Hydrochloric Acid → 2-Amino-6-(2-cyanoethyl)-nicotinic Acid
Reaktionsgleichung
[OH-].[Na+].C[O:4][C:5](=[O:17])[C:6]1[CH:11]=[CH:10][C:9]([CH2:12][CH2:13][C:14]#[N:15])=[N:8][C:7]=1[NH2:16].Cl>CO>[NH2:16][C:7]1[N:8]=[C:9]([CH2:12][CH2:13][C:14]#[N:15])[CH:10]=[CH:11][C:6]=1[C:5]([OH:17])=[O:4]Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
To a solvent mixture of 2N-sodium hydroxide aqueous solution (5 mL) and methanol (5 mL) was added 2-amino-6-(2-cyanoethyl)-nicotinic acid methyl ester (90 mg, 0.439 mmol), and the solution was stirred for 18 hours at room temperature. This mixed solution was neutralized with 5N-hydrochloric acid, then, extracted with ethyl acetate. This organic layer was dried over anhydrous magnesium sulfate, then, the solvent was evaporated in vacuo, and the title compound (68 mg, 0.355 mmol, 81%) was obtained as a yellowish brown solid.
Aufarbeitung
- extractionextracted with ethyl acetate
- dry with materialThis organic layer was dried over anhydrous magnesium sulfate
- customthe solvent was evaporated in vacuo
Quellen und Nachweise
- ORD-Eintrag
- ord-f7c01d8bc5624e4db515dffa190e9139
- Quelldatensatz
- uspto-grants-2011_04
- Patentnummer
- US07932272B2
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