4-Chlorobenzenesulfonamide → HCID 22291407, compound

HRID 967840Notes

Reaction equation

[CH2:1]([C:3]1[N:4]([C:14]2[CH:19]=[CH:18][C:17]([CH2:20][CH2:21][NH:22][C:23](=[O:31])OC3C=CC=CC=3)=[CH:16][CH:15]=2)[CH:5]=[C:6]([C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][N:9]=2)[N:7]=1)[CH3:2].[Cl:32][C:33]1[CH:38]=[CH:37][C:36]([S:39]([NH2:42])(=[O:41])=[O:40])=[CH:35][CH:34]=1>>[Cl:32][C:33]1[CH:34]=[CH:35][C:36]([S:39]([NH:42][C:23]([NH:22][CH2:21][CH2:20][C:17]2[CH:18]=[CH:19][C:14]([N:4]3[CH:5]=[C:6]([C:8]4[CH:13]=[CH:12][CH:11]=[CH:10][N:9]=4)[N:7]=[C:3]3[CH2:1][CH3:2])=[CH:15][CH:16]=2)=[O:31])(=[O:40])=[O:41])=[CH:37][CH:38]=1

Participants

Reactant 2

HCID 668244-Chlorobenzenesulfonamide

HCID 22291387HCID 22291387, compound

Product 1

HCID 22291407HCID 22291407, compound

Procedure

The title compound was prepared according to the procedure described in step 2 of Example 18 from phenyl 2-{4-[2-ethyl-4-(2-pyridinyl)-1H-imidazol-1-yl]phenyl}ethylcarbamate and 4-chlorobenzenesulfonamide. MS (ESI) m/z 510 [M+H]+, 508 [M−H]−, 1H-NMR (CDCl3) □1.17 (3H, t, J=7.3 Hz), 2.65 (2H, q, J=7.7 Hz), 2.80-2.88 (2H, m), 3.42-3.55 (2H, m), 6.78 (1H, br), 7.15-7.28 (4H, m),7.42 (2H, d, J=8.4 Hz), 7.58 (1H, s), 7.71 (1H, t, J=6.0 Hz), 7.80-7.89 (3H, m), 8.51 (1H, d, J=6.0 Hz).

Sources & evidence

ORD record: ord-79188916946d46fe8b9061c115a7a70d
Source dataset: uspto-grants-2005_10
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US06956050B2

Reaction notes

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