Reaktionsgleichung
[C:1]([O:5][C:6]([NH:8][CH:9]1[CH2:14][CH2:13][N:12]([CH2:15][CH:16]2[CH2:21][CH2:20][NH:19][CH2:18][CH2:17]2)[CH2:11][CH2:10]1)=[O:7])([CH3:4])([CH3:3])[CH3:2].[CH3:22][O:23][CH2:24][CH2:25][C:26](O)=[O:27].COC1C=CC(C(O)=O)=CC=1>>[C:1]([O:5][C:6]([NH:8][CH:9]1[CH2:10][CH2:11][N:12]([CH2:15][CH:16]2[CH2:17][CH2:18][N:19]([C:26](=[O:27])[CH2:25][CH2:24][O:23][CH3:22])[CH2:20][CH2:21]2)[CH2:13][CH2:14]1)=[O:7])([CH3:4])([CH3:2])[CH3:3]Komponenten
4
Versuchsvorschrift
Similar procedures as Example 60 are repeated except that 4-(t-butoxycarbonylamino)-1-(4-piperidinylmethyl)piperidine, and 3-methoxypropionic acid are used instead of 4-methoxybenzoic acid in Example 60 as described below to give 4-(t-butoxycarbonylamino)-1-[1-(3-methoxypropionyl)-4-piperidinylmethyl]piperidine.
Quellen und Nachweise
- ORD-Eintrag
- ord-2c95dd9233c64385a9b40a49124510e8
- Quelldatensatz
- uspto-grants-2001_09
- Patentnummer
- US06294555B1
Verknüpfte Notizen
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