反应 #40347

ord-878a69e41b514e08afeac88bdd502b76

反应方程式

O=C=Nc1ccccc1
phenyl isocyanate
Cl.Cl.N=C(N)Nc1nc2c(s1)CNCC2
N-(4,5,6,7-tetrahydro-thiazolo[5,4-c]pyridine-2-yl)-guanidine dihydrochloride
O=C([O-])[O-].[Na+].[Na+]
sodium carbonate
CCN(C(C)C)C(C)C
Diisopropylethylamine
N=C(N)Nc1nc2c(s1)CN(C(=O)Nc1ccccc1)CC2
title compound
N=C(N)Nc1nc2c(s1)CN(C(=O)Nc1ccccc1)CC2
2-guanidino-6,7-dihydro-4H-thiazolo[5,4-c]pyridine-5-carboxylic acid phenyl amide

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    萃取extraction

实验过程

Diisopropylethylamine (0.2 mmol) and, after 5 min, phenyl isocyanate (0.11 mmol) are added to a suspension of N-(4,5,6,7-tetrahydro-thiazolo[5,4-c]pyridine-2-yl)-guanidine dihydrochloride (0.1 mmol) in dimethylformamide (0.5 ml). The reaction mixture is stirred for another 3 hours at room temperature. Then saturated aqueous sodium carbonate solution is added and extraction is carried out with ethyl acetate. The pure title compound is obtained after drying of the combined organic phases over sodium sulphate and removal of the solvent in a vacuum.

来源

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