Tetrahydrofuran → 2-(3-Pyridinylamino)-4-thiazolecarboxylic acid
Reaktionsgleichung
C([O:3][C:4]([C:6]1[N:7]=[C:8]([NH:11][C:12]2[CH:13]=[N:14][CH:15]=[CH:16][CH:17]=2)[S:9][CH:10]=1)=[O:5])C.O1CCCC1.[OH-].[Na+]>CO>[N:14]1[CH:15]=[CH:16][CH:17]=[C:12]([NH:11][C:8]2[S:9][CH:10]=[C:6]([C:4]([OH:5])=[O:3])[N:7]=2)[CH:13]=1Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
2-(Pyridin-3-ylamino)-thiazole-4-carboxylic acid (165 mg) was prepared according to General Procedure C using 2-(pyridin-3-ylamino)-thiazole-4-carboxylic acid ethyl ester in methanol:tetrahydrofuran:2N NaOH (1:1:1, 1.5 mL). The solvents were evaporated and the compound was dried. The crude product was used without further purification.
Aufarbeitung
- customThe solvents were evaporated
- customthe compound was dried
- customThe crude product was used without further purification
Quellen und Nachweise
- ORD-Eintrag
- ord-95270e6983294e26ab93f029557e5b78
- Quelldatensatz
- uspto-grants-2013_08
- Patentnummer
- US08513430B2
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