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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 577366Generated: October 28, 2026

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

https://huagongshe.com/reaction/577366

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 over 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-ylmethoxy)-3,4-dihydroquinazolin-4-one (12.7 g, 70%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09040548B2
Source datasetuspto-grants-2015_05
ORD IDord-02f708c26ba446c18d4565c5b8a75eaf
Source noteuspto-grants-2015_05