Benzenesulfonyl chloride → N-[5-chloro-2-(methylsulfinyl)phenyl]benzenesulfonamide

HRID 70407Notes

Reaction equation

[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([S:9]([CH3:11])=[O:10])=[C:6]([CH:8]=1)[NH2:7].[C:12]1([S:18](Cl)(=[O:20])=[O:19])[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1>>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([S:9]([CH3:11])=[O:10])=[C:6]([NH:7][S:18]([C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)(=[O:20])=[O:19])[CH:8]=1

Participants

Reactant 2

HCID 7369Benzenesulfonyl chloride

HCID 679728505-Chloro-2-(methylsulfinyl)aniline

Product 1

HCID 67972231N-[5-chloro-2-(methylsulfinyl)phenyl]benzenesulfonamide

Procedure

Following General Procedure B, C, the title compound was prepared from 5-chloro-2-(methylsulfinyl)aniline and benzenesulfonyl chloride.

Sources & evidence

ORD record: ord-1865b7742e294e5180831a65e0b07e1d
Source dataset: uspto-grants-2014_09
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US08822530B2

Reaction notes

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