Publicação
Synthesis of diarylamines in the benzo[b]thiophene series by palladium-catalyzed amination and structure-activity relationship as antibacterial agents
| Resumo: | The palladium-catalyzed amination of arylhalides has become an important method for the synthesis of arylamines found in pharmaceuticals. Using this methodology we were able to synthesize several diarylamines in the benzo[b]thiophene series.Here we report the synthesis 01 differently substituted diarylamines derivatives 01 6-bromo or 6-amino- 2,3,5-trimethylbenzo[b]thiophene in good to high yields (50-90%) (Scheme), The amino precursor was prepared from the bromo compound using also a C-N palladium-catalyzed cross-coupling with benzophenone imine, followed by acidic hydrolysis in a 60% overall yield. |
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| Autores principais: | Queiroz, Maria João R.P. |
| Outros Autores: | Ferreira, Isabel C.F.R.; Barbosa, Sandra; Calhelha, Ricardo C.; Estevinho, Leticia M. |
| Ano: | 2004 |
| País: | Portugal |
| Tipo de documento: | documento de conferência |
| Tipo de acesso: | acesso aberto |
| Instituição associada: | Instituto Politécnico de Bragança |
| Idioma: | inglês |
| Origem: | Biblioteca Digital do IPB |
| Resumo: | The palladium-catalyzed amination of arylhalides has become an important method for the synthesis of arylamines found in pharmaceuticals. Using this methodology we were able to synthesize several diarylamines in the benzo[b]thiophene series.Here we report the synthesis 01 differently substituted diarylamines derivatives 01 6-bromo or 6-amino- 2,3,5-trimethylbenzo[b]thiophene in good to high yields (50-90%) (Scheme), The amino precursor was prepared from the bromo compound using also a C-N palladium-catalyzed cross-coupling with benzophenone imine, followed by acidic hydrolysis in a 60% overall yield. |
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