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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 970888생성일: 2026년 10월 25일

Acetonitrile → 4-{[(2-Nitrobenzenesulfonyl)(5,6,7,8-tetrahydro-quinolin-8-yl)-amino]-methyl}-N-pyridin-2-yl-benzamide

https://huagongshe.com/reaction/970888

반응식

참여 물질

역할이름HCID투입량
반응물AcetonitrileHCID 6342—
반응물Potassium CarbonateHCID 11430—
반응물8-(2-Nitrobenzenesulfonyl)amino-5,6,7,8-tetrahydroquinolineHCID 22601394—
용매Ethyl AcetateHCID 8857—
생성물4-{[(2-Nitrobenzenesulfonyl)(5,6,7,8-tetrahydro-quinolin-8-yl)-amino]-methyl}-N-pyridin-2-yl-benzamideHCID 2260144692%

반응 단계

8-[N-(2-nitrobenzenesulfonyl)]amino-5,6,7,8-tetrahydroquinoline (230 mg, 0.69 mmol), 4-Chloromethyl-N-pyridinyl-2-yl-benzamide (170 mg, 0.69 mmol), and K2CO3 (285 mg, 2.06 mmol) were heated to reflux in CH3CN (3 mL) for 24 hours under N2. The reaction mixture was diluted with 200 mL ethyl acetate, and washed with sat. NaHCO3, then brine and dried over Na2SO4. Evaporation of the solvent and purification of the residue by flash chromatography on silica gel using 6% ethyl acetate in CH2Cl2 afforded the title compound (344 mg, 92%) as white foam. 1H NMR (CDCl3) δ 1.61-1.65 (m, 1H), 1.74-1.86 (m, 2H), 2.33-2.37 (m, 1H), 2.59-2.65 (m, 2H), 3.92 (d, 1H, J=16.2), 4.87 (d, 1H, J=16.5 Hz), 5.32 (dd, 1H, J=5.8, 11.3 Hz), 7.04-7.11 (m, 2H), 7.31-7.37 (m, 3H), 7.49-7.67 (m, 3H), 7.73-7.80 (m, 3H), 8.15 (d, 1H, J=7.8 Hz), 8.22 (d, 1H, J=4.2 Hz), 8.31 (d, 1H, J=4.2 Hz), 8.35 (d, 1H, J=8.4 Hz), 8.45 (br, s, 1H); ES-MS m/z 544.1 (M+H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07312234B2
출처 데이터셋uspto-grants-2007_12
ORD IDord-10a5dad64fc040178c7160fec0522316
출처 메모uspto-grants-2007_12