Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | HCID 22750105 | HCID 22750105 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 22750110 | HCID 22750110 | — |
Reaction Steps
A stream of ammonia is passed into a solution of 4-ethoxy-10-nitro-7-oxo-7H-indolizino[7,6,5-de]isoquinoline (5 g) in pyridine (200 cc) until the solution is saturated. The solution obtained is then stirred at a temperature of about 20° C. for 16 hours. The resulting suspension of red crystals is poured into iced water (600 cc). The crystalline precipitate is filtered off and then washed successively with water (5 × 10 cc), ethanol (3 × 10 cc) and then diethyl ether (2 × 20 cc). After drying under reduced pressure (1 mm Hg) at 25° C., 4-amino-10-nitro-7-oxo-7H-indolizino[7,6,5-de]-isoquinoline (4.18 g) is obtained in the form of orange-red crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04137315 |
|---|
| Source dataset | uspto-grants-1979_01 |
|---|
| ORD ID | ord-bd5103d2340f48fd8375cd408b2ac33d |
|---|
| Source note | uspto-grants-1979_01 |
|---|