HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → 2-Acetylpyrrolo[3,4-g]quinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Potassium glycinate | HCID 23673715 | — |
| Reactant | Pyrrolo[3,4-g]quinoline | HCID 67915813 | — |
| Product | 2-Acetylpyrrolo[3,4-g]quinoline | HCID 67915768 | — |
Reaction Steps
The pyrrolo[3,4-g]quinoline derivatives of formula (1) and (2) are prepared by reacting a 7-dimethylaminomethylene-6-oxo-trans-quinoline derivative of formula (7a) or (7b) with potassium glycinate, followed by treatment of the thus formed intermediate product with acetic anhydride. This yields a 2-acetylpyrrolo[3,4-g]quinoline compound. The acetyl group is removed by basic hydrolysis, for example using sodium ethoxide in ethanol. Preparation of the pyrrolo[3,4-g]quinolines of formula (1) is illustrated in Reaction Scheme III: ##STR18## The pyrrolo[3,4-g]quinolines of formula (2) are prepared using the same procedures and starting materials of formula (7b).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04977160 |
| Source dataset | uspto-grants-1990_12 |
| ORD ID | ord-8edac2db2113489ca9ec51802ad705b3 |
| Source note | uspto-grants-1990_12 |