تفاعل #5242
ord-b09968f7a78948329b0580e276d90a67
معادلة التفاعل
المتفاعلات
الكواشف
ظروف التفاعل
المعالجة
- 1أخرىThe reaction was quenched by addition of excess 60% aqueous acetic acid
- 2workup.WAITAfter 30 minutes
- 3workup.ADDITIONthe mixture was diluted with water
- 4تركيزconcentrated
- 5أخرىto remove CH3OH
- 6أخرىThe resulting powder (100 mg) was chromatographed on reverse phase silica gel [
- 7غسيل10 g, flash, stepwise gradient elution
- 8workup.ADDITIONFractions containing the product
- 9تركيزconcentrated under reduced pressure
الإجراء التجريبي
1-(3-Dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (78 mg, 0.41 mmol) was added to a solution of 5-[[(amino)carbonyl]amino-1-(β-D-ribofuranosyl)-1H-imidazole-4-carboxylic acid (19 mg, 0.063 mmol) in water (2 mL) and CH3OH (5 mL) and the mixture was stirred at room temperature overnight. The reaction was quenched by addition of excess 60% aqueous acetic acid. After 30 minutes, the mixture was diluted with water, concentrated to remove CH3OH and lyophilized. The resulting powder (100 mg) was chromatographed on reverse phase silica gel [10 g, flash, stepwise gradient elution: water (200 mL), 10% CH3OH in water (v/v, 100 mL), 20% CH3OH in water (v/v, 100 mL), 10-mL fractions]. Fractions containing the product were combined, concentrated under reduced pressure and lyophilized to give oxanosine: 16 mg (89%).