تفاعل #62327
ord-dadf4429ce544c138b3aeb1a205cd059
معادلة التفاعل
المتفاعلات
الكواشف
لا شيء
المذيبات
ظروف التفاعل
الظروف التفصيلية
See reaction.notes.procedure_details.
المعالجة
- 1استخلاصextracted twice ethyl acetate
- 2غسيلthe resultant organic layer was washed once with saturated brine
- 3تجفيفdried over magnesium sulfate
- 4أخرىThe solvent was evaporated
- 5أخرىthe crude product was purified
- 6أخرىseparated by silica gel column chromatography
الإجراء التجريبي
To a solution of 147 mg of 3-[(E)-2-(4-fluorophenyl)-vinyl]-4-[2-(tetrahydropyran-2-yloxy)-ethoxy]-1H-indazole-1,5-dicarboxylic acid 1-tert-butyl ester 5-ethyl ester in 1.5 mL of tetrahydrofuran was added 1.5 mL of 2N hydrochloric acid, and stirred at room temperature for 19 hours. Thereafter, the reaction solution was added with water and extracted twice 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 87.1 mg of the title compound as a colorless oil.