Ethyl Acetate → 3-phenyl-1H-indazole-5-ol

HRID 2183097

Reaktionsgleichung

Reaktionsgleichung von HRID 2183097
[N+]([C:4]1[CH:5]=[C:6]2[C:10](=[CH:11][CH:12]=1)[NH:9][N:8]=[C:7]2[C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1)([O-])=O.[H][H].C(OCC)(=[O:23])C>[Pd].[Pd].[C]>[C:13]1([C:7]2[C:6]3[C:10](=[CH:11][CH:12]=[C:4]([OH:23])[CH:5]=3)[NH:9][N:8]=2)[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1

Komponenten

6

Reaktionsbedingungen

Temperatur
180 °C

Versuchsvorschrift

To a solution of 5-nitro-3-phenyl-1H-indazole (1.0 g, 4.2 mmol) in ethyl acetate (80 mL) was added palladium on activated carbon (Pd/carbon) then the reaction was subjected to an atmosphere of hydrogen. The reaction was stirred for 3 days when the Pd/carbon was filtered off and the solution concentrated to an oil under vacuo. The oil was then taken up in H2SO4 (6 mL) and water (60 mL) and the suspension was heated in a bomb to 180° C. for 2 days. The reaction was then cooled to room temperature, quenched with NaHCO3 (100 mL) and extracted with ethyl acetate (3×30 mL). The organic layers were combined and dried (Na2SO4) and concentrated to recover the title compound (250mg, 28% yield). 1H NMR (CDCl3) δ 13.0 (s, 1H), 9.20 (s, 1H), 7.91 (s, 1H), 7.88 (s, 1H), 7.50 (t, 2H), 7.41 (d, 1H), 7.36 (t, 1H), 7.28 (s, 1H), 6.96 (dd, 1H); ES-MS (m/z) 195 [M+1]−.

Aufarbeitung

  1. filtrationwas filtered off
  2. concentrationthe solution concentrated to an oil under vacuo
  3. temperatureThe reaction was then cooled to room temperature
  4. customquenched with NaHCO3 (100 mL)
  5. extractionextracted with ethyl acetate (3×30 mL)
  6. dry with materialdried (Na2SO4)
  7. concentrationconcentrated

Quellen und Nachweise

ORD-Eintrag
ord-0bc1bc630e7c4be2ba990b441554481b
Quelldatensatz
uspto-grants-2005_05
Patentnummer
US06897231B2

Verknüpfte Notizen

Wird geladen…