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3-{5-[2-(3,4-dichloro-phenyl)-pent-4-enoylamino]-2-methoxy-phenoxymethyl}-piperidine-1-carboxylic acid tert-butyl ester | 619254-57-8

中文名称
——
中文别名
——
英文名称
3-{5-[2-(3,4-dichloro-phenyl)-pent-4-enoylamino]-2-methoxy-phenoxymethyl}-piperidine-1-carboxylic acid tert-butyl ester
英文别名
Tert-butyl 3-[[5-[2-(3,4-dichlorophenyl)pent-4-enoylamino]-2-methoxyphenoxy]methyl]piperidine-1-carboxylate
3-{5-[2-(3,4-dichloro-phenyl)-pent-4-enoylamino]-2-methoxy-phenoxymethyl}-piperidine-1-carboxylic acid tert-butyl ester化学式
CAS
619254-57-8
化学式
C29H36Cl2N2O5
mdl
——
分子量
563.521
InChiKey
NNPOXHKXWIRSHL-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):
    6.7
  • 重原子数:
    38
  • 可旋转键数:
    11
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.45
  • 拓扑面积:
    77.1
  • 氢给体数:
    1
  • 氢受体数:
    5

文献信息

  • [EN] COMPOUNDS HAVING AFFINITY AT 5HT2C RECEPTOR AND USE THEREOF IN THERAPY<br/>[FR] COMPOSES PRESENTANT UNE AFFINITE AVEC LE RECEPTEUR 5HT2C ET UTILISATION THERAPEUTIQUE DE CEUX-CI
    申请人:GLAXO GROUP LTD
    公开号:WO2003089409A1
    公开(公告)日:2003-10-30
    Compounds of formula (I) or a pharmaceutically acceptable salt thereof are disclosed: wherein R1 is hydrogen, hydroxy, fluoro, chloro, C1-6alkyl, C3-7cycloalkyl, C3-7cycloalkyloxy, C1-6alkoxy or haloC1-6alkoxy; m is 0 when ======= is a double bond and m is 1 when ======= is a single bond; R2 is hydrogen, halogen, cyano, nitro, C1-6alkyl, C3-7cycloalkyl, C3-7cycloalkyloxy, haloC1-6alkyl, C1-6alkoxy, haloC1-6alkoxy, C1-6alkylthio, amino, mono- or di-C1-6alkylamino or an N-linked 4 to 7 membered heterocyclic group; X is -(CH2-CH2)-, -(CH=CH)-, -(CH2)3-, -C(CH3)2-, -(CH=CH-CH2)-, -(CH2-CH=CH)- or a group -(CHR5)- wherein R5 is hydrogen, halogen, hydroxy, cyano, nitro, C1-6alkyl, C3-7cycloalkyl, C3-7cycloalkyloxy, haloC1-6alkyl, C1-6alkoxy, haloC1-6alkoxy or C1-6alkylthio; R3 is halogen, cyano, C1-6alkyl, C3-7cycloalkyl, C3-7cycloalkyloxy, C1-6alkoxy, C1-6alkylthio, hydroxy, amino, mono- or di-C1-6alkylamino, an N-linked 4 to 7 membered heterocyclic group, nitro, haloC1-6alkyl, haloC1-6alkoxy, aryl, arylC1-6alkyl, arylC1-6alkyloxy, arylC1-6alkylthio or COOR6, CONR7R8 or COR9 wherein R6, R7, R8 and R9 are independently hydrogen or C1-6alkyl; p is 0, 1 or 2 or 3; R4 is hydrogen, halogen, hydroxy, cyano, nitro, C1-6alkyl, C1-6alkanoyl, C3-7cycloalkyl, C3-7cycloalkyloxy, haloC1-6alkyl, C1-6alkoxy, haloC1-6alkoxy, C1-6alkylthio, amino, mono- or di-C1-6alkylamino or an N-linked 4 to 7 membered heterocyclic group; Y is oxygen, sulfur, -CH2- or NR10 wherein R10 is hydrogen or C1-6alkyl; D is a single bond, -CH2-, -(CH2)2- or -CH=CH-; and Z is an optionally substituted C-linked 4 to 7 membered heterocyclic group containing at least one nitrogen, an optionally substituted N-linked 4 to 7 membered heterocyclic group, or Z is -NR11R12 where R11 and R12 are independently hydrogen or C1-6alkyl. Methods of preparation and uses thereof in therapy, particularly for CNS disorders such as depression and anxiety, are also disclosed.
