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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2283273Generated: October 31, 2026

2-Aminobenzenesulfonamide → HCID 68785778, compound

https://huagongshe.com/reaction/2283273

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminobenzenesulfonamideHCID 72894—
ReactantHCID 53662657HCID 53662657—
SolventPyridineHCID 1049—
ProductHCID 68785778HCID 6878577836.2%

Reaction Steps

2-Aminobenzene sulfonamide (153 mg, 0.89 mmol) was added in one portion to a solution of 2-(2-chloro-phenyl)-ethenesulfonyl chloride (150 mg, 0.63 mmol) in pyridine (2 mL) at RT. After 30 minutes of stirring, no more starting material was detected by tlc. The reaction mixture was concentrated under reduced pressure and the residue was taken up in ethyl acetate and a small amount of methanol. The organic phase was washed with 1N HCl, saturated sodium bicarbonate, dried over MgSO4, and concentrated under reduced pressure. Purification by preparative tlc afforded the target compound, which was then recrystallized from ethyl acetate/pentane/diethyl ether to afford the title compound (85 mg, 36%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09145380B2
Source datasetuspto-grants-2015_09
ORD IDord-6a4e3d917aae4fe59e3500d047c61601
Source noteuspto-grants-2015_09