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Dibutyl-[3-(2-chloro-4-methyl-phenyl)-5-methyl-1H-pyrazolo[4,3-b]pyridin-7-yl]-amine | 242129-09-5

中文名称
——
中文别名
——
英文名称
Dibutyl-[3-(2-chloro-4-methyl-phenyl)-5-methyl-1H-pyrazolo[4,3-b]pyridin-7-yl]-amine
英文别名
——
Dibutyl-[3-(2-chloro-4-methyl-phenyl)-5-methyl-1H-pyrazolo[4,3-b]pyridin-7-yl]-amine化学式
CAS
242129-09-5
化学式
C22H29ClN4
mdl
——
分子量
384.952
InChiKey
QNPMQRJKYXXYKR-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

反应信息

  • 作为反应物:
    描述:
    Dibutyl-[3-(2-chloro-4-methyl-phenyl)-5-methyl-1H-pyrazolo[4,3-b]pyridin-7-yl]-amine 、 alkaline earth salt of/the/ methylsulfuric acid 在 sodium hydride 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 生成 Dibutyl-[3-(2-chloro-4-methyl-phenyl)-1-ethyl-5-methyl-1H-pyrazolo[4,3-b]pyridin-7-yl]-amine 、 Dibutyl-[3-(2-chloro-4-methyl-phenyl)-2-ethyl-5-methyl-2H-pyrazolo[4,3-b]pyridin-7-yl]-amine
    参考文献:
    名称:
    Synthesis of 3-phenylpyrazolo[4,3-b]pyridines via a convenient synthesis of 4-amino-3-arylpyrazoles and SAR of corticotropin-Releasing factor receptor type-1 antagonists
    摘要:
    3-Phenylpyrazolo[4,3-b]pyridines were synthesized via a cyclization of 4-amino-3-phenylpyrazoles 11-13 with ethyl acetoacetate. These compounds were found to be potent CRF1 antagonists. The 2-alkylpyrazolo[4,3-b]pyridines were more polar but less active than the corresponding 1-alkyl-isomers. (C) 2003 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/s0960-894x(03)00621-8
  • 作为产物:
    参考文献:
    名称:
    Synthesis of 3-phenylpyrazolo[4,3-b]pyridines via a convenient synthesis of 4-amino-3-arylpyrazoles and SAR of corticotropin-Releasing factor receptor type-1 antagonists
    摘要:
    3-Phenylpyrazolo[4,3-b]pyridines were synthesized via a cyclization of 4-amino-3-phenylpyrazoles 11-13 with ethyl acetoacetate. These compounds were found to be potent CRF1 antagonists. The 2-alkylpyrazolo[4,3-b]pyridines were more polar but less active than the corresponding 1-alkyl-isomers. (C) 2003 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/s0960-894x(03)00621-8
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