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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1865503Generated: October 30, 2026

m-Chloroperbenzoic acid → 6-Chloro-pyridine-3-sulfonic acid[3-chloro-4-(naphthalene-2-sulfinyl)-phenyl]-amide

https://huagongshe.com/reaction/1865503

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactant6-Chloro-pyridine-3-sulfonic Acid [3-Chloro-4-(naphthalen-2-ylsulfanyl)phenyl]-amideHCID 23515223—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
Product6-Chloro-pyridine-3-sulfonic acid[3-chloro-4-(naphthalene-2-sulfinyl)-phenyl]-amideHCID 2351522430%

Reaction Steps

To a solution of 6-Chloro-pyridine-3-sulfonic acid [3-chloro-4-(naphthalen-2-ylsulfanyl)-phenyl]-amide (94, 55 mg, 0.12 mmol) in CH2Cl2 (2 mL), was added dropwise a solution of m-chloroperoxybenzoic acid (mCPBA, Aldrich, 36 mg, 0.2 mmol) in CH2Cl2 (1 mL). The resulting mixture was stirred at ambient temperature for 1 hour and diluted with EtOAc (60 mL). The organic layer was washed with saturated aqueous NaHCO3 solution (50 mL), twice with brine solution (50 mL), dried over Na2SO4, and concentrated under vacuum. The crude solid was chromatographed (10-25% EtOAc in hexane) to yield 17 mg (30%) of 103 as an off white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07626033B2
Source datasetuspto-grants-2009_12
ORD IDord-4ceed392dcad4c2a8e39aed390b88c57
Source noteuspto-grants-2009_12