HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl orthoformate → 7-Methoxy-6-benzyloxyquinazolone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl orthoformate | HCID 31214 | — |
| Reactant | 2-Amino-5-(benzyloxy)-4-methoxybenzamide | HCID 59361904 | — |
| Product | 7-Methoxy-6-benzyloxyquinazolone | HCID 67138757 | — |
Reaction Steps
2-Amino-4-methoxy-5-benzyloxybenzamide (JMC, 20, 146) (5 g) was mixed with triethylorthoformate (15 ml) and refluxed overnight. The reaction solution was cooled and triturated with EtOAc (40 ml) then filtered to give 7-methoxy-6-benzyloxyquinazolone (3.2 g). This product was mixed with DIPEA (15 ml) and to the solution was added POCl3 (3 ml) slowly. The reaction mixture was refluxed for 30 minutes and cooled, then poured into a stirred mixture of ice and CHCl3. The solution was further extracted with CHCl3 three times and washed with H2O followed by brine, dried over Na2SO4 and evaporated to give a light brown solid as the chloride for next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07977346B2 |
| Source dataset | uspto-grants-2011_07 |
| ORD ID | ord-fbbf9a4ebf864caf9a2f212d3176c0c9 |
| Source note | uspto-grants-2011_07 |