HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → HCID 14423301, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 14423300 | HCID 14423300 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 14423301 | HCID 14423301 | — |
Reaction Steps
Reduce 6,8,9,10-tetrahydro-10-phenylbenzo[b] [1,8]naphthyridin-5,7-dione (2 mmol) with sodium borohydride (50 mg) in a solvent of ethanol (30 ml) and water (0.25 ml). After 15 minutes, pour the reaction mixture over ice and collect the resulting precipitate on a filter. Reserve the precipitate, and extract the aqueous filtrate with chloroform. Dry the extracts, evaporate the chloroform, and combine the residue with the reserved precipitate to give the product, 10-phenyl-7-hydroxy-6,7,8,9-tetrahydro-benzo[b] [1,8]naphthyridin-5(10H)-one, m.p. 283°-286° C. after crystallization from ethanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05126352 |
| Source dataset | uspto-grants-1992_06 |
| ORD ID | ord-e36b82c3497945678d0fe5fd9537c538 |
| Source note | uspto-grants-1992_06 |