Phenylfurylthieno[2,3-b]pyridyl-methanes. synthesis and reactions of the furan ring transformation

Triarylmethane derivatives with various substituents, phenyl, 5-methyl-2-furyl, and 3-acylamino-thieno[2,3-b]pyrid-2-yl have been obtained for the first time. The behavior of these compounds under protolytic conditions has been studied. It was shown that the character of the protection of the amino...

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Veröffentlicht in:	Chemistry of heterocyclic compounds (New York, N.Y. 1965) N.Y. 1965), 2009-09, Vol.45 (9), p.1105-1116
Hauptverfasser:	Kosulina, D. Yu, Vasilin, V. K, Stroganova, T. A, Sbitneva, E. A, Butin, A. V, Krapivin, G. D
Format:	Artikel
Sprache:	eng
Schlagworte:	(phenyl)(2-acylaminothieno[2,3-b]pyrid-2-yl)carbinols (phenyl)(5-methylfur-2-yl)-(2-acylaminothieno[2,3-b]pyrid-2-yl)methanes 3-amino-2-benzoylthieno[2,3-b]pyridines 4-(3-phenyl-1H-pyrrolo[2',3':4,5]thieno[2,3-b]pyrid-2-yl)-butan-2-ones acylation alkylation Chemistry Chemistry and Materials Science N-[2-(2,5-dioxo-1-phenylhexyl)thieno[2,3-b]pyrid- 3-yl]benzamides Organic Chemistry Pharmacy reduction transformation of the furan ring
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Zusammenfassung:	Triarylmethane derivatives with various substituents, phenyl, 5-methyl-2-furyl, and 3-acylamino-thieno[2,3-b]pyrid-2-yl have been obtained for the first time. The behavior of these compounds under protolytic conditions has been studied. It was shown that the character of the protection of the amino group of the thienopyridine fragment affects the type of transformation of the furan ring.
ISSN:	0009-3122 1573-8353
DOI:	10.1007/s10593-009-0401-9