Tetrahydrofuran → (2R,5S)-3,6-Diethoxy-2-isopropyl-5-(2-[3-methoxy-4-(4-phenyl-butoxy)-phenyl]-ethyl)-2,5dihydro-pyrazine
Reaktionsgleichung
[CH2:1]([O:3][C:4]1[C@@H:5]([CH:13]([CH3:15])[CH3:14])[N:6]=[C:7]([O:10][CH2:11][CH3:12])[CH2:8][N:9]=1)[CH3:2].[CH2:16]([Li])[CH2:17][CH2:18][CH3:19].[CH2:21]1[CH2:25][O:24][CH2:23][CH2:22]1>>[CH2:1]([O:3][C:4]1[C@@H:5]([CH:13]([CH3:15])[CH3:14])[N:6]=[C:7]([O:10][CH2:11][CH3:12])[C@H:8]([CH2:19][CH2:18][C:17]2[CH:16]=[CH:21][C:25]([O:24][CH2:23][CH2:22][CH2:16][CH2:17][C:18]3[CH:14]=[CH:13][CH:5]=[CH:4][CH:19]=3)=[C:7]([O:10][CH3:11])[CH:8]=2)[N:9]=1)[CH3:2]Komponenten
Versuchsvorschrift
To a solution of (R)-3,6-diethoxy-2-isopropyl-2,5-dihydro-pyrazine (2.2 g; 10.4 mmol; Lohr, Birgit et al., Synlett, 1999, 7, 1139-1141) in dry THF (30 ml) at −78° C. there is added n-butyllithium (6.5 ml; 10.4 mmol; 1.6M in n-hexane). After 30 minutes at −78° C. the endproduct of step b) (4.3 g; 10.4 mmol) dissolved in dry THF (15 ml) is added tropwise over a period of 10 minutes. The reaction mixture is allowed to warm up to RT and it is kept at RT for 20 hours. After quenching with saturated aqueous ammonium chloride solution and extraction (2 times) with ethyl acetate the organic phase is dried over MgSO4 and concentrated under reduced pressure. The crude is purified on silica gel using diethylether/n-hexane (1/9) as mobile phase.
Aufarbeitung
- additionis added tropwise over a period of 10 minutes
- customAfter quenching with saturated aqueous ammonium chloride solution and extraction (2 times) with ethyl acetate the organic phase
- dry with materialis dried over MgSO4
- concentrationconcentrated under reduced pressure
- customThe crude is purified on silica gel
Quellen und Nachweise
- ORD-Eintrag
- ord-1ff7ad1a65714c399ebfbea68e6c7bb5
- Quelldatensatz
- uspto-grants-2008_02
- Patentnummer
- US07326801B2
Notizen zur Reaktion
Wird geladen…