تفاعل #69553

ord-21530398d17b4d688e234cdb73de690c

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    استخلاصthe reaction mixture was extracted with ethyl acetate
  2. 2
    تجفيفdried over anhydrous magnesium sulfate
  3. 3
    ترشيحThe mixture was filtered
  4. 4
    workup.DISTILLATIONthe solvent in the filtrate was distilled off under reduced pressure
  5. 5
    أخرىThe residue was purified by silica gel column chromatography (a mixed solvent of n-heptane and ethyl acetate

الإجراء التجريبي

To a N,N-dimethylformamide (6 mL) solution of 3-[2,6-dimethoxy-4-(methoxymethyl)phenyl]-6-methoxypyrazolo[5,1-b][1,3]thiazole-7-amine (400 mg, 1.14 mmol) were added 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide (0.236 mL, 1.33 mmol) and 1-hydroxybenzotriazole (180 mg, 1.33 mmol), and the mixture was stirred at room temperature over one day and night. Water was added to the reaction mixture, and the reaction mixture was extracted with ethyl acetate and dried over anhydrous magnesium sulfate. The mixture was filtered, and then the solvent in the filtrate was distilled off under reduced pressure. The residue was purified by silica gel column chromatography (a mixed solvent of n-heptane and ethyl acetate: n-heptane/ethyl acetate=1/1 then 1/2) to obtain the title compound (404 mg, 0.93 mmol).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08530504B2uspto-grants-2013_09