Benzylamine → HCID 11472167, Verbindung
Reaktionsgleichung
C(OC([N:8]1[CH2:13][CH2:12][C:11](=O)[CH2:10][CH2:9]1)=O)(C)(C)C.[CH2:15]([NH2:22])[C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1.[N+]([C:26]([CH3:34])=[CH:27][C:28]1[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=1)([O-])=O>>[CH2:15]([N:22]1[C:11]2[CH2:10][CH2:9][NH:8][CH2:13][C:12]=2[C:27]([C:28]2[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=2)=[C:26]1[CH3:34])[C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1Komponenten
4
Versuchsvorschrift
The title compound (89.4 mg) was prepared from 0.51 g of 4-oxo-piperidine-1-carboxylic acid tert-butyl ester, 272 μL of benzylamine, and 0.41 g of (2-nitro-propenyl)-benzene. MS (ESI): exact mass calculated for C21H22N2, 302.18; found, m/z 303.2 [M+H]+. 1H NMR (400 MHz, CD3OD): 7.41-7.36 (m, 2H), 7.35-7.30 (m, 2H), 7.28-7.21 (m, 4H), 7.05-7.01 (m, 2H), 5.16 (s, 2H), 4.18 (s, 2H), 3.52 (t, J=6.3 Hz, 2H), 2.89 (t, J=6.3 Hz, 2H).
Quellen und Nachweise
- ORD-Eintrag
- ord-77b094a6f2714a20a94a2fcd87629cc0
- Quelldatensatz
- uspto-grants-2011_03
- Patentnummer
- US07897771B2
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