Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 346738Generated: October 30, 2026

2-Methoxy-4-methylbenzene-1-sulfonyl chloride → 2-Methoxy-4-methyl-N-[2-[(phenylsulfonyl)amino]-4-(1-piperazinyl)phenyl]benzenesulfonamide

https://huagongshe.com/reaction/346738

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Methoxy-4-methylbenzene-1-sulfonyl chlorideHCID 11345048—
ReactantN-(2-amino-5-(4-boc-1-piperazinyl)-phenyl)-benzenesulfonamideHCID 22272479—
Product2-Methoxy-4-methyl-N-[2-[(phenylsulfonyl)amino]-4-(1-piperazinyl)phenyl]benzenesulfonamideHCID 10279475—

Reaction Steps

2-Methoxy-4-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-methoxy-4-methylbenzenesulfonylchloride (53 mg, 0.239 mmol) according to general method 3 to give 80 mg of a purple solid. MS (posES-FIA) m/z=Found: 517.2; Calcd 517.15; 1H NMR δ 7.67–7.37 (m, 6H), 7.10–7.04 (m, 2H), 6.97–6.74 (m, 2H), 6.30 (d, 1H), 4.06 (s, 3H), 3.26–3.09 (m, 8H), 2.37 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07173035B2
Source datasetuspto-grants-2007_02
ORD IDord-b6a40cce6a154e37ba64133e5d0b9fba
Source noteuspto-grants-2007_02