تفاعل #67154

ord-c5c692eec63440c9a7035cf113f07452

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىThe solvent was removed
  2. 2
    أخرىthe residue partitioned between water (5 ml) and dichloromethane (5 ml)
  3. 3
    استخلاصextracted with dichloromethane (20 ml)
  4. 4
    تركيزThe organic layer was concentrated

الإجراء التجريبي

N-(2-chloro-5-{4-(5-methyl-1,3,4-oxadiazol-2-yl)-1-[(4-methylphenyl)sulfonyl]-1H-indazol-6-yl}-3-pyridinyl)methanesulfonamide (16 mg, 0.029 mmol) and 2M sodium hydroxide (1 ml, 2.0 mmol) were placed in isopropanol (5 ml) and the mixture stirred at room temperature overnight. The solvent was removed and the residue partitioned between water (5 ml) and dichloromethane (5 ml). The aqueous was acidified to ˜pH 1 with 2M hydrogen chloride, then extracted with dichloromethane (20 ml). The organic layer was concentrated to give the title compound as a white solid (10 mg).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08524751B2uspto-grants-2013_09