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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 720430생성일: 2026년 10월 24일

1,2-Dimethylhydrazine → 3-Cyano-1-(4-dimethylamino-benzoyl)-pyrrolo[1,2-a]quinoline

https://huagongshe.com/ko/reaction/720430

반응식

참여 물질

역할이름HCID투입량
반응물1,2-DimethylhydrazineHCID 1322—
반응물DimethylformamideHCID 6228—
반응물3-Cyano (4-fluoro-benzoyl)-pyrrolo[1,2-a]quinolineHCID 10267630—
용매WaterHCID 962—
생성물3-Cyano-1-(4-dimethylamino-benzoyl)-pyrrolo[1,2-a]quinolineHCID 2189212325%

반응 단계

A solution of 3-cyano-1-[4-fluoro-benzoyl]-pyrrolo[1,2-a]quinoline (56 mg, 0.18 mmol) and dimethylhydrazine (118 mg, 1.96 mmol) in DMF (5 mL) was refluxed for 24 h. It was diluted with water (50 mL) and extracted with EtOAc (3×20 mL). The combined organic layers were dried, concentrated and the residue was purified by column chromatography (EtOAc/Hexane 6:1) to give 15 mg (25%) of the title compound. 1H NMR (CDCl3): 8.11–8.05–7.95 (m, 3H), 7.82–7.78 (m, 2H), 7.63–7.42 (m, 4H), 7.31 (s, 1H), 6.75 (d, J=9.30 Hz, 2H), 3.14 (s, 6H). MS, 340 (M+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07135480B2
출처 데이터셋uspto-grants-2006_11
ORD IDord-5009080523824638a9d9dbb27028aedd
출처 메모uspto-grants-2006_11