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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1374689생성일: 2026년 10월 25일

Dihydropyrimidine → Boc piperidine dihydropyrimidine

https://huagongshe.com/reaction/1374689

반응식

참여 물질

역할이름HCID투입량
반응물DihydropyrimidineHCID 1056—
반응물PiperidineHCID 8082—
반응물Sodium hydrideHCID 24758—
반응물2-Methoxy-6-methyl-4-(3-chloro-phenyl)-1,4-dihydro-pyrimidine-5-carboxylic acid isopropyl esterHCID 14801742—
반응물tert-Butyl 4-(bromomethyl)piperidine-1-carboxylateHCID 15512811—
촉매Tetrabutylammonium IodideHCID 67553—
용매DimethylformamideHCID 6228—
생성물Boc piperidine dihydropyrimidineHCID 8659664929%

반응 단계

Tetrabutyl ammonium iodide (0.39 mmol) was added to a solution of N-Boc 4-bromomethyl piperidine (0.58 mmol; prepared as described in Bioorganic and Medicinal Chemistry Letters, 9, 2615, (1999)) in dimethylformamide (1 ml) at ambient temperature for 20 minutes. In a second vessel, NaH (0.47 mmol) was added to a solution of 2-methoxy-6-methyl-4-(3-chloro-phenyl)-1,4-dihydro-pyrimidine-5-carboxylic acid isopropyl ester (0.39 mmol) in dimethylformamide (1 ml) at ambient temperature and stirred for 20 minutes. The piperidine solution was then added to the dihydropyrimidine solution and stirred for approximately 2 hours. The reaction was quenched by addition of water, diluted with ethyl acetate, and subsequently washed with water and brine solution. The acetate layer was dried over anhydrous sodium sulfate and concentrated in vacuo. The resulting material was purified via silica gel chromatography utilizing 20% ethyl acetate/hexanes eluent affording the corresponding N Boc piperidine dihydropyrimidine intermediate 195A in 29% yield.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07166603B2
출처 데이터셋uspto-grants-2007_01
ORD IDord-eea2b5cbb7f943a5b718ebdf7413e211
출처 메모uspto-grants-2007_01