Reaktionsgleichung
[CH2:1]([CH:8]([C:12](=O)[CH3:13])[C:9](=O)[CH3:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.Cl.[NH:16]([C:18]1[CH:23]=[CH:22][C:21]([CH2:24][CH2:25][OH:26])=[CH:20][CH:19]=1)[NH2:17]>>[CH2:1]([C:8]1[C:12]([CH3:13])=[N:17][N:16]([C:18]2[CH:19]=[CH:20][C:21]([CH2:24][CH2:25][OH:26])=[CH:22][CH:23]=2)[C:9]=1[CH3:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1Komponenten
3
Versuchsvorschrift
The title compound was prepared according to the procedure described in step 1 of Example 1 from 3-benzylpentane-2,4-dione and 2-(4-hydrazinophenyl)ethanol hydrochloride: 1H-NMR (CDCl3) δ 7.39-7.15 (9H, m), 3.89-3.85 (2H, t, J=6.4 Hz), 3.48 (2H, s), 2.91 (2H, t, J=6.6 Hz), 2.29 (3H, s), 2.21 (3H, s).
Quellen und Nachweise
- ORD-Eintrag
- ord-5c923d99f52c4d209b7bd6a0c0fd651d
- Quelldatensatz
- uspto-grants-2006_02
- Patentnummer
- US07001917B2
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