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

HRID 2205382Notes

Reaction equation

HRID 2205382 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

3

Reactant 2

HCID 7369Benzenesulfonyl chlorideHCID 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-5224408186384c30a4cf737a1a90bc26
Source dataset
uspto-grants-2016_06
Patent number
US09371278B2

Reaction notes

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