反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
PROCEDURE
实验过程
4-[4-(3-Chloro-4-fluorophenyl)-5-oxo-4,5-dihydro-1,2,4-oxadiazol-3-yl]-1,2,5-oxadiazol-3-ylmethyl methanesulfonate (400 mg, 1.02 mmol) was dissolved in anhydrous DMF (10 mL) followed by addition of sodium azide (133 mg, 2.04 mmol). Reaction was stirred for 3 hrs. Consumption of starting material was monitored by TLC and HPLC. The reaction mixture was added to a mixture of (400 μL) bromine/water and stirred for 10 min. DCM was added and the layers were separated. The combined organics were dried with sodium sulfate, filtered, and concentrated in vacuo. The crude residue was purified by flash column chromatography to yield the desired product (225 mg, 65%). MF═C11H5ClFN7O3; LCMS calculated for C11H6ClFN7O3(M+H)+: m/z=338.020.
WORKUP
后处理
- customReaction
- customConsumption of starting material
- additionThe reaction mixture was added to a mixture of (400 μL) bromine/water
- stirringstirred for 10 min
- additionDCM was added
- customthe layers were separated
- dry with materialThe combined organics were dried with sodium sulfate
- filtrationfiltered
- concentrationconcentrated in vacuo
- customThe crude residue was purified by flash column chromatography