Water → 3-(2-Fluorophenyl)-6-(2-Methyl-2H-1,2,4-Triazol-3-Ylmethoxy)-7-(3-Oxocyclobutyl)-1,2,4-Triazolo[4,3-b]Pyridazine

HRID 1369448Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1369448
[Cr](O)(O)(=O)=O.[F:6][C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][C:8]=1[C:13]1[N:17]2[NH:18][C:19](=[O:27])[C:20]([CH:22]3[CH2:25][CH:24]([OH:26])[CH2:23]3)=[CH:21][C:16]2=[N:15][N:14]=1.[CH:28](O)([CH3:30])C.O>CC(C)=O>[F:6][C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][C:8]=1[C:13]1[N:17]2[N:18]=[C:19]([O:27][CH2:30][C:28]3[N:15]([CH3:16])[N:14]=[CH:13][N:17]=3)[C:20]([CH:22]3[CH2:23][C:24](=[O:26])[CH2:25]3)=[CH:21][C:16]2=[N:15][N:14]=1

Komponenten

6

Versuchsvorschrift

8N Chromic acid was added to a solution of 3-(2-fluorophenyl)-7-(3-hydroxycyclobutyl)-1,2,4-triazolo[4,3-b]pyridazin-6-one (0.36 g, 1.2 mmol) in acetone (50 ml) dropwise, until excess was present (red colour remained). The reaction was then stirred for 2 hours before isopropanol was added until the blue colour remained and no excess chromic acid was present. Water (50 ml) was added and the aqueous layer extracted with ethyl acetate (4×50 ml), organic layers were combined, washed with brine (50 ml), dried (MgSO4), filtered and concentrated to give the desired product as a white solid. Data for the title compound: 1H NMR (360 MHz, DMSO) δ3.41 (2H, s), 3.43 (2H, s), 3.73-3.78 (1H, m), 7.42-7.50 (2H, m), 7.64-7.72 (1H, m), 7.83-7.88 (1H, m), 8.38 (1H, s); MS (ES+) m/e 299 [MH]+.

Aufarbeitung

  1. additionwas added until the blue colour
  2. extractionthe aqueous layer extracted with ethyl acetate (4×50 ml), organic layers
  3. washwashed with brine (50 ml)
  4. dry with materialdried (MgSO4)
  5. filtrationfiltered
  6. concentrationconcentrated

Quellen und Nachweise

ORD-Eintrag
ord-ed0ed63cae094c69a1a0a46b18685bf8
Quelldatensatz
uspto-grants-2003_06
Patentnummer
US06579875B1

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