تفاعل #8009

معادلة التفاعل

ethyl chlorocarbonate

THF

hydrochloric acid

sodium borohydride

4-carboxy-6-(3-fluoro-4-methyl-phenyl)-2-isobutyl-2H-pyridazin-3-one

triethylamine

THF

→

title compound

المردود 25.0%

6-(3-fluoro-4-methylphenyl)-4-hydroxy-methyl-2-isobutyl-2H-pyridazin-3-one

المردود 25.0%

المذيبات

water

ظروف التفاعل

المعالجة

1. 1
   ترشيحTriethylamine hydrochloride was filtered off
2. 2
   workup.STIRRINGthe mixture was stirred at room temperature for 10 minutes
3. 3
   استخلاصthe mixture was extracted with ethyl acetate
4. 4
   غسيلThe organic layer was washed with brine
5. 5
   تجفيفdried over anhydrous sodium sulfate
6. 6
   workup.DISTILLATIONThe solvent was distilled off under reduced pressure
7. 7
   أخرىThe residue was purified by column chromatography on silica gel [silica gel 300 g, chloroform/methanol (100/→150/1))

الإجراء التجريبي

To a solution of 4-carboxy-6-(3-fluoro-4-methyl-phenyl)-2-isobutyl-2H-pyridazin-3-one (4.53 g, 14.9 mmol) in THF (40 mL) was added triethylamine (1.66 g, 16.4 mmol). To the ice-cooled mixture was added dropwise a solution of ethyl chlorocarbonate (1.78 g, 16.4 mmol) in THF (5 mL), and the mixture was stirred for 30 minutes. Triethylamine hydrochloride was filtered off. A solution of sodium borohydride (564 mg, 14.9 mmol) in water (1 mL) was added to the filtrate, and then, the mixture was stirred at room temperature for 10 minutes. Thereafter, 2 mol/L hydrochloric acid was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with brine, and dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure. The residue was purified by column chromatography on silica gel [silica gel 300 g, chloroform/methanol (100/→150/1)) to yield the title compound as a colorless crystalline powder (1.08 g, 25.0%).

المصدر