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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1068007Generated: October 31, 2026

m-Chloroperbenzoic acid → N-[(4-chlorophenyl)methyl]-1-(3-methylsulfinylpropyl)-6-(morpholinomethyl)-4-oxo-quinoline-3-carboxamide

https://huagongshe.com/reaction/1068007

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
ReactantN-[(4-chlorophenyl)methyl]-1-(3-methylsulfanylpropyl)-6-(morpholinomethyl)-4-oxo-quinoline-3-carboxamideHCID 16073877—
SolventDichloromethaneHCID 6344—
ProductN-[(4-chlorophenyl)methyl]-1-(3-methylsulfinylpropyl)-6-(morpholinomethyl)-4-oxo-quinoline-3-carboxamideHCID 1607388067.8%

Reaction Steps

A solution of N-(4-chlorobenzyl)-1-[3-(methylsulfanyl)propyl]-6-(4-morpholinylmethyl)-4-oxo-1,4-dihydro-3-quinolinecarboxamide (0.10 gm) from Example No. 61 in dichloromethane (2 mL) at 0° C. is added p-toluenesulfonic acid hydrate (0.04 gm) followed by m-chloroperoxybenzoic acid (˜85%)(0.045 gm). The mixture is stirred for 0.5 hrs. The reaction mixture is diluted with dichloromethane, washed with saturated aqueous sodium sulfite, saturated aqueous sodium bicarbonate, brine, dried (Na2SO4) and concentrated under reduced pressure. The crude product is purified by flash column chromatography eluting with 3% to 9% methanol in dichloromethane. The product fractions are combined and recrystallized from ethyl acetate-methanol-hexanes to afford 0.07 gm of the title compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06248739B1
Source datasetuspto-grants-2001_06
ORD IDord-cfb64910d6fb443ba511e62990da20cc
Source noteuspto-grants-2001_06