Application of design of experiments (DoE) optimization to the one-pot synthesis of 4,6-dihydropteridinones?
Organic & Biomolecular Chemistry Pub Date: 2015-09-01 DOI: 10.1039/C5OB01154J
Abstract
A design of experiments (DoE) analysis of a tandem SnAr-amidation cyclization reaction between 4-chloropyrimidin-5-amine and (S)-N-methylalanine to form (S)-7,8-dimethyl-7,8-dihydropteridin-6(5H)-one is reported. Five reaction variables were optimized using DoE and conversion was improved from 26% to 74%, with a significant reduction in reaction time while retaining high optical purity. The optimized conditions were applied to the synthesis of a wide variety of analogs and the expanded reaction substrate scope included a variety of amino acids and pyrimidines. Products were obtained in isolated yields up to 95% and enantiomeric excess as high as 98%.
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Journal Name：Organic & Biomolecular Chemistry
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CAS no.: 89640-58-4
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