HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Bromoethanol → 3-(2-hydroxyethyl)-6,7-dimethoxy-4(3H)-quinazolinone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Bromoethanol | HCID 10898 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4(1H)-Quinazolinone | HCID 135408753 | — |
| Reactant | 6,7-Dimethoxy-3H-quinazolin-4-one | HCID 135495016 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 3-(2-hydroxyethyl)-6,7-dimethoxy-4(3H)-quinazolinone | HCID 22326622 | — |
Reaction Steps
3-(2-hydroxyethyl)-6,7-dimethoxy-4(3H)-quinazolinone was prepared from 6,7-dimethoxy-4(3H)-quinazolinone (3 g, 14.6 mmol). The quinazolinone was combined with 2-bromoethanol (1.14 mL, 16 mmol), an excess of potassium carbonate (10 g) and heated at reflux in 200 mL acetone. The salts were filtered off and the reaction mixture was concentrated. The residue was dissolved in chloroform and washed with water. The organic layer was dried over Na2SO4, filtered and concentrated, 1.39 g (38%); light brown powder; m.p. 130° C., MS: 250.9 (M+H)+
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06939870B2 |
| Source dataset | uspto-grants-2005_09 |
| ORD ID | ord-148648d487d3477688478062c7640de7 |
| Source note | uspto-grants-2005_09 |