DESCRIPTION T-TYPE CALCIUM CHANNEL BLOCKER
Technical Field
[0001] The present invention relates to T-type calcium channel blockers being optically active dihydropyridine-5-phosphonate derivatives in which the absolute configuration of 4-position on dihydropyridine ring is R-configuration. In addition, the present invention relates to therapeutic or preventive agents against diseases for which T-type calcium channel blockers are effective.
Background Art
[0002] It is known that dihydropyridine-5-phosphonate derivatives (racemate) show oral anti-hypertensive action to be effective for cardiovascular diseases such as angia pectoris, cerebrovascular disease, hypertension or the like (see, for example Patent Documents 1-7).
[0003] The above-mentioned effect is owing to vasodilation mainly based on L-type calcium channel blocking action, and similar to that of L-type calcium antagonists represented by other numeral 1,4-dihydropyridine derivatives,
[0004] Recently, it was found that efonidipine (racemate) being a representative compound of dihydropyridine-5-phosphonate derivatives has T-type calcium channel blocking action in addition to L-type calcium channel blocking action (see, for example, Non-patent Document 1).
[0005] It is reported that the activation of T-type calcium channel participates in occurrence of hypercardia (see, for example Non-patent Document 2), heart failure (see, for example Non-patent Document 2), cardiomyopathy (see, for example Non-patent Document 3), tachyarrhythmia represented by atrial fibrillation (see, for example Non-patent Document 4), arterial sclerosis (see, for example Non-patent Document 5), renal disorder represented by nephritis/nephropathy (see, for example Non-patent Document 6), renal insufficiency (see, for example Non-patent Document 6), inflammation and edema (see, for example Non-patent Document 7), hyper-aldosteronism (see, for example Non-patent Document 8), neurogenic pain (see, for example Non-patent Document 9), and epilepsy (see, for example Non-patent Document 10). Therefore, it is though that T-type calcium channel blockers are effective for therapy or prevention of these diseases.

Patent Document 1: JP 61-30591 A (1986) Patent Document 2: JP 60-69089 A (1985) Patent Document 3: JP 1-275591 A (1989) Patent Document 4: JP 61-63688 A (1986) Patent Document 5: JP 63-233992 A (1988) Patent Document 6: JP 62-169795 A (1987) Patent Document 7: JP 62-169796 A (1987)
Non-patent Document 1: Masumiya H et al.: Eur J Pharmacol 335,p. 15-21 (1997) Non-patent Document 2: Mulder P et al.: J Am Coll Cardiol 29, p.416-421 (1997) Non-patent Document 3: Villame J et al.: Cardiovasc Drugs Ther 15, p.41-48 (2001) Non-patent Document 4: Fareh S et al.: Circulation 100, p.2191-2197 (1999) Non-patent Document 5: Noll G and Luscher TF: Cardiology 89, p.10-15 (1998) Non-patent Document 6: Baylis C et al.: Am J Kidney Dis 38 p.1292-1297 (2001) Non-patent Document 7: Bilici D et al.: Pharmacol Res 44, p.527-531 (2001) Non-patent Document 8. Lenglet S et al.: Endocrinology 143, p. 1748-60 (2002) Non-patent Document 9: McCallum JB et al.: Anesthesiology 98, p.209-216 (2003) Non-patent Document 10: Porcello DM et al.: J Neurophysiol 89, p.177-185 (2003)
[0006] However, dihydropyridine-5-phosphonate derivatives represented by efonidipine (racemate) have a possibility that the influence thereby on vasodilation and cardiac function based on L-type calcium channel blocking action becomes hindrance factors in the therapy of the above-mentioned diseases. In addition, they are liable to cause lowering in Quality of Life, such as headache, flash, dizziness, edema or the like based on vasodilation.
[0007] From the above, it is considered very useful to find T-type calcium channel blockers having a weak or little L-type calcium channel blocking action. [0008] The present inventors eagerly investigated in order to solve the above-mentioned problems. As a result of it, they found that optically active dihydropyridine-5-phosphonate derivatives in which the absolute configuration of 4-position on dihydropyridine ring is R-configuration show a weak or little L-type calcium channel blocking action, and a selective blocking action against T-type calcium channel, and they completed the present invention.
Disclosure of Invention

[0009] That is, the present invention provides the followings:
1, A T-type calcium channel blocker that is optically active 1,4-dihydropyridine
compound, a pharmaceutically acceptable salt thereof or a solvate thereof, of formula
(Formula Removed)
[wherein

R1 and R2 are independently of each other C1-6 alkyl group {the C1-6 alkyl group may be substituted witti phenyl group (the phenyl group may be substituted with C1-6 alkoxy group or halogen atom), C2.6alkenyl group or C2-6 alkynyl group (the C2.6alkenyl group and C2.6 alkynyl group may be substituted with phenyl group (the phenyl group may be substituted with C1-6 alkoxy group or halogen atom))}, or -L1-NR3R4 {R3 and R4 are independently of each other C1-6 alkyl group (the C1-6 alkyl group may be substituted with phenyl group (the phenyl group may be substituted with C1-6 alkoxy group or halogen atom)) or phenyl group (wherein the phenyl group may be substituted with C1-6 alkoxy group or halogen atom), L1 is C2.6alkylene group (the C2.6alkylene group may be substituted with C1-3 alkyl group or phenyl group (the phenyl group may be arbitrarily substituted with halogen atom, C1-3 alkyl group orC1-3 alkoxy group))}, or R1 and R2 together form -CR5R6-CR7R8-, -CR5R6-CR7Re-CR9R10- or -CR5R6-CR7R8-CR9R10-CR11R12- (R5toR12are independently of each other hydrogen atom or C1-6 alkyl group, or any two of them together with the carbon atom bonding them may form 5-, 6-or 7-rnembered ring);
X1 and X2 are independently of each other O or NR13 (R13 is hydrogen atom or C1-6 alkyl group);
Ar is phenyl group, pyridyl group, furyl group or 2,1,3-benzoxadiazoi-4-yl group {the phenyl group, pyridyl group, furyl group and 2,1,3-benzoxadiazol-4-yl group may arbitrarily substituted with one or two substituents selected from NO2, CF3, Br, Cl, F, R (R is C1-20 alkyl group), OH, OR14 (R14 is C1-6 alkyl group), OCHF2, COOR14, NH2, NHR14, NR14R1B (R15 is C1-6 alkyl group), CONH2, CONHR14, CONR14R15, COSR14, SR14, S(0)R14, S(0)2R14, S03H, SO3R14, SO2NH2, SO2NHR14, SO2NR14R15, CN and phenyloxy group}; Ra and Rb are independently of each other C1-6 alkyl group, -L2-NR16R17 {R16andR17are
independently of each other hydrogen atom, C1-6 alkyl group (the C1-6 alkyl group may be substituted with phenyl group (the phenyl group may be substituted with C1-6 alkoxy group or halogen atom)) or phenyl group (the phenyl group may be substituted with C1-6 alkoxy group or halogen atom), L2 is C2.6alkylene group (the C2.6 alkylene group may be arbitrarily substituted with C1-3 alkyl group or phenyl group (the phenyl group may be arbitrarily substituted with halogen atom, C1-3 alkyl group or C1-3 alkoxy group))}, CH20-L2-NR16R17, Ar1 (Ar1 is phenyl group (the phenyl group may be arbitrarily substituted with halogen atom, C1-3 alkyl group or C1-3 alkoxy group)), ChNCHAr1, CH?CH(OH)Ar', CHO, CN, CH2OH, CHOR16, -L2-N(CH2CH2)2NR16 or NR16R17;
