HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 21408185, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 21408197 | HCID 21408197 | — |
| Product | HCID 21408185 | HCID 21408185 | — |
Reaction Steps
10-amino-6,7-dihydro-5-methyl-1,7-dioxo-1H,5H-benzo[ij]quinolizine-2-carboxylic acid (0.02 mole) and acetic anhydride (50 ml.) are stirred and heated on a steam bath for 3 hours. After cooling, the solid precipitate is separated by filtration to give 10-acetamido-6,7-dihydro-5-methyl-1,7-dioxo-1H,5H-benzo[ij]quinolizine-2-carboxylic acid. This product is reduced using sodium borohydride to provide 10-acetamido-6,7-dihydro-7-hydroxy-5-methyl-1-oxo-1H,5H-benzo[ij]quinolizine-2-carboxylic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03985753 |
| Source dataset | uspto-grants-1976_10 |
| ORD ID | ord-c14aae5273334ed4ad682168a19c06b2 |
| Source note | uspto-grants-1976_10 |