Réaction #2254180

ord-d632c73ed8c04d9480f4f695ecf513c4

Équation de réaction

CC(=O)[O-].[Na+]
Sodium acetate
Cl.NO
hydroxylamine hydrochloride
Cc1cc(C=O)sc1C(=O)NCC(F)(F)F
5-formyl-3-methyl-thiophene-2-carboxylic acid (2,2,2-trifluoro-ethyl)-amide
Cc1cc(C=NO)sc1C(=O)NCC(F)(F)F
5-(hydroxyimino-methyl)-3-methyl-thiophene-2-carboxylic acid (2,2,2-trifluoro-ethyl)-amide

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Autrethe reaction is quenched with water
  2. 2
    ExtractionThe reaction mixture is extracted three times with ethyl acetate
  3. 3
    SéchageThe combined organic phases are dried over Na2SO4
  4. 4
    Concentrationconcentrated in vacuo

Mode opératoire

Sodium acetate (90 mg) is added to a solution of hydroxylamine hydrochloride (60 mg) and 5-formyl-3-methyl-thiophene-2-carboxylic acid (2,2,2-trifluoro-ethyl)-amide (190 mg) in THF (5 ml), water (1 ml) and DMSO (1 ml). After 3 hours at room temperature, the reaction is quenched with water. The reaction mixture is extracted three times with ethyl acetate. The combined organic phases are dried over Na2SO4 and concentrated in vacuo to yield 5-(hydroxyimino-methyl)-3-methyl-thiophene-2-carboxylic acid (2,2,2-trifluoro-ethyl)-amide. The crude product obtained (206 mg, yellowish oil) is used without further purification. MS (HPLC/MS): 267 (MH+). Retention time: 2.56 min and 2.64 min (two diastereoisomers).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US09044389B2uspto-grants-2015_06