SYNTHESIS OF FLUORINATED CYCLIC DINUCLEOTIDES

The present invention relates to efficient processes useful in the preparation of fluorinated cyclic dinucleosides, such as [P(R)]-2′-deoxy-2′-fluoro-5′-O-[(R)-hydroxymercaptophosphinyl]-P-thio-β-D-arabino-adenylyl-(3′→5′)-3′-deoxy-3′-fluoroguanosine cyclic nucleotide, which is also known as (2R,5R,...

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Bibliographische Detailangaben
Hauptverfasser: Winston, Matthew S, Peng, Feng, Hiraga, Kaori, Fier, Patrick S, McIntosh, John, Liu, Zhijian, Moore, Jeffrey C, Pan, Weilan, Miller, Steven P, Murphy, Grant S, Obligacion, Jennifer V, Salehi Marzijarani, Nastaran, Marshall, Nicholas M, An, Chihui
Format: Patent
Sprache:eng
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Zusammenfassung:The present invention relates to efficient processes useful in the preparation of fluorinated cyclic dinucleosides, such as [P(R)]-2′-deoxy-2′-fluoro-5′-O-[(R)-hydroxymercaptophosphinyl]-P-thio-β-D-arabino-adenylyl-(3′→5′)-3′-deoxy-3′-fluoroguanosine cyclic nucleotide, which is also known as (2R,5R,7R,8S,10R,12aR,14R,15S,15aR,16R)-7-(2-amino-6-oxo-1,6-dihydro-9H-purin-9-yl)-14-(6-amino-9H-purin-9-yl)-15,16-difluoro-2, 10-bis(sulfanyl)octahydro-2H,10H, 12H-2λ5,10λ5-5,8-methanofuro[3,2-1][1, 3,6,9,11,2,10]pentaoxadiphosphacyclotetradecine-2,10-dione. The present invention also encompasses intermediates useful in the disclosed synthetic processes and the methods of their preparation.