Y is C1-20 alkyl group {the C1-20 alkyl group may be substituted with phenyl group (the phenyl group may be substituted with C1-6 alkoxy group or halogen atom), C2.6 alkenyl group or C2.6 alkynyl group (the C2.6 alkenyl group and C2.6 alkynyl group may be substituted with phenyl group (the phenyl group may be substituted with C1-6 alkoxy group or halogen atom))}, -L3-NR18R19 {R18and R19 are independently of each other C1-6 alkyl group (the C16 alkyl group may be substituted with phenyl group (the phenyl group may be substituted with C1-6 alkoxy group or halogen atom)) or phenyl group (the phenyl group may be substituted with C1-6 alkoxy group or halogen atom), L3 is C2.6 alkylene group (the C2.6 alkylene group may be arbitrarily substituted with C1-3 alkyl group or phenyl group (the phenyl group may be arbitrarily substituted with halogen atom, C1-3 alkyl group or C1-3 alkoxy group))},
(Formula Removed)
(wherein o and p are independently of each other 3 or 4, q is 1, 2 or 3), and * is absolute configuration of R.];
2 The T-type calcium channel blockerthat is optically active 1,4-dihydropyridine compound, a pharmaceutically acceptable salt thereof or a solvate thereof, as set forth in 1., wherein Y is -L3-NR18R19 {R18 and R19are independently of each other C alkyl group (the C1-6 alky! group may be substituted with phenyl group (the phenyl
group may be substituted withC1-6 alkoxy group or halogen atom)) or phenyl group (the phenyl group may be substituted with C1-6 alkoxy group or halogen atom), L3 is C2.6alkylene group (the C2.6alkylene group may be arbitrarily substituted with C1-3 alkyl group or phenyl group (the phenyl group may be arbitrarily substituted with halogen atom,C1-3 alkyl group or C1-3 alkoxy group))},
(Formula Removed)
(wherein o and p are independently of each other 3 or 4, q is 1 , 2 or 3), and Ra is C1-6 alkyl group;
3 The T-type calcium channel blockerthat is optically active 1,4-dihydropyridine compound, a pharmaceutically acceptable salt thereof or a solvate thereof, as set forth in 2., wherein Rb is C1-6 alkyl group, CN or NH2;
4. The T-type calcium channel blocker that is optically active 1 ,4-dihydropyridine
compound, a pharmaceutically acceptable salt thereof or a solvate thereof, as set
forth in 1 ., wherein Y is C1-20 alkyl group {the C1-20 alkyl group may be substituted with
phenyl group (the phenyl group may be substituted with C1-6 alkoxy group or halogen
atom), C2.6 alkenyl group or C2-6 alkynyl group (the C2-6 alkenyl group and C2-6 alkynyl
group may be substituted with phenyl group (the phenyl group may be substituted with
C1-6 alkoxy group or halogen atom))},
Rb is -L2-NR16R17 {R16and R17are independently of each other hydrogen atom, C1-6 alkyl group (the C1-6 alkyl group may be substituted with phenyl group (the phenyl group may be substituted with C1-6 alkoxy group or halogen atom)) or phenyl group (the phenyl group may be substituted with C1-6 alkoxy group or halogen atom), L2 is C2-6 alkylene group (theC2-6 alkylene group may be arbitrarily substituted with C1-3 alkyl group or phenyl group (the phenyl group may be arbitrarily substituted with halogen atom, C1-3 alkyl group or C1-3 alkoxy group))}, CH2O-L2-NR16R17 or -L2-N(CH2CH2)2NR16, and Ra is C1-6 alkyl group;
5. The T-type calcium channel blockerthat is optically active 1,4-dihydropyridine
compound, a pharmaceutically acceptable salt thereof or a solvate thereof, as set forth in 2., 3. or 4., wherein R1 and R2 are independently of each other C1-6 alkyl group (the C1-6 alkyl group may be substituted with phenyl group (the phenyl group may be substituted with C1-6 alkoxy group or halogen atom), C2.6alkenyl group or C2.6alkynyl group (the C2-6 alkenyl group and C2.6alkynyl group may be substituted with phenyl group (the phenyl group may be substituted with C1-6 alkoxy group or halogen atom))}, or R1 and R2 together form -CR5R6-CR7R8-, -CR5R6-CR7R8-CR9R10- or -CR5R6-CR7R8-CR9R10-CR11R12- (R5toR12are independently of each other hydrogen atom or Chalky! group, or any two of them together with the carbon atom bonding them may form 5-, 6-or 7-membered ring); X1 and X2 are both O;
6 The T-type calcium channel blocker that is optically active 1,4-dihydropyridine
compound, a pharmaceutically acceptable salt thereof or a solvate thereof, as set
forth in 5., wherein Ar is phenyl, 3-nitrophenyl, 2-nitrophenyl, 3-chlorophenyl, 2-
chlorophenyl, 3-methoxyphenyl, 2-methoxyphenyl, 2-trifluoromethylphenyl, 2-
trifluoromethylphenyl or 2,3-dichlorophenyl;
7 The T-type calcium channel blocker that is optically active 1,4-dihydropyridine
compound, a pharmaceutically acceptable salt thereof or a solvate thereof, as set
forth in 6., wherein R1 and R2 together form -CH2-C(CH3)2-CH2-, X1 and X2 are both 0,
Ar is 3-nitrophenyl, Ra and Rb are both methyl, and Y is 2-[benzyl(phenyl)amino]ethyl;
8 A pharmaceutical containing the T-type calcium channel blocker as set forth in any
one of 1. to 7.;
9. A therapeutic or preventive agent against a disease for which T-type calcium
channel blocking action is effective, containing the T-type calcium channel blocker as
set forth in any one of 1. to 7.;
10. A therapeutic or preventive agent against hypercardia, containing the T-type
calcium channel blocker as set forth in any one of 1. to 7.;
11. A therapeutic or preventive agent against heart failure, containing the T-type
calcium channel blocker as set forth in any one of 1. to 7.;
12. A therapeutic or preventive agent against cardiomyopathy, containing the T-type
calcium channel blocker as set forth in any one of 1. to 7.;
13. A therapeutic or preventive agent against atrial fibrillation, containing the T-type
calcium channel blocker as set forth in any one of 1. to 7.;
14. A therapeutic or preventive agent against tachycardia-arrhythmia, containing the
T-type calcium channel blocker as set forth in any one of 1. to 7.;
15. A therapeutic or preventive agent against arterial sclerosis, containing the T-type
calcium channel blocker as set forth in any one of 1. to 7.;
16. A therapeutic or preventive agent against nephritis, containing the T-type calcium
channel blocker as set forth in any one of 1. to 7.;
17. A therapeutic or preventive agent against nephropathy, containing the T-type
calcium channel blocker as set forth in any one of 1. to 7.;
18. A therapeutic or preventive agent against renal disorder, containing the T-type
calcium channel blocker as set forth in any one of 1. to 7.;
19. A therapeutic or preventive agent against renal insufficiency, containing the T-type
calcium channel blocker as set forth in any one of 1. to 7.;
20. A therapeutic or preventive agent against edema, containing the T-type calcium
channel blocker as set forth in any one of 1. to 7.;
21. A therapeutic or preventive agent against inflammation, containing the T-type
calcium channel blocker as set forth in any one of 1. to 7.;
22. A therapeutic or preventive agent against hyper-aldosteronism, containing the T-
type calcium channel blocker as set forth in any one of 1. to 7.;
23. A therapeutic or preventive agent against neurogenic pain, containing the T-type
calcium channel blocker as set forth in any one of 1. to 7.; and
24. A therapeutic or preventive agent against epilepsy, containing the T-type calcium
channel blocker as set forth in any one of 1. to 7.
