Reaktionsgleichung
NN.[C:3]([O:9][C:10]([CH3:13])([CH3:12])[CH3:11])(=[O:8])[CH2:4][C:5]([O-:7])=O.[OH2:14].O[N:16]1[C:20]2[CH:21]=CC=CC=2N=[N:17]1.[CH2:25]([N:27]([CH2:30][CH3:31])[CH2:28][CH3:29])[CH3:26].Cl.CN(C)[CH2:35][CH2:36][CH2:37][N:38]=C=NCC>ClCCl>[C:10]([O:9][C:3](=[O:8])[CH2:4][C:5](=[O:7])[NH:17][NH:16][C:20]([CH:21]1[CH2:29][CH2:28][N:27]([C:30]2[CH:31]=[CH:35][CH:36]=[CH:37][N:38]=2)[CH2:25][CH2:26]1)=[O:14])([CH3:13])([CH3:12])[CH3:11]Komponenten
7
Edukt 5
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A mixture of the hydrazine from preparation 35 (2.2 g, 10 mmol), tert-butyl malonate (1.6 g, 10 mmol), 1-hydroxybenzotriazole hydrate (2.02 g, 15 mmol), triethylamine (4.8 ml, 20 mmol) and 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (2.4 g, 12.5 mmol) in dichloromethane (50 ml) was stirred at room temperature for 5 hours. The reaction was diluted with dichloromethane (200 ml), washed with water (150 ml), dried (MgSO4) and evaporated under reduced pressure. The residual oil was purified by column chromatography on silica gel using ethyl acetate as eluant to afford the title compound, as a white solid, 1.4 g.
Aufarbeitung
- washwashed with water (150 ml)
- dry with materialdried (MgSO4)
- customevaporated under reduced pressure
- customThe residual oil was purified by column chromatography on silica gel
Quellen und Nachweise
- ORD-Eintrag
- ord-2ff387fd184f4f2e8c6f2f73124e8925
- Quelldatensatz
- uspto-grants-2006_08
- Patentnummer
- US07084145B2
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