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Molbank 2019, 2019(1), M1045; https://doi.org/10.3390/M1045

3,5-Bis[5-(thiazol-2-yl)thien-2-yl]-4H-1,2,6-thiadiazin-4-one

1
Department of Life Sciences, School of Sciences, European University Cyprus, 6 Diogenis Str., Engomi, P. O. Box 22006, 1516 Nicosia, Cyprus
2
Department of Chemistry, University of Cyprus, P. O. Box 20537, 1678 Nicosia, Cyprus
*
Author to whom correspondence should be addressed.
Received: 21 December 2018 / Revised: 11 January 2019 / Accepted: 13 January 2019 / Published: 15 January 2019
(This article belongs to the Special Issue Heteroatom Rich Organic Heterocycles)
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Abstract

Stille coupling of 3,5-bis(5-bromothien-2-yl)-4H-1,2,6-thiadiazin-4-one (10) with 2-(tri-n-butylstannyl)thiazole and Pd(Ph3P)2Cl2 in PhMe, at ca. 110 °C, for 2 h, gave 3,5-bis[5-(thiazol-2-yl)thien-2-yl]-4H-1,2,6-thiadiazin-4-one (9) in 81% yield. The latter is evaluated for its electronic properties. View Full-Text
Keywords: heterocycle; 1,2,6-thiadiazine; thiazole; Stille coupling; oligomer heterocycle; 1,2,6-thiadiazine; thiazole; Stille coupling; oligomer
This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited (CC BY 4.0).

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Kalogirou, A.S.; Koutentis, P.A. 3,5-Bis[5-(thiazol-2-yl)thien-2-yl]-4H-1,2,6-thiadiazin-4-one. Molbank 2019, 2019, M1045.

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