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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 43650생성일: 2026년 10월 25일

Ammonium formate → Tert-butyl cis(+/-)-4-amino-3-ethoxypiperidine-1-carboxylate

https://huagongshe.com/reaction/43650

반응식

참여 물질

역할이름HCID투입량
반응물Ammonium formateHCID 2723923—
반응물tert-Butyl cis(+/-)-4-(benzylamino)-3-ethoxypiperidine-1-carboxylateHCID 86648597—
촉매PalladiumHCID 23938—
용매MethanolHCID 887—
생성물Tert-butyl cis(+/-)-4-amino-3-ethoxypiperidine-1-carboxylateHCID 8664846777.1%

반응 단계

The same operation as in Example (90d) was performed using tert-butyl cis(±)-4-(benzylamino)-3-ethoxypiperidine-1-carboxylate obtained in Example (112c) (4.06 g, 12.1 mmol), 10% Pd/C (wet, 1.1 g), ammonium formate (2.87 g, 46 mmol) and methanol (30 mL), to obtain 2.28 g of the title compound as a colorless oily substance (94%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08536197B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-cc414890987a4abf9952ae6799d223db
출처 메모uspto-grants-2013_09