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tert-butyl N-[[3-(5-methylsulfanyltriazolo[4,5-d]pyrimidin-3-yl)phenyl]methyl]carbamate | 900185-43-5

中文名称
——
中文别名
——
英文名称
tert-butyl N-[[3-(5-methylsulfanyltriazolo[4,5-d]pyrimidin-3-yl)phenyl]methyl]carbamate
英文别名
——
tert-butyl N-[[3-(5-methylsulfanyltriazolo[4,5-d]pyrimidin-3-yl)phenyl]methyl]carbamate化学式
CAS
900185-43-5
化学式
C17H20N6O2S
mdl
——
分子量
372.451
InChiKey
GUBKKYKSAYJLSL-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):
    2.7
  • 重原子数:
    26
  • 可旋转键数:
    6
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.35
  • 拓扑面积:
    120
  • 氢给体数:
    1
  • 氢受体数:
    7

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

点击查看最新优质反应信息

文献信息

  • TRIAZOLOPYRIMIDINE DERIVATIVES AS GLYCOGEN SYNTHASE KINASE 3 INHIBITORS
    申请人:Love Christopher John
    公开号:US20100160349A1
    公开(公告)日:2010-06-24
    This invention concerns a compound of formula a N-oxide, a pharmaceutically acceptable addition salt, a quaternary amine and a stereochemically isomeric form thereof, wherein ring A represents phenyl, pyridyl, pyrimidinyl, pyridazinyl or pyrazinyl; R 1 represents hydrogen; aryl; formyl; C 1-6 alkylcarbonyl; C 1-6 alkyl; C 1-6 alkyloxycarbonyl; C 1-6 alkyl substituted with formyl, C 1-6 alkylcarbonyl, C 1-6 alkyloxycarbonyl or C 1-6 alkylcarbonyloxy; X represents a direct bond; —(CH 2 ) n3 — or —(CH 2 ) n4 —X 1a —X 1b —; R 2 represents an optionally substituted cyclic system; provided that N,3-diphenyl-3H-1,2,3-triazolo[4,5-d]pyrimidin-5-amine is not included; their use, pharmaceutical compositions comprising them and processes for their preparation.
  • [EN] TRIAZOLOPYRIMIDINE DERIVATIVES AS GLYCOGEN SYNTHASE KINASE 3 INHIBITORS<br/>[FR] DERIVES DE TRIAZOLOPYRIMIDINE COMME INHIBITEURS DE LA GLYCOGENE SYNTHASE KINASE 3
    申请人:JANSSEN PHARMACEUTICA NV
    公开号:WO2006075023A2
    公开(公告)日:2006-07-20
    [EN] This invention concerns a compound of formula (I), a N-oxide, a pharmaceutically acceptable addition salt, a quaternary amine and a stereochemically isomeric form thereof, wherein ring A represents phenyl, pyridyl, pyrimidinyl, pyridazinyl or pyrazinyl; R1 represents hydrogen; aryl; formyl; C1-6alkylcarbonyl; C1-6alkyl; C1-6alkyloxycarbonyl; C1-6alkyl substituted with formyl, C1-6alkylcarbonyl, C1-6alkyloxycarbonyl or C1-6alkylcarbonyloxy; X represents a direct bond; -(CH2)n3- or -(CH2)n4-X1a-X1b-; R2 represents an optionally substituted cyclic system; provided that N,3-diphenyl-3H-1,2,3-triazolo[4,5-d]pyrimidin-5-amine is not included ; their use, pharmaceutical compositions comprising them and processes for their preparation.
    [FR] L'invention concerne un composé de formule (I), un N-oxyde, un sel d'addition pharmaceutique acceptable, un amine quaternaire et sa forme isomérique stéréochimiquement isomère, où l'anneau A représente phényle, pyridyle, pyrimidinyle, pyridazinyle ou pyrazinyle; R1 représente hydrogène; aryle; formyle; C1-6 alkylcarbonyle; C1-6 alkyle; C1-6alkyloxycarbonyle; C1-6ealkyle substitué par formyle, C1-6 alkylcarbonyle, C1-6 alkyloxycarbonyle ou C1-6 alkylcarbonyloxy; X représente une liaison directe; -(CH2)n3- ou -(CH2)n4-X1a-X1b-; R2 représente un système cyclique éventuellement substitué à condition que N,3-diphényl-3H-1,2,3-triazolo[4,5-d]pyrimidine-5-amine ne soit pas inclus; leur utilisation, les compositions pharmaceutiques les contenant et les procédés pour leur préparation.
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