HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 5-Bromo-3,4-dihydro-3-methylquinazolin-2(1H)-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Triphosgene | HCID 94429 | — |
| Reactant | 3-Bromo-2-methylaminomethyl-phenylamine | HCID 18444472 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-Bromo-3,4-dihydro-3-methylquinazolin-2(1H)-one | HCID 18444524 | — |
Reaction Steps
To a solution of 3-bromo-2-methylaminomethyl-phenylamine (1.153 g, 5.36 mmol) in CH2Cl2 (50 ml) was added NEt3 (1.5 ml, 10.76 mmol), triphosgen (555 mg, 1.87 mmol) at 0° C. The reaction was allowed to warm up to room temperature and stirred overnight. After the solvent was removed by using a rotary evaporator, the residue was partitioned between water and ethyl acetate. The organic layer was washed by H2O and brine. After drying over MgSO4, the organic fraction was concentrated in vacuo and resulting brown residue was purified by flash chromatography to give 5-bromo-3-methyl-3,4-dihydro-1H-quinazolin-2-one as white solid. (650 mg, 50%) MS: (M+H)+241.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07196087B2 |
| Source dataset | uspto-grants-2007_03 |
| ORD ID | ord-ef3d47313db143598ad2f5c41dde1193 |
| Source note | uspto-grants-2007_03 |