Réaction #955920

ord-0b2cc6c84c2d43cf8bdebaad00545371

Équation de réaction

CCc1ccc(-c2n[nH]c(=S)[nH]2)c(C)c1
5-(4-ethyl-2-methylphenyl)-2H-1,2,4-triazole-3(4H)-thione
Br.BrCc1ccccn1
2-(bromomethyl)pyridine hydrobromide
CCc1ccc(-c2nc(SCc3ccccn3)n[nH]2)c(C)c1
2-((5-(4-Ethyl-2-methylphenyl)-1H-1,2,4-triazol-3-ylthio)methyl)pyridine
Rendement 39.0%

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Mode opératoire

Prepared in a similar manner to example 1 using 5-(4-ethyl-2-methylphenyl)-2H-1,2,4-triazole-3(4H)-thione (example 10a) and 2-(bromomethyl)pyridine hydrobromide. Yield 39%. 1H NMR (300 MHz, dMSO): δ 1.17-1.22 (t, 3H), 2.46 (s, 3H), 2.60-2.64 (dd, 2H), 4.50 (s, 2H), 7.14-7.18 (m, 2H), 7.27-7.29 (m, 1H), 7.47-7.49 (d, 1H), 7.58 (bd, 1H), 7.72-7.77 (m, 1H), 8.50-8,51 (d, 1H). MS(M+H, 311).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US08968708B2uspto-grants-2015_03