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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1874322생성일: 2026년 10월 27일

Pyridine → N-{3-[(6-aminopyridin-3-yl)oxy]phenyl}-1,3-dimethyl-1H-pyrazole-5-carboxamide

https://huagongshe.com/reaction/1874322

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물2,5-Dimethyl-2H-pyrazole-3-carbonyl chlorideHCID 2736299—
반응물5-(3-Aminophenoxy)pyridin-2-amineHCID 57749166—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물N-{3-[(6-aminopyridin-3-yl)oxy]phenyl}-1,3-dimethyl-1H-pyrazole-5-carboxamideHCID 5774923461.5%

반응 단계

To a solution of 5-(3-aminophenoxy)pyridin-2-amine (975 mg, 4.85 mmol) and pyridine (410 μL, 5.09 mmol) in tetrahydrofuran (10 mL) was added dropwise with stirring under ice-cooling a solution of 1,3-dimethyl-1H-pyrazole-5-carbonyl chloride (807 mg, 5.09 mmol) in tetrahydrofuran (10 mL), and the mixture was stirred at room temperature for 2 hr. The reaction mixture was diluted with water, extracted with ethyl acetate (×3), and the organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate and filtrated. The filtrate was concentrated under reduced pressure, and the residue was purified by column chromatography (silica gel, hexane/ethyl acetate=80/20→40/100) and recrystallized from ethyl acetate-hexane to give the title compound (964 mg, 61%) as a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08304557B2
출처 데이터셋uspto-grants-2012_11
ORD IDord-6d2bdc40125d4c688e4d52cae12fd48c
출처 메모uspto-grants-2012_11