Best Mode for Carrying Out the Invention
[0010] Hereinafter, the present invention is described in further detail.
[0011] In the meantime, "n" means normal, "i" means iso, "s" means secondary, "t"
means tertiary and "c" means cyclo in this specification.
[0012] Each substituent stated in this specification is described.
[0013] Halogen atom includes fluorine atom, chlorine atom, bromine atom and
iodine atom.
[0014] C1-3alkyl group may be a straight-chain alkyl group, branched alkyl group or
C3 cycloalkyl group, and includes for example methyl group, ethyl group, n-propyl
group, i-propyl group and c-propyl group, etc.
[0015] C1-6 alkyl group may be a straight-chain alkyl group, branched alkyl group or
C3-6 cycloalkyl group, and includes for example in addition to the above-mentioned
substituents for C1-3 alkyl group, n-butyl group, i-butyl group, s-butyl group, t-butyl
group, c-butyl group, n-pentyl group, 1-methyl-n-butyl group, 2-methyl-n-butyl group,
3-methyl-n-butyl group, 1,1-dimethyl-n-propyl group, c-pentyl group, 2-methyl-c-butyi group, n-hexyl group, 1-methyt-n-pentyl group, 2-methyl-n-pentyl group, 1,1-dimethyl-n-butyl group, 1-ethyl-n-butyl group, 1,1,2-trimethyl-n-propyl group, c-hexyl group, 1-methyl-c-pentyl group, 1-ethyl-c-butyl group and 1,2-dimethyl-c-butyl group, etc. [0016] C1-20alkyl group may be a straight-chain alkyl group, branched alkyl group or C3-20 cycloalkyl group, and includes for example in addition to the above-mentioned substituents for C1-6alkyl group, n-heptyl group, 2-c-pentylethyl group, n-octyl group, 2-c-hexylethyl group, 3-c-pentyl-n-propyl group, n-nonyl group, 3-c-hexyl-n-propyl group, 4-c-pentyl-n-butyl group, n-decyl group, 4-c-hexyl-n-butyl group, 5-c-pentyl-n-pentyl group, n-undecyl group, 5-c-hexyl-n-pentyl group, 6-c-pentyl-n-hexyl group, n-dodecyl group, n-tridecyl group, n-tetradecyl group, n-pentadecyl group, n-hexadecyl group, n-heptadecyl group, n-octadecyl group, n-nonadecyl group and n-eicosyl, etc. [0017] C2.6alkenyl group includes straight-chain or branched ones, and ethenyi group, 1-propenyl group, 2-propenyl group, 1-methyl-1 -ethenyi group, 1-butenyl group, 2-butenyl group, 3-butenyl group, 2-methyl-1-propenyl group, 2-methyl-2-propenyl group, 1-ethylethenyl group, 1-methyl-1-propenyl group, 1-methyl-2-propenyl group, 1-pentenyl group, 2-pentenyl group, 3-pentenyl group, 4-pentenyl group, 1-n-propylethenyl group, 1-methyl-1-butenyl group, 1-methyl-2-butenyl group, 1-methyl-3-butenyl group, 2-ethyl-2-propenyl group, 2-methyl-1-butenyl group, 2-methyl-2-butenyl group, 2-methyl-3-butenyl group, 3-methyl-1-butenyi group, 3-methyl-2-butenyl group, 3-methyl-3-butenyl group, 1,1-dimethyl-2-propenyl group, 1-i-propylethenyl group, 1,2-dimethyl-1-propenyl group, 1,2-dimethyl-2-propenyl group, 1-hexenyl group, 2-hexenyl group, 3-hexenyl group, 4-hexenyl group, 5-hexenyl group, 1-methyl-1-pentenyl group, 1-methyl-2-pentenyl group, 1-methyl-3-pentenyl group, 1-methyl-4-pentenyl group, 1-n-butylethenyl group, 2-methyl-1-pentenyl group, 2-methyl-2-pentenyl group, 2-methyl-3-pentenyl group, 2-methyl-4-pentenyl group, 2-n-propyl-2-propenyl group, 3-methyl-1-pentenyl group, 3-methyl-2-pentenyl group, 3-methyl-3-pentenyl group, 3-methyl-4-pentenyl group, 3-ethyl-3-butenyl group, 4-methyl-1-pentenyl group, 4-methyl-2-pentenyl group, 4-methyl-3-pentenyl group, 4-methyl-4-pentenyl group, 1,1-dimethyl-2-butenyl group, 1,1-dimethyl-3-butenyl group, 1,2-dimethyl-1-butenyl group, 1,2-dimethyl-2-butenyl group, 1,2-dimethyl-3-butenyl group, 1 -methyl-2-ethyl-2-propenyl group, 1-s-butylethenyl group, 1,3-dimethyl-1-butenyl group, 1,3-dimethyl-2-butenyl group, 1,3-dimethyl-3-butenyl group, 1-i-butylethenyl group, 2,2-dimethyl-3-butenyl group, 2,3-dimethyl-1-butenyl group, 2,3-dimethyl-2-butenyl group, 2,3-dimethyl-3-butenyl group, 2-i-propyl-2-propenyl group,
3,3-dimethyl-1-butenylgroup, 1~ethyl-1-butenyl group, 1-ethyl-2-butenyl group, 1-ethyl-3-butenyl group, 1-n-propyl-1-propenyl group, 1 -n-propyl-2-propenyl group, 2-ethyl-1-butenyl group, 2-ethyl-2-butenyl group, 2-ethyl-3-butenyl group, 1,1,2-trimethyl-2-propenyl group, 1-t-butylethenyl group, 1-methyl-1-ethyl-2-propenyl group, 1~ethyl-2-methyl-1-propenyl group, 1-ethyl-2-methyl-2-propenyl group, 1-i-propyl-1-propenyl group and 1-i-propyl-2-propenyl group, etc.
