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HRID 720430作成日:2026年10月23日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物1,2-DimethylhydrazineHCID 1322—
反応物DimethylformamideHCID 6228—
反応物3-Cyano (4-fluoro-benzoyl)-pyrrolo[1,2-a]quinolineHCID 10267630—
溶媒WaterHCID 962—
生成物3-Cyano-1-(4-dimethylamino-benzoyl)-pyrrolo[1,2-a]quinolineHCID 2189212325%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07135480B2
出典データセットuspto-grants-2006_11
ORD IDord-5009080523824638a9d9dbb27028aedd
出典メモuspto-grants-2006_11