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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1010802Generated: October 30, 2026

Ethyl orthoformate → 7-Methoxy-6-benzyloxyquinazolone

https://huagongshe.com/reaction/1010802

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl orthoformateHCID 31214—
Reactant2-Amino-5-(benzyloxy)-4-methoxybenzamideHCID 59361904—
Product7-Methoxy-6-benzyloxyquinazoloneHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07977346B2
Source datasetuspto-grants-2011_07
ORD IDord-fbbf9a4ebf864caf9a2f212d3176c0c9
Source noteuspto-grants-2011_07