A simple one-pot synthesis of functionalised 6-(indol-3-yl)-2,2′-bipyridine derivatives via multi-component reaction under neat condition
✍ Scribed by Prakasam Thirumurugan; Paramasivan T. Perumal
- Publisher
- Elsevier Science
- Year
- 2009
- Tongue
- French
- Weight
- 389 KB
- Volume
- 50
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
✦ Synopsis
2,2 0 -bipyridine Multi-component reaction 3-Cyanoacetyl indole Neat condition 2,2 0 -Bipyridine Microwave irradiation Cinnamils a b s t r a c t A series of 4-aryl-6-(1H-indol-3-yl)-2,2-bipyridine-5-carbonitrile derivatives were synthesized via a onepot multi-component reaction of aromatic aldehydes, 3-(cyanoacetyl)indole and 2-acetyl pyridine in ammonium acetate by conventional heating and microwave irradiation under solvent-free condition. Also a series of 6,6 0 -di(1H-indol-3-yl)-4,4 0 -diaryl-2,2 0 -bipyridine-5,5 0 -dicarbonitrile derivatives were synthesized using cinnamils, 3-(cyanoacetyl)indole and ammonium acetate. The methodology affords high yields of product at short reaction time.
📜 SIMILAR VOLUMES
A simple and efficient synthesis of 2-(cyclohexylamino)-6,7-dihydro-3-aryl-1H-indole-4(5H)-ones was achieved via a one-pot multi-component reaction of cyclohexyl isocyanide, an aldehyde, a 1,3-dicarbonyl compound, and ammonium acetate in the presence of a catalytic amount of KHSO 4 in acetonitrile.