Sodium ethoxide → 5-Bromo-2-ethylpyrimidine-4-carboxylic acid

HRID 1399927

Reaktionsgleichung

Reaktionsgleichung von HRID 1399927
[Na].[O-]CC.[Na+].Cl.[C:7](=[NH:11])([NH2:10])[CH2:8][CH3:9].[C:12]([OH:20])(=[O:19])/[C:13](=[C:15](\[CH:17]=O)/[Br:16])/Br>C(O)C>[Br:16][C:15]1[C:13]([C:12]([OH:20])=[O:19])=[N:11][C:7]([CH2:8][CH3:9])=[N:10][CH:17]=1

Komponenten

6

Reaktionsbedingungen

Temperatur
55 °C

Versuchsvorschrift

Sodium (356 mg, 15.5 mmol) was carefully added to ethanol (5.9 mL) to prepare sodium ethoxide solution in ethanol. The above freshly prepared ethanol solution (3.5 mL) was added to a stirred suspension of propionimidamide hydrochloride (1.05 g, 9.69 mmol). The mixture was warmed to 55° C., then the heating bath was removed and a solution of mucobromic acid (1 g, 3.87 mmol) in ethanol was added dropwise at a rate which maintained a constant temperature, followed by a further sodium ethoxide solution (2 mL). After cooling, the mixture was filtered and evaporated to a residue which was shaken vigorously with hydrochloric acid (2 M×2.4 mL). The brown precipitate was filtered off and washed with cold water, then freeze-dried to give 5-Bromo-2-ethylpyrimidine-4-carboxylic acid (330 mg, 37%) as a yellow solid. LCMS: 231 [M+1]+, 1H NMR (400 MHz, DMSO-d6): δ 1.25 (t, J=7.6 Hz, 3H), 2.88 (q, J=7.6 Hz, 2H), 9.05 (s, 1H).

Aufarbeitung

  1. customthe heating bath was removed
  2. temperaturemaintained a constant temperature
  3. temperatureAfter cooling
  4. filtrationthe mixture was filtered
  5. customevaporated to a residue which
  6. filtrationThe brown precipitate was filtered off
  7. washwashed with cold water
  8. customfreeze-dried

Quellen und Nachweise

ORD-Eintrag
ord-d196bc86c4364a059f4ee8b0b9033301
Quelldatensatz
uspto-grants-2014_12
Patentnummer
US08906909B2

Verknüpfte Notizen

Wird geladen…