2-Aminobenzenesulfonamide → HCID 178527159, compound

HRID 1767637Notes

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

Reactant 2

HCID 728942-Aminobenzenesulfonamide

HCID 75938Cyclohexanecarbonyl chloride

Product 1

HCID 178527159HCID 178527159, compound

Procedure

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

Sources & evidence

ORD record: ord-b95c672ba4e34438b0de0d59dd5ed219
Source dataset: uspto-grants-2007_06
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US07235548B2

Reaction notes

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