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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 43794생성일: 2026년 10월 24일

Cesium carbonate → Methyl cis(+/-)-3-(4-{[(benzyloxy)carbonyl]amino}-3-methoxypiperidin-1-yl)-4-fluorobenzoate

https://huagongshe.com/ko/reaction/43794

반응식

참여 물질

역할이름HCID투입량
반응물Cesium carbonateHCID 10796—
반응물Binap, (A+-)-HCID 634876—
반응물Methyl 3-bromo-4-fluorobenzoateHCID 7018022—
반응물Benzyl cis(+/-)-[3-methoxypiperidin-4-yl]carbamateHCID 86648490—
촉매palladium(II) acetateHCID 167845—
생성물Methyl cis(+/-)-3-(4-{[(benzyloxy)carbonyl]amino}-3-methoxypiperidin-1-yl)-4-fluorobenzoateHCID 8664874461.5%

반응 단계

The same operation as in Example (42a) was performed using benzyl cis(±)-[3-methoxypiperidin-4-yl]carbamate obtained in Example (160a) (100 mg, 0.38 mmol), methyl 3-bromo-4-fluorobenzoate (264 mg, 1.13 mmol), palladium acetate (25.5 mg, 0.11 mmol), BINAP (141 mg, 0.23 mmol) and cesium carbonate (370 mg, 1.13 mmol), to obtain 97.4 mg of the title compound as a yellow oily substance. mass spectrum (ESI): m/z 417 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08536197B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-255be12eceab457691cdb2f24f685f8f
출처 메모uspto-grants-2013_09