HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 13236317, compound → HCID 13236319, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 13236317 | HCID 13236317 | — |
| Catalyst | HCID 178418390 | HCID 178418390 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 13236319 | HCID 13236319 | 57% |
Reaction Steps
6-[4-(4-Nitrobenzoyl)-1-piperazinyl]-3,4-dihydrocarbostyril (400 mg) was added to 20 ml of methanol and reduced at room temperature at atmospheric pressure using 50 mg of 10% palladium-carbon as a catalyst. After completion of absorption of hydrogen gas the catalyst was removed by filtration. The filtrate was subjected to distillation under reduced pressure and the residue was purified through silica gel column chromatography. Recrystallization from ethanol gave 210 mg of 6-[4-(4-aminobenzoyl)-1-piperazinyl]-3,4-dihydrocarbostyril, m.p. 244°-246° C., pale yellow needles.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04415572 |
| Source dataset | uspto-grants-1983_11 |
| ORD ID | ord-3e68180ff4464aaa86dedbecef1e3e01 |
| Source note | uspto-grants-1983_11 |