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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 561834생성일: 2026년 10월 26일

Sodium Carbonate → N-Cyclopropyl-2,6-bis[(1E)-3-methoxyprop-1-en-1-yl]isonicotinamide

https://huagongshe.com/reaction/561834

반응식

참여 물질

역할이름HCID투입량
반응물Sodium CarbonateHCID 10340—
반응물TriphenylphosphineHCID 11776—
반응물2-[(1E)-3-methoxyprop-1-en-1-yl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolaneHCID 16217443—
반응물2,6-Dichloro-N-cyclopropylisonicotinamideHCID 21510026—
촉매Palladium bromide (PdBr2)HCID 83469—
용매DimethylformamideHCID 6228—
생성물N-Cyclopropyl-2,6-bis[(1E)-3-methoxyprop-1-en-1-yl]isonicotinamideHCID 66761510—

반응 조건

온도100 °C

반응 단계

To a solution of 2,6-dichloro-N-cyclopropylisonicotinamide from Amine 41, Step 1 (I eq.) in DMF (0.08 M) was added (2-[(1E)-3-methoxyprop-1-en-1-yl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (2.7 eq.), palladium bromide (5% loading), triphenylphosphine (10% loading) and sodium carbonate (2 M aqueous solution, 5 eq.). The resulting suspension was heated at 100° C. for 8 h. The reaction mixture was quenched with water and extracted with ether. The combined organic extracts were washed with sat. aq. NaHCO3 and brine. Drying over Na2SO4, filtration and concentration of the filtrate in vacuo afforded the crude product as a red oil. Purification by way of column chromatography (SiO2, 1:1 (v/v) Hex:EtOAc) afforded the title compound as a yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08063105B2
출처 데이터셋uspto-grants-2011_11
ORD IDord-577ce0bfa216420d91f2772d3771d42c
출처 메모uspto-grants-2011_11