Synthesis of potential antimalarials
作者:
John P. Schaefer,
K. S. Kulkarni,
R. Costin,
J. Higgins,
Linda M. Honig,
期刊:
Journal of Heterocyclic Chemistry
(WILEY Available online 1970)
卷期:
Volume 7,
issue 3
页码: 607-613
ISSN:0022-152X
年代: 1970
DOI:10.1002/jhet.5570070321
出版商: Wiley‐Blackwell
数据来源: WILEY
摘要:
AbstractA series of quinoline derivatives containing a 2‐thienyl ring in the 2‐position and CO2H, CH2OH, CHO, CH(OH)CN, CH(OH)CO2H, CO2C2H5, COCH[N(C2H5)2]CO2C2H5, COCH2N(C2H5)2, COCH3,substituents in the 4‐position was synthesized. Both intermediate and target compounds were tested for antimalarial activity. A second series with a 5‐bromo‐2‐thienyl group in the 2‐position and CHOHCH2N(C2H5)2, CHOHCH2N(CH2)6, and CHOHCH2N(CH2C6H5)2substituents in the 4‐position was also prepared, it was found that, although these quinoline methanols were moderately active antimalarials, they exhibited a high degree of phototoxicity. A third series of compounds with 2‐alkyl substituents (methyl,t‐butyl) was also synthesized, and these were found to combine a modest degree of antimalarial activity with low phototoxicity. Several novel synthetic routes to the above compounds were develop
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