反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
产物
AUXILIARIES
试剂、催化剂与溶剂
PROCEDURE
实验过程
Example 1, Alternative Preparation, Step 4: A stirring solution of 2-(trimethylsilyl)ethyl(1R,2S,5R)-2-((S)-3-benzyloxycarbonylamino-2-oxopyrrolidin-1-yl)-5-(cyanomethylamino)cyclohexylcarbamate (400 mg, 0.76 mmol) in dichloromethane (5 mL), was cooled to 0° C. and charged with m-CPBA (372.6 mg, 2.2 eq) in portions. The mixture was stirred at room temperature for 1.5 h. Saturated Na2S2O3 solution (3 mL) and saturated NaHCO3 solution (3 mL) were added and the mixture was stirred at room temperature for 0.5 h. The mixture was diluted with dichloromethane (80 mL), washed with saturated NaHCO3 (20 mL) and brine (20 mL). The solution was dried over anhydrous Na2SO4, filtered, and concentrated in vacuo. The residue obtained was dissolved in methanol (5 mL) and the solution was charged with NH2OH-HCl (262.7 mg, 5 eq). The mixture was stirred at 60° C. for 2.5 h. After cooling to room temperature, the mixture was diluted with dichloromethane (80 mL) and filtered through a pad of celite. The filtrate was washed with saturated NaHCO3 (2×20 mL). The aqueous washes were extracted with dichloromethane (30 mL). The dichloromethane layers were combined and washed with brine (30 mL). The solution was dried over anhydrous Na2SO4, filtered, and concentrated in vacuo to give 2-(trimethylsilyl)ethyl (1R,2S,5R)-2-((S)-3-benzyloxycarbonylamino-2-oxopyrrolidin-1-yl)-5-(hydroxyamino)cyclohexylcarbamate (350 mg, 91%). LC/MS found [M+H]+=507.
WORKUP
后处理
- customExample 1, Alternative Preparation, Step 4
- stirringthe mixture was stirred at room temperature for 0.5 h
- washwashed with saturated NaHCO3 (20 mL) and brine (20 mL)
- dry with materialThe solution was dried over anhydrous Na2SO4
- filtrationfiltered
- concentrationconcentrated in vacuo
- customThe residue obtained
- stirringThe mixture was stirred at 60° C. for 2.5 h
- temperatureAfter cooling to room temperature
- filtrationfiltered through a pad of celite
- washThe filtrate was washed with saturated NaHCO3 (2×20 mL)
- extractionThe aqueous washes were extracted with dichloromethane (30 mL)
- washwashed with brine (30 mL)
- dry with materialThe solution was dried over anhydrous Na2SO4
- filtrationfiltered
- concentrationconcentrated in vacuo