HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 845749Generated: October 29, 2026
HCID 20130164, compound → HCID 20130171, compound
https://huagongshe.com/reaction/845749
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 20130164 | HCID 20130164 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 20130171 | HCID 20130171 | 89.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04760064 |
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| Source dataset | uspto-grants-1988_07 |
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| ORD ID | ord-2dff0494aa0942f7b8d15279ae34033e |
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| Source note | uspto-grants-1988_07 |
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