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1-BOC-4-(4-氨基苯基)哌嗪二盐酸盐 | 193902-64-6

中文名称
1-BOC-4-(4-氨基苯基)哌嗪二盐酸盐
中文别名
1-BOC-4-(4-氨基苯基)-哌嗪双盐酸盐;4-(4-氨基苯基)-1-哌嗪羧酸叔丁酯单盐酸盐
英文名称
1-Boc-4-(4-Aminophenyl)piperazine dihydrochloride
英文别名
tert-butyl 4-(4-aminophenyl)piperazine-1-carboxylate;dihydrochloride
1-BOC-4-(4-氨基苯基)哌嗪二盐酸盐化学式
CAS
193902-64-6
化学式
C15H25Cl2N3O2
mdl
——
分子量
350.3
InChiKey
RXLNINVLZWODOG-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):
    3.17
  • 重原子数:
    22
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.53
  • 拓扑面积:
    58.8
  • 氢给体数:
    3
  • 氢受体数:
    4

安全信息

  • 海关编码:
    2933599090
  • 危险性防范说明:
    P261,P305+P351+P338
  • 危险性描述:
    H302,H315,H319,H335

文献信息

  • Pharmaceutical Compounds
    申请人:Berdini Valerio
    公开号:US20080167309A1
    公开(公告)日:2008-07-10
    The invention provides a compound for use in the prophylaxis or treatment of a disease state or condition mediated by a cyclin dependent kinase, the compound having the formula (I): and salts, tautomers, N-oxides or solvates thereof, wherein A is a bond, C═O, NR g (C═O) or O(C═O) wherein R g is hydrogen or C 1-4 hydrocarbyl optionally substituted by hydroxy or C 1-4 alkoxy; Y is a bond or an alkylene chain of 1, 2 or 3 carbon atoms in length; Q is S or CR 2 ; J is S or CH; provided that one of Q and J is S, and the other of Q and J is not S; when Q is S, there is a double bond between the ring carbon atoms “a” and “b” and a double bond between the ring nitrogen N and J; and when J is S, there is a double bond between Q and the ring carbon atom “a” and a double bond between the ring nitrogen N and the ring carbon atom “b”; and R 1 to R 4 are as defined in the claims.
    本发明提供了一种化合物,用于预防或治疗由细胞周期依赖性激酶介导的疾病状态或病症,该化合物具有以下式子(I)和其盐、互变异构体、N-氧化物或溶剂化物:其中,A是键合、C═O、NRg(C═O)或O(C═O),其中Rg为氢或C1-4烃基,可选地被羟基或C1-4烷氧基取代;Y是长度为1、2或3个碳原子的烷基链或键合;Q是S或CR2;J是S或CH;前提是Q和J中的一个是S,而另一个不是S;当Q是S时,环上碳原子“a”和“b”之间有双键,环氮原子N和J之间也有双键;当J是S时,Q和环上碳原子“a”之间有双键,环氮原子N和环上碳原子“b”之间也有双键;R1至R4如权利要求所定义。
  • THIAZOLE AND ISOTHIAZOLE DERIVATIVES AS PROTEIN KINASE INHIBITORS
    申请人:Astex Therapeutics Limited
    公开号:EP1781647A2
    公开(公告)日:2007-05-09
  • [EN] PHARMACEUTICAL COMPOUNDS<br/>[FR] COMPOSES PHARMACEUTIQUES
    申请人:ASTEX THERAPEUTICS LTD
    公开号:WO2006008545A2
    公开(公告)日:2006-01-26
    The invention provides a compound for use in the prophylaxis or treatment of a disease state or condition mediated by a cyclin dependent kinase, the compound having the formula (I): (I) and salts, tautomers, N-oxides or solvates thereof; wherein A is a bond, C=O, NRg(C=O) or O(C=O) wherein Rg is hydrogen or C1-4 hydrocarbyl optionally substituted by hydroxy or C1-4 alkoxy; Y is a bond or an alkylene chain of 1, 2 or 3 carbon atoms in length; Q is S or CR2; J is S or CH; provided that one of Q and J is S, and the other of Q and J is not S; when Q is S, there is a double bond between the ring carbon atoms “a” and “b” and a double bond between the ring nitrogen N and J; and when J is S, there is a double bond between Q and the ring carbon atom “a” and a double bond between the ring nitrogen N and the ring carbon atom “b”; and R1 to R4 are as defined in the claims.
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