Lithium Hydroxide → 5-Amino-6-chloroimidazo[1,2-a]pyridine-8-carboxylic acid
Reaktionsgleichung
[NH2:1][C:2]1[N:7]2[CH:8]=[CH:9][N:10]=[C:6]2[C:5]([C:11]([O:13]CC)=[O:12])=[CH:4][C:3]=1[Cl:16].[OH-].[Li+]>CO>[NH2:1][C:2]1[N:7]2[CH:8]=[CH:9][N:10]=[C:6]2[C:5]([C:11]([OH:13])=[O:12])=[CH:4][C:3]=1[Cl:16]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
To a stirred solution of ethyl 5-amino-6-chloroimidazo[1,2-a]pyridine-8-carboxylate (Example 1, METHOD A, Step 3, 217 mg, 0.91 mmol) in methanol (5 mL) was added 1N aqueous lithium hydroxide (500 μL) and the mixture was stirred overnight at room temperature. The solvent was removed in vacuo and acidified with 1N hydrochloric acid. The resultant precipitate was collected by filtration to give 165 mg (86%) of the title compound as a white solid.
Aufarbeitung
- customThe solvent was removed in vacuo
- filtrationThe resultant precipitate was collected by filtration
Quellen und Nachweise
- ORD-Eintrag
- ord-6f4e84dcb75f4f718cab610a33144212
- Quelldatensatz
- uspto-grants-2005_10
- Patentnummer
- US06951867B2
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