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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1903189Generated: November 2, 2026

Dimethylformamide → HCID 20468178, compound

https://huagongshe.com/reaction/1903189

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantIsobutyl chloroformateHCID 62365—
ReactantN-[(Oxan-2-yl)methyl]ethanamineHCID 13288216—
ReactantHCID 20467955HCID 20467955—
SolventMethanolHCID 887—
SolventChloroformHCID 6212—
SolventTriethylamineHCID 8471—
ProductHCID 20468178HCID 20468178—

Reaction Steps

Into 100 ml of dimethylformamide were added 3.1 g of 1-benzyl-6-(4-carboxybutoxy)-3,4-dihydrocarbostyril and 1.7 ml of triethylamine. The outside of the reaction vessel containing the above mentioned mixture was ice-cooled and 1.4 ml of isobutyl chloroformate was added dropwise to the mixture under stirring condition. After the addition operation, stirring was continued for 30 minutes and 1.75 g of N-ethyl-N-(2-tetrahydropyranylmethyl)amine was added to the reaction mixture and further stirred at a room temperature for 3 hours. After the reaction was completed, the solvent was removed by distillation and the residue thus obtained was extracted with about 300 ml of chloroform and washed with a diluted NaHCO3 aqueous solution, water, a diluted hydrochloric acid and water in this order. The residue thus obtained was treated by silica-gel column chromatography (solvent used was a mixture of chloroform:methanol=20:1) and the elue thus obtained was concentrated to obtain 2.3 g of 1-benzyl-6-{4-[N-(2-tetrahydropyranylmethyl)-N-ethylaminocarbonyl]butoxy}-3,4-dihydrocarbostyril in the form of a colorless syrupy substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04435404
Source datasetuspto-grants-1984_03
ORD IDord-44a462f0b9df42c8811e2fbdc511fb5b
Source noteuspto-grants-1984_03