Journal
JOURNAL OF COMBINATORIAL CHEMISTRY
Volume 11, Issue 3, Pages 341-344Publisher
AMER CHEMICAL SOC
DOI: 10.1021/cc800167h
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Funding
- Research Council of Shahid Beheshti University
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An efficient one-pot synthesis of novel 8,9-dihydrospiro[chromeno [2,3-d]pyrimidine-5,3'-indoline]-2,2',4, 6(1H,3H,7H)-tetraone derivatives by a three-component condensation reaction of barbituric acids, isatins and cyclohexane-1,3-diones in refluxing water in the presence of P-TSA for 10 h is reported. Two cyclohexane-1,3-diones, three barbituric acids, and eight substituted isatins were chosen for the library validation. Reaction of 5,5-dimethyl-cyclohexane-1,3-dione and acenaphthylene-1,2-dione with barbituric acids resulted in the formation of spiro[acenaphthylene-1,5'-chromeno[2,3,d]pyrmidine] derivatives.
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