HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → 3-(2,6-dimethoxybenzyl)-6-hydroxy-3H-quinazolin-4-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-(Bromomethyl)-1,3-dimethoxybenzene | HCID 15556958 | — |
| Reactant | 3,4-Dihydro-6-hydroxy-4-oxoquinazoline | HCID 135489577 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-(2,6-dimethoxybenzyl)-6-hydroxy-3H-quinazolin-4-one | HCID 19605768 | — |
Reaction Steps
76 mg of sodium hydride (80% in mineral oil) are added to a suspension of 400 mg of 6-hydroxy-3H-quinazolin-4-one in 20 ml of dry dimethylformamide. After stirring for 30 minutes at room temperature, 560 mg of 2,6-dimethoxybenzylbromide are added, and stirring is continued overnight. The solvent is distilled off in vacuo, and the residue partitioned between aqueous pH7-buffer solution and ethyl acetate. The organic phase is separated, dried over magnesium sulfate and evaporated in vacuo. Silica gel chromatography yields a minor amount of the N,O-bis-alkylated product followed by the pure title compound as colourless crystals. mp: 243-245°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05990116 |
| Source dataset | uspto-grants-1999_11 |
| ORD ID | ord-986f5b48d98b426ea1185b247b3c2d8d |
| Source note | uspto-grants-1999_11 |