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    • 3. 发明授权
    • Bicyclic benzamides of 3- or 4-substituted 4-(aminomethyl)-piperidine derivatives
    • 3-或4-取代的4-(氨基甲基) - 哌啶衍生物的双环苯甲酰胺
    • US06635643B2
    • 2003-10-21
    • US09791227
    • 2001-02-22
    • Jean-Paul René Marie André BosmansMichel Anna Jozef De CleynMichel Surkyn
    • Jean-Paul René Marie André BosmansMichel Anna Jozef De CleynMichel Surkyn
    • A61K31495
    • C07D211/42C07D211/44C07D401/06C07D405/06C07D405/12C07D405/14Y02P20/55
    • The present invention of compounds of formula (I) a stereochemically isomeric form thereof, an N-oxide form thereof or a pharmaceutically acceptable acid addition salt thereof, R1 and R2 taken together form a bivalent radical of formula wherein in said bivalent radicals one or two hydrogen atoms may be substituted with C1-6alkyl; R3 is hydrogen or halo; R4 is hydrogen or C1-6alkyl; R5 is hydrogen or C1-6alkyl; L is C3-6cycloalkyl, C5-6cycloalkanone, C2-6alkenyl, or L is a radical of formula —Alk—R6—, Alk—X—R7, —Alk—Y—C(═O)—R9, or —Alk—Y—C(═O)— NR11R12 wherein each Alk is C1-12alkanediyl; and R6 is hydrogen, cyano, C1-6alkylsulfonylamino, C3-6cycloalkyl, C5-6cycloalkanone, or a heterocyclic ringsystem; R7 is hydrogen, C1-6alkyl, hydroxyC1-6alkyl, C3-6cycloalkyl, or a heterocyclic ringsystem; X is O, SO2 or NR8; said R8 being hydrogen or C1-6alkyl; R9 is hydrogen, C1-6alkyl, C3-6cycloalkyl, C1-6alkyloxy or hydroxy; Y is NR10 or a direct bond; said R10 being hydrogen, or C1-6alkyl; R11 and R12 each independently are hydrogen, C1-6alkyl, C3-6cycloalkyl, or R11 and R12 combined with the nitrogen atom may form an optionally substituted pyrrolidinyl, piperidinyl, piperazinyl or 4-morpholinyl ring. Processes for preparing said products, formulations comprising said products and their use as a medicine are disclosed, in particular for treating conditions which are related to impairment of gastric emptying.
    • 本发明的式(I)化合物是其立体化学异构形式,其N-氧化物形式或其药学上可接受的酸加成盐,R 1和R 2一起形成下式的二价基团,其中在 所述二价基团一个或两个氢原子可以被C 1-6烷基取代; R 3是氢或卤素; R 4是氢或C 1-6烷基; R 5是氢或C 1-6烷基; L是C3-6环烷基,C5-6环烷酮,C2-6烯基或L是式-Alk-R6,Alk-XR7,-Alk-YC(= O)-R9的基团, 或-Alk-YC(= O)-NR 11 R 12,其中每个Alk是C 1-12烷二基; R 6是氢,氰基,C 1-6烷基磺酰基氨基,C 3-6环烷基,C 5-6环烷酮或杂环体系; R 7是氢,C 1-6烷基,羟基C 1-6烷基,C 3-6环烷基或杂环环系; X是O,SO 2或NR 8; 所述R 8为氢或C 1-6烷基; R 9是氢,C 1-6烷基,C 3-6环烷基,C 1-6烷氧基或羟基; Y是NR 10或直接键; 所述R 10为氢或C 1-6烷基; R 11和R 12各自独立地为氢,与氮原子结合的C 1-6烷基,C 1-6烷基或R 11和R 12可以形成任选取代的吡咯烷基,哌啶基,哌嗪基或4- 吗啉基环。 公开了用于制备所述产品的方法,包含所述产品的制剂及其作为药物的用途,特别是用于治疗与胃排空的损伤相关的病症。
