Acetic Anhydride → O-Acetyldeoxyacyclovir
Reaktionsgleichung
[OH:1][CH2:2][CH2:3][O:4][CH2:5][N:6]1[CH:14]=[N:13][C:12]2[C:7]1=[N:8][C:9]([NH2:15])=[N:10][CH:11]=2.[C:16](OC(=O)C)(=[O:18])[CH3:17]>CN(C)C1C=CN=CC=1.CN(C)C=O>[C:16]([O:1][CH2:2][CH2:3][O:4][CH2:5][N:6]1[CH:14]=[N:13][C:12]2[C:7]1=[N:8][C:9]([NH2:15])=[N:10][CH:11]=2)(=[O:18])[CH3:17]Komponenten
Reagenzien, Katalysatoren, Lösungsmittel 2
Versuchsvorschrift
A mixture of 0.82 g (3.92 mM) of 9-(2-hydroxyethoxymethyl)-2-amino-9H-purine, 48 mg (0.392 mM) of a 4-dimethylaminopyridine and 0.75 ml (7.84 mM) of acetic anhydride in 18 ml of dry dimethylformamide was stirred at room temperature for two days. The reaction mixture was evaporated in vacuo and the residue dissolved in ethyl acetate and absorbed on silica gel. The solvent was removed by flash evaporation and the residual powder added to a column prepared for flash chromatography. Elution with 5% methanol in dichloromethane gave 1.0 g of a semicrystalline oil which on recrystallization from benzene-hexane gave analytically pure 9-(2-acetoxyethoxymethyl)-2-amino-9H-purine, mpt. 115°-118° C. An additional crop was obtained from the mother liquor.
Aufarbeitung
- customThe reaction mixture was evaporated in vacuo
- dissolutionthe residue dissolved in ethyl acetate
- customabsorbed on silica gel
- customThe solvent was removed by flash evaporation
- additionthe residual powder added to a column
- customprepared for flash chromatography
- washElution with 5% methanol in dichloromethane
- customgave 1.0 g of a semicrystalline oil which
- customon recrystallization from benzene-hexane
Quellen und Nachweise
- ORD-Eintrag
- ord-36d240ac62694166b65b0e5066e56183
- Quelldatensatz
- uspto-grants-1986_09
- Patentnummer
- US04609662
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