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5-benzoyl-4-methylthieno[3,2-c]thiazole | 1209004-08-9

中文名称
——
中文别名
——
英文名称
5-benzoyl-4-methylthieno[3,2-c]thiazole
英文别名
(6-Methylthieno[3,2-d][1,3]thiazol-5-yl)-phenylmethanone;(6-methylthieno[3,2-d][1,3]thiazol-5-yl)-phenylmethanone
5-benzoyl-4-methylthieno[3,2-c]thiazole化学式
CAS
1209004-08-9
化学式
C13H9NOS2
mdl
——
分子量
259.353
InChiKey
KEFAYBBDFFRCTP-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):
    4.4
  • 重原子数:
    17
  • 可旋转键数:
    2
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.08
  • 拓扑面积:
    86.4
  • 氢给体数:
    0
  • 氢受体数:
    4

反应信息

  • 作为产物:
    描述:
    5-benzoyl-4-methyl-3-(1-pyridino)thiophene-2-thiolate 、 丁炔二酸二甲酯5,5-dimethyl-1,3-cyclohexadiene 为溶剂, 反应 36.0h, 以53%的产率得到5-benzoyl-4-methylthieno[3,2-c]thiazole
    参考文献:
    名称:
    Preparation of New Nitrogen-Bridged Heterocycles. 68. One-Pot Synthesis of 4-Substituted 5-Acylthieno[3,2-d]thiazole Derivatives
    摘要:
    The reactions of 5-acyl-3-(1-pyridinio)thiophene-2-thiolates with dimethyl acetylenedicarboxylate in xylene at the reflux temperature afforded the corresponding 2-unsubstituted 5-acylthieno[3,2-d]thiazoles in 25-69% yields together with dimethyl phthalate as another fragmentation product. In a few reactions, the unexpected products, dimethyl 2-[2-acylthieno[2',3':2,3]-1,4-thiazino[4,5-a]pyrrol-8-ylidene]succinate derivatives, were also isolated, though their yields were very low.
    DOI:
    10.3987/com-09-11852
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文献信息

  • Preparation of New Nitrogen-Bridged Heterocycles. 68. One-Pot Synthesis of 4-Substituted 5-Acylthieno[3,2-d]thiazole Derivatives
    作者:Akikazu Kakehi、Hiroyuki Suga、Yukihisa Okumura、Takashi Nishi
    DOI:10.3987/com-09-11852
    日期:——
    The reactions of 5-acyl-3-(1-pyridinio)thiophene-2-thiolates with dimethyl acetylenedicarboxylate in xylene at the reflux temperature afforded the corresponding 2-unsubstituted 5-acylthieno[3,2-d]thiazoles in 25-69% yields together with dimethyl phthalate as another fragmentation product. In a few reactions, the unexpected products, dimethyl 2-[2-acylthieno[2',3':2,3]-1,4-thiazino[4,5-a]pyrrol-8-ylidene]succinate derivatives, were also isolated, though their yields were very low.
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