[0018] C2.6 aikynyl group includes straight-chain or branched ones, and ethynyl group, 1-propynyl group, 2-propynyl group, 1-butynyl group, 2-butynyl group, 3-butynyl group, 1 ~methyl-2-propynyl group, 1-pentynyl group, 2-pentynyl group, 3-pentynyl group, 4-pentynyl group, 1 -methy!-2-butynyl group, 1-methyl-3-butynyl group, 2~methy!-3-butynyl group, 3-methyl-1-butynyl group, 1,1-dimethyl-2-propynyl group, 2~ethyl-2-propynyl group, 1-hexynyl group, 2-hexynyl group, 3-hexynyl group, 4-hexynyl group, 5-hexynyl group, 1-methyl-2-pentynyl group, 1-methyl-3-pentynyl group, 1-methyl-4-pentynyl group, 2-methyl-3-pentynyl group, 2-methyl-4-pentynyl group, 3-methyl-1-pentynyl group, 3-methyl-4-pentynyl group, 4-methyl-1-pentynyl group, 4-methyl-2-pentynyl group, 1,1-dimethyi-2-butynyl group, 1,1-dimethyl-3-butynyl group, 1,2-dimethyl-3-butynyl group, 2,2-dimethyl-3-butynyl group, 3,3-dimethyl-1-butynyl group, 1-ethyl-2-butynyl group, 1-ethyl-3-butynyl group, 1-n-propyl-2-propynyl group, 2-ethyl-3-butynyl group, 1-methyl-1-ethyl-2-propynyl group and 1-i-propyl-2-propynyl group, etc.
[0019] C1- 3 alkoxy group may be a straight-chain alkoxy group, branched alkoxy group or C3 cycloalkoxy group, and includes for example methoxy group, ethoxy group, n-propoxy group, i-propoxy group and c-propoxy group, etc. [0020] C1-6 alkoxy group may be a straight-chain alkoxy group, branched alkoxy group or C3-6 cycloalkoxy group, and includes for example in addition to the above-mentioned substituents for C1-3alkoxy group, n-butoxy group, i-butoxy group, s-butoxy group, t-butoxy group, c-butoxy group, n-pentyloxy group, 1-methyl-n-butoxy group, 2-methyl-n-butoxy group, 3-methyl-n-butoxy group, 1,1 -dimethyl-n-propoxy group, c-pentyloxy group, 2-methyl-c-butoxy group, n-hexyloxy group, 1-methyl-n-pentyloxy group, 2-methyl-n-pentyloxy group, 1,1-dimethyl-n-butoxy group, 1-ethyl-n-butoxy group, 1,1, 2-trimethyl-n-propoxy group, c-hexyloxy group, 1-methyl-c-pentyloxy group, 1-ethyl-c-butoxy group and 1,2-dimethyl-c-butoxy group, etc. [0021] C2.6 afkylene group includes ethylene group, propylene group, butylene group, pentylene group and hexylene group, etc. [0022] 5-, 6- or 7-membered rings include c-pentyl, c-hexyl and c-heptyl, etc.
[0023] Preferable R1 and R2 include the followings in which the latter is more
preferable:
1 R1 and R2 together form -CR5R6-CR7R8-, -CR5R6-CR7R8-CR9R10- or -CR5R6-
CR7R8-CR9R10-CR1tR12- (R6toR12are independently of each other hydrogen atom or
C1-6alkyl group, or any two of them together with the carbon atom bonding them may
form 5-, 6- or 7-membered ring);
2. R1 and R2 together form -CR5R6-CR7R8-CR9R10- (R5toR10are independently of
each other hydrogen atom or C1-6alkyl group);
3. R1 and R2 together form -Ch2-C(Ch3)2-Ch2- or -ChCh3-Ch2-ChCh3-;

4 R1 and R2 are independently of each other C1-6alkyl group {the C1-6alkyl group
may be substituted with phenyl group (the phenyl group may be substituted with C1-6
alkoxy group or halogen atom), C2.6alkenyl group or C2-6alkynyl group (the C2-6alkenyl
group and C2-6alkynyl group may be substituted with phenyl group (the phenyl group
may be substituted with C1-6alkoxy group or halogen atom))};
5 R1 and R'! are independently of each other C1-6 alky! group;
6 R1 and R2 are both methyl group.
[0024] Preferable X1 and X2 include the followings in which the latter is more
preferable:
1 X1 and X2 are both O.
[0025] Preferable Ar includes the followings:
1 Phenyl group, 4-nitrophenyl group, 3-nitrophenyl group, 2-nitrophenyl group, 4-
chlorophenyl group, 3-chlorophenyl group, 2-chlorophenyl group, 4-methoxypheny!
group, 3-methoxyphenyi group, 2-methoxyphenyl group, 4-trifluoromethylphenyl
group, 3-trifluorornethylphenyl group, 2-trifluoromethylphenyl group and 2,3-
dichlorophenyl group;
2 Phenyl group, 3-nitrophenyl group, 2-nitrophenyl group, 3-chlorophenyl group, 2-
chlorophenyl group, 3-methoxyphenyl group, 2-methoxyphenyl group, 3-
trifluoromethylphenyl group, 2-trifluoromethylphenyl group and 2,3-dichlorophenyl
group;
3. Phenyl group, 3-nitrophenyl group, 2-nitrophenyl group, 3-chlorophenyl group, 2-
chlorophenyl group, 3-methoxyphenyl group, 2-methoxyphenyl group, 3-
trifluoromethylphenyl group and 2-trifluoromethylphenyl group;
4, Phenyl group, 3-nitrophenyl group, 2-nitrophenyl group, 3-methoxyphenyl group,
2-methoxyphenyl group, 3-trifluoromethylphenyl group and 2-trifluoromethylphenyl
group.
[0026] Preferable Ra includes the followings:
1 C1-6 alkyl group; more preferably
2, methyl group.
[0027] Preferable Rb includes the followings in which the latter is more preferable:
1 C1-6alkyl group, CN and Nh2;
2 methyl group, CN and Nh2;
3 -L2-NR16R17 {R16and R17are independently of each other hydrogen atom, C1-6 alkyl
group (the C1-6alkyl group may be substituted with phenyl group (the phenyl group
may be substituted with C1-6alkoxy group or halogen atom)) or phenyl group (the
phenyl group may be substituted with C1-6 alkoxy group or halogen atom), L2 is C2.6
aikylene group (the C2.6alkylene group may be arbitrarily substituted with C1-3alkyl
group or phenyl group (the phenyl group may be arbitrarily substituted with halogen
atom, C1-3alkyl group or C1-3 alkoxy group))}, -Ch20-L2-NR16R17and
-L2-N(Ch2Ch2)2NR16;
4 -Ch2O-L2~NR16R17;
5 -Ch2OCh2Ch2Nh2.
