Methanethiol → 2'-Deoxy-2'-methylthiouridine
Reaktionsgleichung
[CH:1]1[C:15](=[O:16])[N:14]=C2[N:3]([C@@H:4]3[O:8][C@H:7]([CH2:9][OH:10])[C@@H:6]([OH:11])[C@@H:5]3O2)[CH:2]=1.[CH3:17][SH:18].[CH3:19]N(C)C(N(C)C)=N>CN(C)C=O>[CH3:19][C@@H:5]1[C@H:6]([OH:11])[C@@H:7]([CH2:9][OH:10])[O:8][C@H:4]1[N:3]1[CH:2]=[CH:1][C:15](=[O:16])[NH:14][C:17]1=[S:18]Komponenten
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
2,2′-Anhydrouridine (15.5 g, 68.2 mmol) [Rao, T. S. and Reese, C. B. (1989) J. Chem. Soc., Chem. Commun., 997], methanethiol (15.7 g, 327 mmol), 1,1,3,3-tetramethylguanidine (39.2 g, 341 mmol) and dimethylforamide (150 ml) were heated together at 60° C. After 12 hr, the reaction mixture was cooled and concentrated under reduced pressure. The residual oil was purified by flash column chromatography on silica gel (300 g). Concentration of the appropriate fractions, which were eluted with CH2Cl2-MeOH (9:1, v/v), and drying of the residue under high vacuum gave 2′-deoxy-2′-methylthiouridine as a pale yellow solid (14.11 g, 75.4%). Attempts to crystallize the solids from ethanol-hexanes (as reported by Imazawa, M., Ueda, T., and Ukita, T. (1975) Chem. Pharm. Bull., 23:604) failed and the material turned into a hygroscopic foam.
Aufarbeitung
- temperaturethe reaction mixture was cooled
- concentrationconcentrated under reduced pressure
- customThe residual oil was purified by flash column chromatography on silica gel (300 g)
- washConcentration of the appropriate fractions, which were eluted with CH2Cl2-MeOH (9:1, v/v)
- customdrying of the residue under high vacuum
Quellen und Nachweise
- ORD-Eintrag
- ord-c0b07e3e95dd4b58908b357ebee70b75
- Quelldatensatz
- uspto-grants-2001_10
- Patentnummer
- US06307040B1
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