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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 43824생성일: 2026년 10월 24일

Cesium carbonate → Methyl 3-(4-benzyloxycarbonylaminopiperidin-1-yl)benzoate

https://huagongshe.com/ko/reaction/43824

반응식

참여 물질

역할이름HCID투입량
반응물Cesium carbonateHCID 10796—
반응물Methyl 3-bromobenzoateHCID 12070—
반응물Binap, (A+-)-HCID 634876—
반응물4-Cbz-aminopiperidineHCID 1514304—
촉매palladium(II) acetateHCID 167845—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
용매1,4-DioxaneHCID 31275—
생성물Methyl 3-(4-benzyloxycarbonylaminopiperidin-1-yl)benzoateHCID 6840599826.6%

반응 조건

온도100 °C

반응 단계

Methyl 3-bromobenzoate (230 mg, 1.07 mmol), palladium acetate (12 mg, 0.054 mmol), BINAP (133 mg, 0.214 mmol) and cesium carbonate (767 mg, 2.35 mmol) were added to a solution of benzyl piperidin-4-yl-carbamate obtained in Example (192b) (248 mg, 0.817 mmol) in 1,4-dioxane (10 mL) and N,N-dimethylformamide (2.5 mL), and the mixture was stirred at 100° C. for 20 hours. The reaction solution was cooled, diluted with ethyl acetate, and washed with brine. The organic layer was dried over magnesium sulfate, and then the solvent was evaporated under reduced pressure. The resulting residue was purified by silica gel column chromatography (elution solvent: hexane/ethyl acetate=3/1) to obtain 80 mg of the title compound as a colorless oily substance (20%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08536197B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-2d442424469f4ef68a66b1df757b2b4d
출처 메모uspto-grants-2013_09