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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 520724생성일: 2026년 10월 25일

Triethylamine → N-(4-((2-(cyclopentanecarboxamido)pyridin-4-yl)oxy)phenyl)-1,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazole-4-carboxamide

https://huagongshe.com/reaction/520724

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Cyclopentanecarbonyl chlorideHCID 78284—
반응물N-(4-((2-aminopyridin-4-yl)oxy)phenyl)-1,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazole-4-carboxamideHCID 73053608—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
용매tetrahydrofuran N,N-dimethylformamideHCID 21974620—
생성물N-(4-((2-(cyclopentanecarboxamido)pyridin-4-yl)oxy)phenyl)-1,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazole-4-carboxamideHCID 7305153032%

반응 조건

온도0 °C

반응 단계

To a suspension of N-(4-((2-aminopyridin-4-yl)oxy)phenyl)-1,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazole-4-carboxamide (100 mg, 0.241 mmol) in THF/DMF (20 mL/1 mL) was added Et3N (0.06 mL, 0.481 mmol). The suspension was cooled to 0° C., a solution of cyclopentanecarbonyl chloride (64.0 mg, 0.481 mmol) in THF (5 mL) was added to the reaction mixture drop wise over 2 hours. The reaction was stirred at rt for 1.5 hours, then diluted with EtOAc (25 mL). The resulted mixture was washed with water (25 mL×3), followed by washing with brine (25 mL), dried over anhydrous Na2SO4, filtered and concentrated in vacuo. The residue was purified by a silica gel column chromatography (DCM/EtOAc/MeOH (v/v)=80/15/1) to give the title compound as a white solid (39 mg, 32%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09326975B2
출처 데이터셋uspto-grants-2016_05
ORD IDord-c27a18b332bc4c7794267f959d1be51d
출처 메모uspto-grants-2016_05