4-t-Butylbenzenesulfonyl chloride → HCID 178441109, compound

HRID 29620Notes

Reaction equation

HRID 29620 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 reaction of 4-t-butylbenzenesulfonyl chloride with (2-Amino-5-chloro-phenyl)-(1H-pyrazol-3-yl)-methanone following the general procedure. MS: m/z 418.1 (M++1). Remove this example—same as [0676 below]

Workup

  1. customRemove this example—same as [0676 below]

Sources & evidence

ORD record
ord-f292bca2a4b9423faf3c18b8cc071bd2
Source dataset
uspto-grants-2008_09
Patent number
US07420055B2

Reaction notes

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