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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 43478생성일: 2026년 10월 25일

Hydrogen chloride-ethyl acetate → Benzyl cis(+/-)-[3-methoxypiperidin-4-yl]carbamate

https://huagongshe.com/reaction/43478

반응식

참여 물질

역할이름HCID투입량
반응물Hydrogen chloride-ethyl acetateHCID 21866389—
반응물tert-Butyl cis(+/-)-4-{[(benzyloxy)carbonyl]amino}-3-methoxypiperidine-1-carboxylateHCID 86648489—
용매MethanolHCID 887—
생성물Benzyl cis(+/-)-[3-methoxypiperidin-4-yl]carbamateHCID 86648490—

반응 단계

tert-Butyl cis(±)-4-{[(benzyloxy)carbonyl]amino}-3-methoxypiperidine-1-carboxylate obtained in Example (40a) (4.28 g, 11.7 mmol) was dissolved in methanol (20 mL). A 4 N hydrochloric acid/ethyl acetate solution (60 mL) was added, and the mixture was stirred at room temperature for 40 minutes. The reaction solution was concentrated under reduced pressure and then saturated aqueous sodium bicarbonate solution was added, followed by extraction with THF. The organic layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure. The resulting compound was used for the next reaction without purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08536197B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-c180fdccb7534d8fabcb7c4c30439f79
출처 메모uspto-grants-2013_09