تفاعل #61877

ord-bb2f4849cf9745ecbfbe67d605536b76

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.STIRRINGThe mixture was further stirred at −5° C. for 30 min
  2. 2
    غسيلthe mixture was washed successively with 10% aqueous citric acid, saturated aqueous sodium hydrogencarbonate
  3. 3
    تجفيفsaturated brine (50 mL) and dried over sodium sulfate
  4. 4
    أخرىThen, methylene chloride was evaporated under reduced pressure
  5. 5
    أخرىThe obtained residue was purified by silica gel column chromatography

الإجراء التجريبي

tert-Butanol (0.85 mL) was dissolved in methylene chloride (17 mL) and chlorosulfonyl isocyanate (0.77 mL) was added at −18° C. The mixture was stirred at the same temperature for 30 min and N-(5-amino-4,6-dimethyl-1-octylindolin-7-yl)-2,2-dimethylpropanamide (1.66 g) and triethylamine (1.24 mL) were added. The mixture was further stirred at −5° C. for 30 min. Methylene chloride (50 mL) was added, and the mixture was washed successively with 10% aqueous citric acid, saturated aqueous sodium hydrogencarbonate, and then saturated brine (50 mL) and dried over sodium sulfate. Then, methylene chloride was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography to give the title compound as crystals (1.9 g).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07429612B2uspto-grants-2008_09