The synthesis of [1]benzopyrano[4,3-b]pyridin-5-ones 4a-f and 4g-j starting from 3-formylcoumarin and 3-cyanocoumarin N-functionalized amidines 3a-f and 3g-j, respectively, was reported. The ring-closure reaction mechanism, under basic or acidic media, was proposed. Furthermore, the reaction of 3-formylamidines 3a,c-f with ammonium acetate gave good yields of 2-substituted [1]benzopyrano[4,3-d]pyrimidin-5-oiies 7. (c) 2005 Elsevier Ltd. All rights reserved.

Substituted coumarin amidines: useful building blocks for the preparation of [1]benzopyrano[4,3-b]pyridin-5-one and [1]benzopyrano[4,3-d]pyrimidin-5-one derivatives / E.M. Beccalli, A. Contini, P. Trimarco. - In: TETRAHEDRON. - ISSN 0040-4020. - 61:21(2005 Apr), pp. 4957-4964. [10.1016/j.tet.2005.03.050]

Substituted coumarin amidines: useful building blocks for the preparation of [1]benzopyrano[4,3-b]pyridin-5-one and [1]benzopyrano[4,3-d]pyrimidin-5-one derivatives

E.M. Beccalli
Primo
;
A. Contini
Secondo
;
P. Trimarco
Ultimo
2005

Abstract

The synthesis of [1]benzopyrano[4,3-b]pyridin-5-ones 4a-f and 4g-j starting from 3-formylcoumarin and 3-cyanocoumarin N-functionalized amidines 3a-f and 3g-j, respectively, was reported. The ring-closure reaction mechanism, under basic or acidic media, was proposed. Furthermore, the reaction of 3-formylamidines 3a,c-f with ammonium acetate gave good yields of 2-substituted [1]benzopyrano[4,3-d]pyrimidin-5-oiies 7. (c) 2005 Elsevier Ltd. All rights reserved.
3-formylcoumarin amidines; 3-cyanocoumarin amidines; enediamino tautomers; Aldols; intramolecuar cyclization
Settore CHIM/06 - Chimica Organica
apr-2005
Article (author)
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/9642
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