首页> 外国专利> Indole derivatives and 2,3 - dihidroindol,Pharmaceutical compositions containing these compounds and the use of such compounds for the preparation of a Medicament for the treatment of disorders sensitive to inhibition of reabsoRcion serotonin 5-ht1a receptor antagonism.

Indole derivatives and 2,3 - dihidroindol,Pharmaceutical compositions containing these compounds and the use of such compounds for the preparation of a Medicament for the treatment of disorders sensitive to inhibition of reabsoRcion serotonin 5-ht1a receptor antagonism.

机译:吲哚衍生物和2,3-二氢吲哚,含有这些化合物的药物组合物以及此类化​​合物在制备药物中的用途,所述药物用于治疗对抑制5-羟色胺5-羟色胺5-ht1a受体拮抗作用敏感的疾病。

摘要

1. An indole or 2,3-dihydroindole derivative having the formula: any of its enantiomers or any mixture thereof, or an acid addition salt thereof, wherein X is -O-, -S-, or -CR4R5-; and Y is -CR6R7-, -CR6R7-CR8R9-, or -CR6=CR7-; or X and Y together form a group -CR4=CR5-, or -CR4=CR5-CR6R7-; Z is-O-, or -S-; W is N, C, or CH; A is a group selected from a group of formula (II), (III) and (IV): wherein the dotted lines mean an optional bond; R1, R2, R3, R12, R13, R14, R15, R16 and R17 are each independently selected from hydrogen, halogen, trifluoromethyl, C1-C4 alkyl, C2-C4 alkenyl, C2-C4 alkynyl, C3-C7 cycloalkyl, C1-C4 alkoxy, hydroxy, formyl, CO-C1-4 alkyl, amino, C1-4 alkylamino, (C1-4)2-dialkylamino, CO-C1-4alkylamino, alkoxycarbonylamino, aminocarbonylamino, alkylaminocarbonylamino, dialkylaminocarbonylamino, nitro and cyano; R4, R5, R6,R7, R8 and R9 are each independently selected form hydrogen and C1-4alkyl; and R11 is selected from hydrogen, C1-4alkyl, C2-4alkenyl, C2-4alkynyl, C3-7cycloalkyl, aryl, aryl-C1-4alkyl, CO-C1-4alkyl and formyl. 2. The compounds according to Claim 1 wherein Z is -O-. 3. The compounds according to Claim 1 wherein Z is -S-. 4. The compounds according to Claim 1 wherein A is a group of formula (II). 5. The compounds according to Claim 1 wherein A is a group of formula (III). 6. The compounds according to Claim 1 wherein A is a group of formula (IV). 7. The compounds according to Claim 2 wherein A is a group of formula (II). 8. The compounds according to Claim 2 wherein A is a group of formula (III). 9. The compounds according to Claim 2 wherein A is a group of formula (IV). 10. The compounds according to Claim 3 wherein A is a group of formula (II). 11. The compounds according to Claim 3 wherein A is a group of formula (III). 12. The compounds according to Claim 3 wherein A is a group of formula (IV). 13. The compounds according to Claims 1 to 12 wherein R4, R5, R6, R7, R8 and R9 is selected from hydrogen or methyl. 