Reaktionsgleichung
[N:1]1([C:5]([C:7]2[CH:8]=[C:9]([Cl:43])[C:10]([O:13][C:14]3[CH:15]=[C:16]([CH:28]=[C:29]([O:31][C@@H:32]([CH3:42])[CH2:33][O:34][Si](C(C)(C)C)(C)C)[CH:30]=3)[C:17]([NH:19][C:20]3[CH:24]=[CH:23][N:22]([CH:25]([CH3:27])[CH3:26])[N:21]=3)=[O:18])=[N:11][CH:12]=2)=[O:6])[CH2:4][CH2:3][CH2:2]1.Cl.C(=O)(O)[O-].[Na+]>CO>[N:1]1([C:5]([C:7]2[CH:8]=[C:9]([Cl:43])[C:10]([O:13][C:14]3[CH:15]=[C:16]([CH:28]=[C:29]([O:31][C@@H:32]([CH3:42])[CH2:33][OH:34])[CH:30]=3)[C:17]([NH:19][C:20]3[CH:24]=[CH:23][N:22]([CH:25]([CH3:27])[CH3:26])[N:21]=3)=[O:18])=[N:11][CH:12]=2)=[O:6])[CH2:2][CH2:3][CH2:4]1Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
3-{[5-(Azetidin-1-ylcarbonyl)-3-chloropyridin-2-yl]oxy}-5-[((1S)-2-{[(1,1-dimethylethyl)(dimethyl)silyl]oxy}-1-methylethyl)oxy]-N-[1-(1-methylethyl)-1H-pyrazol-3-yl]benzamide (142 mg, 0.23 mmol) in methanol (2 mL) was stirred with 3.5M hydrochloric acid (0.2 mL, 0.68 mmol) for 1 hour. The solution was neutralised with saturated sodium bicarbonate solution and the organic solvent was removed under reduced pressure. The residue was extracted with ethyl acetate (3×10 mL), dried (MgSO4), filtered and the solvent removed under reduced pressure. The residue was purified by chromatography on silica, eluting with 75-100% ethyl acetate in hexane, to give the required product as a white foam (99 mg).
Aufarbeitung
- customthe organic solvent was removed under reduced pressure
- extractionThe residue was extracted with ethyl acetate (3×10 mL)
- dry with materialdried (MgSO4)
- filtrationfiltered
- customthe solvent removed under reduced pressure
- customThe residue was purified by chromatography on silica
- washeluting with 75-100% ethyl acetate in hexane
Quellen und Nachweise
- ORD-Eintrag
- ord-b4f367c7b9fd4f05982d55d698f93e91
- Quelldatensatz
- uspto-grants-2010_01
- Patentnummer
- US07642263B2
Verknüpfte Notizen
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