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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1903188Generated: November 2, 2026

Isobutyl chloroformate → 6-{3-[N-ethyl-N-(2-pyridyl)aminocarbonyl]propoxy}carbostyril

https://huagongshe.com/reaction/1903188

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsobutyl chloroformateHCID 62365—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Reactant2-(Ethylamino)pyridineHCID 11804745—
Reactant4-((2-Oxo-1,2-dihydroquinolin-6-yl)oxy)butanoic acidHCID 12866342—
SolventChloroformHCID 6212—
Product6-{3-[N-ethyl-N-(2-pyridyl)aminocarbonyl]propoxy}carbostyrilHCID 12836955—

Reaction Steps

Into 300 ml of chloroform were added 9.9 g of 6-(3-carboxypropoxy)carbostyril and 6.5 ml of DBU. The outside of the reaction vessel containing the abovementioned mixture was ice-cooled and 5.7 ml of isobutyl chloroformate was added dropwise under stirring condition. After the addition operation, stirring was continued for 1 hour at a room temperature and 5.4 g of 2-ethylaminopyridine was added dropwise, then the reaction was continued for 5 hours under stirring condition. The reaction mixture was washed with a diluted NaHCO3 aqueous solution and water, and was concentrated. The residue thus obtained was treated by a silica-gel column chromatography (solvent used was a mixture of chloroform:methanol=20:1) and the elute thus obtained was concentrated then was recrystallized from methanol, to obtain 4.5 g of 6-{3-[N-ethyl-N-(2-pyridyl)aminocarbonyl]propoxy}carbostyril in the form of colorless needle-like crystals. Melting point: 148°-149° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04435404
Source datasetuspto-grants-1984_03
ORD IDord-f80d78a5cf8646e9b40df407ed380c35
Source noteuspto-grants-1984_03