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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 230492Generated: October 25, 2026

5-Fluoro-2-methylbenzenesulphonyl chloride → HCID 10278878, compound

https://huagongshe.com/reaction/230492

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Fluoro-2-methylbenzenesulphonyl chlorideHCID 136286—
ReactantN-(2-amino-5-(4-boc-1-piperazinyl)-phenyl)-benzenesulfonamideHCID 22272479—
ProductHCID 10278878HCID 10278878—

Reaction Steps

5-Fluoro-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 5-fluoro-2-methylbenzenesulfonylchloride (50 mg, 0.239 mmol) according to general method 3 to give 60 mg of a purple solid. MS (posES-FIA) m/z=Found: 505.2; Calcd 505.13; 1H-NMR δ 7.73-7.17 (m, 8H), 6.83 (d, 1H), 6.68 (dd, 1H), 6.50 (dd, 1H), 3.27-3.17 (m, 8H), 2.55 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07566715B2
Source datasetuspto-grants-2009_07
ORD IDord-3ef5a648e1f4441b969f53bab78bc7e4
Source noteuspto-grants-2009_07