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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1903198Generated: November 2, 2026

Dimethylformamide → HCID 20468178, compound

https://huagongshe.com/reaction/1903198

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 20468180HCID 20468180—
ReactantHCID 54008488HCID 54008488—
SolventMethanolHCID 887—
SolventChloroformHCID 6212—
ProductHCID 20468178HCID 20468178—

Reaction Steps

Into 50 ml of dimethylformamide were added 1.9 g of 1-benzyl-6-hydroxy-3,4-dihydrocarbostyril, 1.8 g of K2CO3 and 0.5 g of KI. The mixture was heated at 60°-70° C. under stirring, then 3.4 g of N-ethyl-N-(2-tetrahydropyranylmethyl)-5-chloropentanic acid amide was added dropwise gradually thereto. After the addition operation, the reaction mixture was further stirred at the same temperature for 4 hours. Then the solvent was removed by distillation and the residue thus obtained was dissolved in 200 ml of chloroform and the chloroform layer was washed with a diluted hydrochloric acid, 1% NaOH aqueous solution and water in this order, then dried with anhydrous sodium sulfate. The drying agent was removed by filtratoon, and the mother liquor was concentrated, then the residue thus obtained was treated by a silica-gel column chromatography [solvent used was a mixture of chloroform:methanol=20:1 (v/v)]. 0.6 Grams of 1-benzyl-6-{4-[N-(2-tetrahydropyranylmethyl)-N-ethylaminocarbonyl]butoxy}-3,4-dihydrocarbostyril was obtained as 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-9ef257de176646d09241f62e6b23a622
Source noteuspto-grants-1984_03