0g

The aforementioned ingredients were mixed by a conventional method to obtain 1% ointment.

Preparation Example 5 Suppository:

a compound according to the invention 1g

Witepsol H15* 478g

Witepsol W35* 520g

Polysorbate 80 1cj_ total 1 ,000g

(* trade name of triglyceride type compounds)

The aforementioned ingredients were melt-mixed by a conventional method, poured into suppository containers and cooled to solidify, thereby 1 ,000 suppositories (1g) each containing 1 mg of the active ingredient per a suppository were prepared.

Preparation Example 6 Injection:

a compound according to the invention 1 mg distilled water for injection 5mL

It is used by dissolving when applied.

[Pharmacological Test Example] Effects on the effective refractory period

Method

Beagles were anesthetized with pentobarbital sodium and, under artificially ventilated condition, thoracotomy was conducted along the median and the pericardium was cut open to expose the heart. ECG was recorded using bipolar electrodes attached to the surface of the right atrial free wall, right atrial auricle, and right ventricular free wall. The vagal nerves were stimulated using an electric stimulation device via Nichrome wires inserted into the bilateral vagal nerves in the neck. The conditions for electric stimulation to the vagal nerves were set such that the RR intervals on ECG were prolonged by about 100msec compared with those before the stimulation was started.

Electric current twice as strong as the threshold was used for the electric stimulation to the heart, and premature stimulation S2 was applied after giving 10 serial S1 stimulations at the basic stimulation cyclelength. To determine the effective refractory period, the S1-S2 interval was reduced by 2msec, and the effective refractory period was defined as the point at which responses to premature stimulation S2 were lost.

For evaluation of drug effects, the atrial and ventricular effective refractory periods were determined before drug administration, then each compound was administrated intravenously at the dose of 0.3 mg/kg, and the atrial and ventricular effective refractory periods were determined from 5 min after the administration.

The results were shown as prolongation time in the atrial and ventricular effective refractory periods, i.e. [effective refractory period after administration] - [effective refractory period before administration] (msec).

Table 1 : compound prolongation time in effective refractory period (msec)

(Synthesis Example No.) Atrium ventricle

1 40 5

6 23 0 9 27 3

Results

The compounds of the present invention showed an prolongation effect on the effective refractory period selective for atrium.

Effects of the invention

Compounds according to the present invention exhibit prolongation effect on the effective refractory period selective for atrium, thus can be used as an anti- atrial fibrillation agents and an supraventricular antiarrhythmic agent, and are useful as pharmaceuticals. Further, since compounds according to the present invention have small influence on ventricle, they can contribute to safe treatments of aforementioned arrhythmic conditions.

Claims

1. A benzopyran derivative of the formula (I)

wherein,

R¹ and R² represent each independently a hydrogen atom or a C,„₆alkyl group in which said alkyl group may be optionally substituted with a halogen atom, a hydroxyl group or a C^alkoxy group in which said alkoxy group may be optionally substituted with a fluorine atom,

R³ represents a hydroxyl group or a group,

R⁴ represents a hydrogen atom, or R³ and R⁴ together form a bond,

R⁶ represents a hydrogen atom,

R⁷ represents a hydrogen atom or a C^alkyl group,

X is absent, or represents C=O or SO₂,

R⁸ represents a hydrogen atom or a C_|_₆alkyl group in which said alkyl group may be optionally substituted with a hydroxyl group or a C.,_₆alkoxy group,

Y represents a C₃.₈alkylene group or -(CH₂)_m-CR¹¹R¹²-(CH₂)_n- in which m and n represent each independently 0, 1 , 2, 3 or 4, and m+n is equal to or more than 2; when m represents 0, R >11 and R >12 represent each independently a C,_₆alkyl group, and when m represents those other than 0, R¹¹ and R¹² represent each independently a C,.₃alkyl group or a hydroxyl group, or R¹¹ and R¹² together form a oxygen atom,

R⁵ represents a fluorine atom, a trifluoromethyl group, an amino group, a C^alkylthio group, a C,_₆alkylamino group, a di~C.,_₆alkylamino group, a C^g alkylcarbonylamino group, a C^ alkylsulfonylamino group, an aminocarbonyl group, a alkylcarbonyl group, a group, a C^alkoxycarbonylamino group, an aminosulfonyl group, a O,_₆alkylsulfonyl group, a carboxyl group or a benzoyl group in which said benzoyl group may be optionally substituted with a C.,.₆alkyl group, a C^alkoxy group, a halogen atom, a nitro group or a cyano group, and when R⁹ represents a nitro group,

Y represents a C₄_₈alkylene group, -(CH₂)_m-CR¹¹R¹²-(CH₂)_n- in which m, n, R¹¹ and R¹² are same as the above or -(CH₂)₀-O-(CH₂)_p- in which o and p represent each independently 2, 3 or 4,

R⁵ represents a hydrogen atom, a fluorine atom, a trifluoromethyl group, a hydroxyl group, a formamide group, an amino group, a C^alkoxy group, a C₃.₈ cycloalkyl group, a C,„₆alkylthio group, a C_j.galkylamino group, a group, a C_j.galkylcarbonylamino group, a group, an aminocarbonyl group, a C.,_₆alkylaminocarbonyl group, a group, a group, a group, a C,.₆ alkoxycarbonylamino group, an aminosulfonyl group, a group, a carboxyl group or a benzoyl group in which said benzoyl group may be optionally substituted with a C,.₆alkyl group, a O,.₆alkoxy group, a halogen atom, a nitro group or a cyano group; or a pharmaceutically acceptable salt thereof.

2. The benzopyran derivative or pharmaceutically acceptable salt thereof according to claim 1 , wherein R¹ and R² represent a methyl group, R³ represents a hydroxyl group and R⁴ represents a hydrogen atom.

3. The benzopyran derivative or pharmaceutically acceptable salt thereof according to claim 2, wherein X represents C=O, R⁷ represents a hydrogen atom, and R⁸ represents a methyl group.

4. The benzopyran derivative or pharmaceutically acceptable salt thereof according to claim 2, wherein X is absent, and R⁷ and R⁸ represent a hydrogen atom.

5. The benzopyran derivative or pharmaceutically acceptable salt thereof according to claim 3, wherein R⁹ represents a hydrogen atom.

6. The benzopyran derivative or pharmaceutically acceptable salt thereof according to claim 3, wherein R⁹ represents a nitro group.

7. The benzopyran derivative or pharmaceutically acceptable salt thereof according to claim 4, wherein R⁹ represents a hydrogen atom.

8. The benzopyran derivative or pharmaceutically acceptable salt thereof according to claim 4, wherein R⁹ represents a nitro group.

9. A drug characterized by comprising a benzopyran derivative or pharmaceutically acceptable salt thereof according to claim 1 as an active ingredient.

10. A drug for treating arrhythmia characterized by comprising a benzopyran derivative or pharmaceutically acceptable salt thereof according to claim 1 as an active ingredient.