Hydrochloric Acid → Z-Ser(But)-Ser(But)-OMe
Reaktionsgleichung
[NH:1]([C:12]([O:14][CH2:15][C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1)=[O:13])[C@H:2]([C:9]([OH:11])=O)[CH2:3][O:4][C:5]([CH3:8])([CH3:7])[CH3:6].Cl.[NH2:23][C@H:24]([C:31]([O:33][CH3:34])=[O:32])[CH2:25][O:26][C:27]([CH3:30])([CH3:29])[CH3:28].C(N1CCOCC1)C.C1C=CC2N(O)N=NC=2C=1.C1(N=C=NC2CCCCC2)CCCCC1>CN(C)C=O>[NH:1]([C:12]([O:14][CH2:15][C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1)=[O:13])[C@H:2]([C:9]([NH:23][C@H:24]([C:31]([O:33][CH3:34])=[O:32])[CH2:25][O:26][C:27]([CH3:30])([CH3:29])[CH3:28])=[O:11])[CH2:3][O:4][C:5]([CH3:6])([CH3:7])[CH3:8]Komponenten
8
Edukt 6
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
To 4.43 g of Z-Ser(But)-OH and 3.18 g of HCl.H-Ser(But)-OMe in 30 ml of dimethylformamide are added at 0° 1.89 ml of N-ethylmorpholine, 2.29 g of HOBt and 3.4 g of dicyclohexylcarbodiimide. After standing for 2 hours at 0° and for 15 hours at 20°, the resulting product is filtered off, the filtrate is concentrated by evaporation and taken up in ethyl acetate. After extraction of the solution with sodium bicarbonate, dilute hydrochloric acid and water, the solution is concentrated by evaporation to leave as oil Z-Ser(But)-Ser(But)-OMe; Rf (toluene/acetone 1:1)=0.70.
Aufarbeitung
- filtrationthe resulting product is filtered off
- concentrationthe filtrate is concentrated by evaporation
- extractionAfter extraction of the solution with sodium bicarbonate, dilute hydrochloric acid and water
- concentrationthe solution is concentrated by evaporation
Quellen und Nachweise
- ORD-Eintrag
- ord-648a931901cb4480963112ae3a3deab9
- Quelldatensatz
- uspto-grants-1984_03
- Patentnummer
- US04439425
Notizen zur Reaktion
Wird geladen…