Reaktion #1244269

ord-6db55d18b4a84144a98c14c9038648f7

Reaktionsgleichung

[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
C1CCOC1
THF
O=C1O[C@H]([C@@H](O)CO)C([O-])=C1O.[Na+]
sodium ascorbate
O=[N+]([O-])c1nccn1Cc1cn(CC(O)CF)nn1
pale yellow crystals
Ausbeute 4.2%
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
Ausbeute 4.2%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.ADDITIONthe reaction was poured onto EtOAc
  2. 2
    Waschenwashed with NH4OH
  3. 3
    Sonstigethe material was then purified on a silica gel column
  4. 4
    SonstigeThe material was then further purified via recrystallization

Vorschrift

To a vial was added fluoroazide 17 (690 mg, 5.79 mmol) and 1-propynyl-2-nitroimidazole (876 mg, 5.79 mmol). To this flask was added THF (3 mL), t-BuOH (3 mL), water (3 mL), CuSO4 (185 mg, 1.16 mmol) and sodium ascorbate (1.15 g, 5.79 mmol). After 16 hrs, the reaction was poured onto EtOAc and washed with NH4OH. The organics were combined and the material was then purified on a silica gel column using EtOAc:Hex as the eluent. The material was then further purified via recrystallization using EtOAc:Hex to afford 65 mg (4% yield) of pale yellow crystals. 1H NMR (DMSO-d6, 400 MHz), δ: 4.04 (1H, br d, J=20.4 Hz), 4.20-4.47 (4H, m), 5.53 (1H, br s), 5.66 (2H, s), 7.16, (1H, s), 7.68 (1H, s), 8.05 (1H, s).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07807394B2uspto-grants-2010_10