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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2093094생성일: 2026년 10월 27일

tert-Butyl 4-oxopiperidine-1-carboxylate → 5-Tert-butyl 2-ethyl 6,7-dihydro-1H-pyrrolo[3,2-C]pyridine-2,5(4H)-dicarboxylate

https://huagongshe.com/reaction/2093094

반응식

참여 물질

역할이름HCID투입량
반응물tert-Butyl 4-oxopiperidine-1-carboxylateHCID 735900—
반응물Lithium diisopropylamideHCID 2724682—
반응물Bromoethyl pyruvateHCID 86587973—
용매TetrahydrofuranHCID 8028—
생성물5-Tert-butyl 2-ethyl 6,7-dihydro-1H-pyrrolo[3,2-C]pyridine-2,5(4H)-dicarboxylateHCID 66864309—

반응 단계

A solution of N-boc-4-piperidone (1 eq.) and lithium di-isopropyl amide (1 eq.) in THF was stirred at −78° C. and for 2 hrs. A bromoethyl pyruvate (1.2 eq.) was added to above reaction mixture and stirred for 30 min. Reaction mixture was then quenched with ammonia solution and then extracted with ethyl acetate, dried over sodium sulphate and concentrated to dryness. The residue was then dissolved in dichoromethane and was added silica (100-200 mesh), stirred for overnight at room temperature. Crude was then purified by silica gel column chromatography to yield 5-tert-butyl 2-ethyl 1,4,6,7-tetrahydro-5H-pyrrolo[3,2-c]pyridine-2,5-dicarboxylate.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08440830B2
출처 데이터셋uspto-grants-2013_05
ORD IDord-6f708db8a9684e74b0489fe18c279fe5
출처 메모uspto-grants-2013_05