4-(1,3-Oxazol-5-yl)benzenesulphonyl chloride → N-[4-Chloro-2-(4-methyl-pyridine-3-carbonyl)-phenyl]-4-oxazol-5-yl-benzenesulfonamide

HRID 29617Notes

Reaction equation

HRID 29617 reaction equation
[O:1]1[C:5]([C:6]2[CH:11]=[CH:10][C:9]([S:12](Cl)(=[O:14])=[O:13])=[CH:8][CH:7]=2)=[CH:4][N:3]=[CH:2]1.[NH2:16][C:17]1[CH:22]=[CH:21][C:20]([Cl:23])=[CH:19][C:18]=1[C:24]([C:26]1[CH:27]=[N:28][CH:29]=[CH:30][C:31]=1[CH3:32])=[O:25]>>[Cl:23][C:20]1[CH:21]=[CH:22][C:17]([NH:16][S:12]([C:9]2[CH:10]=[CH:11][C:6]([C:5]3[O:1][CH:2]=[N:3][CH:4]=3)=[CH:7][CH:8]=2)(=[O:14])=[O:13])=[C:18]([C:24]([C:26]2[CH:27]=[N:28][CH:29]=[CH:30][C:31]=2[CH3:32])=[O:25])[CH:19]=1

Participants

3

Reactant 2

HCID 27764154-(1,3-Oxazol-5-yl)benzenesulphonyl chlorideHCID 66660678(2-Amino-5-chloro-phenyl)-(4-methyl-pyridin-3-yl)-methanone

Product 1

HCID 59788628N-[4-Chloro-2-(4-methyl-pyridine-3-carbonyl)-phenyl]-4-oxazol-5-yl-benzenesulfonamide

Procedure

The title compound was prepared using 4-oxazol-5-yl-benzenesulfonyl chloride and (2-amino-5-chloro-phenyl)-(4-methyl-pyridin-3-yl)-methanone according to the general procedure for the preparation of the N-aryl-benzenesulfonamides.

Sources & evidence

ORD record
ord-ca94c62f1bdd478eab24f4c4868e0829
Source dataset
uspto-grants-2008_09
Patent number
US07420055B2

Reaction notes

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