Sodium Hydroxide → Pyrazolo(1,5-a)pyridine-3-carboxylic acid
Reaktionsgleichung
[OH-].[Na+].[N:3]1[N:7]2[CH:8]=[CH:9][CH:10]=[CH:11][C:6]2=[C:5]([C:12]([O:14]CC)=[O:13])[CH:4]=1>C(O)C>[N:3]1[N:7]2[CH:8]=[CH:9][CH:10]=[CH:11][C:6]2=[C:5]([C:12]([OH:14])=[O:13])[CH:4]=1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A 2.5 N aqueous solution of sodium hydroxide (36 mL) was added to a solution of ethyl pyrazolo[1,5-a]pyridine-3-carboxylate (Preparation 22a, 4.3 g, 22.6 mmol) in ethanol (70 mL) and the resulting reaction mixture was heated to reflux for 1 h. After evaporation of the ethanol, the reaction mixture was acidified with 15% aqueous hydrochloric acid solution. The solid formed was filtered, washed with water and diethyl ether and dried to give the title compound (2.81 g, 77%) as a pale pink solid.
Aufarbeitung
- customthe resulting reaction mixture
- temperaturewas heated
- temperatureto reflux for 1 h
- customAfter evaporation of the ethanol
- customThe solid formed
- filtrationwas filtered
- washwashed with water and diethyl ether
- customdried
Quellen und Nachweise
- ORD-Eintrag
- ord-67497fcd245142cc8d6a9400f04a64da
- Quelldatensatz
- uspto-grants-2015_12
- Patentnummer
- US09206183B2
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