HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 12899573, compound → HCID 12899579, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 12899573 | HCID 12899573 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 12899579 | HCID 12899579 | 119.5% |
Reaction Steps
1.0 gram of 4-methyl-7-[3-(4-phenylpiperazinyl)-propoxy]carbostyril dihydrochloride and 0.3 g of palladium black are dispersed in 200 ml of ethanol under hydrogen at a pressure of 2 atmospheres at room temperature and catalytic reduction is carried out at 70°-80° C. for 8 hours. After cooling the reaction mixture, the palladium black is removed by filtration and the mother liquor is concentrated to dryness. The residue is recrystallized from a mixture of methanol-ether to obtain 0.6 g (yield: 60%) of 4-methyl-7-[3-(4-phenylpiperazinyl)-propoxy]-3,4-dihydrocarbostyril.dihydrochloride.dihydrate in the form of colorless crystals with a melting point of 260°-265° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04824840 |
| Source dataset | uspto-grants-1989_04 |
| ORD ID | ord-d951eb478b004c41bc5f1e096d15570f |
| Source note | uspto-grants-1989_04 |