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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 346739Generated: October 28, 2026

HCID 22272473, compound → HCID 22272491, compound

https://huagongshe.com/reaction/346739

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 22272473HCID 22272473—
ReactantN-(2-amino-5-(4-boc-1-piperazinyl)-phenyl)-benzenesulfonamideHCID 22272479—
ProductHCID 22272491HCID 22272491—

Reaction Steps

4-Methoxy-2-methyl-N-[2-[(phenylsulfonyl)amino]-4-(1-piperazinyl)phenyl] benzenesulfonamide was synthesized from N-{2-amino-5-(4-t-butyloxycarbonyl-piperazinyl)-phenyl}benzenesulfonamide and 2-methyl-4-trifluoromethoxybenzenesulfonylchloride (53 mg, 0.455 mmol) according to general method 3 to give before Boc-deprotection 70 mg of a purple solid. MS (posES-FIA) m/z=Found: 571.2; Calcd 571.12; 1H NMR δ 773–7.09 (m, 8H), 6.86 (d, 1H), 6.69 (dd, 1H), 6.48 (d, 1H), 3.29–3.17 (m, 8H), 2.62 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07173035B2
Source datasetuspto-grants-2007_02
ORD IDord-cb5032a31432460aaa7ac736de9454fe
Source noteuspto-grants-2007_02