HCID 22845791, compound → HCID 22845788, compound

HRID 1885521Notes

Reaction equation

HRID 1885521 reaction equation
[N:1]([C@@:4]1([OH:23])[C@@H:8]([CH2:9][O:10]C(=O)C)[O:7][C@@H:6]([N:14]2[CH:22]=[C:20]([CH3:21])[C:18](=[S:19])[NH:17][C:15]2=[O:16])[CH2:5]1)=[N+:2]=[N-:3]>O1CCOCC1.[NH4+].[OH-].CCOCC>[N:1]([C@@:4]1([OH:23])[C@@H:8]([CH2:9][OH:10])[O:7][C@@H:6]([N:14]2[CH:22]=[C:20]([CH3:21])[C:18](=[S:19])[NH:17][C:15]2=[O:16])[CH2:5]1)=[N+:2]=[N-:3]

Participants

5

Reactant 1

HCID 22845791HCID 22845791, compound

Product 1

HCID 22845788HCID 22845788, compound

Reagents, catalysts & solvents 3

HCID 3283Diethyl EtherSolventHCID 14923Ammonium HydroxideSolventHCID 312751,4-DioxaneSolvent

Procedure

3'-Azido-5'-O-acetyl-4-thiothymidine (0.25 g; 0.76 mMol, Example 11) was dissolved in a mixture of 5 mL of dioxane and 5 mL of conc. NH4OH and stirred for 18 hrs. The solvent was removed in vacuo and the residue applied to a silica gel column followed by elution with CHCl3 /EtOAc (3:1 v/v). The appropriate fractions were combined and the solvent removed in vacuo to yield a yellow oil which was dissolved in Et2O, forming crystals upon concentration: 0.16 g (0.56 mMol; 74%).

Workup

  1. customThe solvent was removed in vacuo
  2. washfollowed by elution with CHCl3 /EtOAc (3:1 v/v)
  3. customthe solvent removed in vacuo
  4. customto yield a yellow oil which
  5. customforming crystals upon concentration: 0.16 g (0.56 mMol; 74%)

Sources & evidence

ORD record
ord-f1696fceb1ba4a6a8b8fbdc4dd049404
Source dataset
uspto-grants-1992_09
Patent number
US05145840

Reaction notes

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