14. The compound according to Claim 1 which is 3-[2-[4-(1,4-benzodioxan-5-yl)piperazin-1-yl]ethyl]-5-chloro-1H-indole, 3-[2-[4-(1,4-benzodioxan-5-yl)piperazin-1-yl]ethyl]-5-bromo-1H-indole, 3-[2-[4-(1,4-benzodioxan-5-yl)piperazin-1-yl]ethyl]-2-methyl-1H-indole, 6-chloro-3-[2-[4-(2,2,5-trimethyl-2,3-dihydrobenzofuran-7-yl)piperidin-1-yl]ethyl]-1H-indole, 3-[2-[4-(1,4-benzodioxan-5-yl)piperazin-1-yl]ethyl]-4-chloro-1H-indole, 6-chloro-3-[2-[4-(2,2-dimethyl-2,3-dihydrobenzofuran-7-yl)piperidin-1-yl]-1H-indole, 6-chloro-3-[2-[4-(2,2-dimethyl-2,3-dihydrobenzofuran-7-yl)-1,2,3,6-tetrahydro-1pyridyl]ethyl]-1H-indole, 3-[2-[4-(1,4-benzodioxan-5-yl)piperazin-1-yl]ethyl]-5-fluoro-1H-indole, 3-[2-[4-(1,4-benzodioxan-5-yl)piperazin-1-yl]ethyl]-5-methoxy-1H-indole, 3-[2-[4-(1,4-benzodioxan-5-yl)piperazin-1-yl]ethyl]-1H-indole, 3-[2-[4-(1,4-benzodioxan-5-yl)piperazin-1-yl]ethyl]-6-chloro-1H-indole, 3-[2-[4-(5-chloro-2,2-dimethyl-2,3-dihydrobenzofuran-7-yl)piperazin-1-yl]ethyl]-1H-indole, 6-chloro-3-[2-[4-(5-chloro-3,3-dimethyl-2,3-dihydrobenzofuran-7-yl)piperazin-1-yl]ethyl]-1H-indole, 6-chloro-3-[2-[4-(6-chloro-2,2-dimethyl-3,4-dihydro-2H-1-benzopyran-8-yl)piperazin-1yl]ethyl]-1H-indole, 6-chloro-3-[2-[4-(2,2-dimethyl-2,3-dihydrobenzofuran-7-yl)piperazin-1-yl]ethyl]-1H-indole, 3-[2-[4-(1,4-benzodioxan-5-yl)piperazin-1-yl]ethyl]-5-methyl-1H-indole, or 3-[2-[4-(1,4-benzodioxan-5-yl)piperazin-1-yl]ethyl]-6-methyl-1H-indole, 6-chloro-3-[2-[4-(6-chloro-1,4-benzodioxan-5-yl)piperazin-1-yl]ethyl]-1H-indole, 5-chloro-3-[2-[4-(2,3-dihydrobenzofuran-7-yl)piperazin-1-yl]ethyl]-1H-indole, 3-[2-[4-(2,3-dihydrobenzofuran-7-yl)piperazin-1-yl]ethyl]-5-fluoro-1H-indole, 3-[2-[4-(benzothiophen-7-yl)piperazin-1-yl]ethyl]-5-chloro-1H-indole, 3-[2-[4-(benzothiopyran-8-yl)piperazin-1-yl]ethyl]-5-chloro-1H-indole, 3-[2-[4-(benzothiopyran-8-yl)piperazin-1-yl]ethyl]-5-bromo-1H-indole, 3-[2-[4-(benzothiopyran-8-yl)piperazin-1-yl]ethyl]-6-chloro-1H-indole, 3-[2-[4-(1,4-benzodioxan-5-yl)-1,2,3,6-tetrahydropyridin-1-yl]ethyl]-5-chloro-1H-indole, 3-[2-[4-(1,4-benzodioxan-5-yl)-1,2,3,6-tetrahydropyridan-1-yl]ethyl]-5-fluoro-1H-indole, 3-[2-[4-(1,4-benzodioxan-5-yl)piperidin-1-yl]ethyl]-6-chloro-1H-indole, 3-[2-[4-(1,4-benzodioxan-5-yl)piperidin-1-yl]ethyl]-5-chloro-1H-indole, 3-[2-[4-(1,4-benzodioxan-5-yl)piperidin-1-yl]ethyl]-5-fluoro-1H-indole, 6-chloro-3-[2-[4-(2,3-dihydrobenzofuran-7-yl)-1,2,3,6-tetrahydropyridin-1-yl]ethyl]-1H-indole, 3-[2-[4-(benzofuran-7-yl)-1,2,3,6-tetrahydropyridin-1-yl]ethyl-6-chloro-1H-indole, 3-[2-[4-(benzofuran-7-yl)-1,2,3,6-tetrahydropyridin-1-yl]ethyl]-5-bromo-1H-indole, 3-[2-[4-(benzofuran-7-yl)-1,2,3,6-tetrahydropyridin-1-yl]ethyl]-5-fluoro-1H-indole, 3-[2-[4-(benzofuran-7-yl)piperidin-1-yl]ethyl]-6-chloro-1H-indole, 3-[2-[4-(benzofuran-7-yl)piperidin-1-yl]ethyl]-5-fluoro-1H-indole, 3-[2-[4-(benzofuran-7-yl)piperidin-1-yl]ethyl]-5-bromo-1H-indole, 1-acetyl-3-[2-[4-(1,4-benzodioxan-4-yl)piperazin-1-yl]ethyl]-2,3-dihydro-1H-indole, 1-[2-[4-(1,4-benzodioxan-5-yl)piperazin-1-yl]ethyl]-5-fluoro-1H-indole, 