反应 #40346

ord-a03797be0d6c4f4e9452b66eee9f31f0

反应方程式

O=C([O-])[O-].[Na+].[Na+]
sodium carbonate
O=C(Cl)OCc1ccccc1
Benzyl chloroformate
N=C(N)Nc1nc2c(s1)CNCC2
N-(4,5,6,7-tetrahydro-thiazolo[5,4-c]pyridine-2-yl)-guanidine
CCN(C(C)C)C(C)C
diisopropylethylamine
N=C(N)Nc1nc2c(s1)CN(C(=O)OCc1ccccc1)CC2
title compound
N=C(N)Nc1nc2c(s1)CN(C(=O)OCc1ccccc1)CC2
2-guanidino-6,7-dihydro-4H-thiazolo[5,4-c]pyridine-5-carboxylic acid benzyl ester

反应条件

详细条件
See reaction.notes.procedure_details.

实验过程

Benzyl chloroformate is added to a stirred suspension of N-(4,5,6,7-tetrahydro-thiazolo[5,4-c]pyridine-2-yl)-guanidine (0.1 mmol) and diisopropylethylamine (0.22 mmol) in dimethylformamide (0.7 ml) and the mixture is stirred for another 3 hours at room temperature. After the addition of saturated aqueous sodium carbonate solution extraction is carried out with ethyl acetate; the combined organic phases produce the pure title compound after drying over sodium sulphate and complete evaporation of the solvent.

来源

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