反应 #40344

ord-98496fd20a5141068171bd4a1a3cc0ec

反应方程式

[Na+].[OH-]
caustic soda
CCN(C(C)C)C(C)C
Diisopropylethylamine
CCCCC(=O)Cl
pentanoyl chloride
Cl.Cl.N=C(N)Nc1nc2c(s1)CNCC2
N-(4,5,6,7-tetrahydro-thiazolo[5,4-c]pyridine-2-yl)-guanidine-dihydrochloride
CCCCC(=O)C1NCCc2nc(NC(=N)N)sc21
title compound
CCCCC(=O)C1NCCc2nc(NC(=N)N)sc21
N-(pentanoyl-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.

实验过程

Diisopropylethylamine (0.22 mmol) and then pentanoyl chloride (0.11 mmol) are added to a stirred suspension of N-(4,5,6,7-tetrahydro-thiazolo[5,4-c]pyridine-2-yl)-guanidine-dihydrochloride (0.1 mmol) in dimethylformamide (0.7 ml) and the reaction mixture is stirred for another 16 hours at room temperature. After the addition of 2M caustic soda solution (1 ml) extraction is carried out with ethyl acetate. The combined organic phases produce the pure title compound after drying over sodium sulphate and concentrating to dryness.

来源

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