Water → 2-{[(1-Carbamoyl-1,2-dimethylpropyl)amino]methyl}-5-ethylnicotinic acid

HRID 1723471Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1723471
[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

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

  1. concentrationThe reaction is concentrated in vacuo
  2. dissolutionredissolved in 30 mL water
  3. concentrationadjustment of the pH to 4 with concentrated hydrochloric acid and concentration in vacuo
  4. customgives a gum
  5. dry with materialdried over MgSO4
  6. concentrationconcentrated in vacuo to 6 g foam
  7. customCrystallization from methanol-ether

Quellen und Nachweise

ORD-Eintrag
ord-3ef762d97ea74f6f98a6b5881115b8a3
Quelldatensatz
uspto-grants-1989_08
Patentnummer
US04861887

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