Synthesis of new diheteroarylcarbazoles: a facile and simple route of 3,6-di(pyrazol-4-yl)carbazoles
Synthesis of new diheteroarylcarbazoles: a facile and simple route of 3,6-di(pyrazol-4-yl)carbazoles
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Date
2006-10-23
Authors
Meesala, Ramu
Nagarajan, Rajagopal
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Abstract
A short and facile route to the synthesis of new 3,6-di(pyrazol-4-yl)carbazoles is reported. Dipyrazolylcarbazoles were synthesized in two steps from 3,6-diacetylcarbazoles through a Vilsmeier reaction which led to the formation of carbazolyl-β-chlorovinyl aldehydes, followed by cyclization with hydrazine hydrate. The reaction of the Vilsmeier reagent with hydrazones of diacetylcarbazoles yielded the corresponding pyrazole dicarbaldehydes in good yields. © 2006 Elsevier Ltd. All rights reserved.
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Keywords
β-Chlorovinylaldehydes,
Diheteroarylcarbazoles,
Dipyrazolylcarbazoles,
Hydrazone cyclization,
Vilsmeier reagent
Citation
Tetrahedron Letters. v.47(43)