HCID 57849864, compound → HCID 57849811, compound

Participants

Reaction Steps

Synthesized from 4-(2-bromo-acetyl)-N-cyclopropyl-benzenesulfonamide (150 mg, 0.57 mmol) following multi-step procedure for Example 354 (Compound 5354). MS: 527.1 (M+H+); H1 NMR (MeOH-d4): δ(ppm) 8.18 (dd, 2H), 7.91 (dd, 2H), 8.03 (d, 1H), 7.28 (m, 2H), 7.11 (m, 2H), 5.09 (m, 2H), 3.48 (m, 1H), 2.76 (m, 2H), 2.98 (m, 3H), 1.29 (m, 1H), 0.51 (brs, 1H).

Provenance & Evidence