HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 14423306, compound → HCID 15135971, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 14423306 | HCID 14423306 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 15135971 | HCID 15135971 | — |
Reaction Steps
Charge a Paar bottle with 5,6-dihydro-3-hydroxy-12-phenyl-naphtho[1,2-b] [1,8]naphthyridin-7(12H)-one, an equal weight of 5% Pd on carbon, and ethanol. Pressurize the bottle with hydrogen to about 50 psi, and shake the contents in a Paar apparatus at 25° C. Monitor the progress of hydrogenation by pressure changes or by thin-layer chromatography. When hydrogen uptake ceases, remove catalyst by filtration and ethanol by evaporation. Crystallize the residue to obtain 5,6,8,9,10,11-hexahydro-3-hydroxy-12-phenyl-naphtho[1,2-b] [1,8]naphthyridin-7(12H)-one, m.p. >330° C. after crystallization from C2H5OH.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05126352 |
| Source dataset | uspto-grants-1992_06 |
| ORD ID | ord-5722c2240cc743219d2943445908dbab |
| Source note | uspto-grants-1992_06 |