Carzenide → HCID 58614697, compound

HRID 1364638Notes

Reaction equation

HRID 1364638 reaction equation
[Cl:1][C:2]1[CH:8]=[CH:7][C:5]([NH2:6])=[CH:4][C:3]=1[C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][N:10]=1.[C:15]([C:18]1[CH:23]=[CH:22][C:21]([S:24]([NH2:27])(=[O:26])=[O:25])=[CH:20][CH:19]=1)(O)=[O:16]>>[Cl:1][C:2]1[CH:8]=[CH:7][C:5]([NH:6][C:15](=[O:16])[C:18]2[CH:23]=[CH:22][C:21]([S:24]([NH2:27])(=[O:25])=[O:26])=[CH:20][CH:19]=2)=[CH:4][C:3]=1[C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][N:10]=1

Participants

3

Reactant 2

HCID 8739CarzenideHCID 401519254-Chloro-3-(pyridin-2-yl)aniline

Product 1

HCID 58614697HCID 58614697, compound

Procedure

Procedure G was used to couple 4-chloro-3-(pyridin-2-yl)aniline (30 mg) and 4-carboxybenzenesulfonamide to produce N-(4-chloro-3-(pyridin-2-yl)phenyl)-4-(aminosulfonyl)-benzamide. MS (Q1) 388.0 (M)+.

Sources & evidence

ORD record
ord-aeada592bd244852b7f5ab198c4bba9c
Source dataset
uspto-grants-2011_02
Patent number
US07888364B2

Reaction notes

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