Citric Acid → HCID 86662969, Verbindung
Reaktionsgleichung
[CH:1]#[C:2][CH2:3][NH:4][C@H:5]1[C:9]2[CH:10]=[CH:11][CH:12]=[CH:13][C:8]=2[CH2:7][CH2:6]1.[C:14]([OH:26])(=[O:25])[CH2:15][C:16]([CH2:21][C:22]([OH:24])=[O:23])([C:18]([OH:20])=[O:19])[OH:17]>>[CH:1]#[C:2][CH2:3][NH:4][C@H:5]1[C:9]2[CH:10]=[CH:11][CH:12]=[CH:13][C:8]=2[CH2:7][CH2:6]1.[C:14]([O-:26])(=[O:25])[CH2:15][C:16]([CH2:21][C:22]([O-:24])=[O:23])([C:18]([O-:20])=[O:19])[OH:17]Komponenten
3
Versuchsvorschrift
The experiments conducted in this example are listed below in Table 3. In each of the experiments, rasagiline free base, excipient, and citric acid were combined and mixed. A solid dispersion was prepared from the mixture by dry milling, wet milling, or cryo-grinding the mixture at conditions listed in Table 3 below.
Aufarbeitung
- additionmixed
- customA solid dispersion was prepared from the mixture
- customby dry milling, wet milling
- customcryo-grinding the mixture at conditions
Quellen und Nachweise
- ORD-Eintrag
- ord-6b943e28f8ad4e4a838132c3b71aa459
- Quelldatensatz
- uspto-grants-2014_04
- Patentnummer
- US08691872B2
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