5-Chloro-2,4-difluorobenzenesulphonyl chloride → 5-Chloro-N-(5-chloro-1,3-thiazol-2-yl)-N-(2,4-dimethoxybenzyl)-2,4-difluorobenzenesulfonamide

HRID 1402017Notes

Reaction equation

HRID 1402017 reaction equation
[Cl:1][C:2]1[S:6][C:5]([NH:7][CH2:8][C:9]2[CH:14]=[CH:13][C:12]([O:15][CH3:16])=[CH:11][C:10]=2[O:17][CH3:18])=[N:4][CH:3]=1.[Cl:19][C:20]1[C:21]([F:31])=[CH:22][C:23]([F:30])=[C:24]([S:26](Cl)(=[O:28])=[O:27])[CH:25]=1>>[Cl:19][C:20]1[C:21]([F:31])=[CH:22][C:23]([F:30])=[C:24]([S:26]([N:7]([C:5]2[S:6][C:2]([Cl:1])=[CH:3][N:4]=2)[CH2:8][C:9]2[CH:14]=[CH:13][C:12]([O:15][CH3:16])=[CH:11][C:10]=2[O:17][CH3:18])(=[O:28])=[O:27])[CH:25]=1

Participants

3

Reactant 2

HCID 27735275-Chloro-2,4-difluorobenzenesulphonyl chlorideHCID 577321515-chloro-N-(2,4-dimethoxybenzyl)-1,3-thiazol-2-amine

Product 1

HCID 594366225-Chloro-N-(5-chloro-1,3-thiazol-2-yl)-N-(2,4-dimethoxybenzyl)-2,4-difluorobenzenesulfonamide

Procedure

Prepared according to Preparation 207 using 5-chloro-N-(2,4-dimethoxybenzyl)-1,3-thiazol-2-amine (Preparation 208) and 5-chloro-2,4-difluorobenzenesulfonyl chloride.

Workup

  1. customPrepared

Sources & evidence

ORD record
ord-fba34a2098344ea194ef6d7180bcc297
Source dataset
uspto-grants-2014_12
Patent number
US08907101B2

Reaction notes

Loading…