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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2264178생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/2264178

반응식

참여 물질

역할이름HCID투입량
반응물3-Fluoro-4-(tributylstannyl)pyridineHCID 22273601—
반응물3-Bromo-5-nitro-2,3'-bipyridin-6-amineHCID 59596002—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
촉매HCID 178479804HCID 178479804—
용매DimethylformamideHCID 6228—
생성물3''-Fluoro-5'-nitro-3,2':3',4''-terpyridin-6'-amineHCID 5959600651%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07855202B2
출처 데이터셋uspto-grants-2010_12
ORD IDord-da3ea45afe0640649b9e02357679094a
출처 메모uspto-grants-2010_12