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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 460352생성일: 2026년 10월 24일

Diisopropylethylamine → 1-[3-(3-Fluoro-phenylamino)-6,7-dimethoxy-4H-indeno[1,2-c]pyrazol-1-yl]-2-hydroxy-ethanone

https://huagongshe.com/ko/reaction/460352

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물Benzyloxyacetyl chlorideHCID 177085—
반응물Jnj-10198409HCID 9797370—
용매DimethylformamideHCID 6228—
생성물1-[3-(3-Fluoro-phenylamino)-6,7-dimethoxy-4H-indeno[1,2-c]pyrazol-1-yl]-2-hydroxy-ethanoneHCID 1844544090%

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) (3.6 g, 10.0 mmol), Benzyloxy-acetyl chloride (Compound 27a) (2.2 g, 12.0 mmole) and DMF (50 mL) was added Diisopropylethylamine (5.2 mL, 30 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. Dried over sodium sulfate and removed solvent in vacuo. The crude material was then taken up into ethanol and 0.5 g of Pd/C was added. The reaction was shaken on the hydrogenator over night. The reaction was filtered through Celite and removed solvent in vacuo. Triturated in a small amount of EtOAc. 3.2 g of ˜90% pure material was produced. 300 mg of the crude material was prepped on the Gilson and lyophilization gave Compound 432 as a white powder. MS m/z 384 (M+H)+;

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07196110B2
출처 데이터셋uspto-grants-2007_03
ORD IDord-149543929f314c7a99415f9992e517d4
출처 메모uspto-grants-2007_03