4.5 Article

Efficient Synthesis of 4-Amino-2-methoxy-7,8-dihydropyrido[4,3-d]pyrimidin-5-ones: Practical Access to a Novel Chemotype in the Development of DGAT-1 Inhibitors

期刊

SYNTHESIS-STUTTGART
卷 44, 期 20, 页码 3152-3157

出版社

GEORG THIEME VERLAG KG
DOI: 10.1055/s-0032-1316756

关键词

4-amino-2-methoxy-7,8-dihydropyrido[4,3-d]pyrimidin-5-ones; heterocycle synthesis; DGAT-1 inhibitor; Buchwald amination; aza-Michael addition; Dieckmann-type cyclocondensation

向作者/读者索取更多资源

A practical access to an unprecedented, fused bicyclic 4-amino-2-alkoxy-7,8-dihydropyrido[4,3-d]pyrimidin-5-one scaffold is developed. The synthesis of the potent inhibitor, 2-{4-[4-amino-2-methoxy-5-oxo-7,8-dihydropyrido[4,3-d]pyrimidin-6(5H)-yl]phenyl}-2-methylpropanamide is detailed, with particular emphasis placed on synthetic efficiency and scalability. With the isolation of solid intermediates, the routes described offer clear elements of practicality and facilitate production of the target compound on large scale (>10 g) without chromatography.

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