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N-(5,6,7,8-tetrahydro-6,8,8-trimethyl[1,6]naphthyridin-3-yl)-indole-2-carboxamide | 252901-14-7

中文名称
——
中文别名
——
英文名称
N-(5,6,7,8-tetrahydro-6,8,8-trimethyl[1,6]naphthyridin-3-yl)-indole-2-carboxamide
英文别名
N-(6,8,8-trimethyl-5,7-dihydro-1,6-naphthyridin-3-yl)-1H-indole-2-carboxamide
N-(5,6,7,8-tetrahydro-6,8,8-trimethyl[1,6]naphthyridin-3-yl)-indole-2-carboxamide化学式
CAS
252901-14-7
化学式
C20H22N4O
mdl
——
分子量
334.421
InChiKey
OWLKGISVRXWXGH-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    2.9
  • 重原子数:
    25
  • 可旋转键数:
    2
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.3
  • 拓扑面积:
    61
  • 氢给体数:
    2
  • 氢受体数:
    3

文献信息

  • Tetrahydronaphthyridinyl-carboxamides having anti-convulsant activity
    申请人:SmithKline Beecham p.l.c.
    公开号:US20020143029A1
    公开(公告)日:2002-10-03
    Compounds of formula (I) and pharmaceutically acceptable salts and solvates: 1 where R 1 is hydrogen, C 1-6 alkyl (optionally substituted by hydroxy or C 1-4 alkoxy), phenyl-C 1-4 alkyl-, C 1-6 alkenyl, C 1-6 alkynyl; R 2 is hydrogen or up to three substituents selected from halogen, NO 2 , CN, N 3 , CF 3 O—, CF 3 S—, CF 3 CO—, C 1-6 alkyl, C 1-6 alkenyl, C 1-6 alkynyl, C 1-6 perfluoroalkyl, C 3-6 cycloalkyl, C 3-6 cycloalkyl-C 1-4 alkyl-, C 1-6 alkylO—, C 1-6 alkylCO—, C 3-6 cycloalkylO—, C 3-6 cycloalkylCO—, C 3-6 cycloalkyl-C 1-4 alkylO—, C 3-6 cycloalkyl-C 1-4 alkylCO—, phenyl, phenoxy, benzyloxy, benzoyl, phenyl-C 1-4 alkyl-, C 1-6 alkylS—, C 1-6 alkylSO 2 —, (C 1-4 alkyl) 2 NSO 2 —, (C 1-4 alkyl)NHSO 2 —, (C 1-4 alkyl) 2 NCO—, (C 1-4 alkyl)NHCO— or CONH 2 ; or —NR 5 R 6 where R 5 is hydrogen or C 1-4 alkyl, and R 6 is hydrogen, C 1-4 alkyl, formyl, —CO 2 C 1-4 alkyl or —COC 1-4 alkyl; or two R 2 groups together form a carbocyclic ring that is saturated or unsaturated. R 3 groups and R 4 groups are each independently hydrogen or C 1-6 alkyl and/or the two R 3 groups and/or the two R 4 groups together form a C 3-6 spiroalkyl group, provided that at least one R 3 or R 4 group is not hydrogen; and X is selected from hydrogen, halogen, cyano, alkyl and alkoxy. are useful in the treatment and prophylaxis of epilepsy, migraine, and other disorders.
    公式(I)化合物及其药学上可接受的盐和溶剂化合物:其中R1为氢、C1-6烷基(可选地被羟基或C1-4烷氧基取代)、苯基-C1-4烷基、C1-6烯基、C1-6炔基;R2为氢或最多三个取代基,所选自卤素、NO2、CN、N3、CF3O—、CF3S—、CF3CO—、C1-6烷基、C1-6烯基、C1-6炔基、C1-6全氟烷基、C3-6环烷基、C3-6环烷基-C1-4烷基、C1-6烷氧基、C1-6烷基CO—、C3-6环烷基烷氧基、C3-6环烷基CO—、C3-6环烷基-C1-4烷氧基、C3-6环烷基-C1-4烷基CO—、苯基、苯氧基、苄氧基、苯甲酰基、苯基-C1-4烷基、C1-6烷基S—、C1-6烷基SO2—、(C1-4烷基)2NSO2—、(C1-4烷基)NHSO2—、(C1-4烷基)2NCO—、(C1-4烷基)NHCO—或CONH2;或—NR5R6,其中R5为氢或C1-4烷基,R6为氢、C1-4烷基、甲酰基、—CO2C1-4烷基或—COC1-4烷基;或两个R2基共同形成一个饱和或不饱和的碳环。R3基和R4基各自独立地为氢或C1-6烷基,或两个R3基和/或两个R4基共同形成一个C3-6螺环烷基,前提是至少有一个R3或R4基不是氢;X选自氢、卤素、基、烷基和烷氧基。这些化合物对于治疗和预防癫痫、偏头痛和其他疾病是有用的。
  • TETRAHYDRONAPHTHYRIDINYL-CARBOXAMIDES HAVING ANTI-CONVULSANT ACTIVITY
    申请人:SmithKline Beecham plc
    公开号:EP1084122B1
    公开(公告)日:2003-10-22
  • US6410555B1
    申请人:——
    公开号:US6410555B1
    公开(公告)日:2002-06-25
  • US6762192B2
    申请人:——
    公开号:US6762192B2
    公开(公告)日:2004-07-13
