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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 520712생성일: 2026년 10월 26일

4-Chloropyridine-2-carboxamide → 4-(4-(1,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazole-4-carboxamido)-2-fluorophenoxy)picolinamide

https://huagongshe.com/reaction/520712

반응식

참여 물질

역할이름HCID투입량
반응물4-Chloropyridine-2-carboxamideHCID 303543—
반응물Potassium tert-butoxideHCID 23665647—
반응물N-(3-fluoro-4-hydroxyphenyl)-1,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazole-4-carboxamideHCID 90032660—
용매DimethylformamideHCID 6228—
생성물4-(4-(1,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazole-4-carboxamido)-2-fluorophenoxy)picolinamideHCID 7305326743%

반응 단계

To a solution of N-(3-fluoro-4-hydroxyphenyl)-1,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazole-4-carboxamide (7.18 g, 21.1 mmol) in DMF (200 mL) was added potassium tert-butoxide (7.08 g, 63.2 mmol). The solution was stirred at rt for 20 minutes, followed by the addition of 4-chloropicolinamide (4.27 g, 25.2 mmol). The reaction was heated at 120° C. for 3 hours, then concentrated to 2 mL in vacuo, and diluted with water (60 mL). The precipitate was obtained by filtration, and then washed with water (10 mL). The crude product was purified by a silica gel column chromatography (DCM/EtOAc/MeOH (v/v/v)=1/1/0.05) to give the title compound as a yellow solid (4.15 g, 43% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09326975B2
출처 데이터셋uspto-grants-2016_05
ORD IDord-684510fb3ac7410985397059c7f16ade
출처 메모uspto-grants-2016_05