تفاعل #531657

ord-e15e5995276f4fe89dd59790964cf37c

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىAfter the completion of the reaction
  2. 2
    ترشيحthe precipitate was filtered off
  3. 3
    غسيلwashed with water
  4. 4
    أخرىAfter drying
  5. 5
    أخرىthere were obtained 14 g of raw base which

الإجراء التجريبي

A suspension of 6.87 g of 3,4-dihydroxyphenyl chloromethylketone (trade product) and 8 g of 4-(2-oxobenzimidazolin-1-yl)piperidine (trade product), M.P. 183°-185° C., in 640 ml of methylethyl ketone, in the presence of 1.95 g of dried sodium carbonate and 0.1 g of sodium iodide, was refluxed for 12 hours. After the completion of the reaction, the precipitate was filtered off and washed with water. After drying, there were obtained 14 g of raw base which is transformed in hydrochloride in methanol by addition of hydrochloric ether. There were obtained 8 g of 1-(3,4-dihydroxy phenacyl)-4-(2-oxobenzimidazolin-1-yl)piperidine hydrochloride, white crystals melting at 310°-313° C.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US04264613uspto-grants-1981_04