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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 460351생성일: 2026년 10월 25일

Butanoic acid, 4-chloro-4-oxo-, methyl ester → 4-[3-(3-Fluoro-phenylamino)-6,7-dimethoxy-4H-indeno[1,2-c]pyrazol-1-yl]-4-oxo-butyric acid methyl ester

https://huagongshe.com/reaction/460351

반응식

참여 물질

역할이름HCID투입량
반응물Butanoic acid, 4-chloro-4-oxo-, methyl esterHCID 73888—
반응물DiisopropylethylamineHCID 81531—
반응물Jnj-10198409HCID 9797370—
용매DimethylformamideHCID 6228—
생성물4-[3-(3-Fluoro-phenylamino)-6,7-dimethoxy-4H-indeno[1,2-c]pyrazol-1-yl]-4-oxo-butyric acid methyl esterHCID 58824826—

반응 단계

To a mixture of (6,7-Dimethoxy-1,4-dihydro-indeno[1,2-c]pyrazol-3-yl)-(3-fluoro-phenyl)-amine (Compound 14) (0.50 g, 1.5 mmol), 3-Chlorocarbonyl-propionic acid methyl ester (Compound 26a) (0.277 g, 1.8 mmole) and DMF (1.5 mL) was added Diisopropylethylamine (DIEA) (0.52 mL, 3.0 mmole) at room temperature with stirring. The reaction was stirred at room temperature over night. The reaction was quenched with water and extracted with EtOAc. The solvent was removed via rotovap and the crude material was prepped on the reverse phase HPLC. Lyophilization gave the title compound as a white powder. MS m/z439.9 (M+H)+;

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07196110B2
출처 데이터셋uspto-grants-2007_03
ORD IDord-3032bbf713c84279888a4b6191ba6e7f
출처 메모uspto-grants-2007_03