Réaction #1244269

Équation de réaction

fluoroazide

1-Azido-3-fluoropropan-2-ol

1-propynyl-2-nitroimidazole

THF

sodium ascorbate

→

pale yellow crystals

Rendement 4.2%

1-Fluoro-3-(4-((2-nitro-1H-imidazol-1-yl)methyl)-1H-1,2,3-triazol-1-yl)propan-2-ol

Rendement 4.2%

Solvants

water

t-BuOH

Conditions de réaction

Traitement

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

Mode opératoire

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).

Source