Reacción #322295

ord-7d4b97a983d140cbb2edf104b0e327b0

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroThe title product was prepared
  2. 2
    Otrowith overnight
  3. 3
    OtroThe product was purified
  4. 4
    Otrochromatography and recrystallization from acetonitrile

Procedimiento

The title product was prepared following the procedure of example 3 from 7-amino-1-(4-methyl-1-piperazinyl)-naphthalene (0.15 g, 0.622 mmol) and triethylamine (0.09 mL, 0.68 mmol) and 3,5-dinitrobenzoyl chloride (0.158 g, 0.684 mmol) in acetonitrile (10 mL) with overnight stirring at room temperature. The product was purified using chromatography and recrystallization from acetonitrile to yield 0.17 g (63%) of the title compound: mp 254°-256° C. Analysis calculated for C22H21N5O5 : C, 60.68; H, 4.86; N, 16.08. Found: C, 60.59; H, 4.73; N, 15.88.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05597826uspto-grants-1997_01