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HRID 970621作成日:2026年10月26日

1-(Thien-2-ylcarbonyl)piperazine → 6-Methyl-2-oxo-4-[4-(thiophene-2-carbonyl)-piperazin-1-yl]-1,2-dihydro-quinolin-3-carbonitrile

https://huagongshe.com/reaction/970621

反応式

関与物質

役割名称HCID仕込み量
反応物1-(Thien-2-ylcarbonyl)piperazineHCID 797562—
反応物4-Chloro-6-methyl-2-oxo-1,2-dihydro-quinoline-3-carbonitrileHCID 21081963—
溶媒TolueneHCID 1140—
生成物6-Methyl-2-oxo-4-[4-(thiophene-2-carbonyl)-piperazin-1-yl]-1,2-dihydro-quinolin-3-carbonitrileHCID 2108198392.1%

反応条件

温度110 °C

反応手順

Piperazine-1-yl-thiophen-2-yl-methanone (8.73 g, 41.16 mmol) was added to a solution of Compound 106 (4.5 g, 20.08 mmol) in toluene (50 mL) and heated overnight at 110° C. The solvent was removed under vacuum. The residue was suspended in water, sonicated, and filtered. The crude product was purified by flash chromatography eluting with 0-2% methanol in dichloromethane gradient to yield 7.0 g (92%) of white solids. M.P. 269° C. 1H NMR (DMSO-d6): δ 2.34 (s, 3H), 3.65 (m, 4H), 3.92 (m, 4H), 7.14 (m, 1H), 7.23 (d, J=8.4 Hz, 1H), 7.43 (d, J=8.6 Hz, 1H), 7.49 (d, J=3.5 Hz, 1H), 7.51 (s, 1H), 7.81 (d, J=4.8 Hz, 1H). EIMS m/z 379 (M+1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07312221B2
出典データセットuspto-grants-2007_12
ORD IDord-c70406cb9b074ae2a0e1ffd04cce0359
出典メモuspto-grants-2007_12