Lithium Hydroxide → HCID 68406214, Verbindung
Reaktionsgleichung
[C:1]([C:4]1[S:8][C:7]([N:9]2[CH2:14][CH2:13][C@H:12]([NH:15][C:16]([C:18]3[NH:19][C:20]([CH2:24][CH3:25])=[C:21]([Cl:23])[N:22]=3)=[O:17])[C@H:11]([O:26][CH3:27])[CH2:10]2)=[N:6][C:5]=1[C:28]([O:30]CC)=[O:29])(=[O:3])[CH3:2].[OH-].[Li+]>CO.C1COCC1>[C:1]([C:4]1[S:8][C:7]([N:9]2[CH2:14][CH2:13][C@H:12]([NH:15][C:16]([C:18]3[NH:19][C:20]([CH2:24][CH3:25])=[C:21]([Cl:23])[N:22]=3)=[O:17])[C@H:11]([O:26][CH3:27])[CH2:10]2)=[N:6][C:5]=1[C:28]([OH:30])=[O:29])(=[O:3])[CH3:2]Komponenten
5
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Versuchsvorschrift
Ethyl cis(±)-5-acetyl-2-(4-{[(4-chloro-5-ethyl-1H-imidazol-2-yl)carbonyl]amino}-3-methoxypiperidin-1-yl)-1,3-thiazole-4-carboxylate obtained in Example (190b) (54 mg, 0.11 mmol) was dissolved in methanol (2 ml) and THF (2 ml). A 2 N aqueous lithium hydroxide solution (2 ml) was added, and the mixture was stirred at room temperature overnight. The organic solvent was evaporated under reduced pressure, followed by neutralization with 1 N hydrochloric acid. The resulting solid was collected by filtration and washed with distilled water, to obtain the title compound as a solid.
Aufarbeitung
- customThe organic solvent was evaporated under reduced pressure
- filtrationThe resulting solid was collected by filtration
- washwashed with distilled water
Quellen und Nachweise
- ORD-Eintrag
- ord-1c614474b3514323b5d7b1aa3028ba4c
- Quelldatensatz
- uspto-grants-2015_01
- Patentnummer
- US08927588B2
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