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公开(公告)号:US5708018A
公开(公告)日:1998-01-13
申请号:US592318
申请日:1996-02-02
申请人: Susanne R. Haadsma-Svensson , Bengt R. Andersson , Clas A. Sonesson , Chiu-Hong Lin , R. Nicholas Waters , Kjell A. I. Svensson , Per A. E. Carlsson , Lars O. Hansson , N. Peter Stjernlof
发明人: Susanne R. Haadsma-Svensson , Bengt R. Andersson , Clas A. Sonesson , Chiu-Hong Lin , R. Nicholas Waters , Kjell A. I. Svensson , Per A. E. Carlsson , Lars O. Hansson , N. Peter Stjernlof
IPC分类号: C07D295/08 , A61K31/135 , A61K31/335 , A61K31/357 , A61K31/36 , A61K31/40 , A61K31/42 , A61K31/421 , A61P25/00 , A61P25/18 , A61P25/20 , A61P25/28 , A61P25/30 , A61P43/00 , C07C211/42 , C07C215/42 , C07C217/52 , C07C217/74 , C07C219/26 , C07C223/04 , C07C225/20 , C07C225/22 , C07C229/50 , C07C233/43 , C07C233/44 , C07C237/30 , C07C237/48 , C07C255/54 , C07C255/58 , C07C309/56 , C07C309/65 , C07C309/66 , C07C309/73 , C07C309/76 , C07C311/08 , C07C311/21 , C07C311/37 , C07C311/39 , C07C317/32 , C07C317/36 , C07C323/30 , C07C323/36 , C07D207/32 , C07D207/325 , C07D209/48 , C07D263/32 , C07D295/096 , C07D295/12 , C07D295/135 , C07D317/58 , C07D317/70 , C07D319/14 , C07D319/18 , C07D333/20 , A61K31/165
CPC分类号: C07D207/325 , C07C211/42 , C07C215/42 , C07C217/52 , C07C217/74 , C07C219/26 , C07C223/04 , C07C225/20 , C07C229/50 , C07C233/43 , C07C233/44 , C07C237/48 , C07C255/54 , C07C255/58 , C07C309/65 , C07C309/66 , C07C309/73 , C07C311/08 , C07C311/21 , C07C311/39 , C07C317/36 , C07D209/48 , C07D295/096 , C07D295/135 , C07D317/70 , C07D319/14 , C07D333/20 , C07C2102/08
摘要: Compounds and their pharmaceutically acceptable salts suitable for treating central nervous system disorders associated with the dopamine D3 receptor activity of Formula I: ##STR1## wherein R.sub.1 and R.sub.2 are independently chosen from hydrogen, C.sub.1 -C.sub.8 alkyl, OCH.sub.3, OH, OSO.sub.2 CF.sub.3, OSO.sub.2 CH.sub.3, SOR.sub.5, CO.sub.2 R.sub.5, CONH.sub.2, CONR.sub.5 R.sub.6, COR.sub.5, CN, SO.sub.2 NH.sub.2, SO.sub.2 NR.sub.5 R.sub.6, SO.sub.2 R.sub.5, --OCO--(C.sub.1 -C.sub.6 alkyl), --NCO--(C.sub.1 -C.sub.6 alkyl), --CH.sub.2 O--(C.sub.1 -C.sub.6 alkyl), --CH.sub.2 OH, --CO-Aryl, --NHSO.sub.2 -Aryl, --NHSO.sub.2 --(C.sub.1 -C.sub.6 alkyl), phthalimide, thiophenyl, pyrrol, pyrrolinyl, oxazolyl, or R.sub.1 and R.sub.2 together form --O(CH.sub.2).sub.1-2 O-- or --(CH.sub.2).sub.3-6 -- (except that only one of R.sub.1 and R.sub.2 can be hydrogen or OH in any such compound); R.sub.3 and R.sub.4 are independently chosen from C.sub.2 -C.sub.4 alkenyl, C.sub.3 -C.sub.8 alkynyl, C.sub.3 -C.sub.8 cycloalkyl, --(CH.sub.2).sub.p -- thienyl (where p is 1-4), or C.sub.1 -C.sub.8 alkyl (except where R.sub.1 or R.sub.2 are hydrogen or OH or where both R.sub.1 and R.sub.2 are OCH.sub.3 or a C.sub.1 -C.sub.8 alkyl); R.sub.5 is hydrogen, C.sub.1 -C.sub.8 alkyl, C.sub.2 -C.sub.4 alkenyl, C.sub.3 -C.sub.8 cycloalkyl; and R.sub.6 is C.sub.1 -C.sub.8 alkyl, C.sub.2 -C.sub.4 alkenyl, C.sub.2 -C.sub.8 alkynyl, C.sub.3 -C.sub.8 cycloalkyl, or Aryl.
