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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 346732Generated: October 30, 2026

o-Toluenesulfonyl chloride → HCID 10228032, compound

https://huagongshe.com/reaction/346732

Reaction equation

Participants

RoleNameHCIDCharge
Reactanto-Toluenesulfonyl chlorideHCID 8623—
ReactantN-(2-amino-5-(4-boc-1-piperazinyl)-phenyl)-benzenesulfonamideHCID 22272479—
ProductHCID 10228032HCID 10228032—

Reaction Steps

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 o-toluenesulfonylchloride (46 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: 487.1; Calcd 487.14; 1H-NMR δ 7.74–7.16 (m, 8H), 6.78–6.52 (m, 4H), 3.27–3.16 (m, 8H), 2.58 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07173035B2
Source datasetuspto-grants-2007_02
ORD IDord-05a6795317144925a4b5eaec5e8ad68c
Source noteuspto-grants-2007_02