Reaktionsgleichung
[C:1]1([CH:11]([N:13]2[CH:17]3[C:18](=O)[N:19]([CH2:22][CH2:23][C:24]4[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=4)[CH2:20][CH2:21][CH:16]3[CH2:15][CH2:14]2)[CH3:12])[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][CH:2]=1.CC(C[AlH]CC(C)C)C.C1(C)C=CC=CC=1>C1COCC1>[C:1]1([CH:11]([N:13]2[CH:17]3[CH2:18][N:19]([CH2:22][CH2:23][C:24]4[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=4)[CH2:20][CH2:21][CH:16]3[CH2:15][CH2:14]2)[CH3:12])[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][CH:2]=1Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
To a solution of 4 (4.8 g, 12 mmol) in THF (100 mL) is added slowly 1 M DIBAL in toluene, (50 mL, 50 mmol) at −78° C. The mixture is stirred at room temperature for 1 hour and quenched with 20 mL of water. The solvent is evaporated, the residue is diluted with 100 mL of 1:1 saturated Rochells salt/15% NaOH, and this extracted with EtOAc (4×50 mL). The organic extracts are combined, dried and concentrated under vacuum. The residue is purified by flash chromatography (silica gel; Hexane/EtOAc 1:9) to provide 2.3 g (48%) of the title compound. M+H+=385.26.
Aufarbeitung
- customquenched with 20 mL of water
- customThe solvent is evaporated
- additionthe residue is diluted with 100 mL of 1:1 saturated Rochells salt/15% NaOH
- extractionthis extracted with EtOAc (4×50 mL)
- customdried
- concentrationconcentrated under vacuum
- customThe residue is purified by flash chromatography (silica gel; Hexane/EtOAc 1:9)
Quellen und Nachweise
- ORD-Eintrag
- ord-64c3b14663624cb3bf3c7053b94f6551
- Quelldatensatz
- uspto-grants-2012_06
- Patentnummer
- US08207183B2
Verknüpfte Notizen
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