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A Simple Synthesis of Furo[3′,4′:5,6]pyrido[2,3-d]pyrimidine Derivatives through Multicomponent Reactions in Water

✍ Scribed by Shu-Jiang Tu; Yan Zhang; Hong Jiang; Bo Jiang; Jun-Yong Zhang; Run-Hong Jia; Feng Shi


Publisher
John Wiley and Sons
Year
2007
Tongue
English
Weight
133 KB
Volume
2007
Category
Article
ISSN
1434-193X

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✦ Synopsis


Abstract

A series of furo[3′,4′:5,6]pyrido[2,3‐d]pyrimidine and indeno[2′,1′:5,6]pyrido[2,3‐d]pyrimidine derivatives were synthesized by three‐component reactions involving an aldehyde, 2,6‐diaminopyrimidine‐4(3__H__)‐one, and either tetronic acid or indane‐1,3‐dione in water, under microwave irradiation and traditional heating conditions, without use of any catalyst. This protocol has the advantages of higher yields, lower cost, reduced environmental impact, and convenience of procedure. The synthesis of a class of important compounds in aqueous medium has been achieved. (© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2007)


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## Abstract A series of new 2‐substituted 3‐(4‐chlorophenyl)‐5,8,9‐trimethylthieno[3′,2′: 5,6]pyrido[4,3‐__d__]pyrimidin‐4(3__H__)‐ones **8** were synthesized __via__ an aza‐__Wittig__ reaction. Phosphoranylideneamino derivatives **6a** or **6b** reacted with 4‐chlorophenyl isocyanate to give carbo