Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1064463Generated: October 30, 2026

o-Toluenesulfonyl chloride → HCID 10228032, compound

https://huagongshe.com/reaction/1064463

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 numberUS06969710B2
Source datasetuspto-grants-2005_11
ORD IDord-8725a23d68ab406f91830b7e56264a7f
Source noteuspto-grants-2005_11