Reaktionsgleichung
[C:1]([N:4]1[C:12]2[C:7](=[CH:8][C:9]([OH:14])=[C:10]([Br:13])[CH:11]=2)[CH2:6][CH2:5]1)(=[O:3])[CH3:2].Cl[C:16]([F:22])([F:21])C(OC)=O.C(=O)([O-])[O-].[K+].[K+]>CN(C)C=O>[C:1]([N:4]1[C:12]2[C:7](=[CH:8][C:9]([O:14][CH:16]([F:22])[F:21])=[C:10]([Br:13])[CH:11]=2)[CH2:6][CH2:5]1)(=[O:3])[CH3:2]Komponenten
Versuchsvorschrift
1-Acetyl-6-bromo-5-hydroxyindoline (2 g, 7.8 mmol), methyl 2-chloro-2,2-difluoroacetate (0.82 ml, 7.8 mmol) and potassium carbonate (1.08 g, 7.8 mmol) were suspended in N,N-dimethylformamide (20 mL) under an argon atmosphere and placed in a 65° C. oil bath. After 3 hr, additional methyl 2-chloro-2,2-difluoroacetate (0.3 ml, 2.8 mmol) and potassium carbonate (0.3 g, 2.2 mmol) was added and heated for 18 hr. The solvent was then removed in vacuo and the residue was partitioned between cold 3N HCl and ether. The aqueous layer was extracted three times with ether, the combined organic extracts were washed with brine, dried (Na2SO4), filtered and evaporated. The solid was purified by flash chromatography (2% MeOH/CH2Cl2) to provide the title compound as a white solid
Aufarbeitung
- customplaced in a 65° C.
- temperatureheated for 18 hr
- customThe solvent was then removed in vacuo
- customthe residue was partitioned between cold 3N HCl and ether
- extractionThe aqueous layer was extracted three times with ether
- washthe combined organic extracts were washed with brine
- dry with materialdried (Na2SO4)
- filtrationfiltered
- customevaporated
- customThe solid was purified by flash chromatography (2% MeOH/CH2Cl2)
Quellen und Nachweise
- ORD-Eintrag
- ord-550474a9556d462983b860f2b003f86a
- Quelldatensatz
- uspto-grants-1998_03
- Patentnummer
- US05731477
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