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Hydrochloric Acid → 6-(Dimethylamino)-5-methyl-3-pyridinecarboxylic acid

HRID 502424
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 502424
[CH3:1][N:2]([CH3:12])[C:3]1[C:10]([CH3:11])=[CH:9]C(C#N)=[CH:5][N:4]=1.[OH-].[Na+].Cl.C1C[O:19]CC1.[CH2:21]([OH:23])[CH3:22]>>[CH3:1][N:2]([CH3:12])[C:3]1[C:10]([CH3:11])=[CH:9][C:22]([C:21]([OH:19])=[O:23])=[CH:5][N:4]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 4

HCID 313Hydrochloric AcidHCID 14798Sodium HydroxideHCID 21873804Tetrahydrofuran ethanolHCID 68455945HCID 68455945, Verbindung

Produkt 1

HCID 684549596-(Dimethylamino)-5-methyl-3-pyridinecarboxylic acid

Versuchsvorschrift

The above prepared 6-dimethylamino-5-methyl-nicotinonitrile (0.435 g, 2.70 mmol) was dissolved in 13.6 ml of THF/ethanol=1/1 and treated with 6.75 ml of 2N NaOH (5 eq.). The mixture was refluxed for 30 h; aliquots were taken from time to time and analyzed by MS to follow the disappearance of the amide intermediate. After cooling down to room temperature, the pH was adjusted with HCl to 3. Careful evaporation of the solvents and drying under HV left 1.45 g of the title acid as white solid, contaminated with NaCl, which was used as such for the next step.

Aufarbeitung

  1. temperatureThe mixture was refluxed for 30 h
  2. customCareful evaporation of the solvents
  3. customdrying under HV
  4. waitleft 1.45 g of the title acid as white solid

Quellen und Nachweise

ORD-Eintrag
ord-129956e00932491ca0f2fc902c01cffa
Quelldatensatz
uspto-grants-2010_08
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07772253B2

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