Synthesis of new 1,2-Benzothiazin-3-one Derivatives Designed as Dual Cyclooxygenase-2 and 5-Lipooxygenase Inhibitors



Document title: Synthesis of new 1,2-Benzothiazin-3-one Derivatives Designed as Dual Cyclooxygenase-2 and 5-Lipooxygenase Inhibitors
Journal: Journal of the Brazilian Chemical Society
Database: PERIÓDICA
System number: 000310782
ISSN: 0103-5053
Authors: 1

2
Institutions: 1Universidade Federal do Rio de Janeiro, Faculdade de Farmacia, Rio de Janeiro. Brasil
2Universidade Federal do Rio de Janeiro, Instituto de Quimica, Rio de Janeiro. Brasil
Year:
Season: Abr
Volumen: 9
Number: 2
Pages: 119-130
Country: Brasil
Language: Inglés
Document type: Artículo
Approach: Experimental, aplicado
English abstract In the scope of a research program aiming at the synthesis of new nonsteroidal anti-inflammatory drugs (NSAIDs) acting on the enzymes of the arachidonic acid cascade, we describe in this paper the synthesis of two new series of functionalized alpha,beta-unsaturated 1,2-benzothiazin-3-one derivatives (3a-10a) and (3b-10b), structurally designed as dual cyclooxigenase-2 and 5-lipooxygenase inhibitors by applying rational principles of molecular modification and hybridization. The target compounds (3a-10a) and (3b-10b) were prepared in good overall yields, exploring as the key step of the synthetic route a Knoevenagel-Doebner condensation between substituted benzaldehydes (e.g. 4-methoxy-benzaldehyde) and corresponding 1,2-benzothiazin-3(4H)-one 1,1-dioxide derivatives (17a) and (17b)
Portuguese abstract No âmbito de um programa de pesquisas que visa à síntese de novos fármacos antiinflamatórios não esteróides inibidores de enzimas da cascata do ácido araquidônico, descrevemos neste trabalho a síntese de duas novas séries de derivados 1,2-benzotiazin-3-ônicos alfa,beta-insaturados (3a-10a) e (3b-10b), racionalmente planejados como possíveis inibidores duplos de cicloxigenase-2 (COX-2) e 5-lipoxigenase (5-LO). Os compostos-alvo (3a-10a) e (3b-10b) foram preparados com bons rendimentos globais, explorando como etapa chave da rota sintética empregada uma condensação de Knoevenagel-Doebner entre benzaldeídos substituídos (ex. 4-metoxi-benzaldeído) e o correspondente derivado 1,2-benzotiazin-3(4H)-ona 1,1-dióxido funcionalizado (17a) e (17b)
Disciplines: Química
Keyword: Química farmacéutica,
Derivados de la benzotiazina,
Condensación diastereoselectiva,
Antiinflamatorios no esteroideos
Keyword: Chemistry,
Medicinal chemistry,
Benzothiazin derivatives,
Diastereoselective condensation,
Non steroidal antinflammatory drugs
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