Unknown

Dataset Information

0

Solvent-Free C-3 Coupling of Azaindoles with Cyclic Imines.


ABSTRACT: By direct coupling 7-azaindole and cyclic imines, such as 3,4-dihydroisoquinoline, 6,7-dihydrothieno[3,2-c]pyridine, 3,4-dihydro-?-carboline, and 4,5-dihydro-3H-benz[c]azepine, new 3-substituted 7-azaindole derivatives have been synthesized. The reaction was extended to 4-azaindoles and 6-azaindoles, as electron-rich aromatic compounds. The lowest reactivity was observed in the case of C-3 substitution of 5-azaindole. In this case, the aza-Friedel-Crafts reaction took place by using 10 mol % of p-toluenesulfonic acid (p-TSA) as the catalyst. The role of the acid catalyst can be explained by the different pKa values of the azaindoles. All reactions were performed in solvent-free conditions by using both classical heating and microwave irradiation. In all cases, microwave heating proved to be more convenient to synthesize new C-3-substituted azaindole derivatives.

SUBMITTER: Belasri K 

PROVIDER: S-EPMC6803843 | biostudies-literature | 2019 Oct

REPOSITORIES: biostudies-literature

altmetric image

Publications

Solvent-Free C-3 Coupling of Azaindoles with Cyclic Imines.

Belasri Khadija K   Fülöp Ferenc F   Szatmári István I  

Molecules (Basel, Switzerland) 20191004 19


By direct coupling 7-azaindole and cyclic imines, such as 3,4-dihydroisoquinoline, 6,7-dihydrothieno[3,2-<i>c</i>]pyridine, 3,4-dihydro-β-carboline, and 4,5-dihydro-<i>3H</i>-benz[<i>c</i>]azepine, new 3-substituted 7-azaindole derivatives have been synthesized. The reaction was extended to 4-azaindoles and 6-azaindoles, as electron-rich aromatic compounds. The lowest reactivity was observed in the case of C-3 substitution of 5-azaindole. In this case, the aza-Friedel-Crafts reaction took place  ...[more]

Similar Datasets

| S-EPMC5745074 | biostudies-literature
| S-EPMC6988605 | biostudies-literature
| S-EPMC3904147 | biostudies-literature
| S-EPMC9092949 | biostudies-literature
| S-EPMC5955971 | biostudies-literature
| S-EPMC6664198 | biostudies-literature
| S-EPMC6640803 | biostudies-literature
| S-EPMC3234421 | biostudies-other
| S-EPMC4880406 | biostudies-literature
| S-EPMC10609177 | biostudies-literature