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Hexamethyldisilazane → 2',3'-di-O-methoxycarbonyl-5'-deoxy-5-fluorocytidine

HRID 420836
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 420836
[F:1][C:2]1[C:3]([NH2:9])=[N:4][C:5](=[O:8])[NH:6][CH:7]=1.C[Si](C)(C)N[Si](C)(C)C.COC(O[CH:24]1[O:38][C@H:37]([CH3:39])[C@@H:31]([O:32][C:33]([O:35][CH3:36])=[O:34])[C@H:25]1[O:26][C:27]([O:29][CH3:30])=[O:28])=O.FC(F)(F)S(O[Si](C)(C)C)(=O)=O.C(=O)([O-])O.[Na+]>S([O-])([O-])(=O)=O.[NH4+].[NH4+].ClCCl.O.C(#N)C>[CH3:30][O:29][C:27]([O:26][C@@H:25]1[C@H:31]([O:32][C:33]([O:35][CH3:36])=[O:34])[C@@H:37]([CH3:39])[O:38][C@H:24]1[N:6]1[CH:7]=[C:2]([F:1])[C:3]([NH2:9])=[N:4][C:5]1=[O:8])=[O:28]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

10

Edukt 5

HCID 13838HexamethyldisilazaneHCID 65367Trimethylsilyl triflateHCID 516892Sodium BicarbonateHCID 666573491,2,3-tri-O-methoxycarbonyl-5-deoxy-D-ribofuranoseHCID 178509021HCID 178509021, Verbindung

Produkt 1

HCID 66657440
2',3'-di-O-methoxycarbonyl-5'-deoxy-5-fluorocytidine
Ausbeute 110,1 %

Reagenzien, Katalysatoren, Lösungsmittel 4

HCID 6097028Ammonium SulfateKatalysatorHCID 962WaterLösungsmittelHCID 6342AcetonitrileLösungsmittel3×HCID 6344DichloromethaneLösungsmittel

Versuchsvorschrift

11.6 g (0.090 mole) of 5-fluorocytosine, 19 ml of hexamethyldisilazane and 24 ml of acetonitrile were mixed, and 0.2 g of ammonium sulfate was added to the mixture, which was refluxed for 1 hr. After cooling the reaction mixture to room temperature, 72 ml of acetonitrile was added thereto, followed by subjecting the resulting mixture to distillation to remove about 60 ml of the solvent. The resulting solution was cooled to room temperature, mixed with 27.7 g (0.090 mole) of the compound obtained in Example 1 and 72 ml of acetonitrile, and the resulting mixture was cooled to 20° C. After adding 16.3 ml (0.090 mole) of trimethylsilyl trifluoromethanesulfonate dropwise thereto at 25° C., the reaction mixture was stirred at room temperature overnight, cooled to 10° C., mixed with 45.4 g of sodium hydrogen carbonate, and stirred for 30 min. 9.8 g of water and 72 ml of dichloromethane were added dropwise thereto, the resulting solution was stirred for 2 hrs, filtered, and the isolated solid was washed with 72 ml of dichloromethane. The filtrate was washed with 120 ml of 4% sodium bicarbonate, dried over anhydrous sodium sulfate, filtered, and concentrated under a reduced pressure, to obtain 35.8 g of the title compound.

Aufarbeitung

  1. temperaturewas refluxed for 1 hr
  2. distillationto distillation
  3. customto remove about 60 ml of the solvent
  4. temperatureThe resulting solution was cooled to room temperature
  5. temperaturethe resulting mixture was cooled to 20° C
  6. temperaturecooled to 10° C.
  7. stirringstirred for 30 min
  8. stirringthe resulting solution was stirred for 2 hrs
  9. filtrationfiltered
  10. washthe isolated solid was washed with 72 ml of dichloromethane
  11. washThe filtrate was washed with 120 ml of 4% sodium bicarbonate
  12. dry with materialdried over anhydrous sodium sulfate
  13. filtrationfiltered
  14. concentrationconcentrated under a reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-61b075de1b48453bb52605b985ee7c71
Quelldatensatz
uspto-grants-2012_01
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08097706B2

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