Reaktionsgleichung
[C:1]([N:8]1[CH2:13][CH2:12][NH:11][CH2:10][CH2:9]1)([O:3][C:4]([CH3:7])([CH3:6])[CH3:5])=[O:2].CN(C(ON1N=N[C:24]2[CH:25]=[CH:26][CH:27]=N[C:23]1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F.[C:38]1([CH:44](C)[C:45](O)=[O:46])C=CC=CC=1.[CH3:49]N(C=O)C>C(OCC)C>[CH3:38][CH:44]([N:11]1[CH2:10][CH2:9][N:8]([C:1]([O:3][C:4]([CH3:7])([CH3:6])[CH3:5])=[O:2])[CH2:13][CH2:12]1)[C:45](=[O:46])[C:23]1[CH:24]=[CH:25][CH:26]=[CH:27][CH:49]=1Komponenten
6
Edukt 4
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
To N-BOC-piperazine (0.373 g) in DMF (10 ml) was added HATU (1.14 g) followed by 2-phenylpropionic acid (0.30 ml) and the reaction stirred at RT for 16 h followed by 60° C. for 1 h. The reaction was cooled to RT, then diluted with diethyl ether, washed with water (×3), 2M HCl (×2), saturated aq. NaHCO3 (aq) (×2), dried (Na2SO4) and concentrated in vacuo to give the sub-titled compound (0.25 g).
Aufarbeitung
- waitfollowed by 60° C. for 1 h
- temperatureThe reaction was cooled to RT
- washwashed with water (×3), 2M HCl (×2), saturated aq. NaHCO3 (aq) (×2)
- dry with materialdried (Na2SO4)
- concentrationconcentrated in vacuo
Quellen und Nachweise
- ORD-Eintrag
- ord-16acc7c4cde945e59cce37a822ebe269
- Quelldatensatz
- uspto-grants-2013_09
- Patentnummer
- US08524715B2
Verknüpfte Notizen
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