SCOPUS 정보 검색 플랫폼

Volumn 21, Issue 4, 2010, Pages 426-428

Synthesis and biological evaluation of ethyl 6-alkoxy-7-phenyl-4-hydroxy-3-quinolinecarboxylates against Eimeria tenella

Author keywords

Anticoccidial activity; Eimeria tenella; Ethyl 6 alkoxy 7 phenyl 4 hydroxy 3 quinolinecarboxylate; Synthesis

Indexed keywords

EID: 76349090669 PISSN: 10018417 EISSN: None Source Type: Journal
DOI: 10.1016/j.cclet.2009.12.006 Document Type: Article

Times cited : (2)

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- The data for representative compounds: 5a: yellow solid; yield: 72, melting point: 252-254 °C; 1H NMR (400 MHz, DMSO-d6, δ 12.29 (s, 1H, 8.53 (s, 1H, 7.67 (s, 1H, 7.58 (d, 2H, J, 7.2 Hz, 7.55 (s, 1H, 7.48 (t, 2H, J, 7.2 Hz, J, 7.6 Hz, 7.42-7.40 (m, 1H, 4.22 (q, 2H, J, 7.2 Hz, 4.14 (q, 2H, J, 6.8 Hz, 1.32 (t, 3H, J, 6.8 Hz, 1.29 (t, 3H, J, 6.8 Hz, 13C NMR (400 MHz, DMSO-d6, δ 173.84, 167.83, 152.86, 151.58, 145.02, 138.25, 133.86, 129.45, 129.16, 128.74, 128.08, 127.17, 105.83, 63.88, 58.44, 14.68; IR (KBr, cm-1, 3440, 2979, 2930, 1700, 1613, 1582, 1502, 1469, 1443, 1188; HRMS(ESI, Calcd. for C20H19NO4: 337.1314; Found: 338.1351 (M+H, 360.1204 (M+Na, 5b: yellow solid; yield: 75, melting point: 248-250 °C; 1H NMR (400 MHz, DMSO-d6, δ 12.26 (d, 1H, J, 6.0 Hz, 8.51 (d, 1H, J, 6.4 Hz, 7.65 (s, 1H, 7.54 (d, 2H, J, 8.0 Hz, 7.52 s, 1H
- +). The data left were conserved by the editorial department of Chinese Chemical letters.

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