2,2-Dimethyl-1,3-dioxan-5-ol → 2-(((4-((2,2-Dimethyl-1,3-dioxan-5-yl)oxy)-3-methylpyridin-2-yl)methyl)sulfinyl)-1h-benzimidazole sodium salt
Reaktionsgleichung
COC1OCC(C[O:10][C:11]2[CH:16]=[CH:15][N:14]=[C:13]([CH2:17][S:18]([C:20]3[NH:24][C:23]4[CH:25]=[CH:26][CH:27]=[CH:28][C:22]=4[N:21]=3)=[O:19])[C:12]=2[CH3:29])CO1.[Na:30].COC1OCC(COC2C=CN=C(CS(C3NC4C=CC=CC=4N=3)=O)C=2C)CO1.[CH3:60][C:61]1([CH3:68])[O:66][CH2:65][CH:64](O)[CH2:63][O:62]1>>[Na:30].[CH3:60][C:61]1([CH3:68])[O:66][CH2:65][CH:64]([O:10][C:11]2[CH:16]=[CH:15][N:14]=[C:13]([CH2:17][S:18]([C:20]3[NH:21][C:22]4[CH:28]=[CH:27][CH:26]=[CH:25][C:23]=4[N:24]=3)=[O:19])[C:12]=2[CH3:29])[CH2:63][O:62]1Komponenten
4
Edukt 3
Produkt 1
Versuchsvorschrift
The same procedure as in the steps (6d), (6e), and (6f) of Example 6 was repeated using 2,2-dimethyl-1,3-dioxan-5-ol obtained in the step (9a) to obtain the title compound (530 mg, total yield: 18%) as a light yellow solid.
Aufarbeitung
- customobtained in the step (9a)
Quellen und Nachweise
- ORD-Eintrag
- ord-cf2d85ef1b6046ecac8bf973c8dafada
- Quelldatensatz
- uspto-grants-2012_02
- Patentnummer
- US08124780B2
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