Trimethylsilyl triflate → 4-Chloro-2-(isopropylamino)-1-(2,3,5-tri-O-acetyl-beta-L-ribofuranosyl)-1H-benzimidazole

HRID 1532606Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1532606
[Cl:1][C:2]1[C:10]2[N:9]=[C:8]([NH:11][CH:12]([CH3:14])[CH3:13])[NH:7][C:6]=2[CH:5]=[CH:4][CH:3]=1.C/C(/O[Si](C)(C)C)=N\[Si](C)(C)C.FC(F)(F)S(O[Si](C)(C)C)(=O)=O.C(O[CH:43]1[O:55][C@@H:54]([CH2:56][O:57][C:58](=[O:60])[CH3:59])[C@H:49]([O:50][C:51](=[O:53])[CH3:52])[C@@H:44]1[O:45][C:46](=[O:48])[CH3:47])(=O)C>ClCCCl>[Cl:1][C:2]1[C:10]2[N:9]=[C:8]([NH:11][CH:12]([CH3:14])[CH3:13])[N:7]([C@H:43]3[O:55][C@@H:54]([CH2:56][O:57][C:58](=[O:60])[CH3:59])[C@H:49]([O:50][C:51](=[O:53])[CH3:52])[C@@H:44]3[O:45][C:46](=[O:48])[CH3:47])[C:6]=2[CH:5]=[CH:4][CH:3]=1

Komponenten

6

Versuchsvorschrift

4-Chloro-2-(isopropylamino)-1H -benzimidazole (2.24 g, 10.68 mmol), N,O-bis(trimethylsilyl)acetamide (3.00 mL, 2.47 g, 12.14 mmol), trimethylsilyl trifluoromethanesulfonate (1.2 mL, 1.42 g, 6.00 mmol), 1,2,3,5-tetra-O-acetyl-L-ribofuranose (4.46 g, 14.01 mmol) and 1,2-dichloroethane (35 mL) were used according to general procedure II. The product was purified by silica gel chromatography using 95:5 dichloromethane/acetonitrile to afford 2.34 g (47%) of an off-white foam. MS (EI): m/z 46.82 (M+H).

Aufarbeitung

  1. customThe product was purified by silica gel chromatography

Quellen und Nachweise

ORD-Eintrag
ord-58cd65b4b54a4930875b507888ac2ba7
Quelldatensatz
uspto-grants-2001_03
Patentnummer
US06204249B1

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