反应 #955910

ord-9fd298b8d9da48fda805ce3eee7d4cfa

反应方程式

COc1cc(C)ccc1-c1n[nH]c(=S)[nH]1
5-(2-methoxy-4-methylphenyl)-2H-1,2,4-triazole-3(4H)-thione
Cc1ccc(CCl)nc1
2-(chloromethyl)-5-methylpyridine
COc1cc(C)ccc1-c1nc(SCc2ccc(C)cn2)n[nH]1
2-((5-(2-methoxy-4-methylphenyl)-1H-1,2,4-triazol-3-ylthio)methyl)-5-methylpyridine
收率 14.0%

反应条件

详细条件
See reaction.notes.procedure_details.

实验过程

Prepared in a similar manner to example 1 using 5-(2-methoxy-4-methylphenyl)-2H-1,2,4-triazole-3(4H)-thione (example 1a) and 2-(chloromethyl)-5-methylpyridine (example 2a). Yield 14%. 1H NMR (500 MHz, CDCl3): δ2.29 (s, 3H), 2.41 (s, 3H), 4.00 (s, 3H), 4.51 (s, 2H), 6.75 (s, 1H), 6.90 (s, 1H), 7.40 (s, 1H), 8.1 (d, 1H), 8.4 (s, 1H), 11.5-11.7 (bs, 1H). MS(M+H, 327.1).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US08968708B2uspto-grants-2015_03