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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 520722생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/520722

반응식

참여 물질

역할이름HCID투입량
반응물Iodo benzene diacetateHCID 12217721—
반응물EtOAc CH3CN waterHCID 86658869—
반응물4-(4-(1,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazole-4-carboxamido)phenoxy)picolinamidHCID 117842592—
생성물N-(4-((2-aminopyridin-4-yl)oxy)phenyl)-1,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazole-4-carboxamideHCID 7305360848%

반응 단계

To a solution of 4-(4-(1,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazole-4-carboxamido)phenoxy)picolinamid (1.773 g, 3.998 mmol) in EtOAc/MeCN/H2O (20 mL/20 mL/10 mL) was added iodobenzene diacetate (1.6 g, 4.96 mmol) at 0° C. The reaction was stirred at rt overnight, then concentrated in vacuo and diluted with EtOAc (100 mL). The mixture was washed with saturated aq. NaHCO3 (60 mL), dried over Na2SO4, and concentrated in vacuo. The residue was purified by a silica gel column chromatography (DCM/MeOH (v/v)=30/1) to give the title compound as a yellow solid (799 mg, 48%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09326975B2
출처 데이터셋uspto-grants-2016_05
ORD IDord-6cd25f1834c745f98eb84ae3f774c80b
출처 메모uspto-grants-2016_05