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1,5-Dicyclopropyl-3-(2,5-dimethyl-pyrrol-1-yl)-1H-pyrazole | 1229456-25-0

中文名称
——
中文别名
——
英文名称
1,5-Dicyclopropyl-3-(2,5-dimethyl-pyrrol-1-yl)-1H-pyrazole
英文别名
1,5-dicyclopropyl-3-(2,5-dimethylpyrrol-1-yl)pyrazole
1,5-Dicyclopropyl-3-(2,5-dimethyl-pyrrol-1-yl)-1H-pyrazole化学式
CAS
1229456-25-0
化学式
C15H19N3
mdl
——
分子量
241.336
InChiKey
ZTTDNCTZCOVWKS-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):
    2.8
  • 重原子数:
    18
  • 可旋转键数:
    3
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.53
  • 拓扑面积:
    22.8
  • 氢给体数:
    0
  • 氢受体数:
    1

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

  • 作为产物:
    描述:
    环丙基三氟硼酸钾5-Cyclopropyl-3-(2,5-dimethyl-pyrrol-1-yl)-1H-pyrazole2,2'-联吡啶 、 copper diacetate 、 sodium carbonate 作用下, 以 1,2-二氯乙烷 为溶剂, 以99%的产率得到1,5-Dicyclopropyl-3-(2,5-dimethyl-pyrrol-1-yl)-1H-pyrazole
    参考文献:
    名称:
    Syntheses of 1-substituted-3-aminopyrazoles
    摘要:
    A series of 1-substituted-3-aminopyrazoles were prepared via Chan-Lam coupling reactions, alkylation, and pyrazole ring formation. (C) 2010 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2010.10.073
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文献信息

  • HETEROBICYCLIC CARBOXAMIDES AS INHIBITORS FOR KINASES
    申请人:ARTMANN, III Gerald David
    公开号:US20120245187A1
    公开(公告)日:2012-09-27
    The invention relates to novel organic compounds of formula (I) and their use in the treatment of the animal or human body, to pharmaceutical compositions comprising a compound of formula I and to the use of a compound of formula I for the preparation of pharmaceutical compositions for use in the treatment of protein kinase dependent diseases, especially of proliferative diseases, such as in the treatment of tumour diseases and ocular neovascular diseases.
    本发明涉及一种新型有机化合物(I)及其在动物或人体治疗中的应用,包括含有化合物I的制药组合物以及利用化合物I制备用于治疗蛋白激酶依赖性疾病的制药组合物的应用,特别是在治疗增殖性疾病,如肿瘤疾病和眼部新生血管疾病方面的应用。
  • Heterobicyclic Carboxamides as inhibitors for kinases
    申请人:Artmann, III Gerald David
    公开号:US20100168082A1
    公开(公告)日:2010-07-01
    The invention relates to novel organic compounds of formula (I) and their use in the treatment of the animal or human body, to pharmaceutical compositions comprising a compound of formula I and to the use of a compound of formula I for the preparation of pharmaceutical compositions for use in the treatment of protein kinase dependent diseases, especially of proliferative diseases, such as in the treatment of tumour diseases and ocular neovascular diseases.
    本发明涉及一种新型有机化合物(I)及其在动物或人体治疗中的应用,包括含有化合物I的药物组合物,以及利用化合物I制备用于治疗蛋白激酶依赖性疾病的药物组合物,特别是用于治疗增殖性疾病,如肿瘤疾病和眼部新生血管疾病的治疗。
  • Heterobicyclic carboxamides as inhibitors for kinases
    申请人:Novartis AG
    公开号:US08242125B2
    公开(公告)日:2012-08-14
    The invention relates to novel organic compounds of formula (I) and their use in the treatment of the animal or human body, to pharmaceutical compositions comprising a compound of formula I and to the use of a compound of formula I for the preparation of pharmaceutical compositions for use in the treatment of protein kinase dependent diseases, especially of proliferative diseases, such as in the treatment of tumor diseases and ocular neovascular diseases.
    本发明涉及公式(I)的新型有机化合物及其在动物或人体内治疗中的应用,包括含有公式I化合物的制药组合物,以及公式I化合物用于制备用于治疗蛋白激酶依赖性疾病的制药组合物的应用,特别是用于治疗增殖性疾病,例如治疗肿瘤疾病和眼部新生血管疾病。
  • PYRIDYLOXYINDOLES INHIBITORS OF VEGF-R2 AND USE THEREOF FOR TREATMENT OF DISEASE
    申请人:Novartis AG
    公开号:EP2376478B1
    公开(公告)日:2017-04-19
  • US8242125B2
    申请人:——
    公开号:US8242125B2
    公开(公告)日:2012-08-14
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