Potassium Carbonate → ((2S,5R)-5-(6-Amino-9H-purin-9-yl)-2,5-dihydrofuran-2-yl)methyl acetate

HRID 1030774

Reaktionsgleichung

Reaktionsgleichung von HRID 1030774
C(O[C@@H:5]1[C@@H:9](Br)[C@@H:8]([CH2:11][O:12][C:13](=[O:15])[CH3:14])[O:7][C@H:6]1[N:16]1[CH:24]=[N:23][C:22]2[C:17]1=[N:18][CH:19]=[N:20][C:21]=2[NH2:25])(=O)C.[O-]S(S([O-])=O)=O.[Na+].[Na+].C([O-])([O-])=O.[K+].[K+].[Br-].[Br-].C([N+]1C=CC(C2C=C[N+](CCCCCCC)=CC=2)=CC=1)CCCCCC>C(Cl)Cl.O>[C:13]([O:12][CH2:11][C@H:8]1[O:7][C@@H:6]([N:16]2[C:17]3[N:18]=[CH:19][N:20]=[C:21]([NH2:25])[C:22]=3[N:23]=[CH:24]2)[CH:5]=[CH:9]1)(=[O:15])[CH3:14]

Komponenten

7

Edukt 4

HCID 11430Potassium Carbonate2×HCID 24489Sodium DithioniteHCID 802621,1'-Diheptyl-4,4'-bipyridinium dibromide2×HCID 109825609-(2,5-di-O-acetyl-3-bromo-3-deoxy-beta-D-xylofuranosyl)adenine

Produkt 1

HCID 11022122((2S,5R)-5-(6-Amino-9H-purin-9-yl)-2,5-dihydrofuran-2-yl)methyl acetateAusbeute 83 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 962WaterLösungsmittelHCID 6344DichloromethaneLösungsmittel2×

Versuchsvorschrift

To a solvent mixture of 35 ml of methylene chloride and 15 ml of water were added 500 mg (1.21 mmol) of 9-(2,5-di-O-acetyl-3-bromo-3-deoxy-β-D-xylofuranosyl)adenine, 2.09 g (12.0 mmols) of Na2S2O4 and 995 mg (7.2 mmols) of K2CO3. The mixture was stirred for a while in an argon atmosphere. Then 308 mg (0.6 mmol) of N,N'-diheptyl-4,4'-bipyridinium dibromide was added and the mixture was stirred at 28° C. for 15 hours. Furthermore, 418 mg of Na2S2C4, 380 mg of K2CO3 and 185 mg (0.36 mmol) of N,N'-diheptyl-4,4'-bipyridinium dibromide were supplemented followed by stirring for 24 hours. To the mixture was added 50 ml of methylene chloride. The mixture was fractionated and the organic phase was dried over anhydrous magnesium sulfate. After filtering and concentration, the concentrate was purified by silica gel PTLC [Whatman PLK-5F, developed with ethyl acetate-methanol (8:1)] to give 276 mg (83%) of 5'-O-acetyl-2',3'-didehydro-2',3'-dideoxyadenosine.

Aufarbeitung

  1. stirringthe mixture was stirred at 28° C. for 15 hours
  2. stirringby stirring for 24 hours
  3. dry with materialthe organic phase was dried over anhydrous magnesium sulfate
  4. filtrationAfter filtering
  5. concentrationconcentration
  6. customthe concentrate was purified by silica gel PTLC [Whatman PLK-5F, developed with ethyl acetate-methanol (8:1)]

Quellen und Nachweise

ORD-Eintrag
ord-fe7f1f89f20246688b3021a5b92e411c
Quelldatensatz
uspto-grants-1992_04
Patentnummer
US05106962

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