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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 452633생성일: 2026년 10월 23일

2-Aminopyridine → Methyl 2-(2-pyridylamino)isonicotinate

https://huagongshe.com/ko/reaction/452633

반응식

참여 물질

역할이름HCID투입량
반응물2-AminopyridineHCID 10439—
반응물Potassium Phosphate, TribasicHCID 62657—
반응물Methyl 2-chloropyridine-4-carboxylateHCID 2736842—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
촉매2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 11155794—
용매TolueneHCID 1140—
용매Ethyl AcetateHCID 8857—
생성물Methyl 2-(2-pyridylamino)isonicotinateHCID 6866423265%

반응 단계

A suspension of methyl 2-chloroisonicotinate (1.00 g, 5.83 mmol), 2-aminopyridine (658 mg, 6.99 mmol), tris(dibenzylideneacetone)dipalladium(0) (107 mg, 0.17 mmol), dicyclohexyl(2′,4′,6′-triisopropylbiphenyl-2-yl)phosphine (139 mg, 0.29 mmol) and tripotassium phosphate (3.09 g, 14.6 mmol) in toluene (30 mL) was heated under reflux under an argon atmosphere overnight. After cooling, the reaction mixture was diluted with ethyl acetate, washed with saturated aqueous sodium hydrogen carbonate solution and saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by basic silica gel column chromatography (hexane/ethyl acetate=9/1-2/3) and recrystallized from hexane/ethyl acetate to give the title compound (866 mg, yield 65%) as colorless crystals.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08492378B2
출처 데이터셋uspto-grants-2013_07
ORD IDord-5947a725ed7340a889cf8a5963cb710d
출처 메모uspto-grants-2013_07