تفاعل #713848

ord-a28a05d6b1b04d38a7fa68f924df87bc

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىThe mixture was partitioned between DCM and water
  2. 2
    غسيلThe organic layer was washed with brine
  3. 3
    تجفيفdried over anhydrous sodium sulfate
  4. 4
    تركيزconcentrated under reduced pressure
  5. 5
    أخرىThe residue was purified by silica gel flash chromatography (40-50% ethyl acetate in cyclohexane)

الإجراء التجريبي

DIPEA (51 μL, 0.3 mmol) and then methyl chloroformate (19 μL, 0.25 mmol) were added to a solution of 2-(2,6-dichlorophenyl)-2H-pyrazolo[4,3-c]pyridine-4-ylamine (60 mg, 0.21 mmol) in DCM (2 mL). The reaction was stirred at room temperature until completion as determined by TLC. The mixture was partitioned between DCM and water. The organic layer was washed with brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel flash chromatography (40-50% ethyl acetate in cyclohexane) to afford the title compound as a white solid (35 mg, 49% yield). 1H NMR (400 MHz, DMSO-d6): δ 9.54 (d, J=0.9 Hz, 1H), 7.97 (d, J=7.3 Hz, 1H), 7.86 (d, J=1.4 Hz, 1H), 7.84 (d, J=0.6 Hz, 1H), 7.80-7.78 (m, 1H), 7.72 (dd, J=7.3, 0.9 Hz, 1H), 3.97 (s, 3H). LCMS (Method B): RT=2.71 min, m/z: 337 [M+H+].

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US09309240B2uspto-grants-2016_04