反应详情

Prepared from 2-amino-5-bromo-6-methoxycarbonylpyridine and 4-(N -morpholinylsulfonyl)thiophenol according to General Method 11 step 1 followed by reaction with 2,4-dichlorophenylsulfonyl chloride according to General Method 11 step 2. 1H NMR (CDCl3): 8.04 (1 H, d, J 11 Hz, A-ring CH ortho to SO2NH), 7.62 & 7.42 (2×2 H, 2×d, 2×J 10 Hz, C-ring CH's), 7.43 (1 H, s, A-ring CH ortho to 2×Cl), 7.31 (1 H, d, J 11 Hz, A ring CH ortho to Cl), 7.28 & 7.18 (2×1 H, 2×d, 2×J 11 Hz, pyridyl CH's), 3.89 (3H, s, CH3) 3.72-3.63 (4H, m, CH2OCH2), 2.98-2.88 (4H, m, CH2NCH2). Hplc (Luna 2, Gradient 5): rt 6.00 minutes. LC/MS rt=6.69 minutes, 618/620 (MH+).

1. customrt 6.00 minutes
2. customLC/MS rt=6.69 minutes, 618/620 (MH+)