Реакция #955911

ord-73f3e57ead644a03b570960d8e7b3276

Уравнение реакции

Cc1ccc(-c2n[nH]c(=S)[nH]2)c(C)c1
5-(2,4 dimethylphenyl)-2H-1,2,4-triazole-3(4H)-thione
Br.BrCc1ccccn1
2-(bromomethyl)pyridine hydrobromide
Cc1ccc(-c2nc(SCc3ccccn3)n[nH]2)c(C)c1
2-((5-(2,4-dimethylphenyl)-1H-1,2,4-triazol-3-ylthio)methyl)pyridine
Выход 64.0%

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Методика

Prepared in a similar manner to example 1 using 5-(2,4 dimethylphenyl)-2H-1,2,4-triazole-3(4H)-thione (example 3a) and 2-(bromomethyl)pyridine hydrobromide. Yield 64%. 1H NMR (500 MHz, CDCl3): δ 2.34 (s, 3H), 2.57 (s, 3H), 4.37 (s, 2H), 4.51 (s, 2H), 7.04-7.08 (m, 2H), 7.28-7.31 (m, 1H), 7.41-7.43 (d, 1H), 7.74-7.77 (m, 2H), 8.63-8.64 (d, 1H). MS(M+H, 297); mp=112-114° C.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08968708B2uspto-grants-2015_03