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HRID 561834作成日:2026年10月26日

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

https://huagongshe.com/reaction/561834

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium CarbonateHCID 10340—
反応物TriphenylphosphineHCID 11776—
反応物2-[(1E)-3-methoxyprop-1-en-1-yl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolaneHCID 16217443—
反応物2,6-Dichloro-N-cyclopropylisonicotinamideHCID 21510026—
触媒Palladium bromide (PdBr2)HCID 83469—
溶媒DimethylformamideHCID 6228—
生成物N-Cyclopropyl-2,6-bis[(1E)-3-methoxyprop-1-en-1-yl]isonicotinamideHCID 66761510—

反応条件

温度100 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08063105B2
出典データセットuspto-grants-2011_11
ORD IDord-577ce0bfa216420d91f2772d3771d42c
出典メモuspto-grants-2011_11