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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 434299생성일: 2026년 10월 25일

3-Boc-2,2-dimethyloxazolidine-4-carboxaldehyde, (R)-(+)- → (S)-4-[4-(4-chloro-benzoyl)-piperidin-1-ylmethyl]-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/434299

반응식

참여 물질

역할이름HCID투입량
반응물3-Boc-2,2-dimethyloxazolidine-4-carboxaldehyde, (R)-(+)-HCID 178792—
반응물4-(4-Chlorobenzoyl)PiperidineHCID 2777115—
반응물Sodium triacetoxyborohydrideHCID 5049666—
용매TetrahydrofuranHCID 8028—
생성물(S)-4-[4-(4-chloro-benzoyl)-piperidin-1-ylmethyl]-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl esterHCID 68809159—

반응 단계

To a solution of (R)4-formyl-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester (0.5 g, 2.18 mmol) in tetrahydrofuran (15 ml) is added (4-chloro-phenyl)-piperidin-4-yl-methanone (0.49 g, 2.18 mmol) and sodium triacetoxyborohydride (0.69 g, 3.27 mmol), and the reaction mixture stirred for 3.5 hours at ambient temperature. The solvent is evaporated and the residue partitioned between ethyl acetate (50 ml) and saturated sodium bicarbonate solution (50 ml). The ethyl acetate is dried over magnesium sulphate and evaporated. The crude product is purified by flash silica chromatography (ethyl acetate:hexane, 1:1 elution) to afford (S)-4-[4-(4-chloro-benzoyl)-piperidin-1-ylmethyl]-2,2-dimethyl-oxazoldine-3-carboxylic acid tert-butyl ester, [MH]+437.2.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06670379B2
출처 데이터셋uspto-grants-2003_12
ORD IDord-289e5a0a2c844c5689bd9fe851d1b3ea
출처 메모uspto-grants-2003_12