Acetic Acid → Ethyl 3-(7-ethyl-4-oxo-4,5-dihydroimidazo[1,5-a]quinoxalin-1-yl)propanoate

HRID 576833Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 576833
[C:1]([C:4]1[CH:5]=[C:6]2[C:11](=[CH:12][CH:13]=1)[N:10]1[C:14]([CH2:17][CH2:18][C:19]([O:21][CH2:22][CH3:23])=[O:20])=[N:15][CH:16]=[C:9]1[C:8](=[O:24])[NH:7]2)(=O)[CH3:2].C(O)(=O)C>[OH-].[OH-].[Pd+2].[H][H]>[CH2:1]([C:4]1[CH:5]=[C:6]2[C:11](=[CH:12][CH:13]=1)[N:10]1[C:14]([CH2:17][CH2:18][C:19]([O:21][CH2:22][CH3:23])=[O:20])=[N:15][CH:16]=[C:9]1[C:8](=[O:24])[NH:7]2)[CH3:2]

Komponenten

5

Versuchsvorschrift

A mixture of ethyl 3-(7-acetyl-4-oxo-4,5-dihydroimidazo[1,5-a]-quinoxalin-1-yl)propanoate as synthesized in above Example 183, 131 mg, Pearlman's catalyst 100 mg and acetic acid 5 mL was stirred in hydrogen atmosphere at room temperature for 43 hours. Then 75 mg of Pearlman's catalyst was added and the reaction liquid was mildly heated. Twenty-two hours later, the reaction liquid was filtered through Celite, and 30 mL of water was added to the filtrate. The precipitate was recovered by filtration, washed with water and dried in flowing air under heating to provide 65 mg of the title compound.

Aufarbeitung

  1. customthe reaction liquid
  2. temperaturewas mildly heated
  3. customTwenty-two hours later, the reaction liquid
  4. filtrationwas filtered through Celite, and 30 mL of water
  5. additionwas added to the filtrate
  6. filtrationThe precipitate was recovered by filtration
  7. washwashed with water
  8. customdried
  9. temperatureunder heating

Quellen und Nachweise

ORD-Eintrag
ord-1537c1c9086e45468ece2e54f47b1186
Quelldatensatz
uspto-grants-2015_05
Patentnummer
US09040536B2

Notizen zur Reaktion

Wird geladen…