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HRID 241837생성일: 2026년 10월 27일

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

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl 1-benzyl-4-oxopiperidine-3-carboxylate hydrochlorideHCID 102623—
반응물Formamidine acetateHCID 160693—
반응물Sodium MethoxideHCID 10942334—
용매MethanolHCID 887—
생성물6-benzyl-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidin-4(3H)-oneHCID 13559293564.6%

반응 조건

온도85 °C

반응 단계

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%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08653091B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-2aee3a8fb4a84937a78c3e3c776d8e6e
출처 메모uspto-grants-2014_02