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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1791549Generated: November 1, 2026

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

https://huagongshe.com/reaction/1791549

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormamidine acetateHCID 160693—
ReactantEthyl 2-amino-5-methoxy-4-((1-methylpiperidin-4-yl)methoxy)benzoateHCID 21874813—
Solvent2-MethoxyethanolHCID 8019—
Product6-Methoxy-7-((1-methylpiperidin-4-yl)methoxy)quinazolin-4(3H)-oneHCID 13547037583.7%

Reaction Conditions

Temperature115 °C

Reaction Steps

A solution of ethyl 6-amino-3-methoxy-4-(1-methylpiperidin-4-ylmethoxy)benzoate (16.1 g, 50 mmol) in 2-methoxyethanol (160 ml) containing formamidine acetate (5.2 g, 50 mmol) was heated at 115° C. for 2 hours. Formamidine acetate (10.4 g, 100 mmol) was added in portions every 30 minutes during 4 hours. Heating was prolonged for 30 minutes after the last addition. After cooling, the volatiles were removed under vacuum. The solid was dissolved in ethanol (100 ml) and methylene chloride (50 ml). The precipitate was removed by filtration and the filtrate was concentrated to a final volume of 100 ml. The suspension was cooled to 5° C. and the solid was collected by filtration, washed with cold ethanol followed by ether and dried under vacuum overnight at 60° C. to give 6-methoxy-7-((1-methylpiperidin-4-yl)methoxy)-3,4-dihydroquinazolin-4-one (12.7 g, 70%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07074800B1
Source datasetuspto-grants-2006_07
ORD IDord-1e7f1c8f0d364e399633d11e965d2672
Source noteuspto-grants-2006_07