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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 20233생성일: 2026년 10월 25일

Triethylamine → Benzyl 4-(4-methyl-2-oxotetrahydropyrimidin-1(2H)-yl)piperidin-1-carboxylate

https://huagongshe.com/reaction/20233

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Benzyl 4-isocyanatopiperidine-1-carboxylateHCID 2776273—
반응물4-Bromobutan-2-amine hydrobromideHCID 13555988—
반응물Potassium tert-butoxideHCID 23665647—
용매AcetonitrileHCID 6342—
용매TetrahydrofuranHCID 8028—
생성물Benzyl 4-(4-methyl-2-oxotetrahydropyrimidin-1(2H)-yl)piperidin-1-carboxylateHCID 6842047962%

반응 단계

A solution of benzyl 4-isocyanatopiperidin-1-carboxylate (0.26 g) in acetonitrile (10 mL) was added to a solution of 4-bromobutan-2-amine hydrobromide (0.17 g) and triethylamine (0.10 g) in acetonitrile (10 mL), followed by stirring at room temperature for one hour. Potassium tert-butoxide (0.29 g) and THF (20 mL) were added thereto, and the mixture was further stirred at room temperature for 15 hours. The reaction mixture was concentrated under reduced pressure, and the residue was diluted with water, and extracted with ethyl acetate. The extract was washed with water and saturated saline solution and dried over anhydrous sodium sulfate, and the solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate to ethyl acetate/methanol=10/1) to obtain the title compound (0.15 g, 45%) as a light brown solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07745623B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-dd0ca6057de441808d4ef09f4c6f81e1
출처 메모uspto-grants-2010_06