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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1068003Generated: October 31, 2026

Triphenylphosphine → N-[(4-chlorophenyl)methyl]-1-(2-ethylsulfanylethyl)-6-(morpholinomethyl)-4-oxo-quinoline-3-carboxamide

https://huagongshe.com/reaction/1068003

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
ReactantSulfide, bis(2-hydroxybutyl)HCID 548436—
ReactantHCID 178522870HCID 178522870—
SolventTetrahydrofuranHCID 8028—
ProductN-[(4-chlorophenyl)methyl]-1-(2-ethylsulfanylethyl)-6-(morpholinomethyl)-4-oxo-quinoline-3-carboxamideHCID 16073876—

Reaction Steps

A dry flask containing N-(4-chlorobenzyl)-4-hydroxy-6-(4-morpholinylmethyl)-3-quinolinecarboxamide (0.20 gm) from Preparation No. 40 in dry THF (5 mL) under an argon atmosphere is added triphenylphosphine (393 mg), ethyl 2-hydroxyethylsulfide (0.16 mL) and diethyl azodicarboxylate (0.18 mL). The mixture is stirred at room temperature overnight then concentrated under reduced pressure. The crude product is purified by flash column chromatography eluting with 2% to 6% methanol in dichloromethane and then by recrystallization from ethanolcyclohexane to afford 0.21 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-94118e7b87a449688e80c0a1c478192c
Source noteuspto-grants-2001_06