反应 #1687635

ord-1f3d63b3d76045508493ba53e1f22655

反应方程式

O=C([O-])/C=C/C(=O)[O-]
fumarate
Cc1cnc(-c2cccnc2)s1
88
Cc1cnc(-c2cccnc2)s1
5-Methyl-2-(3-pyridyl)-thiazole
Cc1cnc(C2=CCCN(C)C2)s1
title compound
Cc1cnc(C2=CCCN(C)C2)s1
5-Methyl-2-(1-methyl-1,2,5,6-tetrahydro-3-pyridyl)-thiazole

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他The crude free base obtained

实验过程

The title compound was prepared from 88 (2.2 g, 0.013 mol) by the procedure described in Example 49. The crude free base obtained, 89, was converted to the title fumarate, 90. Yield: 0.8 g (0.0032 mol, 25%). M.P. 159°-160° C. Anal. (C12H16N2O2S)C, H, N.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: USRE036374uspto-grants-1999_11