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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 346646생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/346646

반응식

참여 물질

역할이름HCID투입량
반응물1-(Thien-2-ylcarbonyl)piperazineHCID 797562—
반응물4-Chloro-1,2-dihydro-2-oxoquinoline-3-carbonitrileHCID 2777510—
용매TolueneHCID 1140—
생성물2-Oxo-4-[4-(thiophene-2-carbonyl)-piperazin-1-yl]-1,2-dihydro-quinolin-3-carbonitrileHCID 2108194388%

반응 조건

온도110 °C

반응 단계

Piperazine-1-yl-thiophen-2-yl-methanone (8.0 g, 41 mmol) was added to a solution of Compound 115 (4.1 g, 20 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 6.4 g (88%) of white solids. M.P. 264° C. 1H NMR (DMSO-d6): δ 3.7 (m, 4H), 3.9 (m, 4H), 7.16 (t, J=4.8 Hz, 1H), 7.23 (t, J=5.9 Hz, 1H), 7.31 (d, J=8.6 Hz, 1H), 7.49 (d, J=4.0 Hz, 1H), 7.61 (t, J=8.3 Hz, 1H), 7.8 (m, 2H), 11.90 (b, 1H); EIMS: 364 (M+H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07173036B2
출처 데이터셋uspto-grants-2007_02
ORD IDord-997a2d3835b74e63ace34e99092b8d64
출처 메모uspto-grants-2007_02