反应 #40340

ord-6b14da6e27204bad9338c2861405d99d

反应方程式

[Na+].[OH-]
caustic soda
CCCCCCBr
1-bromohexane
N=C(N)Nc1nc2c(s1)CNCC2
N-(4,5,6,7-tetrahydro-thiazolo[5,4-c]pyridine-2-yl)-guanidine
O=C([O-])[O-].[Cs+].[Cs+]
caesium carbonate
CCCCCCN1CCc2nc(NC(=N)N)sc2C1
title compound
CCCCCCN1CCc2nc(NC(=N)N)sc2C1
N-(5-hexyl-4,5,6,7-tetrahydro-thiazolo[5,4-c]pyridine-2-yl)-guanidine

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    萃取is extracted with ethyl acetate
  2. 2
    干燥the combined organic phases are dried over sodium sulphate
  3. 3
    浓缩concentrated by evaporation

实验过程

1-bromohexane (0.11 mmol) is added to a suspension of N-(4,5,6,7-tetrahydro-thiazolo[5,4-c]pyridine-2-yl)-guanidine (0.1 mmol) and caesium carbonate (0.22 mmol) in dimethylformamide (0.3 ml) and the reaction mixture is stirred overnight at room temperature. After adding 2M caustic soda solution (1 ml) the mixture is extracted with ethyl acetate, the combined organic phases are dried over sodium sulphate and then concentrated by evaporation, the title compound being obtained in pure form.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07727979B2uspto-grants-2010_06