Tetrabutylammonium Fluoride → 2'-O-(2-Methoxyethyl)-5-methyl-uridine
Reaction equation
[Si]([O:18][CH2:19][C@H:20]1[O:24][C@@H:23]([N:25]2[CH:32]=[C:31]([CH3:33])[C:29](=[O:30])[NH:28][C:26]2=[O:27])[C@H:22]([O:34][CH2:35][CH2:36][O:37][CH3:38])[C@@H:21]1[OH:39])(C(C)(C)C)(C1C=CC=CC=1)C1C=CC=CC=1.CCCC[N+](CCCC)(CCCC)CCCC.[F-]>>[CH3:38][O:37][CH2:36][CH2:35][O:34][C@@H:22]1[C@H:21]([OH:39])[C@@H:20]([CH2:19][OH:18])[O:24][C@H:23]1[N:25]1[CH:32]=[C:31]([CH3:33])[C:29](=[O:30])[NH:28][C:26]1=[O:27]Participants
3
Procedure
5′-O-t-Butyldiphenylsilyl-2′-O-(methoxyethyl)-5-methyluridine is treated with TBAF as per the procedure of Example 8 above to give the title compound.
Sources & evidence
- ORD record
- ord-a5eb0643ac4e4b3885a28d3e6c45f048
- Source dataset
- uspto-grants-2003_09
- Patent number
- US06624294B2
Reaction notes
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