(Z)-3,4-Dimethyl-penta-2,4-diene-2-sulfinic acid butyl-methyl-amide | 131196-18-4

• 分子结构分类: 有机化合物 - 有机酸及其衍生物 - 亚磺酸及其衍生物
• 英文名称: (Z)-3,4-Dimethyl-penta-2,4-diene-2-sulfinic acid butyl-methyl-amide
• CAS: 131196-18-4
• 化学式: C₁₂H₂₃NOS
• 分子量: 229.387
• InChiKey: SACOWKKSHRJVHH-QXMHVHEDSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.25
• 重原子数：
  15.0
• 可旋转键数：
  6.0
• 环数：
  0.0
• sp3杂化的碳原子比例：
  0.67
• 拓扑面积：
  20.31
• 氢给体数：
  0.0
• 氢受体数：
  1.0

反应信息

• 作为产物：
  描述：

  2-Butyl-4,5-dimethyl-3,6-dihydro-2H-[1,2]thiazine 1-oxide 、 碘甲烷 在 lithium diisopropyl amide 作用下， 生成 (Z)-3,4-Dimethyl-penta-2,4-diene-2-sulfinic acid butyl-methyl-amide 、 (1R,6S)-2-Butyl-4,5,6-trimethyl-3,6-dihydro-2H-[1,2]thiazine 1-oxide 、 (1R,6R)-2-Butyl-4,5,6-trimethyl-3,6-dihydro-2H-[1,2]thiazine 1-oxide
  参考文献：
  名称：

  Metalation and alkylation of 3,6-dihydrothiazine 1-oxides prepared via Diels-Alder cycloadditions of N-sulfinyl dienophiles

  摘要：

  The deprotonation of various 3,6-dihydrothiazine 1-oxides using LDA or methyllithium has been investigated. It was found that the stability and chemistry of these lithiated heterocycles are highly dependent upon the nature of the ring nitrogen substituent. Thus, N-alkyldihydrothiazine oxides can be metalated at C-6 to give species postulated as 9, which undergo predominantly anti alkylation with alkyl halides. Alternatively, with MeOD, 9 is deuterated at C-6 primarily in a syn mode. N-Silylated heterocycles ring open rapidly and stereoselectively upon metalation to give dienic sulfinamides like 19, which can be reclosed to the starting dihydrothiazine oxides. N-Phenyl-substituted 3,6-dihydrothiazine 1-oxides upon metalation give mixtures of pyrroles and N-S bond cleavage products. Attempts to generate the dianion from NH dihydrothiazine oxide 17 led only to low yields of C-4 alkylated products with alkyl halides.

  DOI：

  10.1021/jo00001a068