[0028] Preferable Y includes the followings in which the latter is more preferable:
1 C1-20 alkyl group {the C1-20 alkyl group may be substituted with phenyl group (the
phenyl group may be substituted with C1-6alkoxy group or halogen atom), C2 - 6 alkenyl
group or C2 - 6 alkynyl group (the C2 - 6 alkenyl group and C2 - 6 alkynyl group may be
substituted with phenyl group (the phenyl group may be substituted with C1 - 6 alkoxy
group or halogen atom))};
2 methyl group, ethyl group, i-propyl group, i-butyl group and methoxyethyl group;
3 -L3-NR18R19 {R18 and R18 are independently of each other C1 - 6 alkyl group (the C1 - 6
alkyl group may be substituted with phenyl group (the phenyl group may be
substituted with C1 - 6 alkoxy group or halogen atom)) or phenyl group (the phenyl group
may be substituted with C1 - 6 alkoxy group or halogen atom), L3 is C2.6 aikylene group
(the C2_6 aikylene group may be arbitrarily substituted with C1 - 3 alkyl group or phenyl
group (the phenyl group may be arbitrarily substituted with halogen atom, C1 - 3 alkyl
group or C1 - 3 alkoxy group))},
(Formula Removed)
(wherein o and p are independently of each other 3 or 4, q is 1, 2 or 3);
(Formula Removed)
active 1,4-dihydropyridine compound used in the present invention is a compound that can form a salt, the pharmaceutically acceptable salt thereof can be also used as an effective component.
[0030] the pharmaceutically acceptable salt includes hydrochlorides, hydrobromides, sulfates, methane sulfoneates, acetates, benzoates, tartrates, phosphates, lactates, maleates, fumaroles, malates, gluconates, salicylates and the like.
[0031] Preferably, hydrochlorides and methane sulfonates may be mentioned. [0032] the solvates are not specifically limited so long as they are pharmaceutically acceptable, and concretely include hydrates and a solvate with ethanol, and the like. [0033] T-type calcium channel blockers that are optically active 1,4-dihydropyridine compound, a pharmaceutically acceptable salt thereof or a solvate thereof used in the present invention, Pharmaceuticals containing the T-type calcium channel blockers, or therapeutic agents against diseases for which T-type calcium channel blocking action is effective, can be generally administered in oral administration forms such as tablets, capsules, powders, granules, pills, syrups and the like, permucosal absorption preparations such as intrarectal administration preparations, transnasal absorption
preparations, transvaginal absorption preparations and the like, transpulmonary absorption preparations, inhalants, ophthalmic solutions, percutaneous absorption preparations or injections. the present preparations can be administered as a simple therapeutic agent or as a mixture with other therapeutic agent. they may be administered as a single item but are generally administered in a form of pharmaceutical composition. these preparations can be produced according to any conventional method by adding pharmacologically and pharmaceutically acceptable additives. that is, for oral preparations, additives such as excipients, lubricants, binders, disintegrators, humectants, plasticizers, coating agents and the like can be used. Oral liquids may be in a form of aqueous or oily suspension, solution, emulsion, syrup, elixir and the like, or be provided as a dry syrup that is prepared with water or other appropriate solvent prior to use. the above-mentioned liquids may contain conventional additives such as suspending agents, perfumes, diluents or emusifiers. When it is administered intrarectally, it can be administered as a suppository. the suppository may contain suitable base ingredients such as cocoa fats, lauric fats, macrogol, glycerogelatin, witepsol, sodium stearate or a mixture thereof, and optionally emulsifiers, suspending agents, preservatives and the like. For the injections, the followings are used: resolvents or solubilizing agents, such as distilled water for injections that can constitute aqueous dosage form or on use-dissolved type dosage form, saline, 5% glucose solution, propylene glycol and the like, pharmaceutical ingredients such as ph adjusters, isotonizing agents, stabilizers and the like.
[0034] When the Pharmaceuticals of the present invention are administered to human, the dosage is determined depending on age or state of the patient. In case where the patient is adult, oral preparations or intrarectal administration is carried out in an amount of about 0.1 mg to 1000 mg per day per body, and an injection is administered in an amount of about 0.05 mg to 500 mg per day per body. these values are merely examples, and the dosage is determined according to the condition of a patient.
[0035] the scene which the present invention is applied includes the scene which the use of the compounds having T-type calcium channel blocking activity is expected to improve the condition of the disease. Concretely, the compounds of the present invention are effective for therapy or prevention of hypercardia, heart failure, cardiomyopathy, tachyarrhythmia represented by atrial fibrillation, arterial sclerosis, renal disorder represented by nephritis/nephropathy, renal insufficiency, inflammation
and edema, hyper-aldosteronism, neurogenic pain, epilepsy, and the like.
[0036] the optically active 1,4-dihydropyridine compounds of formula (1) can be
produced with reference to the methods described in JP 1-113398 A (1989), JP 2-
011592 A (1990), Chem. Pharm. Bull. ,40(9), 2377-2381 (1992) and Chem. Pharm.
Bull. ,40(9), 2370-2376 (1992).
[0037] the production process thereof is shown in Scheme 1.
Scheme 1
(Scheme Removed)
wherein R1, R2, X1, X2, Ra, Rb, Ar, Y and * are defined similarly to the above.
[0038] First of all, styryl phosphonate (2) and optically active aminocrotonic acid derivative (3) are heated in toluene under azeotropic dehydration condition to obtain 1,4-dihydropyridine derivative (1a).
[0039] Next, 1,4-dihydropyridine derivative (1a) is subjected to diastereomer separation with crystallization or chromatography, etc. to obtain (1a-R), and then the (1a-R) is subjected to methoxymethylation to obtain (1b-R), or the (1a) is subjected to methoxymethylation to obtain (1b), and then the (1b) is subjected to diastereomer separation with crystallization or chromatography, etc. to obtain (1b-R).
[0040] then, transesterification is carried out and methoxymethyl group is eliminated with hydrogen chloride to produce optically active 1,4-dihydropyridine compound of formula (1).
[0041] In addition, according to the methods described in JP 59-161392 A (1984), JP 60-69089 A (1985), JP 60-248693 A (1985), JP 60-258194 A (1985), JP 61-30591 A (1986), JP 61-37793 A (1986), JP 61-63688 A (1986), JP 61-210092 A (1986), JP 61-254569 A (1986), JP 62-169795 A (1987), JP 62-169796 A (1987), JP 62-195392 A (1987), JP 63-68591 A (1988), JP 63-233992 (1988), JP 1-113398 A (1989), JP 1-275591 A (1989), Chem. Pharm. Bull.,40(9), p.2362-2369, (1992) and Chem. Pharm. Bull.,40(9), p.2370-2376, (1992), racemic 1,4-dihydropyridine compound is produced, and then optically active 1,4-dihydropyridine compound can be also produced by separating it with hPLC by use of an optically active column.
