Hydrochloric Acid → (E)-3-(6-Amino4-methylpyridin-3-yl)acrylic acid HCl salt

HRID 1710531

Reaktionsgleichung

Reaktionsgleichung von HRID 1710531
[NH2:1][C:2]1[N:7]=[CH:6][C:5](/[CH:8]=[CH:9]/[C:10]([O:12]CC)=[O:11])=[C:4]([CH3:15])[CH:3]=1.[ClH:16]>CC(O)=O>[ClH:16].[NH2:1][C:2]1[N:7]=[CH:6][C:5](/[CH:8]=[CH:9]/[C:10]([OH:12])=[O:11])=[C:4]([CH3:15])[CH:3]=1

Komponenten

4

Edukt 2

HCID 313Hydrochloric AcidHCID 57440845Ethyl (E)-3-(6-amino-4-methylpyridin-3-yl)acrylate

Produkt 1

HCID 67343018(E)-3-(6-Amino4-methylpyridin-3-yl)acrylic acid HCl salt

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 176Acetic AcidLösungsmittel

Reaktionsbedingungen

Temperatur
100 °C

Versuchsvorschrift

To ethyl (E)-3-(6-amino-4-methylpyridin-3-yl)acrylate (1.50 g, 7.3 mmole) was added HOAc (15 mL) and cone. HCl (15 mL). The solution was stirred at 100° C. for 10 hr, cooled to RT, and concentrated to dryness. Trituration with Et2O, filtration and drying under vacuum gave the title compound (1.65 g, quantitative) as a white solid: LCMS (ES) m/e 179.2 (M+H)+; 1H NMR (400 MHz, DMSO-d6) δ 8.37 (s, 1H), 8.28 (br s, 3H), 7.51 (d, J=16.0 Hz, 1H), 6.86 (s, 1H), 6.46 (d, J=16.0 Hz, 1H), 2.41 (s, 3H).

Aufarbeitung

  1. temperaturecooled to RT
  2. concentrationconcentrated to dryness
  3. filtrationTrituration with Et2O, filtration
  4. customdrying under vacuum

Quellen und Nachweise

ORD-Eintrag
ord-8f35b562675b4e38b977c0cacf8d75b6
Quelldatensatz
uspto-grants-2010_09
Patentnummer
US07790716B2

Verknüpfte Notizen

Wird geladen…