Reaktionsgleichung
[F:1][C:2]1[C:11]2[O:10][CH2:9][CH:8]([CH2:12][OH:13])[O:7][C:6]=2[CH:5]=[C:4]([S:14]([CH3:17])(=[O:16])=[O:15])[CH:3]=1.[C:18]1(C)[C:19]([S:24](Cl)(=[O:26])=[O:25])=[CH:20][CH:21]=[CH:22][CH:23]=1.[CH2:29](Cl)Cl>CN(C1C=CN=CC=1)C>[CH3:29][C:22]1[CH:23]=[CH:18][C:19]([S:24]([O:13][CH2:12][CH:8]2[O:7][C:6]3[CH:5]=[C:4]([S:14]([CH3:17])(=[O:16])=[O:15])[CH:3]=[C:2]([F:1])[C:11]=3[O:10][CH2:9]2)(=[O:25])=[O:26])=[CH:20][CH:21]=1Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A solution of [5-fluoro-7-(methylsulfonyl)-2,3-dihydro-1,4-benzodioxin-2-yl]methanol (0.4 g, 1.7 mmol), toluenesulfonyl chloride (0.5 g, 2.6 mmol), TEA (0.4 ml, 2.6 mmol) and 4-DMAP (0.2 g, 1.7 mmol) in DCM (10 ml) was stirred at rt for 1 h. DCM was added and the resulting mixture was washed with HCl (1 N) and brine. The organic phase was dried (Na2SO4) and evaporated to dryness to give the title compound (0.7 g). MS m/z (rel. intensity, 70 eV) 416 (M+, 31), 244 (bp), 243 (26), 231 (19), 91 (70).
Aufarbeitung
- washthe resulting mixture was washed with HCl (1 N) and brine
- dry with materialThe organic phase was dried (Na2SO4)
- customevaporated to dryness
Quellen und Nachweise
- ORD-Eintrag
- ord-17a5df4cda5c49fea3146204156f6994
- Quelldatensatz
- uspto-grants-2013_09
- Patentnummer
- US08524766B2
Verknüpfte Notizen
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