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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1110772Generated: November 2, 2026

Acetic Anhydride → 2-Acetylpyrrolo[3,4-g]quinoline

https://huagongshe.com/reaction/1110772

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantPotassium glycinateHCID 23673715—
ReactantPyrrolo[3,4-g]quinolineHCID 67915813—
Product2-Acetylpyrrolo[3,4-g]quinolineHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04977160
Source datasetuspto-grants-1990_12
ORD IDord-8edac2db2113489ca9ec51802ad705b3
Source noteuspto-grants-1990_12