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3-Methyl-2,3-dihydrothiazolo<4,5-d>pyrimidin-2,7-dithion | 130089-90-6

中文名称
——
中文别名
——
英文名称
3-Methyl-2,3-dihydrothiazolo<4,5-d>pyrimidin-2,7-dithion
英文别名
3-methyl-4H-[1,3]thiazolo[4,5-d]pyrimidine-2,7-dithione
3-Methyl-2,3-dihydrothiazolo<4,5-d>pyrimidin-2,7-dithion化学式
CAS
130089-90-6
化学式
C6H5N3S3
mdl
——
分子量
215.324
InChiKey
PWRYQEDDUBRKLP-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):
    0.8
  • 重原子数:
    12
  • 可旋转键数:
    0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.17
  • 拓扑面积:
    117
  • 氢给体数:
    1
  • 氢受体数:
    3

反应信息

  • 作为反应物:
    描述:
    3-Methyl-2,3-dihydrothiazolo<4,5-d>pyrimidin-2,7-dithionsodium hydroxide 、 sodium dithionite 、 air 作用下, 反应 5.5h, 生成 2-(4-Methylamino-6-thioxo-1,6-dihydro-pyrimidin-5-ylsulfanyl)-acetamide
    参考文献:
    名称:
    Zur Chemie der 4-Amino-thiazolin-2-thione, 2. Mitt.
    摘要:
    6-Amino-thiazolo[4,5-c]isothiazole derivatives 4 are obtained by addition of hydrogen sulfide to the 4-Amino-thiazoline-5-carbonitrile 2 followed by cyclooxidation of the intermediate thioamides 3. In the presence of sodium sulfite the hydrolysis of the 4-amino-2-methylthio-thiazolium salts 5 derived from the title compounds 1 yields the 4-amino-thiazolin-2-ones 6. By their further hydrolysis the 2,4-dioxo-thiazolidin-5-carboxamides 8 are formed. The 2-oxo-and 2-thioxo-thiazolo [4,5-d]pyrimidin-7-ones and -thiones available from 1 undergo ring opening by hydrolysis to give the substituted 4-amino-6-oxo- and 4-amino-6-thioxo-pyrimidine-5-thiols 15a-h and 13i-e. They have been isolated as their disulfides 14 or 5-alkyl derivatives i.e. the substituted 4-amino-5-alkylthiopyrimidin-6-ones and -thiones 16. In analogy, the intermediate 6-amino-7-oxo-thiazolo[4,5-d] pyrimidin-2-thione 18 and the 7-amino-thiazolo[4,5-d]-pyrimidin-2-thione 24 derived from 1 react by ring cleavage to yield the 1,4- and 4,6-diamino-pyrimidin-5-thiole derivatives 22 and 27, respectively, isolated as their disulfides or alkylthio-derivatives. From the pyrimidine 16b the pyrimido[5,4-b]1,4-thiazine derivative 18 can be obtained.
    DOI:
    10.1007/bf00811521
  • 作为产物:
    描述:
    甲酸4-Amino-3-methyl-3-thioxo-Δ4-thiazolin-5-thiocarboxamid 反应 3.0h, 以65%的产率得到3-Methyl-2,3-dihydrothiazolo<4,5-d>pyrimidin-2,7-dithion
    参考文献:
    名称:
    Gewald, K.; Schindler, R., Journal fur praktische Chemie (Leipzig 1954), 1990, vol. 332, # 2, p. 223 - 228
    摘要:
    DOI:
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文献信息

  • Gewald K., Hain U., Schindler R., Gruner M., Monatsh. Chem, 125 (1994) N 10, S 1129-1143
    作者:Gewald K., Hain U., Schindler R., Gruner M.
    DOI:——
    日期:——
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