4-t-Butylbenzenesulfonyl chloride → HCID 178441109, compound

HRID 29629Notes

Reaction equation

HRID 29629 reaction equation
[C:1]([C:5]1[CH:10]=[CH:9][C:8]([S:11](Cl)(=[O:13])=[O:12])=[CH:7][CH:6]=1)([CH3:4])([CH3:3])[CH3:2].[NH2:15][C:16]1[CH:21]=[CH:20][C:19]([Cl:22])=[CH:18][C:17]=1[C:23]([C:25]1[CH:29]=[CH:28][NH:27][N:26]=1)=[O:24]>>[C:1]([C:5]1[CH:10]=[CH:9][C:8]([S:11]([NH:15][C:16]2[CH:21]=[CH:20][C:19]([Cl:22])=[CH:18][C:17]=2[C:23]([C:25]2[CH:29]=[CH:28][NH:27][N:26]=2)=[O:24])(=[O:13])=[O:12])=[CH:7][CH:6]=1)([CH3:4])([CH3:3])[CH3:2]

Participants

3

Reactant 2

HCID 1398824-t-Butylbenzenesulfonyl chlorideHCID 178507589HCID 178507589, compound

Product 1

HCID 178441109HCID 178441109, compound

Procedure

The title compound was prepared by the reacting 4-t-butyl-benzenesulfonyl chloride with (2-amino-5-chloro-phenyl)-(1H-pyrazol-3-yl)-methanone according to the general procedure described for the preparation of (N-aryl-benzenesulfonamides. MS: m/z418 (M++1).

Sources & evidence

ORD record
ord-ea203d18e83646148e252c70be20ee71
Source dataset
uspto-grants-2008_09
Patent number
US07420055B2

Reaction notes

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