773073-13-5Relevant academic research and scientific papers
Demonstration of the feasibility of a direct solid-phase split-pool Biginelli synthesis of 3,4-dihydropyrimidinones
Lusch, Michael J.,Tallarico, John A.
, p. 3237 - 3240 (2004)
(Chemical Equation Presented) A direct, Lewis acid-catalyzed Biginelli synthesis of 3,4-dihydropyrimidinones has been performed on high-capacity polystyrene macrobeads with a polymer O-silyl-attached N-(3-hydroxypropyl)urea. Resin-urea was first reacted separately with either 4-bromo- or 4-chlorobenzaldehyde and LiOTf in MeCN at 80°C. After washing, the beads were pooled and reacted with ethyl acetoacetate and LiOTf in MeCN at 80°C. Formation of only one kind of Biginelli product per bead demonstrated the feasibility of a solid-phase non-Atwal two-step split-and-pool synthesis of 3,4-dihydropyrimidinones.
HETEROARYLCARBOXYLIC ACID ESTER DERIVATIVE
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Page/Page column 28, (2012/11/06)
The present invention provides a hyperglycemic inhibitor having a serine protease inhibitory action, which is a novel prophylactic or therapeutic drug for diabetes. A compound represented by the following formula (I), wherein each symbol is as defined in the description, or a pharmaceutically acceptable salt thereof
