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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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