2-Aminomethyl-1-ethylpyrrolidine → HCID 70251970, Verbindung
Reaktionsgleichung
[CH2:1]([O:11][C:12]1[CH:20]=[C:19]([O:21][CH3:22])[CH:18]=[CH:17][C:13]=1[C:14]([OH:16])=O)/[CH:2]=[C:3](/[CH2:5][CH2:6][CH:7]=[C:8]([CH3:10])[CH3:9])\[CH3:4].[NH2:23][CH2:24][CH:25]1[CH2:29][CH2:28][CH2:27][N:26]1[CH2:30][CH3:31]>>[CH2:30]([N:26]1[CH2:27][CH2:28][CH2:29][CH:25]1[CH2:24][NH:23][C:14](=[O:16])[C:13]1[CH:17]=[CH:18][C:19]([O:21][CH3:22])=[CH:20][C:12]=1[O:11][CH2:1]/[CH:2]=[C:3](/[CH2:5][CH2:6][CH:7]=[C:8]([CH3:9])[CH3:10])\[CH3:4])[CH3:31]Komponenten
3
Versuchsvorschrift
In a manner identical to Example 15, 2-geranyloxy-4-methoxybenzoic acid(1.52 g) was subjected to a condensation reaction with 2-aminomethyl-1-ethylpyrrolidine (0.7 ml), thereby yielding 1.43 g(69%) of the aimed compound.
Quellen und Nachweise
- ORD-Eintrag
- ord-e38acd7718d844f9a9a50866ff1416cc
- Quelldatensatz
- uspto-grants-2000_03
- Patentnummer