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tert-butyl (1S,5S)-3,8-diazabicyclo[3.2.1]octane-8-carboxylate

中文名称
——
中文别名
——
英文名称
tert-butyl (1S,5S)-3,8-diazabicyclo[3.2.1]octane-8-carboxylate
英文别名
——
tert-butyl (1S,5S)-3,8-diazabicyclo[3.2.1]octane-8-carboxylate化学式
CAS
——
化学式
C11H20N2O2
mdl
——
分子量
212.29
InChiKey
HNINFCBLGHCFOJ-IUCAKERBSA-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):
    1.1
  • 重原子数:
    15
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.91
  • 拓扑面积:
    41.6
  • 氢给体数:
    1
  • 氢受体数:
    3

文献信息

  • Mutant IDH1 inhibitors useful for treating cancer
    申请人:THE UNITED STATES OF AMERICA, AS REPRESENTED BY THE SECRETARY, DEPARTMENT OF HEALTH AND HUMAN SERVICE
    公开号:US10703746B2
    公开(公告)日:2020-07-07
    Compounds of Formula I and Formula II and the pharmaceutically acceptable salts thereof are disclosed The variables A, B, Y, Z, X1, X2, R1-4 and R13-18 are disclosed herein. The compounds are useful for treating cancer disorders, especially those involving mutant IDH1 enzymes. Pharmaceutical compositions containing compounds of Formula I or Formula II and methods of treatment comprising administering compounds of Formula I and Formula II are also disclosed.
    公开了式 I 和式 II 的化合物及其药学上可接受的盐 本文公开了变量 A、B、Y、Z、X1、X2、R1-4 和 R13-18。这些化合物可用于治疗癌症疾病,特别是涉及突变 IDH1 酶的疾病。还公开了含有式 I 或式 II 化合物的药物组合物以及包括施用式 I 和式 II 化合物的治疗方法。
  • Thiazole derivatives useful as mutant IDH1 inhibitors for treating cancer
    申请人:THE UNITED STATES OF AMERICA, AS REPRESENTED BY THE SECRETARY, DEPARTMENT OF HEALTH AND HUMAN SERVICES
    公开号:US10836759B2
    公开(公告)日:2020-11-17
    A compound of Formula II or a pharmaceutically acceptable salt thereof, wherein CyN is a cyclic amine group bound via a nitrogen atom; X is C or N; R1 and R2 are each independently a halogen, CN, CF3, CHF2, CH2F, a C1-C10alkyl group, a C1-C10alkoxy group, a di(C1-C5alkyl)amino; m and n are each independently 1, 2, or 3, and represents either a single bond or a double bond, wherein the racemic mixture of 3-(4-(4-chlorophenyl)thiazol-2-yl)-1-(2-ethyl-5-methoxyphenyl)-6-(2-methylprop-1-en-1-yl)-5-(piperazine-1-carbonyl)pyridin-2(1H)-one atropisomers is excluded.
    一种式 II 的化合物或其药学上可接受的盐,其中 CyN 是通过氮原子结合的环胺基;X 是 C 或 N;R1 和 R2 各自独立地是卤素、CN、CF3、CHF2、CH2F、C1-C10 烷基、C1-C10 烷氧基、二(C1-C5 烷基)氨基;m和n各自独立地为1、2或3,代表单键或双键,其中不包括3-(4-(4-氯苯基)噻唑-2-基)-1-(2-乙基-5-甲氧基苯基)-6-(2-甲基丙-1-烯-1-基)-5-(哌嗪-1-羰基)吡啶-2(1H)-酮异构体的外消旋混合物。
  • EP3475276B1
    申请人:——
    公开号:EP3475276B1
    公开(公告)日:2021-03-31
  • NAPHTHYRIDINONE COMPOUNDS USEFUL AS T CELL ACTIVATORS
    申请人:Bristol-Myers Squibb Company
    公开号:EP3814347A1
    公开(公告)日:2021-05-05
  • THIAZOLE DERIVATIVES USEFUL AS MUTANT IDH1 INHIBITORS FOR TREATING CANCER
    申请人:THE UNITED STATED OF AMERICA AS REPRESENTED BY THE SECRETARY, DEPARTMENT OF HEALTH AND HUMAN SERVICE
    公开号:US20190241551A1
    公开(公告)日:2019-08-08
    A compound of Formula II or a pharmaceutically acceptable salt thereof, wherein CyN is a cyclic amine group bound via a nitrogen atom; X is C or N; R 1 and R 2 are each independently a halogen, CN, CF 3 , CHF 2 , CH 2 F, a C 1 -C10alkyl group, a C1-C 10 alkoxy group, a di(C 1 -C 5 alkyl)amino; m and n are each independently 1, 2, or 3, and represents either a single bond or a double bond, wherein the racemic mixture of 3-(4-(4-chlorophenyl)thiazol-2-yl)-1-(2-ethyl-5-methoxyphenyl)-6-(2-methylprop-1-en-1-yl)-5-(piperazine-1-carbonyl)pyridin-2(1H)-one atropisomers is excluded.
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