4-Chlorobenzenesulfonyl chloride → 4-chloro-N-[5-chloro-2-(methylthio)phenyl]benzenesulfonamide

HRID 2205385

Reaction equation

HRID 2205385 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][CH:13]=1>>[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][CH:13]=1

Participants

3

Reactant 2

HCID 73984-Chlorobenzenesulfonyl chlorideHCID 27945775-Chloro-2-(methylthio)aniline

Product 1

HCID 474192324-chloro-N-[5-chloro-2-(methylthio)phenyl]benzenesulfonamideYield 68%

Procedure

Following General Procedure B, the title compound (150 mg, 68%) was prepared from 5-Chloro-2-methylsulfanyl-phenylamine (110 mg, 0.64 mmol) and 4-Chloro-benzenesulfonyl chloride (134 mg, 0.64 mmol).

Sources & evidence

ORD record
ord-93a6e49dcde9458b857ebec1932cd7ad
Source dataset
uspto-grants-2016_06
Patent number
US09371278B2

Linked notes

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