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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 520815생성일: 2026년 10월 26일

Potassium Carbonate → 3-[2-(1-t-Butyloxycarbonyl piperidin-4-yloxy)pyridin-5-yl]-1-(morpholin-4-yl)prop-2-ene-1-one

https://huagongshe.com/reaction/520815

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물AcryloylmorpholineHCID 98723—
반응물tert-Butyl 4-((5-bromopyridin-2-yl)oxy)piperidine-1-carboxylateHCID 21914479—
촉매palladium(II) acetateHCID 167845—
용매DimethylformamideHCID 6228—
생성물3-[2-(1-t-Butyloxycarbonyl piperidin-4-yloxy)pyridin-5-yl]-1-(morpholin-4-yl)prop-2-ene-1-oneHCID 9004272291.5%

반응 단계

A solution of t-butyl 4-(5-bromo pyridin-2-yloxy)piperidine-1-carboxylate (1 gram, 2.80 mmoles), 4-acryloylmorpholine (0.63 gram, 4.46 mmoles), palladium acetate (13 mg, 0.061 mmoles) tri(o-tolyl)phosphine (25.6 mg, 0.084 mmoles) and potassium carbonate (0.62 g, 4.49 mmoles) in DMF (15 mL) was stirred for 3 hours at 140° C. The progress of the reaction was monitored by thin layer chromtography. After completion of reaction, the mass was quenched on to chilled water (30 mL) and the product was extracted with ethyl acetate (3×15 mL). The resulting organic layer was washed with water, dried over sodium sulfate and concentrated under vacuum. The residue, thus obtained, was purified by flash chromatography using ethyl acetate:n-hexane in the ratio of 1:1 to afford the title compound (1.07 grams).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09328092B2
출처 데이터셋uspto-grants-2016_05
ORD IDord-68b517314f804299a5a85ee2f2a0fa9c
출처 메모uspto-grants-2016_05