반응 #45839

반응 방정식

citric acid

Triethylamine

cyclopentanecarbonyl chloride

2-amino-5-phenyl-4-fluoro-3-hydroxy-6-methylbenzonitrile

→

compound

수율 72.0%

4-Amino-5-cyano-2-fluoro-6-methylbiphenyl-3-yl cyclopentanecarboxylate

수율 72.0%

용매

acetonitrile

반응 조건

후처리

1. 1
   기타the solvent was evaporated away under reduced pressure
2. 2
   workup.ADDITIONEthyl acetate was added to the resulting residue
3. 3
   세척by washing with saturated brine
4. 4
   건조The organic layer was dried over anhydrous magnesium sulfate
5. 5
   기타the solvent was evaporated away under reduced pressure
6. 6
   기타The resulting residue was purified by preparative TLC (ethyl acetate

실험 절차

Under nitrogen atmosphere, 2-amino-5-phenyl-4-fluoro-3-hydroxy-6-methylbenzonitrile (I-41) (200 mg, 0.83 mmol) was dissolved in acetonitrile (10 ml), and cooled at 0° C. Triethylamine (138 μl, 1.36 mmol) and cyclopentanecarbonyl chloride (138 μl, 1.36 mmol) were dropwise added to the solution, followed by stirring at room temperature for 2 hours. 10% citric acid was added to the reaction liquid, and the solvent was evaporated away under reduced pressure. Ethyl acetate was added to the resulting residue, followed by washing with saturated brine. The organic layer was dried over anhydrous magnesium sulfate, and the solvent was evaporated away under reduced pressure. The resulting residue was purified by preparative TLC (ethyl acetate:n-hexane=1:3, v/v) to obtain the entitled compound (200 mg, 72%) as a colorless oil.

출처