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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 845749Generated: October 29, 2026

HCID 20130164, compound → HCID 20130171, compound

https://huagongshe.com/reaction/845749

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 20130164HCID 20130164—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
SolventDimethylformamideHCID 6228—
ProductHCID 20130171HCID 2013017189.7%

Reaction Steps

To a solution of 1-(4-benzyloxycarbonylmethoxybenzoyl)-6-[4-(3,4-dimethoxybenzoyl)-1-piperazinyl]-3,4-dihydrocarbostyril (4 g) in a mixture of DMF (30 ml) and ethanol (30 ml) was added 10% palladium on carbon (500 mg) and the mixture was hydrogenated at room temperature and atmospheric pressure. After completion of reaction, the catalyst was filtered off and the filtrate was evaporated under reduced pressure. The residue was dissolved in dichloromethane. The solution was washed with water, dried and evaporated under reduced pressure. The resultant residue was purified by silica-gel column chromatography (eluent:dichloromethane:methanol=100:2 to 1:1) to give 1-(4-carboxymethoxybenzoyl)-6-[4-(3,4-dimethoxybenzoyl)-1-piperazinyl]-3,4-dihydrocarbostyril (3.1 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04760064
Source datasetuspto-grants-1988_07
ORD IDord-2dff0494aa0942f7b8d15279ae34033e
Source noteuspto-grants-1988_07