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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1425262생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1425262

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08927588B2
출처 데이터셋uspto-grants-2015_01
ORD IDord-ce39f08fe00e4433aea11174ec7b1f40
출처 메모uspto-grants-2015_01