摘要翻译: PCT No.PCT / US94 / 08046 Sec。 371日期:1996年5月14日 102(e)日期1996年5月14日PCT提交1994年7月21日PCT公布。 公开号WO95 / 04713 日期1995年2月16日化合物及其药学上可接受的盐适用于治疗与式I的多巴胺D3受体活性相关的中枢神经系统疾病:其中R1和R2独立地选自氢,C1-C8烷基,OCH3,OH ,(C 1 -C 6烷基),-NCO-(C 1 -C 6烷基),-CH 2 O-(C 1 -C 6烷基), - (C 1 -C 6)烷氧基羰基, 烷基),-CH 2 OH,-CO-芳基,-NHSO 2 - 芳基,-NHSO 2 - (C 1 -C 6烷基),邻苯二甲酰亚胺,噻吩基,吡咯,吡咯烷基,恶唑基或R 1和R 2一起形成-O(CH 2) - 或 - (CH 2)3-6 - (除了R1和R2中只有一个可以是任何这样的化合物中的氢或OH); R 3和R 4独立地选自C 2 -C 4烯基,C 3 -C 8炔基,C 3 -C 8环烷基, - (CH 2)p - 噻吩基(其中p为1-4)或C 1 -C 8烷基(除了其中R 1或R 2为 氢或OH或其中R 1和R 2均为OCH 3或C 1 -C 8烷基); R5是氢,C1-C8烷基,C2-C4烯基,C3-C8环烷基; 并且R 6是C 1 -C 8烷基,C 2 -C 4烯基,C 2 -C 8炔基,C 3 -C 8环烷基或芳基。
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公开(公告)号:US5639778A
公开(公告)日:1997-06-17
申请号:US522290
申请日:1995-09-07
申请人: Bengt R. Andersson , Per A. E. Carlsson , Lars O. Hansson , Clas A. Sonesson , N. Peter Stjernlof , Kjell A. I. Svensson , R. Nicholas Waters , Susanne R. Haadsma-Svensson
发明人: Bengt R. Andersson , Per A. E. Carlsson , Lars O. Hansson , Clas A. Sonesson , N. Peter Stjernlof , Kjell A. I. Svensson , R. Nicholas Waters , Susanne R. Haadsma-Svensson
IPC分类号: A61K31/34 , A61K31/343 , A61K31/40 , A61K31/403 , A61P25/00 , A61P43/00 , C07D209/58 , C07D209/60 , C07D307/92 , C07D307/93 , C07D409/12 , C07D491/04 , C07D491/052 , C07D493/04 , A61K31/33
CPC分类号: C07D209/58 , C07D209/60 , C07D307/92 , C07D307/93 , C07D409/12 , C07D491/04
摘要: A compound of formula (I) and pharmaceutically acceptable salts thereof, where Z is R.sub.3 and X and Y form (a), or X is R.sub.3 and Y and Z form (a) or (b); R.sub.1 and R.sub.2 are independently hydrogen, C.sub.1-6 alkyl, C.sub.3-7 cycloalkyl, --CH.sub.2 --C.sub.3-7 cycloalkyl, phenyl (optionally substituted with halogen or C.sub.1-6 alkyl), -thiophenyl (optionally substituted with halogen or C.sub.1-6 alkyl), or C.sub.1-6 alkyl phenyl; R.sub.3 are independently hydrogen, halogen, --O--C.sub.1-6 alkyl or C.sub.1-6 alkyl; R.sub.4 is a valence bond, CH.sub.2 or oxygen; R.sub.5 and R.sub.6 are independently hydrogen, sulfur, --S--C.sub.1-6 alkyl, halogen, CON(R.sub.3).sub.2, --COCF.sub.3, --CO--C.sub.1-6 alkyl, --CO phenyl, oxygen, --CHO, CN except that when Y and Z form (b), R.sub.1 and R.sub.2 are hydrogen or a C.sub.1-6 alkyl and R.sub.3 is hydrogen, then at least one of R.sub.5 and R.sub.6 must be other than hydrogen. These compounds and derivatives thereof exhibit dopamine-receptor stimulating activity in mammals. ##STR1##
摘要翻译: PCT No.PCT / US94 / 02800 Sec。 371 1995年9月7日第 102(e)1995年9月7日PCT PCT 1994年3月21日PCT公布。 出版物WO94 / 21608 1994年9月29日一种式(I)化合物及其药学上可接受的盐,其中Z为R 3,X和Y为(a),或X为R 3,Y和Z为(a)或(b)。 R 1和R 2独立地是氢,C 1-6烷基,C 3-7环烷基,-CH 2 -C 3-7环烷基,苯基(任选被卤素或C 1-6烷基取代) - 噻吩基(任选地被卤素或C 1-6烷基 )或C 1-6烷基苯基; R 3独立地是氢,卤素,-O-C 1-6烷基或C 1-6烷基; R4是价键,CH2或氧; R 5和R 6独立地是氢,硫,-S-C 1-6烷基,卤素,CON(R 3)2,-COCF 3,-CO-C 1-6烷基,-CO苯基,氧,-CHO, 和Z形式(b)中,R 1和R 2是氢或C 1-6烷基,R 3是氢,则R 5和R 6中的至少一个必须不是氢。 这些化合物及其衍生物在哺乳动物中表现出多巴胺受体刺激活性。 (a)
(a) (b)
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