Synthesis 2015; 47(11): 1656-1660
DOI: 10.1055/s-0034-1380189
paper
© Georg Thieme Verlag Stuttgart · New York

Tin(II) Chloride Catalyzed Synthesis of New Pyrazolo[5,4-b]quinolines under Solvent-Free Conditions

Ahmad Poursattar Marjani
Department of Chemistry, Faculty of Science, Urmia University, Urmia 57154, Iran   Email: jkhalafi@yahoo.com   Email: j.khalafi@urmia.ac.ir
,
Jabbar Khalafy*
Department of Chemistry, Faculty of Science, Urmia University, Urmia 57154, Iran   Email: jkhalafi@yahoo.com   Email: j.khalafi@urmia.ac.ir
,
Fatemeh Salami
Department of Chemistry, Faculty of Science, Urmia University, Urmia 57154, Iran   Email: jkhalafi@yahoo.com   Email: j.khalafi@urmia.ac.ir
,
Mahsa Mohammadlou
Department of Chemistry, Faculty of Science, Urmia University, Urmia 57154, Iran   Email: jkhalafi@yahoo.com   Email: j.khalafi@urmia.ac.ir
› Author Affiliations
Further Information

Publication History

Received: 12 November 2014

Accepted after revision: 12 February 2015

Publication Date:
12 March 2015 (online)


Abstract

A series of new pyrazolo[5,4-b]quinoline derivatives were synthesized in good yields by tin(II) chloride dihydrate catalyzed cyclocondensation of 5-amino-3-(arylamino)-1H-pyrazole-4-carbonitriles with cyclohexane-1,3-dione or dimedone. The synthetic procedure can be carried out by means of simple operations under convenient solvent­-free conditions.

Supporting Information