4-(Phenylsulfonyl)aniline → HCID 69891125, compound

HRID 2306728Notes

Reaction equation

HRID 2306728 reaction equation
[C:1]1([S:7]([C:10]2[CH:16]=[CH:15][C:13]([NH2:14])=[CH:12][CH:11]=2)(=[O:9])=[O:8])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[Cl:17][C:18]1[C:27]2[C:22](=[CH:23][CH:24]=[C:25]([C:28]3[O:29][C:30]([CH3:33])=[N:31][N:32]=3)[CH:26]=2)[N:21]=[CH:20][N:19]=1>>[ClH:17].[C:1]1([S:7]([C:10]2[CH:16]=[CH:15][C:13]([NH:14][C:18]3[C:27]4[C:22](=[CH:23][CH:24]=[C:25]([C:28]5[O:29][C:30]([CH3:33])=[N:31][N:32]=5)[CH:26]=4)[N:21]=[CH:20][N:19]=3)=[CH:12][CH:11]=2)(=[O:8])=[O:9])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1

Participants

3

Reactant 2

HCID 5166664-(Phenylsulfonyl)anilineHCID 226097254-Chloro-6-(5-methyl-1,3,4-oxadiazol-2-yl)quinazoline

Product 1

HCID 69891125HCID 69891125, compound

Procedure

The title compound was prepared according to Procedure A from 4-benzenesulphonylaniline and 4-chloro-6-(5-methyl-1,3,4-oxadiazol-2-yl)-quinazoline; δH [2H6]DMSO 11.63(1H, bs), 9.42(1H, s), 8.95(1H, s), 8.56(1H, d), 8.10(6H, m), 7.70(4H, m), 2.65(3H, s); m/z (M+1+) 444.

Sources & evidence

ORD record
ord-08bb46ee539a4fc2a98d787aa63b0c2f
Source dataset
uspto-grants-2004_12
Patent number
US06828320B2

Reaction notes

Loading…