反应 #1810808

ord-dfa80a1a88114ecb8b1374df58ae837b

反应方程式

CI
methyliodide
CNC(=S)N(C)C1CCC(NC(=O)OCc2ccccc2)CC1
[4-(1,3-dimethyl-thioureido)-cyclohexyl]carbamic acid benzylester
I
hydroiodide
CN=C(SC)N(C)C1CCC(NC(=O)OCc2ccccc2)CC1
[4-(1,2,3-Trimethyl-isothioureido)-cyclohexyl]-carbamic acid benzylester

溶剂

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他The mixture obtained
  2. 2
    温度is refluxed for 2.5 hours
  3. 3
    其他solvent is evaporated

实验过程

0.18 ml of methyliodide are added to a solution of 0.64 g [4-(1,3-dimethyl-thioureido)-cyclohexyl]carbamic acid benzylester in 30 ml of AcCN. The mixture obtained is refluxed for 2.5 hours and solvent is evaporated. [4-(1,2,3-Trimethyl-isothioureido)-cyclohexyl]-carbamic acid benzylester in the form of a hydroiodide is obtained.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07485632B2uspto-grants-2009_02