Title of article
Microwave-accelerated Dimroth rearrangement for the synthesis of 4-anilino-6-nitroquinazolines. Application to an efficient synthesis of a microtubule destabilizing agent
Author/Authors
Alicia Foucourt، نويسنده , , Carole Dubouilh-Benard، نويسنده , , Elizabeth Chosson، نويسنده , , Cécile Corbière، نويسنده , , Catherine Buquet، نويسنده , , Mauro Iannelli، نويسنده , , Bertrand Leblond، نويسنده , , Francis Marsais، نويسنده , , Thierry Besson، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2010
Pages
8
From page
4495
To page
4502
Abstract
A useful and rapid access to 4-anilino-6-nitroquinazolines was investigated in a multi-gram scale via microwave-accelerated condensation and Dimroth rearrangement of the starting anilines with imines obtained by reaction of anthranilonitriles with formamide dimethylacetal. A novel short and efficient route to Azixa™ (EPi28495, MPC-6827), a microtubule destabilizing agent and apoptosis inducer, was performed with success demonstrating that well controlled parameters offer comfortable using of microwave technology with safe and environmental benefits.
Keywords
4-Anilinoquinazolines , Dimroth rearrangement , Microwave-assisted synthesis
Journal title
Tetrahedron
Serial Year
2010
Journal title
Tetrahedron
Record number
1100931
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