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HRID 1465468생성일: 2026년 10월 27일

Ethyl Acetate → Tert-butyl 4-(6-cyanopyridin-3-yl)piperazine-1-carboxylate

https://huagongshe.com/reaction/1465468

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl AcetateHCID 8857—
반응물Potassium CarbonateHCID 11430—
반응물tert-Butyl piperazine-1-carboxylateHCID 143452—
반응물5-Bromopyridine-2-carbonitrileHCID 817154—
용매DimethylformamideHCID 6228—
생성물Tert-butyl 4-(6-cyanopyridin-3-yl)piperazine-1-carboxylateHCID 6703021174%

반응 조건

온도120 °C

반응 단계

To a solution of 5-bromopyridine-2-carbonitrile (551.3 mg, 3.012 mmol) in anhydrous dimethylformamide (6.0 ml) were added tert-butyl piperazine-1-carboxylate (670.6 mg, 3.601 mmol) and potassium carbonate (829.0 mg, 5.998 mmol). The mixture was stirred at 120° C. for 63 hrs and cooled to room temperature. Ethyl acetate (30 ml) was added, and the precipitate was collected by filtration. Water (30 ml) was added to the filtrate, and the precipitated solid was collected by filtration and dried under reduced pressure to give tert-butyl 4-(6-cyanopyridin-3-yl)piperazine-1-carboxylate (642.9 mg, yield 74.0%) as a slightly yellow solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08999989B2
출처 데이터셋uspto-grants-2015_04
ORD IDord-a5d1d698b94045d8850b11c2a3c02f10
출처 메모uspto-grants-2015_04