This submission belongs to the session c. Bioorganic Chemistry and Natural Products of the event The 4th International Electronic Conference on Synthetic Organic Chemistry
Published date
11 Sep, 2000
Citation
Ramachandra S. Hosmane, Huan-Ming Chen, Synthesis of 1-(2'-Deoxy-ß-D-ribofuranosyl)-1H-imidazo[4,5-d]pyridazine-4,7(5 H,6H)-dion: a Potentially Beneficial Building Block for Antisense Applications, in Proceedings of The 4th International Electronic Conference on Synthetic Organic Chemistry, 1 November–30 November 2000, MDPI: Basel, Switzerland, doi: 10.3390/ecsoc-4-01926
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Synthesis of 1-(2'-Deoxy-ß-D-ribofuranosyl)-1H-imidazo[4,5-d]pyridazine-4,7(5 H,6H)-dion: a Potentially Beneficial Building Block for Antisense Applications
Huan-Ming Chen 1
Ramachandra S. Hosmane 1
1. Laboratory for Drug Design and Synthesis Department of Chemistry & Biochemistry University of Maryland, Baltimore County 1000 Hilltop Circle, Baltimore, Maryland 21250, USA
Abstract
Synthesis of the title compound,1-(2'-deoxy-ß-D-ribofuranosyl)-1H-imidazo[4,5-d]pyridazine- -4,7(5H,6H)-dione (1), is reported. It was synthesized in five steps, commencing with methyl 1-(ß-D-ribofuranosyl)imidazo-4,5-dicarboxylate (2). The 3',5'-hydroxyl groups of 2 was protected with a bis-silylating agent to form 3, which was then converted into the corresponding 2'-thionocarbonate derivative 5. The reduction of the latter with tri-n-butyltin hydride (to form 6), followed by silyl deprotection with tetra-n-btylammonium fluoride, afforded 7. Treatment of the latter with hydrazine hydrate yielded the target nucleoside 1.
Keywords
Synthesis
Nucleoside Analogue
Imidazo[4,5-d]pyridazine
2'-Deoxy Nucleoside Analogue
Synthesis of 1-(2'-O-Methyl-ß -D-Ribofuranosyl)-1H-imidazo[4,5-d]pyridazine-4,7(5H,6H)-dion: an Attractive Building Block for Antisense and Triple-helical Applications
A Model Study for a Novel Synthetic Approach to 2-Carboxyinosines