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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 43, 2013 - Issue 5
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Original Articles

Four-Component Synthesis of Star-Shaped 2-(Indol-3-yl)pyridine Derivatives in One Pot

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Pages 705-718 | Received 26 Aug 2010, Published online: 13 Nov 2012
 

Abstract

A protocol for the synthesis of star-shaped 2-(indol-3-yl)pyridine derivatives 4, neat, in the presence of iodine as a catalyst was developed (method A). Based on this strategy, compounds 4-aryl-2-(1H-indol-3-yl)-6-arylnicotinonitriles 6 were synthesized from 3-(cynonoacetyl)indole 1, aromatic aldehyde 2, aromatic ketone 5, and AcONH4 under the conditions of both methods A (solvent free) and B (using AcOH as solvent). The compounds 4-aryl-2-(1H-indol-3-yl)-6-(thiophen-2-yl)nicotinonitriles 8 were also prepared under the conditions of method B.

GRAPHICAL ABSTRACT

Notes

a Isolated yield.

b DDQ (50 mol%) was added.

a Reaction conditions: 3-(cyanoacetyl)indole 1 (1 mmol), aromatic aldehyde 2 (1 mmol), 3-acetylpyridine 3 (1 mmol), AcONH4 (1.5 g), iodine (0.1 mmol), 120 °C, neat.

b Isolated yield.

c Detected by LC-MS.

a Isolated yield.

b Reaction conditions: Method A: 3-(cyanoacetyl)indole 1 (1 mmol), aromatic aldehyde 2 (1 mmol), aromatic ketone 5 (1 mmol), AcONH4 (1.5 g), iodine (0.1 mmol), 120 °C, neat; Method B: 3-(cyanoacetyl)indole 1 (1 mmol), aromatic aldehyde 2 (1 mmol), aromatic ketone 5 (1 mmol), AcONH4 (1.5 mmol), iodine (0.1 mmol), AcOH (1.5 ml), refluxing temperature.

a Reaction conditions: 3-(cyanoacetyl)indole 1 (1 mmol), aromatic aldehyde 2 (1 mmol), 1-(thiophen-2-yl)ethanonene 7 (1 mmol), AcONH4 (1.5 mmol), iodine (0.1 mmol), AcOH (1.5 ml), refluxing temperature.

b Isolated yield.

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