Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1064465Generated: October 30, 2026

4-Butoxybenzenesulfonyl Chloride → HCID 10187338, compound

https://huagongshe.com/reaction/1064465

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Butoxybenzenesulfonyl ChlorideHCID 517990—
ReactantN-(2-amino-5-(4-boc-1-piperazinyl)-phenyl)-benzenesulfonamideHCID 22272479—
ProductHCID 10187338HCID 10187338—

Reaction Steps

4-Butoxy-N-[2-[(phenylsulfonyl)amino]-4-(1-piperazinyl)phenyl]benzenesulfonamide was synthesized from N-{2-amino-5-(4-t-butyloxycarbonyl-piperazinyl)-phenyl}benzenesulfonamide and 4-n-butoxybenzenesulfonylchloride (59 mg, 0.239 mmol) according to general method 3 to give 70 mg of a purple solid. MS (posES-FIA) m/z=Found: 545.2. Calcd 545.18. 1H-NMR δ 7.73-7.45 (m, 7H), 6.95-6.91 (m, 2H), 6.72-6.70 (m, 1H), 4.00 (t, 2H), 3.29-3.24 (m, 8H), 1.79-1.70 (m, 2H), 1.55-1.43 (m, 2H), 0.97 (t, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06969710B2
Source datasetuspto-grants-2005_11
ORD IDord-0b87eb9552df4972b5d4d27adc16e74e
Source noteuspto-grants-2005_11