    • 4. 发明授权
    • Gastrokinetic monocyclic benzamides of 3- or 4-substituted 4-(aminomethyl)-piperidine derivatives
    • 3-或4-取代的4-(氨基甲基) - 哌啶衍生物的胃动力单环苯甲酰胺
    • US06452013B1
    • 2002-09-17
    • US09462287
    • 2000-01-05
    • Jean-Paul René Marie André BosmansMichel Anna Jozef De CleynMichel Surkyn
    • Jean-Paul René Marie André BosmansMichel Anna Jozef De CleynMichel Surkyn
    • C07D21100
    • C07D211/42C07D211/44C07D401/06C07D405/06C07D405/12C07D405/14Y02P20/55
    • The present invention of compounds of formula (I) a stereochemically isomeric form thereof, an N-oxide form thereof or a pharmaceutically acceptable acid addition salt thereof, R1 is C1-6alkyloxy, C2-6alkenyloxy or C2-6alkynyl-oxy; R2 is hydrogen, C1-6alkyl C1-6alkyloxy; R3 is hydrogen or halo; R4 is hydrogen or C1-6alkyl; R5 is hydrogen or C1-6alkyl; L is C3-6cycloalkyl, C5-6cycloalkanone, C2-6alkenyl, or L is a radical of formula —Alk—R6—, Alk—X—R7, -Alk-Y—C(═O)—R9, or -Alk-Y—C(═O)—NR11R12 wherein each Alk is C1-12alkanediyl; and R6 is hydrogen, cyano, C1-6alkylsulfonylamino, C3-6cycloalkyl, C5-6cycloalkanone, or a heterocyclic ringsystem; R7 is hydrogen, C1-6alkyl, hydroxyC1-6alkyl, C3-6cycloalkyl, or a heterocyclic ringsystem; X is O, S, SO2 or NR8; said R8 being hydrogen or C1-6alkyl; R9 is hydrogen, C1-6alkyl, C3-6cycloalkyl, C1-6alkyloxy or hydroxy; Y is NR10 or a direct bond; said R10 being hydrogen, or C1-6alkyl; R11 and R12 each independently are hydrogen, C1-6alkyl, C3-6cycloalkyl, or R11 and R12 combined with the nitrogen atom may form an optionally substituted pyrrolidinyl, piperidinyl, piperazinyl or 4-morpholinyl ring. Processes for preparing said products, formulations comprising said products and their use as a medicine are disclosed, in particular for treating conditions which are related to impairment of gastric emptying.
    • 本发明的式(I)化合物是其立体化学异构形式,其N-氧化物形式或其药学上可接受的酸加成盐,R 1是C 1-6烷氧基,C 2-6烯氧基或C 2-6炔基氧基; R2是氢,C1-6烷基C1-6烷氧基; R3是氢或卤素; R4是氢或C1-6烷基; R5是氢或C1-6烷基; L是C3-6环烷基,C5-6环烷酮,C2-6烯基或L是式-Alk-R6-,Alk-X-R7,-Alk-YC(= O)-R9或-Alk-YC( = O)-NR 11 R 12,其中每个Alk是C 1-12烷二基; R6为氢,氰基,C1-6烷基磺酰基氨基,C3-6环烷基,C5-6环烷酮或杂环环系; R7是氢,C1-6烷基,羟基C1-6烷基,C3-6环烷基或杂环环系; X是O,S,SO 2或NR 8; 所述R8为氢或C1-6烷基; R9是氢,C1-6烷基,C3-6环烷基,C1-6烷氧基或羟基; Y是NR10或直接键; 所述R 10为氢或C 1-6烷基; R 11和R 12各自独立地为氢,C 1-6烷基,C 3-6环烷基或R 11和R 12与氮原子结合可以形成任选取代的吡咯烷基,哌啶基,哌嗪基或4-吗啉基环。 公开了用于制备所述产品的方法,包含所述产品的制剂及其作为药物的用途,特别是用于治疗与胃排空的损伤相关的病症。