    公式(I)的化合物或其药学上可接受的盐被披露:其中R1是氢,羟基,,C1-6烷基,C3-7环烷基,C3-7环烷氧基,C1-6烷氧基或卤代C1-6烷氧基;当=======是双键时,m为0,当=======是单键时,m为1;R2是氢,卤素,基,硝基,C1-6烷基,C3-7环烷基,C3-7环烷氧基,卤代C1-6烷基,C1-6烷氧基,卤代C1-6烷氧基,C1-6烷基,基,单或双C1-6烷基基或N-连接的4至7成员杂环基;X是-(CH2- )-,-(CH=CH)-,-( )3-,-C(CH3)2-,-(CH=CH- )-,-( -CH=CH)-或一个基团-(CHR5)-其中R5是氢,卤素,羟基,基,硝基,C1-6烷基,C3-7环烷基,C3-7环烷氧基,卤代C1-6烷基,C1-6烷氧基,卤代C1-6烷氧基或C1-6烷基;R3是卤素,基,C1-6烷基,C3-7环烷基,C3-7环烷氧基,C1-6烷氧基,C1-6烷基,羟基,基,单或双C1-6烷基基,N-连接的4至7成员杂环基,硝基,卤代C1-6烷基,卤代C1-6烷氧基,芳基,芳基C1-6烷基,芳基C1-6烷氧基,芳基C1-6烷基或COOR6,CONR7R8或COR9其中R6,R7,R8和R9独立地是氢或C1-6烷基;p是0,1,2或3;R4是氢,卤素,羟基,基,硝基,C1-6烷基,C1-6烷酰基,C3-7环烷基,C3-7环烷氧基,卤代C1-6烷基,C1-6烷氧基,卤代C1-6烷氧基,C1-6烷基,基,单或双C1-6烷基基或N-连接的4至7成员杂环基;Y是氧,,- -或NR10其中R10是氢或C1-6烷基;D是单键,- -,-( )2-或-CH=CH-;Z是含有至少一个氮的可选择取代的C-连接的4至7成员杂环基,可选择取代的N-连接的4至7成员杂环基,或Z是-NR11R12其中R11和R12独立地是氢或C1-6烷基。还披露了其制备方法和在治疗中的用途,特别是用于中枢神经系统疾病如抑郁症和焦虑症。
  • Compounds having affinity at 5ht2C receptor and use thereof in therapy
    申请人:Damiani Federica
    公开号:US20050203079A1
    公开(公告)日:2005-09-15
    Compounds of formula (I) or a pharmaceutically acceptable salt thereof are disclosed: wherein R 1 is hydrogen, hydroxy, fluoro, chloro, C 1-6 alkyl, C 3-7 cycloalkyl, C 3-7 cycloalkyloxy, C 1-6 alkoxy or haloC 1-6 alkoxy; m is 0 when is a double bond and m is 1 when is a single bond; R 2 is hydrogen, halogen, cyano, nitro, C 1-6 alkyl, C 3-7 cycloalkyl, C 3-7 cycloalkyloxy, haloC 1-6 alkyl, C 1-6 alkoxy, haloC 1-6 alkoxy, C 1-6 alkylthio, amino, mono- or di-C 1-6 alkylamino or an N-linked 4 to 7 membered heterocyclic group; X is —(CH 2 —CH 2 )—, —(CH═CH)—, —(CH 2 ) 3 —, —C(CH 3 ) 2 —, —(CH═CH—CH 2 )—, —(CH 2 —CH═CH)— or a group —(CHR 5 )— wherein R 5 is hydrogen, halogen, hydroxy, cyano, nitro, C 1-6 alkyl, C 3-7 cycloalkyl, C 3-7 cycloalkyloxy, haloC 1-6 alkyl, C 1-6 alkoxy, haloC 1-6 alkoxy or C 1-6 alkylthio; R 3 is halogen, cyano, C 1-6 alkyl, C 3-7 cycloalkyl, C 3-7 cycloalkyloxy, C 1-6 alkoxy, C 1-6 alkylthio, hydroxy, amino, mono- or di-C 1-6 alkylamino, an N-linked 4 to 7 membered heterocyclic group, nitro, haloC 1-6 alkyl, haloC 1-6 