تفاعل #91021

ord-72d1cb29de514e8b92eda89af5958294

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىThe mixture was partitioned between 1M HCl (5 mL) and DCM (10 mL)
  2. 2
    أخرىthe phases were separated
  3. 3
    أخرىThe organic solvent was removed in vacuo
  4. 4
    أخرىthe residue was purified by silica gel chromatography (40 g, 0-20% IPA in isohexane)

الإجراء التجريبي

2 M Lithium hydroxide (554 μL, 1.11 mmol) was added to a solution of 4-(3,5-diisopropoxy-4-ethoxybenzamido)-2-fluorobenzoate (3) (320 mg, 0.740 mmol) in THF (5 mL) and the mixture was stirred at RT for 20 h. The mixture was partitioned between 1M HCl (5 mL) and DCM (10 mL) and the phases were separated. The organic solvent was removed in vacuo and the residue was purified by silica gel chromatography (40 g, 0-20% IPA in isohexane) to afford 4-(3,5-diisopropoxy-4-ethoxybenzamido)-2-fluorobenzoic acid (AAA-064) as a white solid (176 mg, 56%): m/z 420 [M+H]+ (ES+), 418 [M−H]− (ES−). 1H-NMR (400 MHz, DMSO-d6) δ: 13.03 (1H, br s), 10.45 (1H, s), 7.88 (1H, t), 7.81 (1H, dd), 7.61 (1H, dd), 7.22 (2H, s), 4.65 (2H, sep), 4.00 (2H, q), 1.29 (12H, d), 1.26 (3H, t).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US09447028B2uspto-grants-2016_09