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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 450472생성일: 2026년 10월 24일

Aldoxime → 2-Fluoro-4-(2-(3-methylisoxazol-5-yl)pyridin-4-yloxy)benzenamine

https://huagongshe.com/ko/reaction/450472

반응식

참여 물질

역할이름HCID투입량
반응물AldoximeHCID 7863—
반응물TriethylamineHCID 8471—
반응물ChlorosuccinimideHCID 31398—
반응물4-(2-Ethynylpyridin-4-yloxy)-2-fluorobenzenamineHCID 59825583—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물2-Fluoro-4-(2-(3-methylisoxazol-5-yl)pyridin-4-yloxy)benzenamineHCID 5982558123.1%

반응 조건

온도130 °C

반응 단계

Acetaldoxime (0.078 g, 1.321 mmol) and triethylamine (0.246 ml, 1.761 mmol) were added to a solution of 4-(2-ethynylpyridin-4-yloxy)-2-fluorobenzenamine (0.201 g, 0.881 mmol) in THF (4 mL) in a microwave reaction vial. To this solution was added 1-chloropyrrolidine-2,5-dione (0.176 g, 1.32 mmol) and the mixture was stirred at 130° C. for 45 min under microwave irradiation. An additional 1.5 eq each of acetaldoxime and 1-chloropyrrolidine-2,5-dione were added and the reaction heated for an additional 45 min at 130° C. This process was repeated one more time. The mixture was poured into a biphasic solution of water (40 mL) and EtOAc (30 mL). The organic layer was separated and the aqueous layer was extracted with EtOAc (2×20 ml). The combined organics were washed with brine, dried (Na2SO4), concentrated in vacuo and purified by column chromatography (EtOAc-hexanes) to afford 2-fluoro-4-(2-(3-methylisoxazol-5-yl)pyridin-4-yloxy)benzenamine (58 mg, 23% yield) as light red colored residue. MS (ESI) m/z: 286.1 (M+H+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08486951B2
출처 데이터셋uspto-grants-2013_07
ORD IDord-6ae99d6367eb4e3ab7485053c800488d
출처 메모uspto-grants-2013_07