Reaktion #417954

ord-3375b08b5c3a432fb130c603ea376af9

Reaktionsgleichung

C[C@@]1(n2ccc(=O)[nH]c2=O)O[C@@](COC(=O)c2ccccc2)(N=[N+]=[N-])[C@](O)(C(=O)c2ccccc2)[C@]1(O)C(=O)c1ccccc1
4′-Azido-1′-methyl-2′,3′,5′-O-tribenzoyluridine
C[C@@]1(n2ccc(=O)[nH]c2=O)O[C@@](CO)(N=[N+]=[N-])[C@@H](O)[C@H]1O
( 54 )
Ausbeute 46.2%
C[C@@]1(n2ccc(=O)[nH]c2=O)O[C@@](CO)(N=[N+]=[N-])[C@@H](O)[C@H]1O
4′-azido-1′-methyluridine
Ausbeute 46.2%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeThe solvent was removed
  2. 2
    Sonstigethe residue was purified on a silica gel column (DCM/MeOH=50:1 to 30:1)

Vorschrift

4′-Azido-1′-methyl-2′,3′,5′-O-tribenzoyluridine (37-7) (0.20 g, 0.34 mmol) was dissolved in saturated methanolic ammonia (50 mL), and the mixture was stirred at R.T. for 14 hours. The solvent was removed, and the residue was purified on a silica gel column (DCM/MeOH=50:1 to 30:1) to give (54) as a white solid (47 mg, 46.0%). 1H NMR (CD3OD, 400 MHz) δ8.15 (d, J=8.4 Hz, 1H), 5.63 (d, J=8.4 Hz, 1H), 4.73 (d, J=5.6 Hz, 1H), 4.17 (d, J=5.2 Hz, 1H), 3.67 (d, J=12.0 Hz, 1H), 3.55 (d, J=12.0 Hz, 1H), 1.76 (s, 3H); ESI-negative-MS: m/z=298.1 [M−H]+, 597.2 [2M+H]+.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08877731B2uspto-grants-2014_11