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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 43972생성일: 2026년 10월 25일

Cesium carbonate → Ethyl cis(+/-)-3-(4-{benzyl[(benzyloxy)carbonyl]amino}-3-methoxypiperidin-1-yl)-5-methylbenzoate

https://huagongshe.com/reaction/43972

반응식

참여 물질

역할이름HCID투입량
반응물Cesium carbonateHCID 10796—
반응물1,4-DioxaneHCID 31275—
반응물Ethyl 3-bromo-5-methylbenzoateHCID 20086624—
반응물Benzyl benzyl[cis(+/-)-3-methoxypiperidin-4-yl]carbamateHCID 86712358—
촉매palladium(II) acetateHCID 167845—
용매DimethylformamideHCID 6228—
생성물Ethyl cis(+/-)-3-(4-{benzyl[(benzyloxy)carbonyl]amino}-3-methoxypiperidin-1-yl)-5-methylbenzoateHCID 8664885358.1%

반응 단계

The same operation as in Example (42a) was performed using benzyl benzyl[cis (±)-3-methoxypiperidin-4-yl] carbamate obtained in Example (259c) (150 mg, 0.42 mmol), ethyl 3-bromo-5-methylbenzoate obtained in Example (259e) (103 mg, 0.42 mmol), palladium acetate (10 mg, 0.04 mmol), (±)-BINAP (53 mg, 0.08 mmol), cesium carbonate (303 mg, 0.93 mmol), 1,4-dioxane (6 mL) and DMF (1.5 mL), to obtain 126 mg of the title compound as a yellow oily substance (57%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08536197B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-c6bb4212968e4789aba76182a35e8fc8
출처 메모uspto-grants-2013_09