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Water → 3'-Azido-2',3'-dideoxyuridine 5'-monophosphate

HRID 467264
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 467264
C(CC[O:5][P:6]([O-])([O-:8])=[O:7])#N.[N:10]([C@@H:13]1[C@@H:17]([CH2:18][OH:19])[O:16][C@@H:15]([N:20]2[CH:27]=[CH:26][C:24](=[O:25])[NH:23][C:21]2=[O:22])[CH2:14]1)=[N+:11]=[N-:12].C1(N=C=NC2CCCCC2)CCCCC1.O>N1C=CC=CC=1.[OH-].[K+]>[P:6]([O:19][CH2:18][C@H:17]1[O:16][C@@H:15]([N:20]2[CH:27]=[CH:26][C:24](=[O:25])[NH:23][C:21]2=[O:22])[CH2:14][C@@H:13]1[N:10]=[N+:11]=[N-:12])([OH:8])([OH:7])=[O:5]
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Komponenten

7

Edukt 4

HCID 962WaterHCID 10868DicyclohexylcarbodiimideHCID 55262NavuridineHCID 4064087beta-Cyanoethyl phosphate

Produkt 1

HCID 1594863'-Azido-2',3'-dideoxyuridine 5'-monophosphateAusbeute 73 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 1049
Pyridine
Lösungsmittel
2×
HCID 14797Potassium HydroxideLösungsmittel

Versuchsvorschrift

A freshly prepared pyridinium salt of 2-cyanoethylphosphate (8.05 g, 23.64 mmol) was added to a solution of 3'-azido-2',3'-dideoxyuridine (2.50 g, 9.7 mmol) in dry pyridine (50 ml) and evaporated to dryness at 30° C. The concentrated residue was dissolved in pyridine (50 ml) and the solution again evaporated to dryness. The process was repeated twice and then the residue obtained was dissolved in dry pyridine (50 ml). Dicyclohexylcarbodiimide (8.08 g, 39.1 mmol) was added to the solution. The reaction mixture was stirred for 48 hours at room temperature. Water (10 ml) was added and the solution was then filtered to remove dicyclohexylurea. The clear solution was evaporated to dryness. The residue obtained was then dissolved in 1N KOH (250 ml) and heated for 15 minutes at 100° C. The cold solution was passed through a column of acidic Dowex 50 (H+), the effluent brought to pH 9 and passed through a column of Dowex (1×4 Cl-). A linear gradient elution of 0.015N HCl to 0.15N HCl resulted in 3'-azido-2',3'-dideoxyuridine-5'-monophosphate with a 73% yield.

Aufarbeitung

  1. customevaporated to dryness at 30° C
  2. dissolutionThe concentrated residue was dissolved in pyridine (50 ml)
  3. customthe solution again evaporated to dryness
  4. customthe residue obtained
  5. filtrationthe solution was then filtered
  6. customto remove dicyclohexylurea
  7. customThe clear solution was evaporated to dryness
  8. customThe residue obtained
  9. temperatureheated for 15 minutes at 100° C
  10. washA linear gradient elution of 0.015N HCl to 0.15N HCl
  11. customresulted in 3'-azido-2',3'-dideoxyuridine-5'-monophosphate with a 73% yield

Quellen und Nachweise

ORD-Eintrag
ord-68ca896be8d043ec87e3ddc71e971c91
Quelldatensatz
uspto-grants-1992_10
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05159067

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