1-[2-[4-(1,4-benzodioxan-5-yl)piperazin-1-yl]ethyl]-6-chloro-1H-indole, 1-[2-[4-(1,4-benzodioxan-5-yl)piperazin-1-yl]ethyl]-1H-indole, 1-[2-[4-(2,3-dihydrobenzofuran-7-yl)piperazin-1-yl]ethyl]-1H-indole, 3-[2-[4-(1,4-benzodioxan-5-yl)piperazin-1-yl]ethyl]-2,3-dihydro-1H-indole, 3-[2-[4-(1,4-benzodioxan-5-yl)piperazin-1-yl]ethyl]-2,3-dihydro-5-fluoro-1H-indole, 3-[2-[4-(1,4-benzodioxan-5-yl)piperazin-1-yl]ethyl]-5-chloro-2,3-dihydro-1H-indole, 3-[2-[4-(1,4-benzodioxan-5-yl)piperazin-1-yl]ethyl]-1-butyl-1H-indole, 1-allyl-3-[2-[4-(1,4-benzodioxan-5-yl)piperazin-1-yl]ethyl-lH-indole, 3-[2-[4-(1,4-benzodioxan-5-yl)piperazin-1-yl]ethyl]-1-propargyl-1H-indole, 3-[2-[4-(1,4-benzodioxan-5-yl)piperazin-1-yl]ethyl]-2,3-dihydro-1-methyl-1H-indole, 3-[2-[4-(1,4-benzodioxan-5-yl)piperazin-1-yl]ethyl]-1-benzyl-2,3-dihydro-1H-indole, 1-allyl-3-[2-[4-(1,4-benzodioxan-5-yl)piperazin-1-yl]ethyl]-2,3-dihydro-1H-indole, 1-acetyl-3-[2-[4-(1,4-benzodioxan-5-yl)piperazin-1-yl]ethyl]-1H-indole, 3-[2-[4-(benzo-1,4-dithian-5-yl)piperazin-1-yl]ethyl]-5-chloro-1H-indole, 3-[2-[4-(benzo-1,4-dithian-5-yl)piperazin-1-yl]ethyl]-6-chloro-1H-indole, 3-[2-[4-(benzo-1,4-dithian-5-yl)piperazin-1-yl]ethyl]-5-fluoro-1H-indole, 3-[2-[4-(benzo-1-thia-4-oxan-5-yl)piperazin-1-yl]ethyl]-5-chloro-1H-indole, 3-[2-[4-(benzo-1-thia-4-oxan-5-yl)piperazin-1-yl]ethyl]-6-chloro-1H-indole, and 3-[2-[4-(benzo-1-thia-4-oxan-5-yl)piperazin-1-yl]ethyl]-5-fluoro-1H-indole,or an acid addition salt thereof. 15. A pharmaceutical composition comprising a compound according to Claims 1 to 14 or a pharmaceutically acceptable acid addition salt thereof and at least one pharmaceutically acceptable carrier or diluent. 16. The use of a compound according to Claims 1 to 14 or a pharmaceutically acceptable acid addition salt thereof for the preparation of a medicament for the treatment of a disorder or disease responsive to the inhibition of serotonin reuptake and antagonism of 5-HT1A-receptors. 17. The use of a compound according to Claim 16 wherein the medicament is for the treatment of affective disorders, including depression, psychosis, anxiety disorders including general anxiety disorder, panic disorder and obsessive compulsive disorder. 18. A method for the treatment of a disorder or disease of living animal body, including a human, which is responsive to the inhibition of serotonin reuptake and antagonism of 5-HT1A-receptors comprising administering to such animal, including a human, a therapeutically effective amount of a compound according to Claims 1 to 14 or a pharmaceutically acceptable acid addition salt thereof. 19. A method of treatment according to Claim 18 where the disorder or disease is an affective disorder, including depression, psychosis, anxiety disorders including general anxiety disorder, panic disorder and obsessive compulsive disorder.
