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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1042293Generated: October 31, 2026

6-bromo-7-methyl-8-nitroquinazolin-4(3H)-one → 8-amino-7-methylquinazolin-4(3H)-one

https://huagongshe.com/reaction/1042293

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-bromo-7-methyl-8-nitroquinazolin-4(3H)-oneHCID 135894579—
SolventEthanolHCID 702—
Product8-amino-7-methylquinazolin-4(3H)-oneHCID 135742263—

Reaction Steps

6-Bromo-7-methyl-8-nitroquinazolin-4(3H)-one (4.8 g, 17 mmol) was suspended in EtOH (500 ml) and degassed using a vacuum line. The mixture was then evacuated with nitrogen and 10% Pd/C (1.4 g) was added under a positive flow of nitrogen. The reaction was then placed under a hydrogen atmosphere with a large balloon while stirring. After 4 days, the reaction was filtered through a pad of celite. The filtrate was reduced under vacuum and the residue was triturated with ether to give 8-amino-7-methylquinazolin-4(3H)-one as an off white solid. MS Found: (ESI pos. ion) m/z 176 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08557830B2
Source datasetuspto-grants-2013_10
ORD IDord-55b717dc38ab4a9198acf8b84d5c1a2c
Source noteuspto-grants-2013_10