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[4-[3-chloro-4-(trifluoromethoxy)phenyl]-2-{[(1,3,6-trimethyl-2,4-dioxo-1,2,3,4-tetrahydrofuro[2,3-d]pyrimidin-5-yl)acetyl]imino}-1,3-thiazol-3(2H)-yl]methyl 2,2-dimethylpropanoate | 1383138-87-1

中文名称
——
中文别名
——
英文名称
[4-[3-chloro-4-(trifluoromethoxy)phenyl]-2-{[(1,3,6-trimethyl-2,4-dioxo-1,2,3,4-tetrahydrofuro[2,3-d]pyrimidin-5-yl)acetyl]imino}-1,3-thiazol-3(2H)-yl]methyl 2,2-dimethylpropanoate
英文别名
[4-[3-chloro-4-(trifluoromethoxy)phenyl]-2-[2-(1,3,6-trimethyl-2,4-dioxofuro[2,3-d]pyrimidin-5-yl)acetyl]imino-1,3-thiazol-3-yl]methyl 2,2-dimethylpropanoate
[4-[3-chloro-4-(trifluoromethoxy)phenyl]-2-{[(1,3,6-trimethyl-2,4-dioxo-1,2,3,4-tetrahydrofuro[2,3-d]pyrimidin-5-yl)acetyl]imino}-1,3-thiazol-3(2H)-yl]methyl 2,2-dimethylpropanoate化学式
CAS
1383138-87-1
化学式
C27H26ClF3N4O7S
mdl
——
分子量
643.04
InChiKey
KEBRKXBVCOABCL-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):
    5.6
  • 重原子数:
    43
  • 可旋转键数:
    8
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.37
  • 拓扑面积:
    147
  • 氢给体数:
    0
  • 氢受体数:
    11

反应信息

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文献信息

  • 2-AMINO-4-ARYLTHIAZOLE COMPOUNDS AS TRPA1 ANTAGONISTS
    申请人:Glenmark Pharmaceuticals, S.A.
    公开号:US20140051667A1
    公开(公告)日:2014-02-20
    The present invention is related to 2-amino-4-arylthiazole derivatives as TRPA (Transient Receptor Potential subfamily A) modulators. In particular, compounds described herein are useful for treating or preventing diseases, conditions and/or disorders modulated by TRPA1 (Transient Receptor Potential subfamily A, member 1). Also provided herein are processes for preparing compounds described herein, intermediates used in their synthesis, pharmaceutical compositions thereof, and methods for treating or preventing diseases, conditions and/or disorders modulated by TRPA1.
    本发明涉及2-氨基-4-芳基噻唑衍生物作为TRPA(瞬时受体电位亚家族A)调节剂。特别地,本文所描述的化合物可用于治疗或预防由TRPA1(瞬时受体电位亚家族A,成员1)调节的疾病、病况和/或疾患。本文还提供了制备所述化合物的过程、用于其合成的中间体、其制药组合物以及治疗或预防由TRPA1调节的疾病、病况和/或疾患的方法。
  • 2-amino-4-arylthiazole compounds as TRPA1 antagonists
    申请人:Kumar Sukeerthi
    公开号:US08592398B2
    公开(公告)日:2013-11-26
    The present invention is related to 2-amino-4-arylthiazole derivatives as TRPA (Transient Receptor Potential subfamily A) modulators. In particular, compounds described herein are useful for treating or preventing diseases, conditions and/or disorders modulated by TRPA1 (Transient Receptor Potential subfamily A, member 1). Also provided herein are processes for preparing compounds described herein, intermediates used in their synthesis, pharmaceutical compositions thereof, and methods for treating or preventing diseases, conditions and/or disorders modulated by TRPA1.
    本发明涉及2-氨基-4-芳基噻唑衍生物作为TRPA(瞬时受体电位亚家族A)调节剂。特别地,本文所描述的化合物对于治疗或预防由TRPA1(瞬时受体电位亚家族A,成员1)调节的疾病、状况和/或紊乱是有用的。本文还提供了制备所述化合物的过程,用于其合成的中间体,其制药组合物以及治疗或预防由TRPA1调节的疾病、状况和/或紊乱的方法。
  • 2-AMINO-4-ARYLTHIAZOLE COMPOUNDS AS TRPAI ANTAGONISTS
    申请人:Kumar Sukeerthi
    公开号:US20120157411A1
    公开(公告)日:2012-06-21
    The present invention is related to 2-amino-4-arylthiazole derivatives as TRPA (Transient Receptor Potential subfamily A) modulators. In particular, compounds described herein are useful for treating or preventing diseases, conditions and/or disorders modulated by TRPA1 (Transient Receptor Potential subfamily A, member 1). Also provided herein are processes for preparing compounds described herein, intermediates used in their synthesis, pharmaceutical compositions thereof, and methods for treating or preventing diseases, conditions and/or disorders modulated by TRPA1.
    本发明涉及2-氨基-4-芳基噻唑衍生物作为TRPA(瞬时受体电位亚家族A)调节剂。具体来说,本文描述的化合物对于治疗或预防由TRPA1(瞬时受体电位亚家族A,成员1)调节的疾病、症状和/或疾病具有用处。本文还提供了制备所述化合物的方法,用于合成它们的中间体,它们的药物组成物,以及治疗或预防由TRPA1调节的疾病、症状和/或疾病的方法。
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