机译:1.具有下式的吲哚或2,3-二氢吲哚衍生物或其任何对映异构体或其任何混合物或其酸加成盐,其中X为-O-,-S-或-CR 4 R < 5>-; Y为-CR 6 R 7-,-CR 6 R 7 -CR 8 R 9或-CR 6 = CR 7-。 X或Y一起形成-CR 4 = CR 5-或-CR 4 = CR 5 -CR 6 R 7-。 Z为-O-或-S-; W是N,C或CH; A是选自式(II),(III)和(IV)的组的基团:其中虚线表示任选的键; R 1,R 2,R 3,R 12,R 13,R 14,R 15,R 16和R 17各自独立地选自氢,卤素,三氟甲基,C1-C4烷基,C2-C4烯基,C2-C4炔基,C3-C7环烷基,C1-C4烷氧基,羟基,甲酰基,CO-C1-4烷基,氨基,C1-4烷基氨基,(C1 -4)2-二烷基氨基,C 1 -C 1-4烷基氨基,烷氧基羰基氨基,氨基羰基氨基,烷基氨基羰基氨基,二烷基氨基羰基氨基,硝基和氰基; R 4,R 5,R 6,R 7,R 8和R 9各自独立地选自氢和C 1-4烷基。 R 11选自氢,C 1-4烷基,C 2-4烯基,C 2-4炔基,C 3-7环烷基,芳基,芳基-C 1-4烷基,C 1 -C 1-4烷基和甲酰基。 2.根据权利要求1的化合物,其中Z是-O-。 3.根据权利要求1的化合物,其中Z是-S-。 4.根据权利要求1的化合物,其中A是式(II)的基团。 5.根据权利要求1的化合物,其中A是式(III)的基团。 6.根据权利要求1的化合物,其中A是式(IV)的基团。 7.根据权利要求2的化合物,其中A是式(II)的基团。 8.根据权利要求2的化合物,其中A是式(III)的基团。 9.根据权利要求2的化合物,其中A是式(IV)的基团。 10.根据权利要求3的化合物,其中A是式(II)的基团。 11.根据权利要求3的化合物,其中A是式(III)的基团。 12.根据权利要求3的化合物,其中A是式(IV)的基团。 13.根据权利要求1至12的化合物,其中R 4,R 5,R 6,R 7,R 8和R 9选自氢或甲基。 14.根据权利要求1的化合物,其为3- [2- [4-(1,4-苯并二恶烷-5-基)哌嗪-1-基]乙基] -5-氯-1H-吲哚,3- [2 -[[4-(1,4-苯并二恶烷-5-基)哌嗪-1-基]乙基] -5-溴-1H-吲哚,3- [2- [4-(1,4-苯并二恶烷-5-基] )哌嗪-1-基]乙基] -2-甲基-1H-吲哚,6-氯-3- [2- [4-(2,2,5-三甲基-2,3-二氢苯并呋喃-7-基)哌啶-1-基]乙基] -1H-吲哚,3- [2- [4-(1,4-苯并二恶烷-5-基)哌嗪-1-基]乙基] -4-氯-1H-吲哚,6-氯-3- [2- [4-(2,2-二甲基-2,3-二氢苯并呋喃-7-基)哌啶-1-基] -1H-吲哚,6-氯-3- [2- [4- (2,2-二甲基-2,3-二氢苯并呋喃-7-基)-1,2,3,6-四氢-1吡啶基]乙基] -1H-吲哚,3- [2- [4-(1,4-苯并二恶烷-5-基)哌嗪-1-基]乙基] -5-氟-1H-吲哚,3- [2- [4-(1,4-苯并二恶烷-5-基)哌嗪-1-基]乙基] -5-甲氧基-1H-吲哚,3- [2- [4-(1,4-苯并二恶烷-5-基)哌嗪-1-基]乙基] -1H-吲哚,3- [2- [4-( 