HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formic Acid → HCID 86733651, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formic Acid | HCID 284 | — |
| Reactant | HCID 86733645 | HCID 86733645 | — |
| Product | HCID 86733651 | HCID 86733651 | — |
Reaction Steps
2,1 g of cis-6-(4-aminophenyl)-8,9-dimethoxy-2-methyl-1,2,3,4,4a,10b-hexahydro-benzo[c][1,6] naphthyridine are heated to 100° for 21/2 hours in 50 ml of 90% formic acid. The reaction solution is evaporated to dryness in a vacuum, the resulting residue is made alkaline with a dilute potash solution and this aqueous phase is extracted with methylene chloride. After drying and concentrating the organic phase by evaporation, the title compound is obtained as a yellow oil and crystallizes after the addition of ethanol in the form of yellowish prisms having a melting point of 140°-145°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03966938 |
| Source dataset | uspto-grants-1976_06 |
| ORD ID | ord-f99931aa2c1e4b62b8ce03c23c378b4d |
| Source note | uspto-grants-1976_06 |