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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1064461Generated: October 26, 2026

Ethenesulfonyl chloride, 2-phenyl- → N-[2-({[(E)-2-Phenylethenyl]sulfonyl}amino)-5-(1-piperazinyl)phenyl]benzenesulfonamide

https://huagongshe.com/reaction/1064461

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthenesulfonyl chloride, 2-phenyl-HCID 107500—
ReactantN-(2-amino-5-(4-boc-1-piperazinyl)-phenyl)-benzenesulfonamideHCID 22272479—
ProductN-[2-({[(E)-2-Phenylethenyl]sulfonyl}amino)-5-(1-piperazinyl)phenyl]benzenesulfonamideHCID 22272438—

Reaction Steps

N-[2-({[(E)-2-Phenylethenyl]sulfonyl}amino)-5-(1-piperazinyl)phenyl]benzenesulfonamide was synthesized from N-{2-amino-5-(4-t-butyloxycarbonyl-piperazinyl)-phenyl}benzenesulfonamide and β-styrenesulfonylchloride (48 mg, 0.239 mmol according to general method 3 to give before Boc-deprotection 160 mg of a purple solid. MS (posES-FIA) m/z=Found: 499.2. Calcd 499.14. 1H-NMR δ 8.26 (d, 1H), 8.04 (d, 1H), 7.75-7.38 (m, 8H), 7.22 (d, 1H, J=15.4 Hz), 7.16 (d, 1H), 6.97 (d, 1H), J=15.4 Hz), 6.78 (dd, 1H), 6.68 (d, 1H), 3.68 (app t, 2H), 3.39 (app t, 2H), 3.28-3.21 (m, 4H),

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06969710B2
Source datasetuspto-grants-2005_11
ORD IDord-1757380f2cbf4f76b5c046681ce447bf
Source noteuspto-grants-2005_11