反应详情

To the 2'-O-propylcytidine reaction mixture of Example 82 in an ice bath was added pyridine (60 ml) and trimethylsilyl chloride (60 ml). The reaction was stirred for 30 mins followed by the addition of benzoyl chloride (55 ml). The resulting reaction mixture was stirred for 2.5 hrs and then cooled in an ice bath. H2O (100 ml) and conc. NH4OH (100 ml) were added. After stirring for 30 mins, the reaction mixture was evaporated and the residue partition between H2O and CH2Cl2. The organic phase was washed once with dil Na2CO3, once with dil HCl, dried over MgSO4 and evaporated. The resulting residue was loaded on a silica gel column (150 g) and eluted with first CH2Cl2 then 5 to 10% MeOH in CH2Cl2 as the elution solvent. The product containing fractions were evaporated to a foam. The foam was crystallized from EtOAc/Hexanes to give the product (6.5 g total) in several crystal batches.

1. customThe resulting reaction mixture
2. stirringwas stirred for 2.5 hrs
3. temperaturecooled in an ice bath
4. stirringAfter stirring for 30 mins
5. customthe reaction mixture was evaporated
6. customthe residue partition between H2O and CH2Cl2
7. washThe organic phase was washed once with dil Na2CO3, once with dil HCl
8. dry with materialdried over MgSO4
9. customevaporated
10. washeluted with first CH2Cl2
11. additionThe product containing fractions
12. customwere evaporated to a foam
13. customThe foam was crystallized from EtOAc/Hexanes
14. customto give the product (6.5 g total) in several crystal batches