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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 346558Generated: October 29, 2026

Ammonia → 6-Methoxy-7-((1-methylpiperidin-4-yl)methoxy)quinazolin-4(3H)-one

https://huagongshe.com/reaction/346558

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
Reactant6-Methoxy-7-(1-methylpiperidin-4-ylmethoxy)-3-((pivaloyloxy)methyl)-3,4-dihydroquinazolin-4-oneHCID 10993445—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
Product6-Methoxy-7-((1-methylpiperidin-4-yl)methoxy)quinazolin-4(3H)-oneHCID 13547037590.9%

Reaction Steps

A saturated solution of ammonia in methanol (14 ml) was added to a solution of 6-methoxy-7-(1-methylpiperidin-4-ylmethoxy)-3-((pivaloyloxy)methyl)-3,4-dihydroquinazolin-4-one (1.38 g, 3.3 mmol) in methanol (5 ml). After stirring for 20 hours at ambient temperature, the suspension was diluted with methylene chloride (10 ml). The solution was filtered. The filtrate was evaporated under vacuum and the residue was triturated with ether, collected by filtration, washed with ether and dried under vacuum to give 6-methoxy-7-(1-methylpiperidin-4-ylmethoxy)-3,4-dihydroquinazolin-4-one (910 mg, 83%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07173038B1
Source datasetuspto-grants-2007_02
ORD IDord-0aa21963222d4df18ec829592e358bc9
Source noteuspto-grants-2007_02