4-Chloro-3-methylbenzene-1-sulfonyl chloride → 4-chloro-N-[5-chloro-2-(methylthio)phenyl]-3-methylbenzenesulfonamide

HRID 332204

Reaction equation

HRID 332204 reaction equation
[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([S:9][CH3:10])=[C:6]([NH2:8])[CH:7]=1.[Cl:11][C:12]1[CH:17]=[CH:16][C:15]([S:18](Cl)(=[O:20])=[O:19])=[CH:14][C:13]=1[CH3:22]>>[Cl:11][C:12]1[CH:17]=[CH:16][C:15]([S:18]([NH:8][C:6]2[CH:7]=[C:2]([Cl:1])[CH:3]=[CH:4][C:5]=2[S:9][CH3:10])(=[O:20])=[O:19])=[CH:14][C:13]=1[CH3:22]

Participants

3

Reactant 2

HCID 2210014-Chloro-3-methylbenzene-1-sulfonyl chlorideHCID 27945775-Chloro-2-(methylthio)aniline

Product 1

HCID 573786444-chloro-N-[5-chloro-2-(methylthio)phenyl]-3-methylbenzenesulfonamideYield 59.6%

Procedure

Following General Procedure B, the title compound (205 mg, 59%) was prepared from 5-chloro-2-methylsulfanyl-phenylamine (165 mg, 0.95 mmol) and 4-chloro-3-methyl-benzenesulfonyl chloride (215 mg, 0.95 mmol).

Sources & evidence

ORD record
ord-f619f678d9fc4b7b9a7ecfec951e6e37
Source dataset
uspto-grants-2014_11
Patent number
US08877804B2

Linked notes

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