تفاعل #682977

ord-4e5480f451d54182a4b5b1775d3e9eee

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    استخلاصthe reaction mixture was extracted with EtOAc
  2. 2
    غسيلThe organic layer was washed with NaHCO3, water and brine
  3. 3
    تجفيفdried over anhydrous sodium sulfate
  4. 4
    ترشيحfiltered off
  5. 5
    تركيزconcentrated in vacuo

الإجراء التجريبي

To a solution of 4-borono-2-fluorobenzoic acid (160 mg, 0.870 mmol), (R)-1-(2-fluorophenylsulfonyl)piperidin-3-amine (225 mg, 0.870 mmol), and DIEA (456 μL, 2.61 mmol) in THF (1450 μL) and DMF (1450 μL) was added HOAt (237 mg, 1.740 mmol) and EDC (417 mg, 2.175 mmol). After 3 h stirring at room temperature, the reaction mixture was extracted with EtOAc. The organic layer was washed with NaHCO3, water and brine, dried over anhydrous sodium sulfate, filtered off, and concentrated in vacuo yielding (R)-3-fluoro-4-(1-(2-fluorophenylsulfonyl)piperidin-3-ylcarbamoyl)phenylboronic acid, which was used in next step reaction without purification. LCMS (m/z): 425.2 (MH+), 0.72 min.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US09242996B2uspto-grants-2016_01