Diisopropylethylamine → HCID 67386290, Verbindung
Reaktionsgleichung
[C:1]([NH:8][C@@H:9]([C:11]([OH:13])=O)[CH3:10])([O:3][C:4]([CH3:7])([CH3:6])[CH3:5])=[O:2].F[B-](F)(F)F.N1(OC(N(C)C)=[N+](C)C)C2C=CC=CC=2N=N1.Cl.[C:37]([CH:39]1[CH2:42][NH:41][CH2:40]1)#[N:38].C(N(CC)C(C)C)(C)C>ClCCl.C(OCC)(=O)C.O>[C:4]([O:3][C:1](=[O:2])[NH:8][C@H:9]([CH3:10])[C:11]([N:41]1[CH2:42][CH:39]([C:37]#[N:38])[CH2:40]1)=[O:13])([CH3:5])([CH3:6])[CH3:7]Komponenten
Edukt 4
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 3
Versuchsvorschrift
Boc-D-alanine (1.0 g, 5.29 mmol) and O-benzotriazol-1-yl-N,N,N′,N′-tetramethyluronium tetrafluoroborate (1.87 g, 5.81 mmol) were dissolved in dichloromethane. 3-Cyanoazetidine hydrochloride (0.94 g, 7.93 mmol) and then N,N-diisopropylethylamine (2.3 mL, 13.2 mmol) were added and the mixture was stirred at room temperature for 16 h. Water and ethyl acetate were added and the layers were separated. The aqueous layer was extracted once more with ethyl acetate. The combined organic layers were washed with sodium chloride solution, dried over sodium sulfate and concentrated. The residue was purified by silica gel chromatography (ethyl acetate/hexanes) to provide 0.91 g (68%) of [(R)-2-(3-cyano-azetidin-1-yl)-1-methyl-2-oxo-ethyl]-carbamic acid tert-butyl ester.
Aufarbeitung
- customthe layers were separated
- extractionThe aqueous layer was extracted once more with ethyl acetate
- washThe combined organic layers were washed with sodium chloride solution
- dry with materialdried over sodium sulfate
- concentrationconcentrated
- customThe residue was purified by silica gel chromatography (ethyl acetate/hexanes)
Quellen und Nachweise
- ORD-Eintrag
- ord-51eb93e1791f447d9359d801e6fd4044
- Quelldatensatz
- uspto-grants-2013_08
- Patentnummer
- US08518945B2
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