Diethyl Ether → HCID 57153373, Verbindung
Reaktionsgleichung
[C:1]1([N:7]2[CH2:11][CH2:10][C:9](=O)[C:8]2=[O:13])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[NH2:14][N:15]1[CH2:19][CH2:18][CH2:17][CH:16]1[CH2:20][O:21][CH3:22].CCOCC>C1C=CC=CC=1>[CH3:22][O:21][CH2:20][CH:16]1[CH2:17][CH2:18][CH2:19][N:15]1[N:14]=[C:9]1[CH2:10][CH2:11][N:7]([C:1]2[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=2)[C:8]1=[O:13]Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A solution of the product of Example 61 and chiral 1-amino-2-methoxymethylpyrrolidine (SAMP or RAMP; 1 equiv) in benzene is refluxed under Dean-Stark conditions for 20 h. After cooling, Et2O is added and the mixture is washed with water. The organic layer is dried (MgO4) and evaporated to give a residue which is chromatographed on silica gel to give the title compound.
Aufarbeitung
- temperatureAfter cooling
- washthe mixture is washed with water
- customThe organic layer is dried (MgO4)
- customevaporated
- customto give a residue which
- customis chromatographed on silica gel
Quellen und Nachweise
- ORD-Eintrag
- ord-7cd4eb49a4a64bc196af6fa9a1c1c900
- Quelldatensatz
- uspto-grants-1994_05
- Patentnummer
- US05314886
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