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7-Chloro-1-(3-cyano-4-methylphenyl)-4-hydroxy-2-oxoquinoline-3-carbonitrile | 1016641-86-3

中文名称
——
中文别名
——
英文名称
7-Chloro-1-(3-cyano-4-methylphenyl)-4-hydroxy-2-oxoquinoline-3-carbonitrile
英文别名
——
7-Chloro-1-(3-cyano-4-methylphenyl)-4-hydroxy-2-oxoquinoline-3-carbonitrile化学式
CAS
1016641-86-3
化学式
C18H10ClN3O2
mdl
——
分子量
335.749
InChiKey
RZODDURBUFJNFY-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):
    3.6
  • 重原子数:
    24
  • 可旋转键数:
    1
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.06
  • 拓扑面积:
    88.1
  • 氢给体数:
    1
  • 氢受体数:
    4

上下游信息

  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

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文献信息

  • QUINOLINONE DERIVATIVES
    申请人:Kesteleyn Bart Rudolf Romanie
    公开号:US20100087649A1
    公开(公告)日:2010-04-08
    HIV inhibitory compounds of formula (I) including the stereoisomeric forms thereof, the pharmaceutically acceptable salts, and pharmaceutically acceptable solvates thereof; wherein R 1 is cyano; R 2 is H, C 1-6 alkyl, trifluoromethyl, amino, mono- or di-C 1-6 alkylamino, C 1-6 alkylamino wherein the C 1-6 alkyl group can be substituted; X 1 is CH or N; R 3 is phenyl or pyridyl, each unsubstituted or substituted; R 4 is H, C 1-6 alkyl, (C 1-6 alkylcarbonylamino)C 1-6 alkyl-, Ar, potionally substituted thienyl, furanyl, pyridyl, pyrimidyl, pyrazinyl, pyrrolyl, pyrazolyl, imidazolyl, triazolyl, oxazolyl, thiazolyl, halo, trifluoromethyl, hydroxy, C 1-6 alkyloxy, —OPO(OH) 2 , amino, aminocarbonyl, cyano, —Y 1 —R 6 , —Y 1 -Alk-R 6 , or —Y 1 -Alk-Y 2 —R 7 ; R 3 is H, halo, hydroxy or C 1-6 alkyloxy; or R 4 and R 5 form —O—CH 2 —O—; Y 1 is O or NR 8 ; Y 2 is O or NR 9 ; Alk is bivalent C 1-6 alkyl; R 6 is pyrrolidinyl, piperidinyl, morpholinyl, piperazinyl, 4-C 1-6 alkylpiperazinyl, 4-(C 1-6 alkylcarbonyl)piperazinyl, pyridyl, or imidazolyl; R 7 is H, C 1-6 alkyl, hydroxyC 1-6 alkyl, C 1-6 alkylcarbonyl; R 8 and R 9 are H or C 1-6 alkyl; Ar is optionally substituted phenyl; pharmaceutical compositions comprising the above compounds (I) as active ingredient.
  • [EN] QUINOLINONE DERIVATIVES<br/>[FR] DÉRIVÉS DE QUINOLINONE
    申请人:TIBOTEC PHARM LTD
    公开号:WO2008037784A1
    公开(公告)日:2008-04-03
    [EN] HIV inhibitory compounds of formula (I) including the stereoisomeric forms thereof, the pharmaceutically acceptable salts, and pharmaceutically acceptable solvates thereof; wherein R1 is cyano; R2 is H, C1-6alkyl, trifluoromethyl, amino, mono- or di-C1-6alkylamino, C1-6alkylamino wherein the C1-6alkyl group can be substituted; X1 is CH or N; R3 is phenyl or pyridyl, each unsubstituted or substituted; R4 is H, C1-6alkyl, (C1-6alkylcarbonyla mino)C1-6alkyl-, Ar, potionally substituted thienyl, furanyl, pyridyl, pyrimidyl, pyrazinyl, pyrrolyl, pyrazolyl, imidazolyl, triazo lyl, oxazolyl, thiazolyl, halo, trifluoromethyl, hydroxy, C1-6alkyloxy, -OPO(OH)2, amino, aminocarbonyl, cyano, -Y1-R6, -Y1-Alk-R6, or -Y1-Alk-Y2-R7; R5 is H, halo, hydroxy or C1-6alkyloxy; or R4 and R5 form -O-CH2-O-; Y1 is O or NR8; Y2 is O or NR9; Alk is bivalent C1-6alkyl; R6 is pyrrolidinyl, piperidinyl, morpho linyl, piperazinyl, 4-C1 -6alkylpiperazinyl, 4-(C1-6alkylcarbonyl)piperazinyl, pyridyl, or imidazolyl; R7 is H, C1-6alkyl, hydroxyC1 -6alkyl, C1
    [FR] La présente invention concerne des composés inhibiteurs du VIH, de formule (I), y compris les formes stéréoisomères, les sels pharmaceutiquement acceptables et les solvates pharmaceutiquement acceptables de ceux-ci. Dans cette formule, R1 représente cyano; R2 représente H, alkyle C1-6, trifluorométhyle, amino, mono- ou di-alkylamino C1-6, alkylamino C1-6, le groupe alkyle C1-6 pouvant être substitué; X1 représente CH ou N; R3 représente phényle ou pyridyle, chacun substitué ou non; R4 représente H, alkyle C1-6, (alkylcarbonylamino C1-6)C1-6alkyle, Ar, thiényle, furanyle, pyridyle, pyrimidyle, pyrazinyle, pyrrolyle, pyrazolyle, imidazolyle, triazolyle, oxazolyle, thiazolyle, halo, trifluorométhyle, hydroxy, alkyloxy C1-6, -OPO(OH)2, amino, aminocarbonyle, cyano, -Y1-R6, -Y1-Alk-R6 ou -Y1-Alk-Y2-R7
  • WO2008/37784
    申请人:——
    公开号:——
    公开(公告)日:——
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