4-Aminoacetanilide → HCID 87373884, compound

Participants

Reaction Steps

The title compound was prepared from 3′-benzyl-3-methyl-2′-methylthio-4′-oxo-4-phenyl-3H,4′H-[2,5′]bithiazolyliden-3′-ium p-toluenesulfonate and 4′-aminoacetanilide in a manner similar to that described in Example 1. 1H-NMR (CDCl3): δ 7.56 (2H, d), 7.42–7.47 (5H, m), 7.24–7.34 (5H, m), 7.12 (1H, s), 6.97 (2H, d), 6.30 (1H, s), 5.15 (2H, s), 3.49 (3H, s), 2.17 (3H, s); MS(ESI): 513 (MH+).

Provenance & Evidence