    • 6. 发明授权
    • Gastrokinetic monocyclic benzamides of 3-or 4-substituted 4-(aminoethyl)-piperidine derivatives
    • 3-或4-取代的4-(氨基乙基) - 哌啶衍生物的胃动力单环苯甲酰胺
    • US06750349B2
    • 2004-06-15
    • US10162802
    • 2002-06-05
    • Jean-Paul René Marie André BosmansMichel Anna Jozef De CleynMichel Surkyn
    • Jean-Paul René Marie André BosmansMichel Anna Jozef De CleynMichel Surkyn
    • A61K21100
    • C07D211/42C07D211/44C07D401/06C07D405/06C07D405/12C07D405/14Y02P20/55
    • The present invention of compounds of formula (I) a stereochemically isomeric form thereof, an N-oxide form thereof or a pharmaceutically acceptable acid addition salt thereof, R1 is C1-6alkyloxy, C2-6alkenyloxy or C2-6alkynyl-oxy; R2 is hydrogen, C1-6alkyl C1-6alkyloxy; R3 is hydrogen or halo; R4 is hydrogen or C1-6alkyl; R5 is hydrogen or C1-6alkyl; L is C3-6cycloalkyl, C5-6cycloalkanone, C2-6alkenyl, or L is a radical of formula —Alk—R6—, Alk-X—R7, —Alk—Y—C(═O)—R9, or —Alk—Y—C(═O)—NR11R12 wherein each Alk is C1-12alkanediyl; and R6 is hydrogen, cyano, C1-6alkylsulfonylamino, C3-6cycloalkyl, C5-6cycloalkanone, or a heterocyclic ringsystem; R7 is hydrogen, C1-6alkyl, hydroxyC1-6alkyl, C3-6cycloalkyl, or a heterocyclic ringsystem; X is O, S, SO2 or NR8; said R8 being hydrogen or C1-6alkyl; R9 is hydrogen, C1-6alkyl, C3-6cycloalkyl, C1-6alkyloxy or hydroxy; Y is NR10 or a direct bond; said R10 being hydrogen, or C1-6alkyl; R11 and R12 each independently are hydrogen, C1-6alkyl, C3-6cycloalkyl, or R11 and R12 combined with the nitrogen atom may form an optionally substituted pyrrolidinyl, piperidinyl, piperazinyl or 4-morpholinyl ring. Processes for preparing said products, formulations comprising said products and their use as a medicine are disclosed, in particular for treating conditions which are related to impairment of gastric emptying.
    • 本发明的式(I)化合物是其立体化学异构形式,其N-氧化物形式或其药学上可接受的酸加成盐,R 1是C 1-6烷氧基,C 2-6烯基氧基或C 2-6炔基氧基; R 2是氢,C 1-6烷基C 1-6烷氧基; R 3是氢或卤素; R 4是氢或C 1-6烷基; R 5是氢或C 1-6烷基; L是C3-6环烷基,C5-6环烷酮,C2-6烯基或L是式-Alk-R6,Alk-XR7,-Alk-YC(= O)-R9的基团, ,或-Alk-YC(= O)-NR 11 R 12,其中每个Alk是C 1-12烷二基; R 6是氢,氰基,C 1-6烷基磺酰基氨基,C 3-6环烷基,C 5-6环烷酮或杂环体系; R 7是氢,C 1-6烷基,羟基C 1-6烷基,C 3-6环烷基或杂环环系; X是O,S,SO 2或NR 8; 所述R 8为氢或C 1-6烷基; R 9是氢,C 1-6烷基,C 3-6环烷基,C 1-6烷氧基或羟基; Y是NR 10或直接键; 所述R 10为氢或C 1-6烷基; R 11和R 12各自独立地为氢,与氮原子结合的C 1-6烷基,C 1-6烷基或R 11和R 12可以形成任选取代的吡咯烷基,哌啶基,哌嗪基或4- 吗啉基环。 公开了用于制备所述产品的方法,包含所述产品的制剂及其作为药物的用途,特别是用于治疗与胃排空的损伤相关的病症。
    • 7. 发明授权
