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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 535343Generated: October 30, 2026

Acetic Acid → 6-benzyl-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidin-4(3H)-one

https://huagongshe.com/reaction/535343

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantEthyl 1-benzyl-4-oxopiperidine-3-carboxylate hydrochlorideHCID 102623—
ReactantFormamidine acetateHCID 160693—
ReactantSodium MethoxideHCID 10942334—
SolventMethanolHCID 887—
SolventSodium HydroxideHCID 14798—
Product6-benzyl-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidin-4(3H)-oneHCID 135592935—

Reaction Conditions

Temperature85 °C

Reaction Steps

A mixture of ethyl 1-benzyl-4-oxopiperidine-3-carboxylate hydrochloride (50.0 g, 0.168 mol), formamidine acetate (16.2 g, 0.201 mol), 4.37 M of sodium methoxide in methanol (190 mL) and methanol (200 mL, 5 mol) was heated to 85° C. for 16 hour in a 350 ml sealed reaction vessel. The mixture was allowed to cool and reduced in vacuo. The residue was dissolved in 1N NaOH (150 ml) and poured over ice. Glacial acetic acid was added to the mixture until the pH of the mixture was 7 and a tan solid precipitated out the solid was filtered, washed with water and cold ether, and dried on high vacuum to yield the title compound as a tan solid; (26.2 g, 61.4%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08859545B2
Source datasetuspto-grants-2014_10
ORD IDord-2fd67665d17644f8881f2e4abf84d66b
Source noteuspto-grants-2014_10