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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 225475생성일: 2026년 10월 25일

Dimethylformamide dimethyl acetal → tert-butyl 3-[(dimethylamino)methylene]-4-oxotetrahydro-1(2H)-pyridinecarboxylate

https://huagongshe.com/reaction/225475

반응식

참여 물질

역할이름HCID투입량
반응물Dimethylformamide dimethyl acetalHCID 78373—
반응물tert-Butyl 4-oxopiperidine-1-carboxylateHCID 735900—
생성물tert-butyl 3-[(dimethylamino)methylene]-4-oxotetrahydro-1(2H)-pyridinecarboxylateHCID 53395404—

반응 단계

A mixture of 1-tert-butoxycarbonyl piperidine-4-one and N,N-dimethylformamide dimethylacetal was stirred for 6 hours heated to reflux to give 1-tert-butoxycarbonyl-3-[(dimethylamino)methylene]piperidine-4-one. A mixture of the obtained 1-tert-butoxycarbonyl-3-[(dimethylamino)methylene]piperidine-4-one, 2-hydrazinoethanol and MeOH was stirred for two hours heated to reflux to give a mixture of 2-(5-tert-butoxycarbonyl-4,5,6,7-tetrahydro-2H-pyrazolo[4,3-c]pyridine-2-yl)ethanol and 2-(5-tert-butoxycarbonyl-4,5,6,7-tetrahydro-1H-pyrazolo[4,3-c]pyridine-1-yl)ethanol. A mixture of the obtained mixture, 4M HCl-EtOAc solution and EtOH was stirred for two hours at room temperature to give a mixture of 2-(4,5,6,7-tetrahydro-2H-pyrazolo[4,3-c]pyridine-2-yl)ethanol dihydrochloride and 2-(4,5,6,7-tetrahydro-1H-pyrazolo[4,3-c]pyridine-1-yl)ethanol dihydrochloride.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07557112B2
출처 데이터셋uspto-grants-2009_07
ORD IDord-953adb0e737a46aaa32b36c89166e09a
출처 메모uspto-grants-2009_07