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| 1190874-37-3

中文名称
——
中文别名
——
英文名称
——
英文别名
——
化学式
CAS
1190874-37-3
化学式
C15H23ClN4O2
mdl
——
分子量
326.826
InChiKey
JRPJZXWBKQRBHV-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:
    在 bromomethyl-ortho-nitrophenyl linked Tentagel resin 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 生成 tert-butyl 4-[3-chloro-5-(methylsulfonyloxymethyl)-2-pyridyl]piperazine-1-carboxylate
    参考文献:
    名称:
    Novel CXCR3 antagonists with a piperazinyl-piperidine core
    摘要:
    High-throughput screening of an encoded combinatorial aryl piperazine library led to the identification of a novel series of potent piperazinyl-piperidine based CXCR3 antagonists. Analogs of the initial hit were synthesized via solid and solution phase methods to probe the influence of structure on the CXCR3 binding of these molecules. Various functional groups were found to contribute to the overall potency and essential molecular features were identified. (C) 2009 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2009.07.020
  • 作为产物:
    描述:
    三苯基膦 作用下, 以 四氢呋喃 为溶剂, 生成
    参考文献:
    名称:
    Novel CXCR3 antagonists with a piperazinyl-piperidine core
    摘要:
    High-throughput screening of an encoded combinatorial aryl piperazine library led to the identification of a novel series of potent piperazinyl-piperidine based CXCR3 antagonists. Analogs of the initial hit were synthesized via solid and solution phase methods to probe the influence of structure on the CXCR3 binding of these molecules. Various functional groups were found to contribute to the overall potency and essential molecular features were identified. (C) 2009 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2009.07.020
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