    • Bicyclic benzamides of 3- or 4-substituted 4-(aminomethyl)-piperidine derivatives
    • 3-或4-取代的4-(氨基甲基) - 哌啶衍生物的双环苯甲酰胺
    • US07790750B2
    • 2010-09-07
    • US11584732
    • 2006-10-20
    • Jean-Paul René Marie André BosmansMichel Anna Jozef De CleynMichel Surkyn
    • Jean-Paul René Marie André BosmansMichel Anna Jozef De CleynMichel Surkyn
    • A61K31/445C07D407/02
    • C07D211/42C07D211/44C07D401/06C07D405/06C07D405/12C07D405/14Y02P20/55
    • The present invention of compounds of formula (I) a stereochemically isomeric form thereof, an N-oxide form thereof or a pharmaceutically acceptable acid addition salt thereof, R1 and R2 taken together form a bivalent radical of formula wherein in said bivalent radicals one or two hydrogen atoms may be substituted with C1-6alkyl; R3 is hydrogen or halo; R4 is hydrogen or C1-6alkyl; R5 is hydrogen or C1-6alkyl; L is C3-6cycloalkyl, C5-6cycloalkanone, C2-6alkenyl, or L is a radical of formula -Alk-R6—, Alk-X—R7, -Alk-Y—C(═O)—R9, or -Alk-Y—C(═O)—NR11R12 wherein each Alk is C1-12alkanediyl; and R6 is hydrogen, cyano, C1-6alkylsulfonylamino, C3-6cycloalkyl, C5-6cycloalkanone, or a heterocyclic ringsystem; R7 is hydrogen, C1-6alkyl, hydroxyC1-6alkyl, C3-6cycloalkyl, or a heterocyclic ringsystem; X is O, S, SO2 or NR8; said R8 being hydrogen or C1-6alkyl; R9 is hydrogen, C1-6alkyl, C3-6cycloalkyl, C1-6alkyloxy or hydroxy; Y is NR10 or a direct bond; said R10 being hydrogen, or C1-6alkyl; R11 and R12 each independently are hydrogen, C1-6alkyl, C3-6cycloalkyl, or R11 and R12 combined with the nitrogen atom may form an optionally substituted pyrrolidinyl, piperidinyl, piperazinyl or 4-morpholinyl ring. Processes for preparing said products, formulations comprising said products and their use as a medicine are disclosed, in particular for treating conditions which are related to impairment of gastric emptying.
    • 式(I)化合物的本发明是其立体化学异构形式,其N-氧化物形式或其药学上可接受的酸加成盐,R1和R2一起形成下式的二价基团:其中在所述二价基团中,一个或两个 氢原子可以被C 1-6烷基取代; R3是氢或卤素; R4是氢或C1-6烷基; R5是氢或C1-6烷基; L是C3-6环烷基,C5-6环烷酮,C2-6链烯基或L是式-Alk-R6-,Alk-X-R7,-Alk-Y-C(= O)-R9或-Alk- Y-C(= O)-NR 11 R 12,其中每个Alk是C 1-12烷二基; R6为氢,氰基,C1-6烷基磺酰基氨基,C3-6环烷基,C5-6环烷酮或杂环环系; R7是氢,C1-6烷基,羟基C1-6烷基,C3-6环烷基或杂环环系; X是O,S,SO 2或NR 8; 所述R8为氢或C1-6烷基; R9是氢,C1-6烷基,C3-6环烷基,C1-6烷氧基或羟基; Y是NR10或直接键; 所述R 10为氢或C 1-6烷基; R 11和R 12各自独立地为氢,C 1-6烷基,C 3-6环烷基或R 11和R 12与氮原子结合可以形成任选取代的吡咯烷基,哌啶基,哌嗪基或4-吗啉基环。 公开了用于制备所述产品的方法,包含所述产品的制剂及其作为药物的用途,特别是用于治疗与胃排空的损伤相关的病症。
    • 9. 再颁专利
