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5-[(3-Chloro-4-fluorophenyl)methyl]-1,3-thiazol-2-amine | 893724-17-9

中文名称
——
中文别名
——
英文名称
5-[(3-Chloro-4-fluorophenyl)methyl]-1,3-thiazol-2-amine
英文别名
——
5-[(3-Chloro-4-fluorophenyl)methyl]-1,3-thiazol-2-amine化学式
CAS
893724-17-9
化学式
C10H8ClFN2S
mdl
MFCD06496550
分子量
242.704
InChiKey
XCLVAYKNTWGKSJ-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):
    3.3
  • 重原子数:
    15
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.1
  • 拓扑面积:
    67.2
  • 氢给体数:
    1
  • 氢受体数:
    4

反应信息

  • 作为反应物:
    参考文献:
    名称:
    Novel and potent inhibitors of stearoyl-CoA desaturase-1. Part I: Discovery of 3-(2-hydroxyethoxy)-4-methoxy-N-[5-(3-trifluoromethylbenzyl)thiazol-2-yl]benzamide
    摘要:
    A series of structurally novel stearoyl-CoA desaturase-1 (SCD-1) inhibitors has been identified by optimizing a hit from our corporate library. Preliminary structure-activity relationship (SAR) studies led to the discovery of the highly potent and orally bioavailable thiazole-based SCD-1 inhibitor, 3-(2-hydroxyethoxy)-4-methoxy-N-[5-(3-trifluoromethylbenzyl)thiazol-2-yl]benzamide (23a). (C) 2009 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2009.05.119
  • 作为产物:
    描述:
    3-(3-chloro-4-fluoro-phenyl)-propionaldehyde硫脲N-氯代丁二酰亚胺L-脯氨酸 作用下, 以 二氯甲烷乙醇 为溶剂, 以55%的产率得到5-[(3-Chloro-4-fluorophenyl)methyl]-1,3-thiazol-2-amine
    参考文献:
    名称:
    Novel and potent inhibitors of stearoyl-CoA desaturase-1. Part I: Discovery of 3-(2-hydroxyethoxy)-4-methoxy-N-[5-(3-trifluoromethylbenzyl)thiazol-2-yl]benzamide
    摘要:
    A series of structurally novel stearoyl-CoA desaturase-1 (SCD-1) inhibitors has been identified by optimizing a hit from our corporate library. Preliminary structure-activity relationship (SAR) studies led to the discovery of the highly potent and orally bioavailable thiazole-based SCD-1 inhibitor, 3-(2-hydroxyethoxy)-4-methoxy-N-[5-(3-trifluoromethylbenzyl)thiazol-2-yl]benzamide (23a). (C) 2009 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2009.05.119
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