2-Amino-4-chlorobenzenesulphonamide → HCID 59635817, compound

HRID 2283372Notes

Reaction equation

HRID 2283372 reaction equation
[NH2:1][C:2]1[CH:7]=[C:6]([Cl:8])[CH:5]=[CH:4][C:3]=1[S:9]([NH2:12])(=[O:11])=[O:10].[CH3:13][O:14][C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][C:16]=1/[CH:21]=[CH:22]/[S:23](Cl)(=[O:25])=[O:24]>>[Cl:8][C:6]1[CH:5]=[CH:4][C:3]([S:9]([NH2:12])(=[O:11])=[O:10])=[C:2]([NH:1][S:23](/[CH:22]=[CH:21]/[C:16]2[CH:17]=[CH:18][CH:19]=[CH:20][C:15]=2[O:14][CH3:13])(=[O:25])=[O:24])[CH:7]=1

Participants

3

Reactant 2

HCID 777902-Amino-4-chlorobenzenesulphonamideHCID 55280297HCID 55280297, compound

Product 1

HCID 59635817HCID 59635817, compound

Procedure

The title compound was synthesized as described for Example 226 a) starting from 2-amino-4-chlorobenzenesulfonamide and (E)-2-(2-methoxyphenyl)ethenesulfonyl chloride.

Sources & evidence

ORD record
ord-b471dc3d0fdd4167b20c4cce867377c8
Source dataset
uspto-grants-2015_09
Patent number
US09145380B2

Reaction notes

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