반응 #822447

반응 방정식

5,7-dichloro-3-(4-methoxy-phenyl)-3-methyl-1H-quinoline-2,4-dione

1-methylpiperazine

→

compound

수율 32.0%

5-chloro-3-(4-methoxy-phenyl)-3-methyl-7-(4-methyl-piperazine-1-yl)-1H-quinoline-2,4-dione

수율 32.0%

반응 조건

후처리

1. 1
   온도was heated
2. 2
   온도at reflux temperature overnight
3. 3
   기타Excessive 1-methylpiperazine was removed by evaporation in vacuo
4. 4
   workup.ADDITIONThe residue was diluted with water (50 mL)
5. 5
   기타resulting suspension
6. 6
   추출was extracted with ethyl acetate (50 mL×3)
7. 7
   세척The organic layer was washed with brine (50 ml×2)
8. 8
   건조dried over anhydrous MgSO4
9. 9
   농축concentrated under reduced pressure

실험 절차

A mixture of 5,7-dichloro-3-(4-methoxy-phenyl)-3-methyl-1H-quinoline-2,4-dione (0.10 g, 0.29 mmol) and 1-methylpiperazine (3.0 mL) was heated at reflux temperature overnight. Excessive 1-methylpiperazine was removed by evaporation in vacuo. The residue was diluted with water (50 mL), and resulting suspension was extracted with ethyl acetate (50 mL×3). The organic layer was washed with brine (50 ml×2), dried over anhydrous MgSO4, and concentrated under reduced pressure. The pure objective compound (38 mg, 32%) was obtained as yellow solid by a flash column chromatography (CH2Cl2:MeOH=20:1): 1H NMR (200 MHz, CDCl3) δ 1.82 (s, 3H, CH3), 2.33 (s, 3H, NCH3), 2.44-2.65 (m, 4H, 2×NCH2), 2.88-2.91 (m, 4H, 2×NCH2), 3.74 (s, 3H, OCH3), 6.43 (d, J=1.8 Hz, 1H, ArH) 6.54 (d, J=1.8 Hz, 1H, ArH), 6.80 (d, J=9.0 Hz, 1H, ArH), 7.19 (d, J=9.0 Hz, 1H, ArH), 9.23 (s, 1H, NH); m.p. 201-202° C.; MS(EI) m/e 413 [M+]; HRMS m/e cacld. for C22H24N3O3Cl1 413.1506, found 413.1516.

출처