Water → 2-{[(1-Carbamoyl-1,2-dimethylpropyl)amino]methyl}-5-ethylnicotinic acid
Reaktionsgleichung
[C:1]([C:4]([NH:9][CH2:10][C:11]1[N:21]=[CH:20][C:19]([CH2:22][CH3:23])=[CH:18][C:12]=1[C:13]([O:15]CC)=[O:14])([CH3:8])[CH:5]([CH3:7])[CH3:6])(=[O:3])[NH2:2].[OH-].[Na+].O>CO.C(OCC)(=O)C.O1CCCC1>[C:1]([C:4]([NH:9][CH2:10][C:11]1[N:21]=[CH:20][C:19]([CH2:22][CH3:23])=[CH:18][C:12]=1[C:13]([OH:15])=[O:14])([CH3:8])[CH:5]([CH3:7])[CH3:6])(=[O:3])[NH2:2]Komponenten
7
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 3
Versuchsvorschrift
A solution of 5.6 g of ethyl 2-{[(1-carbamoyl-1,2-dimethylpropyl)amino]methyl}-5-ethylnicotinate (0.0174 mol) in 30 mL of methanol containing 2 g of NaOH (0.05 mol) and 10 mL water is stirred at room temperature for two hours and 30 minutes. The reaction is concentrated in vacuo and redissolved in 30 mL water; adjustment of the pH to 4 with concentrated hydrochloric acid and concentration in vacuo gives a gum. This residue is dissolved in a mixture of ethyl acetate, tetrahydrofuran, and methanol, dried over MgSO4, and concentrated in vacuo to 6 g foam. Crystallization from methanol-ether affords 3.1 g product, mp 180°-181° C.
Aufarbeitung
- concentrationThe reaction is concentrated in vacuo
- dissolutionredissolved in 30 mL water
- concentrationadjustment of the pH to 4 with concentrated hydrochloric acid and concentration in vacuo
- customgives a gum
- dry with materialdried over MgSO4
- concentrationconcentrated in vacuo to 6 g foam
- customCrystallization from methanol-ether
Quellen und Nachweise
- ORD-Eintrag
- ord-35237f6859104417a1d2abddb1dc1b5b
- Quelldatensatz
- uspto-grants-1991_07
- Patentnummer
- US05034532
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