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2-methyl-4-[(S)-2,3,3-trimethyl-2-butyl]-1,4-benzodiazepin-5(3H)-one | 512827-94-0

中文名称
——
中文别名
——
英文名称
2-methyl-4-[(S)-2,3,3-trimethyl-2-butyl]-1,4-benzodiazepin-5(3H)-one
英文别名
4-[(2S)-3,3-dimethylbutan-2-yl]-2-methyl-3H-1,4-benzodiazepin-5-one
2-methyl-4-[(S)-2,3,3-trimethyl-2-butyl]-1,4-benzodiazepin-5(3H)-one化学式
CAS
512827-94-0
化学式
C16H22N2O
mdl
——
分子量
258.363
InChiKey
QDANCCJEARVQSF-LBPRGKRZSA-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):
    3.1
  • 重原子数:
    19
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    32.7
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    描述:
    methyl 2-chloro-2-(4-methylphenyl-hydrazono)acetate2-methyl-4-[(S)-2,3,3-trimethyl-2-butyl]-1,4-benzodiazepin-5(3H)-one三乙胺 作用下, 以 氯仿 为溶剂, 反应 7.0h, 以22%的产率得到methyl (3aS)-5-[(2S)-3,3-dimethylbutan-2-yl]-3a-methyl-3-(4-methylphenyl)-6-oxo-4H-[1,2,4]triazolo[4,3-a][1,4]benzodiazepine-1-carboxylate
    参考文献:
    名称:
    Diastereoselective nitrilimine cycloaddition to the CN bond of enantiopure 1,4-benzodiazepinones
    摘要:
    Enantiopure 1,4-benzodiazepin-4-one 1 and 1,4-benzodiazepin-6-ones 2 were reacted with hydrazonoyl chloride 8 in the presence of various basic agents. The diastereoselective 1,3-dipolar cycloaddition between the C=N double bond of 1 or 2 and the nitrilimine intermediate 9 gave the enantiopure [1,2,4]triazolo[4,3-a][1,4]benzo diazepinones 10-13. (C) 2002 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0957-4166(02)00663-8
  • 作为产物:
    描述:
    Benzamide, 2-nitro-N-[(1S)-1,2,2-trimethylpropyl]- 在 盐酸sodium hydroxide四丁基硫酸氢铵铁粉potassium carbonate溶剂黄146 、 sodium nitrite 作用下, 以 乙醇甲苯 为溶剂, 反应 13.5h, 生成 2-methyl-4-[(S)-2,3,3-trimethyl-2-butyl]-1,4-benzodiazepin-5(3H)-one
    参考文献:
    名称:
    Diastereoselective nitrilimine cycloaddition to the CN bond of enantiopure 1,4-benzodiazepinones
    摘要:
    Enantiopure 1,4-benzodiazepin-4-one 1 and 1,4-benzodiazepin-6-ones 2 were reacted with hydrazonoyl chloride 8 in the presence of various basic agents. The diastereoselective 1,3-dipolar cycloaddition between the C=N double bond of 1 or 2 and the nitrilimine intermediate 9 gave the enantiopure [1,2,4]triazolo[4,3-a][1,4]benzo diazepinones 10-13. (C) 2002 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0957-4166(02)00663-8
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文献信息

  • Diastereoselective nitrilimine cycloaddition to the CN bond of enantiopure 1,4-benzodiazepinones
    作者:Giorgio Molteni、Gianluigi Broggini、Tullio Pilati
    DOI:10.1016/s0957-4166(02)00663-8
    日期:2002.11
    Enantiopure 1,4-benzodiazepin-4-one 1 and 1,4-benzodiazepin-6-ones 2 were reacted with hydrazonoyl chloride 8 in the presence of various basic agents. The diastereoselective 1,3-dipolar cycloaddition between the C=N double bond of 1 or 2 and the nitrilimine intermediate 9 gave the enantiopure [1,2,4]triazolo[4,3-a][1,4]benzo diazepinones 10-13. (C) 2002 Elsevier Science Ltd. All rights reserved.
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