HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 13064824, compound → HCID 13064850, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 13064824 | HCID 13064824 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | HCID 178418390 | HCID 178418390 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 13064850 | HCID 13064850 | — |
Reaction Steps
1.5 Gram of 6-{1-oxo-4-[4-(4-nitrophenyl)piperazinyl]-butyl}-3,4-dihydrocarbostyril and 0.3 g of 5%-palladium-carbon were dispersed in 150 ml of ethanol and catalytically reduced under 2 kg/cm2 of hydrogen gas for 5 hours. The reaction mixture was filtered and the mother liquor was concentrated under a reduced pressure. The residue thus obtained was recrystallized from methanol to obtain 0.7 g of 6-{1-hydroxy-4-[4-(4-aminophenyl)-1-piperazinyl]butyl}-3,4-dihydrocarbostyril in brown powdery crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04619932 |
| Source dataset | uspto-grants-1986_10 |
| ORD ID | ord-def0ba61aedd4d10aa9949bb65b49c38 |
| Source note | uspto-grants-1986_10 |