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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 580281생성일: 2026년 10월 25일

Diethyl oxalacetate → Diethyl furo[3,2-b]pyridine-5,6-dicarboxylate

https://huagongshe.com/reaction/580281

반응식

참여 물질

역할이름HCID투입량
반응물Diethyl oxalacetateHCID 66951—
반응물3-Azidofuran-2-carbaldehydeHCID 4153776—
반응물3-Aminofuran-2-carbaldehydeHCID 12210211—
촉매PiperidineHCID 8082—
용매EthanolHCID 702—
생성물Diethyl furo[3,2-b]pyridine-5,6-dicarboxylateHCID 1375250424%

반응 단계

3-Amino-2-formylfuran, prepared from 3-azido-2-formylfuran (8.9 g 0.065 mol) is dissolved in ethanol and to this solution diethyl oxalacetate (12.23 g, 0.065 mol) and ten drops of piperidine are added. In addition pulverized 3 A° molecular sieve is added and the reaction stirred at 65°-60° C. for three hours, then additional diethyl oxalacetate (2.2 g) is added. The reaction is essentially complete after 12 hours at 55°-60° C. On cooling the reaction is filtered, and the filtrate concentrated and then dissolved in ethyl acetate, water washed, then brine washed, dried over anhydrous magnesium sulfate and stripped to dryness. The residue is dissolved in 3:1 hexane:ethyl acetate and passed through a flash chromatographic column in two stages. First it is filtered by vacuum through a four to five inch pad of silica from which the last three fractions containing the required product are collected and combined. These combined fractions are then passed through a six inch column eluting under pressure with ethyl acetate:hexane 3:1 and 2.1. Diethyl furo[3,2-b]pyridine-5,6-dicarboxylate 4.15 g (24%) is obtained after crystallization from hexane-ether, of mp 60°-64° C., and with a mass spectrum m/e of 264.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04752323
출처 데이터셋uspto-grants-1988_06
ORD IDord-658303faffc34e65b52fba38e477c186
출처 메모uspto-grants-1988_06