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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1421050Generated: October 26, 2026

6-methoxy-7-(2-(N-methyl-N-(6-methylpyrimidin-4-yl)amino)ethoxy)-3-((pivaloyloxy)methyl)-3,4-dihydroquinazolin-4-one → 6-methoxy-7-(2-(N-methyl-N-(6-methylpyrimidinyl)amino)ethoxy)-3,4-dihydroquinazolin-4-one

https://huagongshe.com/reaction/1421050

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-methoxy-7-(2-(N-methyl-N-(6-methylpyrimidin-4-yl)amino)ethoxy)-3-((pivaloyloxy)methyl)-3,4-dihydroquinazolin-4-oneHCID 22625087—
SolventAmmoniaHCID 222—
Product6-methoxy-7-(2-(N-methyl-N-(6-methylpyrimidinyl)amino)ethoxy)-3,4-dihydroquinazolin-4-oneHCID 135744735183.1%

Reaction Steps

A solution of 6-methoxy-7-(2-(N-methyl-N-(6-methylpyrimidin-4-yl)amino)ethoxy)-3-((pivaloyloxy)methyl)-3,4-dihydroquinazolin-4-one (365 mg, 0.8 mmol) in methanolic ammonia (30 ml of a 3M solution) was stirred at ambient temperature for 16 hours. The volatiles were removed by evaporation, the residue was triturated with ether, the solid was collected by filtration, washed with ether and dried under vacuum to give 6-methoxy-7-(2-(N-methyl-N-(6-methylpyrimidinyl)amino)ethoxy)-3,4-dihydroquinazolin-4-one (250 mg, 92%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06071921
Source datasetuspto-grants-2000_06
ORD IDord-24b99ac54d214b8aadee2b5423c51edb
Source noteuspto-grants-2000_06