2-Aminobenzenesulfonamide → HCID 178527159, compound

HRID 496126Notes

Reaction equation

HRID 496126 reaction equation
[NH2:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[S:8]([NH2:11])(=[O:10])=[O:9].[CH:12]1([C:18](Cl)=O)[CH2:17][CH2:16][CH2:15][CH2:14][CH2:13]1>>[CH:12]1([C:18]2[NH:11][S:8](=[O:9])(=[O:10])[C:3]3[CH:4]=[CH:5][CH:6]=[CH:7][C:2]=3[N:1]=2)[CH2:17][CH2:16][CH2:15][CH2:14][CH2:13]1

Participants

3

Reactant 2

HCID 728942-AminobenzenesulfonamideHCID 75938Cyclohexanecarbonyl chloride

Product 1

HCID 178527159HCID 178527159, compound

Procedure

2-Aminobenzenesulfonamide was transformed by Method E (using cyclohexanecarbonyl chloride).

Sources & evidence

ORD record
ord-d7a62e79769f4ed1b834568a17ebc9ef
Source dataset
uspto-grants-2005_09
Patent number
US06943159B1

Reaction notes

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