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HRID 2264178作成日:2026年10月26日

3-Fluoro-4-(tributylstannyl)pyridine → 3''-Fluoro-5'-nitro-3,2':3',4''-terpyridin-6'-amine

https://huagongshe.com/reaction/2264178

反応式

関与物質

役割名称HCID仕込み量
反応物3-Fluoro-4-(tributylstannyl)pyridineHCID 22273601—
反応物3-Bromo-5-nitro-2,3'-bipyridin-6-amineHCID 59596002—
触媒Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
触媒HCID 178479804HCID 178479804—
溶媒DimethylformamideHCID 6228—
生成物3''-Fluoro-5'-nitro-3,2':3',4''-terpyridin-6'-amineHCID 5959600651%

反応手順

An oven dried resealable Schlenk tube was charged with 3-bromo-5-nitro-2,3′-bipyridin-6-amine (4.51 g, 15.3 mmol), 3-fluoro-4-(tributylstannyl)pyridine (11.8 g, 30.6 mmol) and dimethylformamide (150 mL). The Schienk tube was subjected to three cycles of evacuation-backfilling with argon, and bis(triphenylphosphino)-palladium (II) chloride (1.1 g, 1.53 mmol) and copper (I) iodide (291 mg, 1.53 mmol) were added. After three new cycles of evacuation-backfilling with argon, the Schlenk tube was capped and placed in a 160° C. oil bath. After 3 h, the solvent was evaporated and the crude residue was treated with 2N hydrogen chloride (130 mL) aqueous solution for 45 minutes. The aqueous solution was washed with ethyl acetate and then neutralised with 6N sodium hydroxide aqueous solution. The solution was extracted with ethyl acetate, dried (MgSO4) and evaporated. The residue was purified by silica gel flash chromatography (95:5 dichloromethane/methanol) to give the title compound (2.39 g, 51%) as a solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07855202B2
出典データセットuspto-grants-2010_12
ORD IDord-da3ea45afe0640649b9e02357679094a
出典メモuspto-grants-2010_12