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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 43941생성일: 2026년 10월 24일

Cesium carbonate → Methyl cis(+/-)-5-(4-{[(benzyloxy)carbonyl]amino}-3-methoxypiperidin-1-yl)thiophene-2-carboxylate

https://huagongshe.com/ko/reaction/43941

반응식

참여 물질

역할이름HCID투입량
반응물Cesium carbonateHCID 10796—
반응물Ethyl 5-bromothiophene-2-carboxylateHCID 605723—
반응물Binap, (A+-)-HCID 634876—
반응물Benzyl cis(+/-)-[3-methoxypiperidin-4-yl]carbamateHCID 86648490—
촉매palladium(II) acetateHCID 167845—
용매TolueneHCID 1140—
용매Ethyl AcetateHCID 8857—
생성물Methyl cis(+/-)-5-(4-{[(benzyloxy)carbonyl]amino}-3-methoxypiperidin-1-yl)thiophene-2-carboxylateHCID 8664882360.4%

반응 조건

온도110 °C

반응 단계

A suspension of ethyl 5-bromothiophene-2-carboxylate obtained in Example (244a) (100 mg, 0.45 mmol), benzyl cis(±)-(3-methoxypiperidin-4-yl)-carbamate obtained in Example (40b) (143 mg, 0.54 mmol), palladium acetate (10 mg, 0.05 mmol), BINAP (28 mg, 0.05 mmol) and cesium carbonate (206 mg, 0.63 mmol) in toluene was stirred at 110° C. for 39 hours. The reaction solution was diluted with ethyl acetate, washed with water and brine, and then dried over anhydrous magnesium sulfate. Following filtration, the filtrate was concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (elution solvent: hexane/ethyl acetate=2/1) to obtain 110 mg of the title compound as a yellow oily substance (60%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08536197B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-bf2627a8c0c149f688c086ae44623de2
출처 메모uspto-grants-2013_09