Reaktion #163119

ord-7940004b756542eaad89362ec64f14a3

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeThe reaction was partitioned with water, layers
  2. 2
    Trocknenorganic layer was dried over Na2SO4
  3. 3
    Filtrationfiltered
  4. 4
    Einengenconcentrated in vacuo
  5. 5
    SonstigeThe crude residue obtained
  6. 6
    Filtrationwas purified by a silica gel filtration
  7. 7
    Sonstigeto give

Vorschrift

To a solution of 6-fluoronicotinic acid (10 g, 70.9 mmol) in DCM (200 ml), was added N,O-Dimethylhydroxylamine hydrochloride (7.3 g, 74.8 mmol), N-(3-Dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride (15 g, 78.5 mmol), and triethylamine (22 ml, 156 mmol). The reaction mixture was allowed to stir at room temperature for 16 hours. The reaction was partitioned with water, layers were cut, and organic layer was dried over Na2SO4, filtered, and concentrated in vacuo. The crude residue obtained was purified by a silica gel filtration using EtOAc-DCM (4:1) to give 7.2 g (55% isolated yield) of the title compound. 1H NMR: 8.48 (s, 1H) 8.21 (t, J=8.29 Hz, 1H) 7.27 (dd, J=8.29, 3.01 Hz, 1H) 3.54 (s, 3H) 3.27 (s, 3H).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08835465B2uspto-grants-2014_09