Reaktion #955913

ord-86ad03731c764746948377210ac17f5f

Reaktionsgleichung

CCc1ccc(-c2n[nH]c(=S)[nH]2)cc1
5-(4-ethylphenyl)-2H-1,2,4-triazole-3(4H)-thione
Br.BrCc1ccccn1
2-(bromomethyl)pyridine hydrobromide
CCc1ccc(-c2nc(SCc3ccccn3)n[nH]2)cc1
2-((5-(4-Ethylphenyl)-1H-1,2,4-triazol-3-ylthio)methyl)pyridine
Ausbeute 71.0%

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Vorschrift

Prepared in a similar manner to example 1 using 5-(4-ethylphenyl)-2H-1,2,4-triazole-3(4H)-thione (example 4a) and 2-(bromomethyl)pyridine hydrobromide. Yield 71%. 1H NMR (500 MHz, dMSO): δ 1.18-1.22 (t, 3H), 2.64-2.66 (t, 2H), 4.52 (s, 2H), 7.30-7.88 (m, 8H), 14.3 (bs, 1H). MS(M+H, 297).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08968708B2uspto-grants-2015_03