US2016348109A1PendingUtilityA1

Post-synthetic chemical modification of rna at the 2'-position of the ribose ring via "click" chemistry

Assignee: SIRNA THERAPEUTICS INCPriority: Jan 22, 2010Filed: Aug 11, 2016Published: Dec 1, 2016
Est. expiryJan 22, 2030(~3.5 yrs left)· nominal 20-yr term from priority
C12N 15/1137C12N 15/113C12N 2310/321C12N 2330/30C12N 2310/14C07D 209/48C07C 217/52C07H 21/02C07D 295/088C07C 217/40C12N 2310/141C07D 207/08C07C 2601/02C07D 211/22C07D 211/44C07D 207/12C07D 211/46
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Claims

Abstract

This invention relates to a 2′-modified RNA agent comprising at least one RNA strand containing a 2′-O substituent having an alkyne functional group attaching to the O atom at the 2′-position on one or more ribose rings, wherein the 2′-O substituent is located at one or more of positions 2, 3, 4, 7, 8, 9, 10, 11, 13, 14, and 16, from 5′-end of the RNA strand. This invention also relates to a 2′-modified RNA agent comprising at least one RNA strand containing a 2′-O substituent having a triazole functional group attaching to the O atom at the 2′-position on one or more ribose rings, wherein the 2′-O substituent is located at one or more of positions 2, 3, 4, 7, 8, 9, 10, 11, 13, 14, and 16, from 5′-end of the RNA strand.

Claims

exact text as granted — not AI-modified
What is claimed is: 
     
         1 . A process for introducing 2′-modifications into RNA, said process comprises a) obtaining RNA with an alkyne functional group at the 2′-position on at least one ribose ring; b) creating a solution of RNA in a solvent; and c) adding an organic azide and a metal catalyst to the solution to form a reaction and creating a 2′-modified RNA.

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