Efficient continuous-flow synthesis of novel 1,2,3-triazole-substituted β-aminocyclohexanecarboxylic acid derivatives with gram-scale production

被引:31
作者
Oetvoes, Sandor B. [1 ]
Georgiades, Adam [1 ]
Mandity, Istvan M. [1 ]
Kiss, Lorand [1 ]
Fueloep, Ferenc [1 ]
机构
[1] Univ Szeged, Inst Pharmaceut Chem, H-6720 Szeged, Hungary
关键词
beta-amino acids; click chemistry; continuous-flow; copper; flow chemistry; triazoles; AZIDE-ALKYNE CYCLOADDITION; CLICK CHEMISTRY; MEDICINAL CHEMISTRY; 1,4-DISUBSTITUTED 1,2,3-TRIAZOLES; 1,3-DIPOLAR CYCLOADDITIONS; HUISGEN CYCLOADDITION; CHEMICAL-SYNTHESIS; TERMINAL ALKYNES; AMINO ACIDS; COPPER;
D O I
10.3762/bjoc.9.172
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The preparation of novel multi-substituted 1,2,3-triazole-modified beta-aminocyclohexanecarboxylic acid derivatives in a simple and efficient continuous-flow procedure is reported. The 1,3-dipolar cycloaddition reactions were performed with copper powder as a readily accessible Cu(I) source. Initially, high reaction rates were achieved under high-pressure/high-temperature conditions. Subsequently, the reaction temperature was lowered to room temperature by the joint use of both basic and acidic additives to improve the safety of the synthesis, as azides were to be handled as unstable reactants. Scale-up experiments were also performed, which led to the achievement of gram-scale production in a safe and straightforward way. The obtained 1,2,3-triazole-substituted beta-aminocyclohexanecarboxylates can be regarded as interesting precursors for drugs with possible biological effects.
引用
收藏
页码:1508 / 1516
页数:9
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