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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 872996생성일: 2026년 10월 24일

Iodo benzene diacetate → N-(5-((2-aminopyridin-4-yl)oxy)pyridin-2-yl)-1,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazole-4-carboxamide

https://huagongshe.com/ko/reaction/872996

반응식

참여 물질

역할이름HCID투입량
반응물Iodo benzene diacetateHCID 12217721—
반응물4-((6-(1,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazole-4-carboxamido)pyridin-3-yl)oxy)picolinamideHCID 73053266—
반응물EtOAc CH3CN waterHCID 86658869—
생성물N-(5-((2-aminopyridin-4-yl)oxy)pyridin-2-yl)-1,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazole-4-carboxamideHCID 7305362777%

반응 단계

To a solution of 4-((6-(1,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazole-4-carboxamido)pyridin-3-yl)oxy)picolinamide (60 mg, 0.13 mmol) in EtOAc/MeCN/H2O (2 mL/2 mL/1 mL) was added iodobenzene diacetate (54 mg, 0.16 mmol) at 0° C. The reaction was stirred at rt for 2 hours, then concentrated in vacuo. The resulted residue was dissolved in EtOAc (10 mL), washed with saturated aq. NaHCO3, and then dried over anhydrous Na2SO4. The organic solution was concentrated in vacuo to give the title compound as a yellow solid (43 mg, 77%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08975282B2
출처 데이터셋uspto-grants-2015_03
ORD IDord-69c0f0e0fab1401fb64d181061d6c418
출처 메모uspto-grants-2015_03