Reaktion #2152136

ord-1ba7caedd20548f48c28148b6ec480aa

Lösungsmittel

Reaktionsbedingungen

Temperatur
75°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    FiltrationThe reaction mixture was filtered while hot and
  2. 2
    Einengenconcentrated under reduced pressure
  3. 3
    workup.ADDITIONCH2Cl2 (40 mL) was added
  4. 4
    ExtraktionThe aq. layer was extracted with CH2Cl2 (2×20 mL)
  5. 5
    Trocknenextracts were dried over MgSO4
  6. 6
    Filtrationfiltered
  7. 7
    Sonstigethe solvents were removed under reduced pressure

Vorschrift

In a flame dried round-bottomed flask equipped with a magnetic stir bar and under inert atmosphere (N2), a mixture of 1-[5-(2-methyl-[1,3]dioxolan-2-yl)-thiophen-2-ylmethyl]-3-nitro-1H-pyrazole (230 mg, 0.78 mmol), iron powder (132 mg, 2.34 mmol) and NH4Cl (210 mg, 3.85 mmol) in a mixture of EtOH (4.0 mL) and water (2.0 mL) was stirred at 75° C. for 30 min. The reaction mixture was filtered while hot and concentrated under reduced pressure. CH2Cl2 (40 mL) was added followed by 1M NaOH (40 mL). The aq. layer was extracted with CH2Cl2 (2×20 mL) and the combined org. extracts were dried over MgSO4, filtered, and the solvents were removed under reduced pressure to give the title compound as a red oil. LC-MS-conditions 02: tR=0.69 min; [M+H]+=266.38.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08288419B2uspto-grants-2012_10