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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 80635생성일: 2026년 10월 25일

Sodium hydride → 4-(3-Methoxycarbonyl-[1,2,4]triazol-1-yl)-piperidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/80635

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물1-(tert-Butoxycarbonyl)-4-(methanesulfonyloxy)piperidineHCID 4184869—
반응물HCID 178418794HCID 178418794—
용매DimethylformamideHCID 6228—
생성물4-(3-Methoxycarbonyl-[1,2,4]triazol-1-yl)-piperidine-1-carboxylic acid tert-butyl esterHCID 57708407—

반응 단계

To a solution of 1H-[1,2,4]triazole-3-carboxylic acid ethyl ester (1.05 g, 8.23 mmol) in dimethylformamide (50 mL) was added sodium hydride (60%, 0.395 g, 9.88 mmol). The solution was stirred at room temperature for 20 minutes followed by 1 hour at 70° C. 4-methanesulfonyloxy-piperidine-1-carboxylic acid tert-butyl ester (2.3 g, 8.23 mmol) was then added in a single portion and heated at 70° C. for 40 hours. The solution was cooled to 0° C. and the salt precipitate was removed by filtration. The filtrate was diluted with dichloromethane and washed with water, brine, dried over sodium sulfate, filtered and concentrated in vacuo. The residue was purified by flash chromatograph on silica gel with Hexanes and EtOAc to afford the desired product. 1H NMR (CDCl3): δ 8.18 (1H, s), 4.40 (1H, m), 4.22 (2H, m), 3.96 (3H, s), 2.82 (2H, m), 2.12 (2H, m), 1.94 (2H, m), 1.41 (9H, s).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08846675B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-c6ee8b84d5e34e3ea897045e3e8729c8
출처 메모uspto-grants-2014_09