Pyridine-Based Heterocycles. Synthesis of New Pyrido [4,34,5]thieno[2,3-d]pyrimidines and Related Heterocycles 英文参考文献.docVIP
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Pyridine-Based Heterocycles. Synthesis of New Pyrido [4,34,5]thieno[2,3-d]pyrimidines and Related Heterocycles 英文参考文献
Molecules 2010, 15, 2651-2666; doi:10.3390/moleculeOPEN ACCESS
molecules
ISSN 1420-3049
/journal/molecules
Article
Pyridine-Based Heterocycles. Synthesis of New Pyrido
[4,3:4,5]thieno[2,3-d]pyrimidines and Related Heterocycles
Hussein El-Kashef 1,*, Abdel-Rahman Farghaly 1, Ahmed Al-Hazmi 2, Thierry Terme 3 and
Patrice Vanelle 3,*
1
Chemistry Department, Faculty of Science, Assiut University, 71516 Assiut, Egypt
2
Chemistry Department, Faculty of Science, Ibb University, Yemen
3
Laboratoire Pharmaco-Chimie Radicalaire, Faculté de Pharmacie, Universités d’Aix-Marseille I, II
et III-CNRS, UMR 6264, Laboratoire Chimie Provence, 27 Bd J. Moulin, 13385 Marseille cedex 5,
France
? Authors to whom correspondence should be addressed; E-Mails: elkashef@.eg (H.E.-K.);
patrice.vanelle@univmed.fr (P.V.).
Received: 11 March 2010; in revised form: 31 March 2010 / Accepted: 6 April 2010 /
Published: 12 April 2010
Abstract: The synthesis of the title compounds was achieved using ethyl 2-amino-6-
methyl-4,5,6,7-tetrahydrothieno[2,3-c]pyridine-3-carboxylate (1) as starting material. The
reaction of the amino ester 1 with phenylisothiocyanate in boiling ethanol afforded the
thiourea derivative 5. The cyclization reactions of 5 under different reaction conditions led
to different pyridothienopyrimidine derivatives. Other reactions of the latter derivatives
leading to pyrido[4,3:4,5]thieno[2,3-d]triazolo[1,5-a]pyrimidines are also presented.
Keywords: pyrimidines; pyridines; thienopyrimidines; fused pyrimidines; fused pyridines
1. Introduction
Fused pyridine ring systems have received considerable attention due to their diverse biological
activity. In particular, pyrido[4,3:4,5]thieno[2,3-d]pyrimidin-4(3H)-ones were reported to be used for
the prophylaxis and therapy of cerebral ischemia [1,2], and as central nervous system agents [3]. Other
derivatives also act as 5-HT1A receptor antagonists and serotonin reuptake inhibi
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