  • [EN] TETRAHYDRONAPHTHYRIDINYL-CARBOXAMIDES HAVING ANTI-CONVULSANT ACTIVITY<br/>[FR] TETRAHYDRONAPHTYRIDINYL-CARBOXAMIDES PRESENTANT UNE ACTIVITE ANTI-CONVULSIVANTE
    申请人:SMITHKLINE BEECHAM PLC
    公开号:WO1999065903A1
    公开(公告)日:1999-12-23
    (EN) Compounds of formula (I) and pharmaceutically acceptable salts and solvates: where R1 is hydrogen, C1-6alkyl (optionally substituted by hydroxy or C1-4alkoxy), phenyl-C1-4alkyl-, C1-6alkenyl, C1-6alkynyl; R2 is hydrogen or up to three substituents selected from halogen, NO2, CN, N3, CF3O-, CF3S-, CF3SO2-, CF3CO-, C1-6alkyl, C1-6alkenyl, C1-6alkynyl, C1-6perfluoroalkyl, C3-6cycloalkyl, C3-6cycloalkyl-C1-4alkyl-, C1-6alkylO-, C1-6alkylCO-, C3-6cycloalkylO-, C3-6cycloalkylCO-, C3-6cycloalkyl-C1-4alkylO-, C3-6cycloalkyl-C1-4alkylCO-, phenyl, phenoxy, benzyloxy, benzoyl, phenyl-C1-4alkyl-, C1-6alkylS-, C1-6alkylSO2-, (C1-4alkyl)2NSO2-, (C1-4alkyl)NHSO2-, (C1-4alkyl)2NCO-, (C1-4alkyl)NHCO- or CONH2; or -NR5R6 where R5 is hydrogen or C1-4alkyl, and R6 is hydrogen, C1-4alkyl, formyl, -CO2C1-4alkyl or -COC1-4alkyl; or two R2 groups together form a carbocyclic ring that is saturated or unsaturated, optionally interrupted by O or NH; R3 groups and R4 groups are each independently hydrogen or C1-6alkyl and/or the two R3 groups and/or the two R4 groups together form a C3-6spiroalkyl group, provided that at least one R3 or R4 group is not hydrogen; and X is selected from hydrogen, halogen, cyano, alkyl and alkoxy, are useful in the treatment and prophylaxis of epilepsy, migraine, and other disorders.(FR) La présente invention concerne des composés représentés par la formule générale (I) ainsi que certains de leurs sels et solvates pharmaceutiquement acceptés. Ces composés conviennent au traitement et à la prophylaxie de l'épilepsie, de la migraine et d'autres troubles. En l'occurrence, R1 est hydrogène, C1-6alkyle (éventuellement substitué par hydroxy ou C1-4alcoxy), phényle-C1-4alkyle-, C1-6alcényle, C1-6alkynyle; R2 est hydrogène ou un maximum de trois substituants choisis parmi halogène, NO2, CN, N3, CF3O-, CF3S-, CF3SO2-, CF3CO-, C1-6alkyle, C1-6alcényle, C1-6alkynyle, C1-6perfluoroalkyle, C3-6cycloalkyle, C3-6cycloalkyle-C1-4alkyle-, C1-6alkyleO-, C1-6alkyleCO-, C3-6cycloalkyleO-, C3-6cycloalkyleCO-, C3-6cycloalkyle-C1-4alkyleO-, C3-6cycloalkyle-C1-4alkyleCO-, phényle, phénoxy, benzyloxy, benzoyl, phényle-C1-4alkyle-, C1-6alkyleS-, C1-6alkyleSO2-, (C1-4alkyle)2NSO2-, (C1-4alkyle)NHSO2-, (C1-4alkyle)2NCO-, (C1-4alkyle)NHCO- ou CONH2; ou -NR5R6 auquel cas R5 est hydrogène ou C1-4alkyle, et R6 est hydrogène, C1-4alkyle, formyle, -CO2C1-4alkyle ou -COC1-4alkyle; ou deux groupes R2 forment ensemble un cycle carbocyclique qui est saturé ou insaturé, éventuellement interrompu par O ou NH; les groupes R3 et R4 sont chacun indépendamment hydrogène ou C1-6alkyle et/ou les deux groupes R3 et/ou les deux groupes R4 forment ensemble un groupe C3-6spiroalkyle, à condition que l'un au moins du groupe R3 ou R4 ne soit pas hydrogène; et X est hydrogène, halogène, cyano, alkyle ou alcoxy.
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