2-n-Propyl-(1)-nitro-2-thiopseudoharnstoff | 2986-27-8

• 分子结构分类: 有机化合物 - 有机1,3-偶极化合物 - 烯丙基型1,3-偶极有机化合物
• 英文名称: 2-n-Propyl-(1)-nitro-2-thiopseudoharnstoff
• 英文别名: propyl N'-nitrocarbamimidothioate
• CAS: 2986-27-8
• 化学式: C₄H₉N₃O₂S
• 分子量: 163.2
• InChiKey: TXRDUVSDKSFMKM-UHFFFAOYSA-N

物化性质

• 沸点：
  246.9±23.0 °C(Predicted)
• 密度：
  1.39±0.1 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  1.4
• 重原子数：
  10
• 可旋转键数：
  3
• 环数：
  0.0
• sp3杂化的碳原子比例：
  0.75
• 拓扑面积：
  110
• 氢给体数：
  1
• 氢受体数：
  4

反应信息

• 作为产物：
  描述：

  alkaline earth salt of/the/ methylsulfuric acid 在 硫酸 作用下， 生成 2-n-Propyl-(1)-nitro-2-thiopseudoharnstoff
  参考文献：
  名称：

  The Preparation and Reactions of 2-Alkyl-1-(or 3)-nitro-2-thiopseudourea. Part I. Reaction with Amines¹

  摘要：

  DOI：

  10.1021/ja01636a042

文献信息

• Thiolytic decomposition of the carcinogen N-methyl-N'-nitro-N-nitrosoguanidine. A change in rate-limiting step with nucleophile basicity controls alkylating activity
  作者：Taina Santala、James C. Fishbein

  DOI：10.1021/ja00049a017

  日期：1992.11

  The kinetics of the reaction of seven alkanethiolates with N-methyl-N'-nitro-N-nitrosoguanidine over the pH range 3-8.5 at 40-degrees-C, ionic strength 1 M (KCl), are reported. Plots of k(obs) against total thiol concentration are linear, and the slopes of these plots change as a function of pH. The changes in slope with pH are well-described by a rate law for decomposition of MNNG that is first-order in thiolate ion and first-order in neutral MNNG. Rate constants k2' for the reaction of the thiolates are determined. There is no significant buffer catalysis of the reactions of any of the thiolates in the pH range studied. In the case of the reactions of propanethiolate and trifluoroethanethiolate, two products, methylnitroguanidine (MNG) and the thiol ((RS)-N-nitroformamidine) adducts 1, were found to account quantitatively (98 +/- 3%) for the nitroguanidine skeleton of the starting material. In the case of the other five thiolates, the percent yield of MNG was determined. The yields of MNG are independent of thiolate ion concentration or buffer concentration. The yield of MNG changes from 5% for the reaction of propanethiolate, the most basic thiolate, to 90% for the reaction of pentafluoropropanethiolate, the least basic thiolate. On the basis of the yields of MNG, which indicate the extent of reaction at the nitroso nitrogen for the different thiolates, specific second-order rate constants for the thiolate ion reaction at the nitroso nitrogen, k(DN), and for the thiolate ion reaction at the guanidino carbon, k(DA), are calculated from the total second-order rate constant, k2'. The plot of log k(DN) against pK(aRSH) is linear with a slope beta(nuc) = 0.54 +/- 0.02. A similar plot for log k(DA) shows a downward break with decreasing thiol pK(a). The plot is consistent with a reaction that involves an anionic intermediate, T-, the formation of which is rate-limiting for basic thiolates and the decomposition of which is rate-limiting for weakly basic thiolates. Limiting values of beta(nuc) consistent with the data were determined to be beta(nuc) = 0.70 +/- 0.12 and 2.4 +/- 0.2 for rate-limiting formation and breakdown reactions, respectively. The latter value is attributed to a late transition state for leaving group expulsion with a large imbalance in which C-N double bond formation lags behind leaving group expulsion. The results represent a good chemical model for the recently reported chemoprotective denitrosation reaction between glutathione and MNNG that is catalyzed by a glutathione S-transferase.