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1-(3-Chloropropyl)-3-fluoropiperidine | 1228631-66-0

中文名称
——
中文别名
——
英文名称
1-(3-Chloropropyl)-3-fluoropiperidine
英文别名
——
1-(3-Chloropropyl)-3-fluoropiperidine化学式
CAS
1228631-66-0
化学式
C8H15ClFN
mdl
——
分子量
179.665
InChiKey
QTUMAWXLAZSQPL-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):
    2.1
  • 重原子数:
    11
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    3.2
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    描述:
    methyl 1-(2-(3-chlorophenyl)-2-oxoethyl)-4-hydroxy-1H-pyrrole-2-carboxylate 、 1-(3-Chloropropyl)-3-fluoropiperidinepotassium carbonate 、 sodium iodide 作用下, 以 乙腈 为溶剂, 反应 24.0h, 生成
    参考文献:
    名称:
    Pyrrolo[1,2-a]pyrazine and pyrazolo[1,5-a]pyrazine: Novel, potent, and selective series of Vasopressin1b receptor antagonists
    摘要:
    Novel series of pyrrole-pyrazinone and pyrazole-pyrazinone have been identified as potent and selective Vasopressin(1b) receptor antagonists. Exploration of the substitution pattern around the core of these templates allowed generation of compounds with high inhibitory potency at the Vasopressin(1b) receptor, including examples that showed good selectivity with respect to Vasopressin(1a), Vasopressin(2), and Oxytocin receptor subtypes. (C) 2010 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2010.07.037
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文献信息

  • Pyrrolo[1,2-a]pyrazine and pyrazolo[1,5-a]pyrazine: Novel, potent, and selective series of Vasopressin1b receptor antagonists
    作者:Roberto Arban、Federica Bianchi、Alberto Buson、Susanna Cremonesi、Romano Di Fabio、Gabriella Gentile、Fabrizio Micheli、Alessandra Pasquarello、Alfonso Pozzan、Luca Tarsi、Silvia Terreni、Federica Tonelli
    DOI:10.1016/j.bmcl.2010.07.037
    日期:2010.9
    Novel series of pyrrole-pyrazinone and pyrazole-pyrazinone have been identified as potent and selective Vasopressin(1b) receptor antagonists. Exploration of the substitution pattern around the core of these templates allowed generation of compounds with high inhibitory potency at the Vasopressin(1b) receptor, including examples that showed good selectivity with respect to Vasopressin(1a), Vasopressin(2), and Oxytocin receptor subtypes. (C) 2010 Elsevier Ltd. All rights reserved.
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