Реакция #955915

ord-c290744ad245432db13df4a3a2ad5758

Уравнение реакции

S=c1[nH]nc(-c2cc3ccccc3o2)[nH]1
5-(benzofuran-2-yl)-2H-1,2,4-triazole-3(4H)-thione
Br.BrCc1ccccn1
2-(bromomethyl)pyridine hydrobromide
Cc1cc(-c2nc(SCc3ccccn3)n[nH]2)oc1C
2-((5-(4,5-dimethylfuran-2-yl)-1H-1,2,4-triazol-3-ylthio)methyl)pyridine
Выход 59.0%

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Методика

Prepared in a similar manner to example 1 using 5-(benzofuran-2-yl)-2H-1,2,4-triazole-3(4H)-thione (example 6a) and 2-(bromomethyl)pyridine hydrobromide. Yield 59%. 1H NMR (500 MHz, CDCl3): δ 4.37 (s, 2H), 7.26-7.34 (m, 5H), 7.4-7.42 (d,1H), 7.55-7.57 (d, 1H), 7.65-7.67 (d, 1H), 7.75 (t, 1H), 8.62 (s, 1H). MS(M+H, 309).

Источник

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