Réaction #1244270

ord-425f22919fbe43d5b1b51fe388e54b05

Équation de réaction

[N-]=[N+]=NCC(O)CF
fluoroazide
[N-]=[N+]=NCC(O)CF
1-Azido-3-fluoropropan-2-ol
CC#Cn1ccnc1[N+](=O)[O-]
1-propynyl-2-nitroimidazole
O=[N+]([O-])c1nccn1Cc1cn(CC(O)CF)nn1
1-Fluoro-3-(4-((2-nitro-1H-imidazol-1-yl)methyl)-1H-1,2,3-triazol-1-yl)propan-2-ol

Conditions de réaction

Température
60°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    AutreThe material is then purified on a silica gel column
  2. 2
    AutreThe material is then further purified via recrystallization
  3. 3
    AutreHex to afford pale yellow crystals

Mode opératoire

To a vial is added fluoroazide 17 (5.79 mmol) and 1-propynyl-2-nitroimidazole (5.79 mmol). The solution is heated at 60° C. overnight. The material is then purified on a silica gel column using EtOAc:Hex as the eluent. The material is then further purified via recrystallization using EtOAc:Hex to afford pale yellow crystals.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07807394B2uspto-grants-2010_10