Réaction #1098653

ord-61a3f4899ecf4967905b06e0d242f95b

Équation de réaction

C#CCn1ccnc1[N+](=O)[O-]
alkyne
C#CCn1ccnc1[N+](=O)[O-]
2-Nitro-1-(prop-2-ynyl)-1H-imidazole
[N-]=[N+]=NC(CO)CF
29
[N-]=[N+]=NC(CO)CF
2-Azido-3-fluoropropan-1-ol
→
O=[N+]([O-])c1nccn1Cc1cn(C(CO)CF)nn1
1
O=[N+]([O-])c1nccn1Cc1cn(C(CO)CF)nn1
3-Fluoro-2-(4-((2-nitro-1H-imidazol-1-yl)methyl)-1H-1,2,3-triazol-1-yl)propan-1-ol

Réactifs

C#CCn1ccnc1[N+](=O)[O-]
alkyne
C#CCn1ccnc1[N+](=O)[O-]
2-Nitro-1-(prop-2-ynyl)-1H-imidazole
[N-]=[N+]=NC(CO)CF
29
[N-]=[N+]=NC(CO)CF
2-Azido-3-fluoropropan-1-ol

Réactifs

Aucun

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

Mode opératoire

To a vial is added alkyne 10 (1.9 g, 12.6 mmol) and 29 (1.5 g, 12.6 mmol). The solution is heated at 60° C. overnight. The material is then purified on a silica gel column using 10% MeOH:CH2Cl2 as the eluent. The material is then further purified via recrystallization using EtOAc:Hex to afford 1 as a solid.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07977361B2uspto-grants-2011_07