Réaction #1005983

ord-4e77e4ed071943b69d634f2cdf0361f0

Équation de réaction

CN(CCCCCl)C(=O)n1cnc(-c2ccccc2)c1
Compound 47
CN(CCCCCl)C(=O)n1cnc(-c2ccccc2)c1
N-(4-chlorobutyl)-N-methyl-4-phenyl-1H-imidazole-1-carboxamide
CCCC[N+](CCCC)(CCCC)CCCC.[N-]=[N+]=[N-]
tetra-n-butylammonium azide
CN(CCCCN=[N+]=[N-])C(=O)n1cnc(-c2ccccc2)c1
N-(4-azidobutyl)-N-methyl-4-phenyl-1H-imidazole-1-carboxamide

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Températurethe reaction was refluxed for 8 h
  2. 2
    Autresolvent was evaporated on Rotavapor
  3. 3
    Autreto give a crude compound which
  4. 4
    Autreon purification by Biotage SP1

Mode opératoire

Compound 47 (4.3) (1 mmol) was taken in anhydrous acetone (25 mL) and tetra-n-butylammonium azide (2 mmol) was added and the reaction was refluxed for 8 h. The reaction was cooled to RT and solvent was evaporated on Rotavapor to give a crude compound which on purification by Biotage SP1 provided pure N-(4-azidobutyl)-N-methyl-4-phenyl-1H-imidazole-1-carboxamide (48/4.4).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US09271962B2uspto-grants-2016_03