تفاعل #62327

ord-dadf4429ce544c138b3aeb1a205cd059

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    استخلاصextracted twice ethyl acetate
  2. 2
    غسيلthe resultant organic layer was washed once with saturated brine
  3. 3
    تجفيفdried over magnesium sulfate
  4. 4
    أخرىThe solvent was evaporated
  5. 5
    أخرىthe crude product was purified
  6. 6
    أخرىseparated 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.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07429609B2uspto-grants-2008_09