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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 970472생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/970472

반응식

참여 물질

역할이름HCID투입량
반응물1-(Thien-2-ylcarbonyl)piperazineHCID 797562—
반응물4-Chloro-1-(4-fluorobenzyl)-2-oxo-1,2-dihydro-quinoline-3-carbonitrileHCID 21081957—
용매TolueneHCID 1140—
생성물1-(4-Fluorobenzyl)-2-oxo-4-[4-(thiophene-2-carbonyl)-piperazin-1-yl]-1,2-dihydro-quinolin-3-carbonitrileHCID 2108188797%

반응 조건

온도120 °C

반응 단계

Piperazine-1-yl-thiophen-2-yl-methanone (234 mg, 1.19 mmol) was added to a solution of Compound 8 (170 mg, 0.54 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 247 mg (97%) of white solids. M.P. 258° C. 1H NMR (DMSO-d6): δ 3.69 (m, 4H), 3.94 (m, 4H), 5.47 (s, 2H), 7.16 (m, 3H), 7.28 (m, 3H), 7.43 (d, J=8.5 Hz, 1H), 7.50 (d, J=3.3 Hz, 1H), 7.64 (t, J=7.25, 2H), 7.81 (d, J=4.8 Hz, 1H) 7.95 (d, J=7.5 Hz, 1H). EIMS m/z 473 (M+1), 495 (M+23). Anal. (C26H21FN4O2S) C, H, N.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07312220B2
출처 데이터셋uspto-grants-2007_12
ORD IDord-2b65e26d6be749b396d7e8b6859ae13e
출처 메모uspto-grants-2007_12