Methanesulfonyl chloride → HCID 135890156, compound

Participants

Reaction Steps

The title compound was prepared by reacting the compound of example 81 with mesyl chloride in the same manner as that of example 50. 1H NMR (CDCl3) δ: 8.39 (1H, d), 7.43 (1H, dd), 7.06 (1H, d), 4.18 (2H, t), 3.20 (3H, s), 2.68 (2H, q), 2.58 (2H, q), 2.00 (2H, m), 1.28 (3H, t), 1.14 (6H, t).

Provenance & Evidence