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HRID 346576作成日:2026年10月26日

1-(Thien-2-ylcarbonyl)piperazine → 1-Methyl-2-Oxo-4-[4-(Thiophen-2-Ylcarbonyl)piperazin-1-Yl]-1,2-Dihydroquinoline-3-Carbonitrile

https://huagongshe.com/reaction/346576

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-1-methyl-2-oxo-1,2-dihydroquinoline-3-carbonitrileHCID 2785748—
溶媒TolueneHCID 1140—
生成物1-Methyl-2-Oxo-4-[4-(Thiophen-2-Ylcarbonyl)piperazin-1-Yl]-1,2-Dihydroquinoline-3-CarbonitrileHCID 2108192498%

反応条件

温度120 °C

反応手順

Piperazine-1-yl-thiophen-2-yl-methanone (600 mg, 3.06 mmol) was added to a solution of Compound 3 (319 mg, 1.46 mmol) in toluene (40 mL) and heated overnight at 120° C. The solvent was removed under vacuum. The residue was suspended in water, sonicated, and filtered to yield 540 mg (98%) of white solids. M.P. 247° C. 1H NMR (DMSO-d6): δ 3.58 (s, 3H), 3.63 (m, 4H), 3.92 (m, 4H), 7.16 (t, J=4.8 Hz, 1H), 7.33 (t, J=7.5 Hz, 1H), 7.48 (d, J=3.5 Hz, 1H), 7.59 (d, J=8.5 Hz, 1H), 7.75 (t, J=7.25, 2H), 7.79 (d, J=4.8 Hz, 1H) 7.92 (d, J=7.5 Hz, 1H). EIMS m/z 379 (M+1), 401 (M+23). Anal. (C20H18N4O2S) C, H, N.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07173036B2
出典データセットuspto-grants-2007_02
ORD IDord-e8a83815c6a24df4bcc906fcea4d816f
出典メモuspto-grants-2007_02