HuagongsheHuagongshe Chemistry Print Report · For research reference only
6-bromo-7-methyl-8-nitroquinazolin-4(3H)-one → 8-amino-7-methylquinazolin-4(3H)-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 6-bromo-7-methyl-8-nitroquinazolin-4(3H)-one | HCID 135894579 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 8-amino-7-methylquinazolin-4(3H)-one | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08557830B2 |
| Source dataset | uspto-grants-2013_10 |
| ORD ID | ord-55b717dc38ab4a9198acf8b84d5c1a2c |
| Source note | uspto-grants-2013_10 |