Journal of Chemistry

A Facile Synthesis of 6-Amino-4-Aryl-3-Methyl-2,4- Dihydropyrano [2,3-C] Pyrazole-5-Carbonitriles in Aqueous Medium

Author & Affiliation:
ROHIT. R. WAKODKAR
Department of chemistry, Saraswati Bhuwan College of Science, Aurangabad, 431004 (M.S.) (India)
GAJANAN SANAP
Department of chemistry, Saraswati Bhuwan College of Science, Aurangabad, 431004 (M.S.) (India)
MAZAHAR FAROOQUI
Department of Chemistry, Dr. Rafiq Zakaria College for Women, Aurangabad (India)
DEEPAK D. KAYANDE
Department of chemistry, Saraswati Bhuwan College of Science, Aurangabad, 431004 (M.S.) (India)
Keyword:
Pyranopyrazoles, Tetra n-butyl ammonium bromide (TBAB) Aqueous medium, Multicomponent reactions
Issue Date:
March 2018
Abstract:

A convenient four-component synthesis of 6-amino-4-alkyl/aryl-3-methyl-2,4-dihydropyrano[2,3- c]pyrazole-5-carbonitriles.They are widely used for industrial purposes and also exhibit a broad range of antimicrobial activity. They are synthesized by using ethylacetoacetate, hydrazine hydrate, malononitrile, and various aldehydes using Tetra n-butyl ammonium bromide (TBAB) as a catalyst and water as solvent under mild reaction conditions. This method has several advantages such as high yield, mild reaction condition, operational simplicity, easy work-up procedure with environment friendly nature.

Pages:
50-56
ISSN:
2319-8036 (Online) - 0973-3450 (Print)
Source:
DOI:
http://dx.doi.org/10.22147/juc/140201

Copy the following to cite this article:

R. R. Wakodkar; G. Sanap; M. Farooqui; D. D. Kayande, "A Facile Synthesis of 6-Amino-4-Aryl-3-Methyl-2,4- Dihydropyrano [2,3-C] Pyrazole-5-Carbonitriles in Aqueous Medium", Journal of Ultra Chemistry, Volume 14, Issue 2, Page Number 50-56, 2018

Copy the following to cite this URL:

R. R. Wakodkar; G. Sanap; M. Farooqui; D. D. Kayande, "A Facile Synthesis of 6-Amino-4-Aryl-3-Methyl-2,4- Dihydropyrano [2,3-C] Pyrazole-5-Carbonitriles in Aqueous Medium", Journal of Ultra Chemistry, Volume 14, Issue 2, Page Number 50-56, 2018

Available from: http://www.journalofchemistry.org/paper/880/

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