Síntese de novas azinas trifluormetil substituídas e derivados a partir de reações de heterociclização de trifluoracetil enol éteres com diamino arenos

• Ano de defesa: 2013
• Autor(a) principal: Andrighetto, Rosalia
• Tipo de documento: Tese
• Tipo de acesso: Acesso aberto
• Idioma: por
• Instituição de defesa: Universidade Federal de Santa Maria; BR; Química; UFSM; Programa de Pós-Graduação em Química
• Palavras-chave em Português: Química; Quinolinas; CNPQ::CIENCIAS EXATAS E DA TERRA::QUIMICA
• Link de acesso: http://repositorio.ufsm.br/handle/1/4258

The present research describes the study of synthetic strategies for obtaining of polyheterocyclic systems trifluoromethyl substituted from simple precursors: 4-alkoxy-1,1,1-trifluoroalk-3-en-2-ones (1), of formula F3C-C(O)-CH=C(R1)-OR, where R1 = H, CH3, C6H5, 4-FC6H4, 4-BrC6H4, 4-CH3C6H4, 4-OCH3C6H4, 2-furyl, 2-thienyl and R = Me, Et, and three diamino arenes: 1,3-phenylenediamine (1,3-FDA), 2,6-diaminopyridine (2,6-DAP) and 2,6-diaminotoluene (2,6-DAT). Considering the biological importance and employment of amino-quinolines as the starting material for the synthesis of new heterocycles, as well as, it is known that there is difficulty in relation to the control of regiochemistry reactions involving the synthesis of pyridine ring structures with aryl-geminal CF3- substituted, studies were directed to establish protocols for cyclocondensation reactions of [3+3] type. Was evaluated the synthesis of a new series of 1,7-phenanthrolines, 7-aminoquinolines, acridines, 2-amino-1,8-naphthyridines, antiridines and derivatization reactions. Initially, the reactions between 1 and 1,3-FDA, at a molar ratio of 1:1, were developed. The bis-enaminoneswere preferably obtained, in 32 41 % yields, instead of aminoquinolines 2. Whereas, reactions employing 1 and 2,6-DAP, at a molar ratio of 1:1, produced 2-amino-1,8-naphthyridines 4 (26 73 %). Following, the reactions of 1 and 2,6-DAT, furnished enaminones 9, in 46 70 % yields, which were subjected to reactions carried out in the presence of a strongly acidic medium (PPA), affording the corresponding new series of tetrasubstituted quinolines 10 (86 93 % yields). Finally, was evaluated the behavior of the compounds 4 and 10 in reactions with 1, diazotization, halogenation and N-acylation reactions. C-oxidation side chain reactions demonstrated the possibility of C H allylic bond oxidation (8-Me) when only two non-linked (free) carbonyl groups are attached to the nitrogen atom (7-NR2) at the β-position of the CH3 substituent (8-Me), affording the corresponding carbaldehyde (7-formyl-quinoline) in satisfactory yield (79 %).