2-(5-mercapto-4-phenyl-4H-1,2,4-triazol-3-yl)-N-(thiazol-2-yl)acetamide | 1142922-92-6

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 唑类
• 英文名称: 2-(5-mercapto-4-phenyl-4H-1,2,4-triazol-3-yl)-N-(thiazol-2-yl)acetamide
• 英文别名: 2-(4-phenyl-5-sulfanylidene-1H-1,2,4-triazol-3-yl)-N-(1,3-thiazol-2-yl)acetamide
• CAS: 1142922-92-6
• 化学式: C₁₃H₁₁N₅OS₂
• 分子量: 317.395
• InChiKey: WOQIDMXQPXAVME-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.9
• 重原子数：
  21
• 可旋转键数：
  4
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.08
• 拓扑面积：
  130
• 氢给体数：
  2
• 氢受体数：
  5

反应信息

• 作为产物：
  描述：

  1-(3-(2'-thiazolylamino)-3-oxopropane)-4-phenylthiosemicarbazide 在 sodium hydroxide 作用下， 以 水 为溶剂， 反应 0.5h， 以62%的产率得到2-(5-mercapto-4-phenyl-4H-1,2,4-triazol-3-yl)-N-(thiazol-2-yl)acetamide
  参考文献：
  名称：

  Synthesis and reactions of thiosemicarbazides, triazoles, and Schiff bases as antihypertensive α-blocking agents

  摘要：

  Methyl 2-(thiazol-2-ylcarbamoyl)acetate was synthesized and used as starting material. It was treated with hydrazine hydrate to afford the hydrazide, which was reacted with nitromethane and formaldehyde to give the saturated nitropyrimidine. The hydrazide was reacted with phenyl isothiocyanate to afford the thiosemicarbazide, which was cyclized with ethyl bromoacetate, sodium hydroxide, or sulfuric acid to afford N-phenylthiazolidinone, N-phenyltriazole, and thiadiazolyl derivatives. The methyl 2-(thiazol-2-ylcarbamoyl)acetate was coupled with diazonium salts of aniline, 4-chloroaniline, 4-bromoaniline, or 4-aminobenzenesulfonamide to afford the carbamoyl acetates, which were reacted with 2-aminobenzimidazole, 1,2,4,5-tetrachlorophthalic anhydride, and hydrazine hydrate to afford the corresponding thiazolylmalonamide, tetrachloroisoindolylimide, and tri-azole derivatives. Schiff bases and imides are newly synthesized candidates obtained via simple condensation of the hydrazide with aldehydes, 2,3-pyridinedicarboxylic anhydride, or 1,8-naphthalenedicarboxylic anhydride. The pharmacological screening showed that many of these compounds have good antihypertensive alpha-blocking activity and low toxicity.

  DOI：

  10.1007/s00706-008-0896-2