Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1068028Generated: November 1, 2026

Dichloromethane → N-[(4-chlorophenyl)methyl]-1-[(4-chlorophenyl)sulfanylmethyl]-6-(morpholinomethyl)-4-oxo-quinoline-3-carboxamide

https://huagongshe.com/reaction/1068028

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantCesium carbonateHCID 10796—
ReactantBenzene, 1-chloro-4-((chloromethyl)thio)-HCID 23610—
ReactantHCID 178513551HCID 178513551—
SolventDimethylformamideHCID 6228—
ProductN-[(4-chlorophenyl)methyl]-1-[(4-chlorophenyl)sulfanylmethyl]-6-(morpholinomethyl)-4-oxo-quinoline-3-carboxamideHCID 16073907—

Reaction Conditions

Temperature105 °C

Reaction Steps

A suspension of N-(4-chlorobenzyl-4-hydroxy-6-(4-morpholinylmethyl)-3-quinolinecarboxamide (0.25 gm) from Preparation No. 40 and cesium carbonate (0.39 gm) in DMF (3 mL) is treated with chloromethyl 4-chlorophenyl sulfide (0.13 mL). The mixture is tightly capped and heated to 105° C. for 2 hrs. The reaction mixture is allowed to cool to room temperature, diluted with dichloromethane (50 mL), washed with water (2×10 mL), brine, dried (Na2SO4) and concentrated under reduced pressure. The crude product is purified by flash column chromatography eluting with 1% to 3% methanol in dichloromethane and then by trituration with ethyl acetate to afford 0.26 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-05c6bed423404959bb0ca97049edf8ce
Source noteuspto-grants-2001_06