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l‐ Proline Catalyzed Synthesis of Highly Functionalized 4‐Hydroxy‐ 4H ‐chromene‐pyrazoles and 4‐Hydroxy‐ 4H ‐chromene‐barbiturates in Aqueous Medium
Author(s) -
Subba Reddy Chitreddy V,
Sumathi Shanmugam
Publication year - 2020
Publication title -
chemistryselect
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.437
H-Index - 34
ISSN - 2365-6549
DOI - 10.1002/slct.202001949
Subject(s) - chemistry , barbituric acid , catalysis , alkoxy group , malononitrile , solvent , hydrolysis , yield (engineering) , aldol condensation , proline , aldol reaction , organic chemistry , combinatorial chemistry , amino acid , materials science , biochemistry , alkyl , metallurgy
A simple and efficient method for the synthesis of novel 4‐hydroxy‐4 H ‐chromene‐pyrazoles and 4‐hydroxy‐4 H ‐chromene‐barbiturates was developed from the reaction of 2‐ethoxy‐2 H ‐chromene chalcones with pyrazolin‐5‐one and barbituric acid catalyzed by l ‐proline in water. The developed protocol is applicable for the construction of biologically important 4 H ‐chromenes from easily accessible chalcones having various substituents. This reaction proceeds through Aldol condensation, Michael addition and hydrolysis reactions followed by the elimination of ethoxy group. This methodology offers cleaner conversion, a shorter reaction time and high yields. For the first time, we report the synthesis of novel 4‐hydroxy‐4 H ‐chromenes from 2‐ethoxy‐2 H ‐chromene chalcones and pyrazolin‐5‐one/barbituric acid using l ‐proline (72 – 86 % yield in 6 h) . Water was used as the solvent for all the compounds it represents a green synthetic protocol.