تفاعل #4652

ord-a3fc75976eb84e38ac08b331292e5971

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىThe catalyst is then removed by filtration
  2. 2
    تركيزthe filtrate is concentrated by evaporation under reduced pressure
  3. 3
    أخرىThe crystals so obtained
  4. 4
    أخرىare isolated by filtration
  5. 5
    أخرىdried in vacuo

الإجراء التجريبي

A solution of 23 g of crude 1-[N-[2-(3-carbamoyl-4-hydroxyphenoxy)ethyl]-benzylamino]-3-[4-(2-hydroxyethoxy)phenoxy]-2-propanol in 500 ml of methanol is hydrogenated, under normal conditions, with the addition of 2 g of 5% palladium on carbon catalyst, until hydrogen absorption has ceased. The catalyst is then removed by filtration and the filtrate is concentrated by evaporation under reduced pressure. The crystalline residue is stirred in a mixture of 50 ml of methanol and ether. The crystals so obtained are isolated by filtration and dried in vacuo, affording 1-[2-(3-carbamoyl-4-hydroxyphenoxy)ethylamino]-3-[4-(2-hydroxyethoxy)phenoxy]-2-propanol with a melting point of 150°-151° C. Reaction with the equivalent amount of hydrogen chloride, as solution in methanol, affords the hydrochloride with a melting point of 205°-206° C.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US04727067uspto-grants-1988_02