تفاعل #62326
ord-ec0353e48ca847c1983b4272642af2e5
معادلة التفاعل
المتفاعلات
الكواشف
المذيبات
ظروف التفاعل
المعالجة
- 1workup.STIRRINGstirred at 50° C. for 17 hours
- 2workup.STIRRINGstirred for 3 hours at room temperature and for 2 hours at 50° C.
- 3workup.STIRRINGfurther stirred at 50° C. for 4 hours
- 4استخلاصextracted twice with ethyl acetate
- 5غسيلthe resultant organic layer was washed once with saturated brine
- 6تجفيفdried over magnesium sulfate
- 7أخرىThe solvent was evaporated
- 8أخرىthe crude product was purified
- 9أخرىseparated by silica gel column chromatography
الإجراء التجريبي
To a solution of 200 mg of 3-[(E)-2-(4-fluorophenyl)-vinyl]-4-hydroxy-1H-indazole-1,5-dicarboxylic acid 1-tert-butyl ester 5-ethyl ester in 13 mL of N,N-dimethylformamide were added 196.5 mg of 2-(2-bromoethoxy)-tetrahydropyran and 306.3 mg of cesium carbonate, stirred for 1 hour and 30 minutes at room temperature, stirred at 50° C. for 17 hours, added with 196.5 mg of 2-(2-bromoethoxy)-tetrahydropyran and 306.3 mg of cesium carbonate, stirred for 3 hours at room temperature and for 2 hours at 50° C., added with 554 mg of 2-(2-bromoethoxy)-tetrahydropyran, and further stirred at 50° C. for 4 hours. Then, the reaction solution was added saturated aqueous ammonium chloride, extracted twice with ethyl acetate, and the resultant organic layer was washed once with saturated brine and dried over magnesium sulfate. The solvent was evaporated, and the crude product was purified and separated by silica gel column chromatography, to afford 147 mg of the title compound as a colorless oil.