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Efficient Synthesis of 4-Arylmethylene-3-methylisoxazol-5(4H)-one Derivatives Catalyzed by Malic Acid
被引:6
|作者:
Tahmasabi, Sayed Zakaria
[1
]
Kiyani, Hamzeh
[1
,2
,3
]
Samimi, Heshmat Allah
[1
]
机构:
[1] Shahrekord Univ, Fac Sci, Dept Chem, Shahrekord, Iran
[2] Damghan Univ, Sch Chem, Damghan, Iran
[3] Shahrekord Univ, Fac Sci, Dept Chem, POB 88186-34141, Shahrekord, Iran
关键词:
Aryl;
heteroaryl aldehydes;
green conditions;
heterocyclization;
isoxazol-5(4H)-ones;
malic acid;
anti-Alzheimer;
3-COMPONENT SYNTHESIS;
3,4-DISUBSTITUTED ISOXAZOL-5(4H)-ONES;
ISOXAZOLONE DERIVATIVES;
EXPEDITIOUS SYNTHESIS;
GREEN SYNTHESIS;
FRUIT JUICE;
ISOXAZOLE-5(4H)-ONES;
INHIBITORS;
EXTRACT;
OXIDE;
D O I:
10.2174/1570178619666220903155012
中图分类号:
O62 [有机化学];
学科分类号:
070303 ;
081704 ;
摘要:
The efficient, straightforward, and green procedure was established in the direction of synthesis of 4-arylmethylene-3-methylisoxazol-5(4H)-one derivatives using the malic acid, which acted as the catalyst for the three-component heterocyclization reaction. In this reaction, aryl/heteroaryl aldehydes, hydroxylamine hydrochloride, and ethyl acetoacetate/ethyl benzoylacetate were applied as the reactants. The reaction was optimized to attain the best conditions for the synthesis of target heterocyclic compounds in a single step route. The best results were obtained from optimization experiments using 10 mol% malic acid as the catalyst, water solvent, and 50 degrees C temperature. The noticeable features of this process are the simplicity of the experimental procedure, the easy separation of the pure compounds from the product mixture, the simplicity of operation, avoidance of any hazardous organic solvents, no use of chromatographic purification techniques, clean reaction profiles, high yields, relatively short reaction time, and eco-friendliness.
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页码:167 / 174
页数:8
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