HuagongsheHuagongshe Chemistry Print Report · For research reference only
Magnesium Bromide → 4-[(3-Chloro-2-fluorophenyl)amino]-7-hydroxyquinazoline-6-carbaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Magnesium Bromide | HCID 82241 | — |
| Reactant | 4-[(3-Chloro-2-fluorophenyl)amino]-7-methoxyquinazoline-6-carbaldehyde | HCID 11573492 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 4-[(3-Chloro-2-fluorophenyl)amino]-7-hydroxyquinazoline-6-carbaldehyde | HCID 136368411 | 100.6% |
Reaction Conditions
| Temperature | 130 °C |
|---|
Reaction Steps
Solid anhydrous magnesium bromide (3.66 g, 19.9 mmol) was carefully added to a stirred solution of 4-[(3-chloro-2-fluorophenyl)amino]-7-methoxyquinazoline-6-carbaldehyde (2.0 g, 6.04 mmol) in pyridine (30 ml) at room temperature. The resulting suspension was heated at 130° C. for 16 hours, cooled to room temperature and concentrated to dryness to give a yellow solid. This was suspended in water (100 ml), collected by filtration and washed several times with water. The resulting yellow solid was dried to a constant weight in a vacuum oven at 40° C. to give 4-[(3-chloro-2-fluorophenyl)amino]-7-hydroxyquinazoline-6-carbaldehyde, (1.93 g, 100%); Mass Spectrum: (M+H)+ 318.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07632840B2 |
| Source dataset | uspto-grants-2009_12 |
| ORD ID | ord-7b91894a25284a28a3c94f01ea21d098 |
| Source note | uspto-grants-2009_12 |