Solvent-free synthesis of ethereally substituted blocked monosaccharides and the selective hydrolysis thereof
AssigneeGreenwich Pharmaceuticals Incorporated
InventorSudershan K. Arora
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AssigneeGreenwich Pharmaceuticals Incorporated
InventorSudershan K. Arora
Estimating the term…
A solvent-free method for synthesizing an ethereally-substituted, blocked monosaccharide comprising the steps of: 1) mixing, in the absence of solvent, a partially blocked monosaccharide unblocked at one position, an alkyl halide or a substituted alkyl halide, and an anhydrous alkali base; 2) heating the mixture to a temperature sufficient to allow the mixture to react; 3) maintaining the mixture at a suitable temperature for a time sufficient to form an ethereally-substituted blocked monosaccharide and drive off any water produced; 4) removing any unreacted alkyl halide or substituted alkyl halide from the mixture; 5) recovering the ethereally-substituted blocked monosaccharide product from the mixture; and, optionally, 6) selectively hydrolyzing the ethereally-substituted blocked monosaccharide product to remove one or more of the acetal blocking groups.
A solvent-free method for synthesizing 1,2:5,6-di-O-isopropylidene-3-O-3'-(N',N'-dimethylamino-n-propyl)-.alpha., D-glucofuranose comprising the steps of:
A solvent-free synthesis to prepare 1,2:5,6-di-O-isopropylidene-3-O-3'-(N',N'-dimethylamino-n-propyl)-.alpha., D-glucofuranose by the following reaction:
Dependencies are inferred from the claim text.