RESUMO
A sequential three-component reaction of 3,5-diarylidenepiperidin-4-one, malononitrile, and amine (such as aromatic amine, cyclopropanamine, and NH(4)OAc) in acetic acid under microwave irradiation has been developed. In this one-pot reaction, a series of new N-substituted 2-amino-1,6-naphthyridine derivatives were synthesized with excellent yields. This method has the advantages of operational simplicity and increased safety for small-scale fast synthesis of N-aryl 2-amino-1,6-naphthyridines for biomedical screening.
Assuntos
Técnicas de Química Combinatória/métodos , Micro-Ondas , Naftiridinas/síntese química , RadiaçãoRESUMO
A series of new heterocyclic compounds, involving pyrimido[4,5-b][1,6]-, benzo[b][1,6]-, pyrazolo[3,4-b][1,6]naphthyridine, and aza-benzo[b]fluorene skeletons were successfully synthesized via the reaction of structurally diverse 3,5-dibenzylidenepiperidin-4-one with various enamine-likes (2,6-diaminopyrimidin-4(3H)-one, 3-amino-5,5-dimethylcyclohex-2-enone, 3-methyl-1-phenyl-1H-pyrazol-5-amine and 1H-benzo[d]imidazol-2-amine) in glycol under microwave irradiation. This method has the advantages of short synthetic route, operational simplicity, and increased safety for small-scale fast synthesis for biomedical screening.
Assuntos
Micro-Ondas , Naftiridinas/síntese química , Modelos Moleculares , Estrutura Molecular , Naftiridinas/químicaRESUMO
A series of new polycyclic-fused isoxazolo[5,4-b]pyridines were obtained by a one-pot tandem reaction under microwave irradiation in water. Without any use of additional reagent or catalyst, the synthetic protocol represents a green one and makes this methodology suitable for library synthesis in drug discovery efforts.
Assuntos
Técnicas de Química Combinatória/métodos , Isoxazóis/síntese química , Piridinas/síntese química , Bibliotecas de Moléculas Pequenas/síntese química , Técnicas de Química Combinatória/economia , Isoxazóis/química , Micro-Ondas , Estrutura Molecular , Piridinas/química , Bibliotecas de Moléculas Pequenas/química , Fatores de Tempo , Água/químicaRESUMO
A new mild base-catalyzed Mannich reaction of aromatic aldehydes with 1,2-diphenylethanone and hetero-arylamines including pyridin-2-amine and pyrimidin-2-amine is described. In this reaction, a series of new beta-aminoketones were stereoselectively synthesized in water by controlling the steric hindrance of the substrates under microwave heating. This method has the advantages of a short synthetic route, operational simplicity, increased safety for small-scale high-speed synthesis, and minimal environmental impact.
Assuntos
Aminas/química , Calefação , Cetonas/síntese química , Bases de Mannich/química , Micro-Ondas , Aldeídos/química , Benzoína/análogos & derivados , Benzoína/química , Catálise , Cetonas/química , Estrutura Molecular , Estereoisomerismo , Água/químicaRESUMO
A new and efficient strategy for the synthesis of benzo[e][1,4]thiazepin-2(1H,3H,5H)-ones via a microwave-assisted multi-component reaction in aqueous media is described.
Assuntos
Micro-Ondas , Tiazepinas/síntese química , Água/química , Aldeídos/química , Compostos de Anilina/química , Química Verde , Especificidade por Substrato , Temperatura , Tiazepinas/química , Tiazolidinas/química , Tioglicolatos/químicaRESUMO
A series of new 3-pyrimidin-5-ylpropanamides was selectively synthesized via a microwave-assisted, chemoselective reaction of arylidene-Meldrum's acid, 6-hydroxypyrimidin-4(3H)-one, and structurally diverse amines including (S or R)-1-phenylethanamine, cyclohexanamine, and cyclopentanamine depended on nature of solvents. In this reaction, the utilization of HOAc as a solvent leads to 3-pyrimidin-5-ylpropanamides, whereas water as reaction media results in the spiro[5.5]undecane-1,5,9-triones from same starting materials. This method has the advantages of short synthetic route, operational simplicity, increased safety for small-scale high-speed synthesis, and minimal environment impact.