HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → Benafentrine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 86733645 | HCID 86733645 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | Benafentrine | HCID 3084603 | — |
Reaction Steps
1.0 g of cis-6-(4-aminophenyl)-1,2,3,4,4a,10b-hexahydro-8,9-dimethoxy-2-methyl-benzo[c][1,6]naphthyridine (produced as in Example 5) is heated to 60° in a mixture of 2 cc of pyridine and 2 cc of acetic anhydride for 2 hours. The reaction mixture is then evaporated to dryness in a vacuum and the residue is crystallized from acetone. M.P. 173°-175°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03966938 |
| Source dataset | uspto-grants-1976_06 |
| ORD ID | ord-8c740cdc30ba4804a2cf37abeb9dbb7d |
| Source note | uspto-grants-1976_06 |