[0042] hereinafter, the present invention is described based on examples to which
the present invention is not limited at all.
[0043] Racemic efonidipine synthesized according to the method described in JP
63-233992 A (1988) was collected with hPLC through optically active isomer
separation column to obtain R-form and S-form of efonidipine (1,4-dihydro-2,6-
dimethyl-5-(5,5-dimethyl-2-oxo-1,3,2-dioxaphosphorinan-2-yl)-4-(3-nitrophenyl)-3-
pyridine carboxylic acid 2-[benzyl (phenyl) amino] ethylester) that was used as
examples.
hPLC Collection Condition
Column: ChIRALCEL OC (manufactured by Daicel Chemical Industries, Ltd.)
Column size: 20 c mo x 50 cm
Eluent: methanol
Column temperature: room temperature
Flow rate: 760 rnL/min.
[0044] In the meantime, compounds as examples other than the above-mentioned
efonidipine compound were synthesized as follows:
[0045] the compounds that 5-position of dihydropyridine ring is diethylphosphonyl
(Z2) were synthesized with reference to the production process described in JP 60-
69089 A (1985) and JP 60-248693 A (1985).
[0046] the compounds that 5-position of dihydropyridine ring is 5,5-dimethyl-2-oxo-
1,3,2-dioxaphosphorinan-2-yl (Z1) were synthesized with reference to the production
process described in JP 62-169795 A (1987) and Chem. Pharm. Bull., 40(9), p.2362-
2369 (1992).
[0047] the compounds that 5-position of dihydropyridine ring is 4,6-dimethyl-2-oxo-
1,3,2-dioxaphosphorinan-2-yl (Z3, Z4) were synthesized with reference to the
production process described in JP 63-68591 A (1988) and Chem. Pharm. Bull., 40(9),
p 2370-2376 (1992).
[0048] In addition, the following compound (1-a) was produced according to the
process shown below.
(Scheme Removed)
[0049] After 8.05 g (19.3 mmoi) of compound (3), 1.64 g (21.3 mmol) of ammonium acetate and 80 ml of ethanol were mixed, the resulting mixture was refluxed with heating for 45 minutes. To the obtained reaction solution, 7.23 g (21.3 mmol) of compound (2) was added, and the resulting mixture was further refluxed with heating for 3 hours. After cooling, the solvent was distilled off under a reduced pressure, and 100 ml of toluene and 50 ml of 10% sodium carbonate aqueous solution were added, then the resulting mixture was shaken and allowed to stand and thereby separated into phases. the organic phase was washed with 20% sodium chloride solution, dried over magnesium sulfate (anhydrous), and then the solvent was distilled off under a reduced pressure. the residue was purified with silica gel chromatography (hexane-ethyl acetate 4:1, V/V to ethyl acetate) to obtain 6.04 g (yield 42%) of compound (4) as yellow amorphous. (Compound (3) was produced according to the method described in EP0599220A1.)
mS m/z: 738 (m* +1), 1h-NmR (CDCI3) d (ppm): 0.87 (3h, s), 1.08 (3h, s), 2.39 (3h, d), 2.42 (2h, t), 3.51-3.73 (4h, m), 3.69 (3h, s), 4.21-4.31 (2h, m), 4.56 (1h, d), 4.70 (1h, d), 4.93 (1h, d), 7.17-7.49 (16h, m), 7.62 (1h, d), 8.02 (1h, d), 8.11 (1h, m). [0050] After 500 mg (0.678 mmol) of compound (4) was dissolved in 5 ml of methanol, 500 mg (1.37 mmol) of 10% hCI-meOh was added thereto and the resulting mixture was refluxed with heating for 2.5 hours. After cooling on standing, the solvent was distilled off under a reduced pressure, and 20 ml of chloroform and 10 ml of 10% sodium carbonate aqueous solution were added, then the resulting mixture was shaken and allowed to stand and thereby separated into phases. the organic phase was washed with water, dried over magnesium sulfate (anhydrous), and then the solvent was distilled off under a reduced pressure. the residue was purified with silica gel chromatography (hexane-ethyl acetate 20:1 to ethyl acetate, then chloroform-methanol 5:1, V/V) to obtain 216 mg (yield 64%) of compound (1-a) as yellow oily product.
mS m/z: 495 (m+), 1h-NmR (CDCI3) 6 (ppm): 0.89 (3h, s), 1.04 (3h, s), 2.46 (3h, d), 3.00-3.03(2h, m), 3.54-3.74 <4h, m), 3.68 (3h, s), 4.09-4.27 (2h, m), 4.61 (1h, d), 4.66 (1h, d), 4.89 (1h, d), 7.40 (1h, dd), 7.65 (1h, d), 8.01 (1h, d), 8.10 (1h, m), 8.47 (1h, brm).
Pharmacological Test Example 1 (effect on L-type and T-type Ca (calcium) channel expressed in mammalian cells (BhK cells)) Test method
(Example Removed)
Results
[0052] the optically active R-form of efonidipine showed concentration-dependent inhibition in a concentration of 0.1 j^m or more for T-type Ca channel, and did not show any inhibition for L-type Ca channel even in a concentration of 10 jxm. On the other hand, the S-form showed a strong inhibition for L-type Ca channel that is as high as 55.6±7.1% in 1 nm. From these results, it was found that R-form of efonidipine has a high selectivity for T-type Ca channel.
[0053] In addition, L-type Ca channel inhibition was shown only by one optically active S-form, whereas T-type Ca channel inhibition was shown by both optically active forms to equal level. this suggests that if 1,4-dihydropyridine compound showing T-type Ca channel blocking effect in a form of racemate is found, the one (R-form) of the optically active products will be a compound having a high selectivity for T-type Ca channel.
Pharmacological Test Example 2 (effect on T-type Ca channel expressed in
mammalian cells (BhK cells))
Test method
[0054] Similarly to the procedure of Pharmacological Test Example 1, the
compounds of formula Ar
were measured for T-type Ca channel inhibition in a drug concentration of 10 µm, and the results are shown in table described below.
[0055] In the meanwhile, Z1 to Z4, Y1 to Y7, B1 and A1 to A7 used in the table mean the kind of substituents of the compounds as follows:
(Example Removed)
[0056] As the above-mentioned compounds in a form of racemate showed T-type calcium channel inhibition, it is assumed that the one of the optically active product (R-form shows no L-type calcium channel inhibition) becomes a compound showing a selective T-type calcium channel inhibition.
Preparation Example 1
[0057] Granules containing the following components were prepared.
Components Compound of formula (1) 10 mg
Lactose 700 mg
Cornstarch 274 mg
hPC-L 16 mg
1000mg
the compound of formula (1) and lactose were passed through 60-mesh sieve.
Cornstarch was passed through 120-mesh sieve. these components were mixed in
a twin-cylinder mixer. hydroxypropylcellulose having a low viscosity (hPC-L) was
added to the mixed powders, the resulting mixture was kneaded, granulated
(extrusion granulation, bore 0.5 to 1 mm), and then dried. the obtained dried
granules were passed through a vibrating screen (12/60 mesh) to obtain an intended
granules.
