Reaktion #71077

ord-dc3e7320b40841f094207f6ed0cbde80

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 (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 mixture of 2-[2-(2-methyl-[1,3]dioxolan-2-yl)-thiazol-4-ylmethyl]-4-nitro-2H-[1,2,3]triazole (86 mg, 0.29 mmol), iron powder (49 mg, 0.87 mmol) and NH4Cl (78 mg, 1.45 mmol) in a mixture of EtOH (1.0 mL) and water (0.5 mL) was stirred at 75° C. for 60 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=0.68 min; [M+H]+=268.25.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08536209B2uspto-grants-2013_09