alkoxy, aryl, arylC 1-6 alkyl, arylC 1-6 alkyloxy, arylC 1-6 alkylthio or COOR 6 , CONR 7 R 8 or COR 9 wherein R 6 , R 7 , R 8 and R 9 are independently hydrogen or C 1-6 alkyl; p is 0, 1 or 2 or 3; R 4 is hydrogen, halogen, hydroxy, cyano, nitro, C 1-6 alkyl, C 1-6 alkanoyl, C 3-7 cycloalkyl, C 3-7 cycloalkyloxy, haloC 1-6 alkyl, C 1-6 alkoxy, haloC 1-6 alkoxy, C 1-6 alkylthio, amino, mono- or di-C 1-6 alkylamino or an N-linked 4 to 7 membered heterocyclic group; Y is oxygen, sulfur, —CH 2 — or NR 10 wherein R 10 is hydrogen or C 1-6 alkyl; D is a single bond, —CH 2 —, —(CH 2 ) 2 — or —CH═CH—; and Z is an optionally substituted C-linked 4 to 7 membered heterocyclic group containing at least one nitrogen, an optionally substituted N-linked 4 to 7 membered heterocyclic group, or Z is —NR 11 R 12 where R 11 and R 12 are independently hydrogen or C 1-6 alkyl. Methods of preparation and uses thereof in therapy, particularly for CNS disorders such as depression and anxiety, are also disclosed.
    公开了化学式(I)或其药学上可接受的盐的化合物:其中R1是氢,羟基,,C1-6烷基,C3-7环烷基,C3-7环烷氧基,C1-6烷氧基或卤代C1-6烷氧基; 当是双键时,m为0,当是单键时,m为1; R2是氢,卤素,基,硝基,C1-6烷基,C3-7环烷基,C3-7环烷氧基,卤代C1-6烷基,C1-6烷氧基,卤代C1-6烷氧基,C1-6基,基,单基或二基C1-6烷基基或N-连接的4至7成员杂环基; X是—(CH2— )—,—(CH═CH)—,—( )3—,—C(CH3)2—,—(CH═CH— )—,—( —CH═CH)—或一个—(CHR5)—基团,其中R5是氢,卤素,羟基,基,硝基,C1-6烷基,C3-7环烷基,C3-7环烷氧基,卤代C1-6烷基,C1-6烷氧基,卤代C1-6烷氧基或C1-6基; R3是卤素,基,C1-6烷基,C3-7环烷基,C3-7环烷氧基,C1-6烷氧基,C1-6基,羟基,基,单基或二基C1-6烷基基,N-连接的4至7成员杂环基,硝基,卤代C1-6烷基,卤代C1-6烷氧基,芳基,芳基C1-6烷基,芳基C1-6烷氧基,芳基C1-6基或COOR6,CONR7R8或COR9,其中R6,R7,R8和R9独立地为氢或C1-6烷基; p为0、1、2或3; R4是氢,卤素,羟基,基,硝基,C1-6烷基,C1-6酰基,C3-7环烷基,C3-7环烷氧基,卤代C1-6烷基,C1-6烷氧基,卤代C1-6烷氧基,C1-6基,基,单基或二基C1-6烷基基或N-连接的4至7成员杂环基; Y是氧,,— —或NR10,其中R10是氢或C1-6烷基; D是单键,— —,—( )2—或—CH═CH—; Z是一个可选择取代的含有至少一个氮的C-连接的4至7成员杂环基,一个可选择取代的N-连接的4至7成员杂环基,或Z是—NR11R12,其中R11和R12独立地为氢或C1-6烷基。还公开了制备方法及其在治疗中的用途,特别是在中枢神经系统疾病如抑郁症和焦虑症中的应用。
  • COMPOUNDS HAVING AFFINITY AT 5HT2C RECEPTOR AND USE THEREOF IN THERAPY
    申请人:GLAXO GROUP LIMITED
    公开号:EP1497265B1
    公开(公告)日:2009-02-18
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