Preparation Example 2
[0058] Powders for filling into capsules containing the following components were
prepared.
Components Compound of formula (1) 10mg
Lactose 79 mg
Cornstarch 10mg
magnesium stearate 1 mg
100mg
the compound of formula (1) and lactose were passed through 60-mesh sieve. Cornstarch was passed through 120-mesh sieve. these components were mixed with magnesium stearate in a twin-cylinder mixer. 100 mg of 10 times powders were filled into No. 5 hard gelatin capsule. Preparation Example 3
[0059] Granules for filling into capsules containing the following components were
prepared.
Components Compound of formula (1) 15mg
Lactose 90 mg
Cornstarch 42 mg
hPC-I 3mg
150mg
the compound of formula (1) and lactose were passed through 60-mesh sieve. Cornstarch was passed through 120-mesh sieve. these components were mixed in a twin-cylinder mixer. hydroxypropylcellulose having a low viscosity (hPC-L) was added to the mixed powders, the resulting mixture was kneaded, granulated, and then dried. the obtained dried granules were passed through a vibrating screen (12/60 mesh) to obtain an intended granules. 150 mg of the granules were filled into No. 4 hard gelatin capsule. Preparation Example 4
[0060] Tablets containing the following components were prepared.
Components Compound of formula (1) 10mg
Lactose 90 mg
Fine crystalline cellulose 30 mg
magnesium stearate 5 mg
CmC-Na 15 mg
150mg
the compound of formula (1), lactose, fine crystalline cellulose and CmC-Na (carboxymethylcellulose sodium salt) were passed through 60-mesh sieve and mixed one another. magnesium stearate was added to the mixed powders to obtain mixed powders for preparation. the powders were subjected to direct compression to obtain 150 mg of tablets. Preparation Example 5
[0061] Intravenous preparations were prepared as follows.
Compound of formula (1) 100mg
Saturated fatty acid glyceride 1000 ml
Generally, the solution containing the above-mentioned components was intravenously administered to a patient in a rate of 1 ml per minute.
Industrial Applicability
[0062] As the compounds of the present invention have selective T-type calcium channel blocking effect, it is assumed that these compounds can be used for therapy of hypercardia, heart failure, cardiomyopathy, tachycardia-arrhythmia represented by atrial fibrillation, arterial sclerosis, renal disorder represented by nephritis/nephropathy, renal insufficiency, inflammation and edema, hyper-aldosteronism, neurogenic pain, or epilepsy, without adverse effect on blood pressure, cardiac function and Quality of Life. therefore, the present invention can provide therapeutic agents for the above-mentioned diseases with effectiveness, safety and Quality of Life, and thus it is very useful for example in the art of medical treatment and medicine.

CLAIMS
1. A T-type calcium channel blocker that is optically active 1,4-dihydropyridine compound, a pharmaceutically acceptable salt thereof or a solvate thereof, of formula
(Formula Removed)
[wherein

R1 and R2 are independently of each other C1- 6alkyl group {the C1- 6 alkyl group may be substituted with phenyl group (the phenyl group may be substituted with C1- 6alkoxy group or halogen atom), C2.6alkenyl group or C2- 6 alkynyl group (the C2- 6alkenyl group and C2.6alkynyl group may be substituted with phenyl group (the phenyl group may be substituted with C1- 6alkoxy group or halogen atom))}, or -L1-NR3R4 {R3 and R4 are independently of each other C1- 6 alkyl group (the C1- 6 alkyl group may be substituted with phenyl group (the phenyl group may be substituted with C1- 6alkoxy group or halogen atom)) or phenyl group (wherein the phenyl group may be substituted with C1- 6alkoxy group or halogen atom), L1 is C2- 6alkylene group (the C2- 6 alkylene group may be substituted with C1- 3alkyl group or phenyl group (the phenyl group may be arbitrarily substituted with halogen atom, C1- 3 alkyl group or C1- 3alkoxy group))}, or R1 and R2 together form -CR5R6-CR7R8-, -CR5R6-CR7R8-CR9R10- or -CR5R6-CR7R8-CR9R10-CR11R12- (R5toR12are independently of each other hydrogen atom or C1- 6 alkyl group, or any two of them together with the carbon atom bonding them may form 5-, 6-or 7-membered ring);
X1 and X2 are independently of each other O or NR13 (R13 is hydrogen atom or C1- 6 alkyl group);
Ar is phenyl group, pyridyl group, furyl group or 2,1,3-benzoxadiazol-4-yl group {the phenyl group, pyridyl group, furyl group and 2,1,3-benzoxadiazol-4-yl group may arbitrarily substituted with one or two substituents selected from NO2, CF3, Br, Cl, F, R (R is C1- 20 alkyi group), OH, OR14 (R14 is C1- 6 alkyl group), OCHF2, COOR14, NH2, NHR14, NR14R15 (R15 is C1- 6 alkyl group), CONH2, CONHR14, CONR14R15, COSR14, SR14, S(O)R14, S(0)2R14, SO3H, S03R14, SO2NH2l SO2NHR14, SO2NR14R15, CN and phenyloxy group};
Ra and Rb are independently of each other C1-6 alkyl group, -L2-NR16R17 {R16 and R17 are independently of each other hydrogen atom, C1-6alkyl group (the C1-6alkyl group may be substituted with phenyl group (the phenyl group may be substituted with C1-6 alkoxy group or halogen atom)) or phenyl group (the phenyl group may be substituted with C1-6alkoxy group or halogen atom), L2 is C2- 6 alkylene group (the C2- 6alkylene group may be arbitrarily substituted with C1-3 alkyl group or phenyl group (the phenyl group may be arbitrarily substituted with halogen atom, C1-3alkyl group or C1-3alkoxy group))}, CH2O-L2-NR16R17, Ar1 (Ar1 is phenyl group (the phenyl group may be arbitrarily substituted with halogen atom, C1-3alkyl group or C1-3alkoxy group)), CH=CHAr1, CH2CH(OH)Ar1, CHO, CN, CH2OH, CHOR16, -L2-N(CH2CH2)2NR16 or NR16R17;
Y is C1-20 alkyl group {the C2- 6alkyl group may be substituted with phenyl group (the phenyl group may be substituted with C1- 6alkoxy group or halogen atom), C2- 6 alkenyl group or C2.6 alkynyl group (the C2- 6 alkenyl group and C2- 6 alkynyl group may be substituted with phenyl group (the phenyl group may be substituted with C1- 6alkoxy group or halogen atom))}, -L3-NR18R19 {R18and R19are independently of each other C1- 6alkyl group (the C1- 6alkyl group may be substituted with phenyl group (the phenyl group may be substituted with C1- 6alkoxy group or halogen atom)) or phenyl group (the phenyl group may be substituted with C1- 6alkoxy group or halogen atom), L3 is C2.6 alkylene group (the C2- 6alkylene group may be arbitrarily substituted with C1- 3 alkyl group or phenyl group (the phenyl group may be arbitrarily substituted with halogen atom, C1- 3 alkyl group or C1- 3 alkoxy group))},
(Formula Removed)
(wherein o and p are independently of each other 3 or 4, q is 1 , 2 or 3), and * is absolute configuration of R.]