1,4-苯并二恶烷-5-基)哌嗪-1-基]乙基] -6-氯-1H-吲哚,3- [2- [4-(5-氯-2,2-二甲基-2,3-二氢苯并呋喃-7-基)哌嗪-1-基]乙基] -1H-吲哚,6-氯-3- [2- [4-(5-氯-3,3-二甲基-2,3-二氢苯并呋喃-7-基)哌嗪-1-基]乙基] -1H-吲哚,6-氯-3- [2- [ 4-(6-氯-2,2-二甲基-3,4-二氢-2H-1-苯并吡喃-8-基)哌嗪-1基]乙基] -1H-吲哚,6-氯-3- [2- [ 4-(2,2-二甲基-2,3-二氢苯并呋喃-7-基)哌嗪-1-基]乙基] -1H-吲哚,3- [2- [4-(1,4-苯并二恶烷-5-基] )哌嗪-1-基]乙基] -5-甲基-1H-吲哚或3- [2- [4-(1,4-苯并二恶烷-5-基)哌嗪-1-基]乙基] -6-甲基-1H-吲哚,6-氯-3- [2- [4-(6-氯-1,4-苯并二恶烷-5-基)哌嗪-1-基]乙基] -1H-吲哚,5-氯-3 -[[2- [4-(2,3-二氢苯并呋喃-7-基)哌嗪-1-基]乙基] -1H-吲哚,3- [2- [4-(2,3-二氢苯并呋喃-7-基)哌嗪-1-基]乙基] -5-氟-1H-吲哚,3- [2- [4-(苯并噻吩-7-基)哌嗪-1-基]乙基] -5-氯-1H-吲哚,3 -[[2- [4-(苯并噻喃-8-基)哌嗪-1-基]乙基] -5-氯-1H-吲哚,3- [2- [4-(苯并噻喃-8-基)哌嗪-1- [基]乙基] -5-溴-1H-吲哚,3- [2- [4-(苯并噻喃-8-基)哌嗪-1-基]乙基] -6-氯-1H-吲哚,3- [2- [4-(1,4-苯并二恶烷-5-基)-1,2,3,6-四氢吡啶-1-基]乙基] -5-氯-1H-吲哚,3- [2- [4-(1,4-苯并二恶烷-5-基)-1,2,3,6-四氢吡啶-1-基]乙基] -5-氟-1H-吲哚,3- [2- [4-(1,4-苯并二恶烷-5-基)哌啶-1-基]乙基] -6-氯-1H-吲哚,3- [2- [4-(1,4-苯并二恶烷-5-基)哌啶-1-基]乙基] -5-氯-1H-吲哚,3- [2- [4-(1,4-苯并二恶烷-5] -基)哌啶-1-基]乙基] -5-氟-1H-吲哚,6-氯-3- [2- [4-(2,3-二氢苯并呋喃-7-基)-1,2,3, 6-四氢吡啶-1-基]乙基] -1H-吲哚,3- [2- [4-(苯并呋喃-7-基)-1,2,3,6-四氢吡啶-1-基]乙基-6-氯-1H-吲哚,3- [2- [4-(苯并呋喃-7-基)-1,2,3,6-四氢吡啶-1-基]乙基] -5-溴-1H-吲哚,3- [2 -[[4-(苯并呋喃-7-基)-1,2,3,6-四氢吡啶-1-基]乙基] -5-氟-1H-吲哚,3- [2- [4-(苯并呋喃-7-基)哌啶-1-基]乙基] -6-氯-1H-吲哚,3- [2- [4-(苯并呋喃-7-基)哌啶- 1-基]乙基] -5-氟-1H-吲哚,3- [2- [4-(苯并呋喃-7-基)哌啶-1-基]乙基] -5-溴-1H-吲哚,1-乙酰基-3- [2- [4-(1,4-苯并二恶烷-4-基)哌嗪-1-基]乙基] -2,3-二氢-1H-吲哚,1- [2- [4-(1, 