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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 43601생성일: 2026년 10월 23일

Methanol → cis(+/-)-Benzyl (1-carbamoyl-3-methoxypiperidin-4-yl)carbamate

https://huagongshe.com/ko/reaction/43601

반응식

참여 물질

역할이름HCID투입량
반응물MethanolHCID 887—
반응물Trimethylsilyl isocyanateHCID 70696—
반응물Hydrogen chloride-ethyl acetateHCID 21866389—
반응물tert-Butyl cis(+/-)-4-{[(benzyloxy)carbonyl]amino}-3-methoxypiperidine-1-carboxylateHCID 86648489—
용매Ethyl AcetateHCID 8857—
생성물cis(+/-)-Benzyl (1-carbamoyl-3-methoxypiperidin-4-yl)carbamateHCID 13173086081%

반응 단계

A 4 N hydrochloric acid/ethyl acetate solution (30 ml, 120 mmol) was added to a solution of tert-butyl cis(±)-4-{[(benzyloxy)carbonyl]amino}-3-methoxypiperidine-1-carboxylate obtained in Example (103a) in ethyl acetate (10 mL). The mixture was stirred for 45 minutes and the solvent was evaporated under reduced pressure. The residue was diluted with dichloromethane, washed with a 1 N aqueous sodium hydroxide solution and brine, dried over anhydrous magnesium sulfate, and then concentrated under reduced pressure. Trimethylsilyl isocyanate (0.86 g, 7.5 mmol) was added to the resulting residue, and the mixture was stirred at room temperature for 15 hours. Methanol (1 mL) was added, followed by stirring for 30 minutes. The precipitated solid was filtered off and washed with dichloromethane to obtain 1.44 g of the title compound as a colorless solid (81%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08536197B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-cdd9ad254116463698dae8d73b8a1ec2
출처 메모uspto-grants-2013_09