2 The T-type calcium channel blocker that is optically active 1 ,4-dihydropyridine compound, a pharmaceutically acceptable salt thereof or a solvate thereof, according
to claim 1, wherein Y is -L3-NR18R19 {R18 and R19 are independently of each other C1-6 alkyl group (the C1-6alkyl group may be substituted with phenyl group (the phenyl group may be substituted with C1-6alkoxy group or halogen atom)) or phenyl group (the phenyl group may be substituted with C1-6alkoxy group or halogen atom), L3 is C2.6alkylene group (the C2.6alkylene group may be arbitrarily substituted with C1-3alkyl group or phenyl group (the phenyl group may be arbitrarily substituted with halogen atom, C1-3alkyl group or C1-3alkoxy group))},
(Formula Removed)
(wherein o and p are independently of each other 3 or 4, q is 1, 2 or 3), and Ra is C1-6 alkyl group,
3 The T-type calcium channel blocker that is optically active 1,4-dihydropyridine
compound, a pharmaceutically acceptable salt thereof or a solvate thereof, according
to claim 2, wherein Rb is C1-6 alkyl group, CN or NH2.
4 The T-type calcium channel blocker that is optically active 1,4-dihydropyridine
compound, a pharmaceutically acceptable salt thereof or a solvate thereof, according
to claim 1, wherein Y is C1-20 alkyl group {the C1-20 alkyl group may be substituted with
phenyl group (the phenyl group may be substituted with C1-6 alkoxy group or halogen
atom), C2-6alkenyl group or C2.6 alkynyl group (the C2-6 alkenyl group and C2.6 alkynyl
group may be substituted with phenyl group (the phenyl group may be substituted with
C1-6 alkoxy group or halogen atom))},
Rb is -L2-NR16R17 {R16 and R17are independently of each other hydrogen atom, C1-6alkyl group (the C1-6alkyl group may be substituted with phenyl group (the phenyl group may be substituted with C1-6 alkoxy group or halogen atom)) or phenyl group (the phenyl group may be substituted with C1-6 alkoxy group or halogen atom), L2 is C2.6 alkylene group (the C2.6 alkylene group may be arbitrarily substituted with C1-3alkyl group or phenyl group (the phenyl group may be arbitrarily substituted with halogen
atom, C1-3 alkyl group or C1-3 alkoxy group))}, CH2O-L2-NR16R17 or -L2-N(CH2CH2)2NR16,
and
Ra is C1-6 alkyl group.
5 The T-type calcium channel blocker that is optically active 1,4-dihydropyridine
compound, a pharmaceutically acceptable salt thereof or a solvate thereof, according
to claim 2, 3 or 4, wherein R1 and R2 are independently of each other C1- 6 alkyl group
{the C1-6 alkyl group may be substituted with phenyl group (the phenyl group may be
substituted with C1-6alkoxy group or halogen atom), C2- 6alkenyl group or C2 -6alkynyl
group (the C2- 6 alkenyl group and C2- 6alkynyl group may be substituted with phenyl
group (the phenyl group may be substituted with C2- 6alkoxy group or halogen atom))},
or R1 and R2 together form -CR5R6-CR7R8-, -CR5R6-CR7R8-CR9R10- or -CR5R6-CR7R8-
CR9R10-CR11R12- (R5to R12are independently of each other hydrogen atom or C1-6alkyl
group, or any two of them together with the carbon atom bonding them may form 5-, 6-
or 7-membered ring);
X1 and X2 are both O.
6 The T-type calcium channel blocker that is optically active 1,4-dihydropyridine
compound, a pharmaceutically acceptable salt thereof or a solvate thereof, according
to claim 5, wherein Ar is phenyl, 3-nitrophenyl, 2-nitrophenyl, 3-chlorophenyl, 2-
chlorophenyl, 3-methoxyphenyl, 2-methoxyphenyl, 2-trifluoromethylphenyl, 2-
trifluoromethylphenyl or 2,3-dichlorophenyl.
7 The T-type calcium channel blocker that is optically active 1,4-dihydropyridine
compound, a pharmaceutically acceptable salt thereof or a solvate thereof, according
to claim 6, wherein R1 and R2 together form -CH2-C(CH3)2-CH2-, X1 and X2 are both O,
Ar is 3-nitrophenyl, Ra and Rb are both methyl, and Y is 2-[benzyl(phenyl)amino]ethyl.
8 A pharmaceutical containing the T-type calcium channel blocker according to
any one of claims 1 to 7.
9 A therapeutic or preventive agent against a disease for which T-type calcium
channel blocking action is effective, containing the T-type calcium channel blocker
according to any one of claims 1 to 7.
10. A therapeutic or preventive agent against hypercardia, containing the T-type calcium channel blocker according to any one of claims 1 to 7.
11 A therapeutic or preventive agent against heart failure, containing the T-type
calcium channel blocker according to any one of claims 1 to 7.
12 A therapeutic or preventive agent against cardiomyopathy, containing the T-
type calcium channel blocker according to any one of claims 1 to 7.

13. A therapeutic or preventive agent against atrial fibrillation, containing the T-type
calcium channel blocker according to any one of claims 1 to 7.
14. A therapeutic or preventive agent against tachycardia-arrhythmia, containing
the T-type calcium channel blocker according to any one of claims 1 to 7.
15. A therapeutic or preventive agent against arterial sclerosis, containing the T-
type calcium channel blocker according to any one of claims 1 to 7.
16. A therapeutic or preventive agent against nephritis, containing the T-type
calcium channel blocker according to any one of claims 1 to 7.
17 A therapeutic or preventive agent against nephropathy, containing the T-type calcium channel blocker according to any one of claims 1 to 7.
18. A therapeutic or preventive agent against renal disorder, containing the T-type
calcium channel blocker according to any one of claims 1 to 7.
19. A therapeutic or preventive agent against renal insufficiency, containing the T-
type calcium channel blocker according to any one of claims 1 to 7,
20. A therapeutic or preventive agent against edema, containing the T-type calcium
channel blocker according to any one of claims 1 to 7.
21. A therapeutic or preventive agent against inflammation, containing the T-type
calcium channel blocker according to any one of claims 1 to 7.
22. A therapeutic or preventive agent against hyper-aldosteronism, containing the
T-type calcium channel blocker according to any one of claims 1 to 7.
23. A therapeutic or preventive agent against neurogenic pain, containing the T-
type calcium channel blocker according to any one of claims 1 to 7.
24. A therapeutic or preventive agent against epilepsy, containing the T-type
calcium channel blocker according to any one of claims 1 to 7.