반응 #1687635

ord-1f3d63b3d76045508493ba53e1f22655

반응 방정식

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

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타The crude free base obtained

실험 절차

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.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: USRE036374uspto-grants-1999_11