HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → Pyrrolo(4,3,2-de)(1,2,4)triazolo(3,4-a)isoquinoline, 4,6-dihydro-8-methyl-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Pyrrolo(4,3,2-de)isoquinolin-5(1H)-one, 3,4-dihydro-, hydrazone, monohydrochloride | HCID 3041086 | — |
| Product | Pyrrolo(4,3,2-de)(1,2,4)triazolo(3,4-a)isoquinoline, 4,6-dihydro-8-methyl- | HCID 3041158 | — |
Reaction Steps
5-Hydrazino-1,3-dihydropyrrolo[4,3,2-de]isoquinoline hydrochloride (50 mg), described in Example 8, is heated at reflux with 3 ml of acetic anhydride for 2 hours. The mixture is cooled and then poured into a saturated solution of sodium bicarbonate. The resulting precipitate is collected and then dissolved in methanol. This solution is rendered acidic by the addition of HCl in ether. The mixture is treated with charcoal and concentrated to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03978066 |
| Source dataset | uspto-grants-1976_08 |
| ORD ID | ord-a7bb1d60d56f46199cfb1b62a51a5100 |
| Source note | uspto-grants-1976_08 |