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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 241837Generated: October 25, 2026

Ethyl 1-benzyl-4-oxopiperidine-3-carboxylate hydrochloride → 6-benzyl-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidin-4(3H)-one

https://huagongshe.com/reaction/241837

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 1-benzyl-4-oxopiperidine-3-carboxylate hydrochlorideHCID 102623—
ReactantFormamidine acetateHCID 160693—
ReactantSodium MethoxideHCID 10942334—
SolventMethanolHCID 887—
Product6-benzyl-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidin-4(3H)-oneHCID 13559293564.6%

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) was heated at 85° C. for 16 hour in a 350 mL sealed reaction vessel. The mixture was allowed to cool and concentrated 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 numberUS08653091B2
Source datasetuspto-grants-2014_02
ORD IDord-2aee3a8fb4a84937a78c3e3c776d8e6e
Source noteuspto-grants-2014_02