2-(Bromomethyl)pyridine hydrobromide → HCID 57330885, compound

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Reaction Steps

Prepared in a similar manner to example 1 using 5-(4,5-dimethylfuran-2-yl)-2H-1,2,4-triazole-3(4H)-thione (example 5a) and 2-(bromomethyl)pyridine hydrobromide. Yield 27%. 1H NMR (500 MHz, dMSO): δ 1.98 (s, 3H), 2.28 (s, 3H), 4.37 (s, 2H), 6.76 (s, 1H), 7.3 (m, 1H), 7.45 (d, 1H), 7.75 (t, 1H), 8.6 (s, 1H). MS (M+H, 287).

Provenance & Evidence