HCID 19609792, compound → HCID 86641440, compound

HRID 547999Notes

Reaction equation

HRID 547999 reaction equation
[Br:1][C:2]1[C:3]([OH:13])=[C:4]([C:8]([CH3:12])=[C:9]([Cl:11])[CH:10]=1)[C:5]([OH:7])=O.[Cl:14][C:15]1[CH:21]=[C:20]([S:22]([C:25]([F:28])([F:27])[F:26])(=[O:24])=[O:23])[CH:19]=[CH:18][C:16]=1[NH2:17]>>[Br:1][C:2]1[C:3]([OH:13])=[C:4]([C:8]([CH3:12])=[C:9]([Cl:11])[CH:10]=1)[C:5]([NH:17][C:16]1[CH:18]=[CH:19][C:20]([S:22]([C:25]([F:28])([F:26])[F:27])(=[O:24])=[O:23])=[CH:21][C:15]=1[Cl:14])=[O:7]

Participants

3

Reactant 2

HCID 19609792HCID 19609792, compoundHCID 57432758HCID 57432758, compound

Product 1

HCID 86641440HCID 86641440, compound

Procedure

3-Bromo-5-chloro-N-(2-chloro-4-trifluoromethanesulfonylphenyl)-2-hydroxy-6-methylbenzamide is synthesized from 3-bromo-5-chloro-2-hydroxy-6-methylbenzoic acid and 2-chloro-4-(trifluoromethanesulfonyl)aniline by General Procedure F.

Sources & evidence

ORD record
ord-dcd59ee9853d481fa080e1e9dfce9e8a
Source dataset
uspto-grants-2011_05
Patent number
US07939690B2

Reaction notes

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