Reaktion #2152221

ord-e2b992bfbc41446297e550114937362b

Lösungsmittel

Reaktionsbedingungen

Temperatur
85°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 (10 mL) was added
  4. 4
    ExtraktionThe aq. layer was extracted with CH2Cl2 (2×10 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 0.1M solution of 2-(2-methyl-[1,3]dioxolan-2-yl)-4-(3-nitro-pyrazol-1-ylmethyl)-thiazole (160 mg, 0.54 mmol), iron powder (91 mg, 1.62 mmol) and NH4Cl (146 mg, 2.70 mmol) in a mixture of EtOH (2.0 mL) and water (1.0 mL) was stirred at 85° C. for 30 min. The reaction mixture was filtered while hot and concentrated under reduced pressure. CH2Cl2 (10 mL) was added followed by 1N NaOH (10 mL). The aq. layer was extracted with CH2Cl2 (2×10 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 an oil. LC-MS-conditions 02: tR=0.60 min; [M+H]+=267.30.

Quelle

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