    • Bicyclic benzamides of 3-or 4-substituted 4-(aminomethyl)-piperidine derivatives
    • 3-或4-取代的4-(氨基甲基) - 哌啶衍生物的双环苯甲酰胺
    • USRE40793E1
    • 2009-06-23
    • US11259719
    • 2005-10-26
    • Jean-Paul Renë Marie Andrë BosmansMichel Anna Jozef DeCleynMichel Surkyn
    • Jean-Paul Renë Marie Andrë BosmansMichel Anna Jozef DeCleynMichel Surkyn
    • A61K31/495A61K31/445C07D401/00C07D211/06C07D237/28
    • C07D211/42C07D211/44C07D401/06C07D405/06C07D405/12C07D405/14Y02P20/55
    • The present invention of compounds of formula (I) a stereochemically isomeric form thereof, an N-oxide form thereof or a pharmaceutically acceptable acid addition salt thereof, R1 and R2 taken together form a bivalent radical of formula wherein in said bivalent radicals one or two hydrogen atoms may be substituted with C1-6alkyl; R3 is hydrogen or halo; R4 is hydrogen or C1-6alkyl; R5 is hydrogen or C1-6alkyl; L is C3-6cycloalkyl, C5-6cycloalkanone, C2-6alkenyl, or L is a radical of formula —Alk—R6—, Alk—X—R7, —Alk—Y—C(═O)—R9, or —Alk—Y—C (═O)—NR11R12 wherein each Alk is C1-12alkanediyl; and R6 is hydrogen, cyano, C1-6alkylsulfonylamino, C3-6cycloalkyl, C5-6cycloalkanone, or a heterocyclic ring-system; R7 is hydrogen, C1-6alkyl, hydroxyC1-6alkyl, C3-6cycloalkyl, or a heterocyclic ringsystem; X is O, SO2 or NR8; said R8 being hydrogen or C1-6alkyl; R9 is hydrogen, C1-6alkyl, C3-6cycloalkyl, C1-6alkyloxy or hydroxy; Y is NR10 or a direct bond; said R10 being hydrogen, or C1-6alkyl; R11 and R12 each independently are hydrogen, C1-6alkyl, C3-6cycloalkyl, or R11 and R12 combined with the nitrogen atom may form an optionally substituted pyrrolidinyl, piperidinyl, piperazinyl or 4-morpholinyl ring. Processes for preparing said products, formulations comprising said products and their use as a medicine are disclosed, in particular for treating conditions which are related to impairment of gastric emptying.
    • 式(I)化合物的本发明是其立体化学异构形式,其N-氧化物形式或其药学上可接受的酸加成盐,R1和R2一起形成下式的二价基团:其中在所述二价基团中,一个或两个 氢原子可以被C 1-6烷基取代; R3是氢或卤素; R4是氢或C1-6烷基; R5是氢或C1-6烷基; L是C3-6环烷基,C5-6环烷酮,C2-6烯基或L是式-Alk-R6-,Alk-X-R7,-Alk-YC(-O)-R9或-Alk-YC( -O)-NR 11 R 12,其中每个Alk是C 1-12烷二基; R6为氢,氰基,C1-6烷基磺酰基氨基,C3-6环烷基,C5-6环烷酮或杂环环系; R7是氢,C1-6烷基,羟基C1-6烷基,C3-6环烷基或杂环环系; X是O,SO 2或NR 8; 所述R8为氢或C1-6烷基; R9是氢,C1-6烷基,C3-6环烷基,C1-6烷氧基或羟基; Y是NR10或直接键; 所述R 10为氢或C 1-6烷基; R 11和R 12各自独立地为氢,C 1-6烷基,C 3-6环烷基或R 11和R 12与氮原子结合可以形成任选取代的吡咯烷基,哌啶基,哌嗪基或4-吗啉基环。 公开了用于制备所述产品的方法,包含所述产品的制剂及其作为药物的用途,特别是用于治疗与胃排空的损伤相关的病症。