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HRID 1958101作成日:2026年10月25日

Nicotinic Acid → N-(5-bromo-6-(2,2,2-trifluoroethoxy)pyridin-3-yl)nicotinamide

https://huagongshe.com/reaction/1958101

反応式

関与物質

役割名称HCID仕込み量
反応物Nicotinic AcidHCID 938—
反応物DiisopropylethylamineHCID 81531—
反応物O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
反応物5-Bromo-6-(2,2,2-trifluoroethoxy)-pyridin-3-ylamineHCID 67281044—
溶媒DimethylformamideHCID 6228—
生成物N-(5-bromo-6-(2,2,2-trifluoroethoxy)pyridin-3-yl)nicotinamideHCID 67280716—

反応手順

To a solution of nicotinic acid (454 mg, 3.69 mmol) in DMF (33 mL) were added successively TBTU (1.18 g, 3.69 mmol), N,N-diisopropylethylamine (3.16 mL, 18.4 mmol) and 5-bromo-6-(2,2,2-trifluoroethoxy)pyridin-3-amine (1 g, 3.69 mmol). The brown mixture was stirred under argon for 3 h at room temperature. After evaporation of DMF, the brown oil was partitioned between ethyl acetate (50 mL) and 1M NaOH (30 mL). The aqueous layers were back-extracted with ethyl acetate (1×50 mL). The organic parts were washed with water (2×25 mL) and brine (25 mL), then dried over MgSO4 and concentrated in vacuo. The crude material was purified by flash chromatography (silica gel, 40 g, 10% to 100% ethyl acetate in heptane) to deliver the desired product as a white solid (580 mg; 42%); MS (EI): 376.1; 378.0 (M+H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08410107B2
出典データセットuspto-grants-2013_04
ORD IDord-369192810d434ddebb4acf29dccaad68
出典メモuspto-grants-2013_04