4-苯并二恶烷-5-基)哌嗪-1-基]乙基] -5-氟-1H-吲哚,1- [2- [4-(1,4-苯并二恶烷-5-基)哌嗪-1-基]乙基] -6-氯-1H-吲哚,1- [2- [4-(1,4-苯并二恶烷-5-基)哌嗪-1-基]乙基] -1H-吲哚,1- [2- [4 -(2,3-二氢苯并呋喃-7-基)哌嗪-1-基]乙基] -1H-吲哚,3- [2- [4-(1,4-苯并二恶烷-5-基)哌嗪-1-基]乙基] -2,3-二氢-1H-吲哚,3- [2- [4-(1,4-苯并二恶烷-5-基)哌嗪-1-基]乙基] -2,3-二氢-5-氟-1H-吲哚,3- [2- [4-(1,4-苯并二恶烷-5-基)哌嗪-1-基]乙基] -5-氯-2,3-二氢-1H-吲哚,3- [ 2- [4-(1,4-苯并二恶烷-5-基)哌嗪-1-基]乙基] -1-丁基-1H-吲哚,1-烯丙基-3- [2- [4-(1,4-苯并二恶烷-5-基)哌嗪-1-基]乙基-1H-吲哚,3- [2- [4-(1,4-苯并二恶烷-5-基)哌嗪-1-基]乙基] -1-炔丙基-1H-吲哚,3- [2- [4-(1,4-苯并二恶烷-5-基)哌嗪-1-基]乙基] -2,3-二氢-1-甲基-1H-吲哚,3- [2- [4-(1,4-苯并二恶烷-5-基)哌嗪-1-基]乙基] -1-苄基-2,3-二氢-1H-吲哚,1-烯丙基-3- [2- [ 4-(1,4-苯并二恶烷-5-基)哌嗪-1-基]乙基] -2,3-二氢-1H-吲哚,1-乙酰基-3- [2- [4-(1,4-苯并二恶烷) -5-基)哌嗪-1-基]乙基] -1H-吲哚,3- [2- [4-(苯并-1,4-二噻吩基5-基)哌嗪-1-基]乙基] -5-氯-1H-吲哚,3- [2- [4-(苯并-1,4-二苯-5-基)哌嗪-1-基]乙基] -6-氯-1H-吲哚,3- [2- [ 4-(苯并-1,4-二噻吩-5-基)哌嗪-1-基]乙基] -5-氟-1H-吲哚,3- [2- [4-(苯并-1-噻吩-4-恶烷) -5-基)哌嗪-1-基] -5-氯-1H-吲哚,3- [2- [4-(苯并-1-噻-4-氧杂-5-基)哌嗪-1-基]乙基] -6-氯-1H-吲哚和3- [2- [4-(苯并-1-噻吩-4-氧杂-5-基]哌嗪-1-基]乙基] -5-氟-1H -吲哚或其酸加成盐。 15.一种药物组合物,其包含根据权利要求1至14的化合物或其药学上可接受的酸加成盐和至少一种药学上可接受的载体或稀释剂。 16.根据权利要求1至14的化合物或其药学上可接受的酸加成盐在制备用于治疗对5-HT1A受体的5-羟色胺再摄取和拮抗具有响应性的病症或疾病的药物中的用途。 。 17.权利要求16的化合物的用途,其中所述药物用于治疗情感障碍,包括抑郁症,精神病,包括一般性焦虑症,焦虑症和强迫症的焦虑症。 18.一种对5-HT 1A受体的5-羟色胺再摄取和拮抗作用有响应的,对包括人在内的活体动物疾病或疾病的治疗方法,包括对包括人在内的这种动物进行治疗性治疗。 15.有效量的根据权利要求1至14的化合物或其药学上可接受的酸加成盐。 19.根据权利要求18所述的治疗方法,其中,所述疾病是包括抑郁症,精神病,包括一般性焦虑症,恐慌症和强迫症在内的焦虑症。

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