Réaction #640522

ord-bdc05eaa34b34a0ab1fd3859f5f40060

Équation de réaction

Nc1nonc1-c1nc2ccccc2[nH]1
4-(1H-benzimidazol-2-yl)-furazan-3-ylamine
O=C([O-])[O-].[K+].[K+]
potassium carbonate
ICOc1ccccc1
iodomethoxy benzene
Nc1nonc1-c1nc2ccccc2n1COc1ccccc1
title compound
Nc1nonc1-c1nc2ccccc2n1COc1ccccc1
4-(1-Phenoxymethyl-1H-benzimidazol-2-yl)-furazan-3-ylamine

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    AutreEvaporation of the solvent under reduced pressure
  2. 2
    Autrepartitioning of the resulting residue between water and ethyl acetate
  3. 3
    Séchageby drying of the organic solution over sodium sulphate and chromatography of the residue

Mode opératoire

To a solution of 4-(1H-benzimidazol-2-yl)-furazan-3-ylamine (0.10 g, 0.497 mmol) is added potassium carbonate (0.172 g, 1.24 mmol) and iodomethoxy benzene (0.128 g, 0.546 mmol). The mixture is stirred over night. Evaporation of the solvent under reduced pressure and partitioning of the resulting residue between water and ethyl acetate followed by drying of the organic solution over sodium sulphate and chromatography of the residue gives the title compound as a colorless solid, m.p. 171-173° C.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: USRE042890E1uspto-grants-2011_11