تفاعل #63497

ord-8a99252617924af7b5e6e37583a9b8a9

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.ADDITIONare added
  2. 2
    أخرىthe organic phase is separated
  3. 3
    تجفيفdried with sodium sulfate
  4. 4
    أخرىAfter evaporation and chromatography

الإجراء التجريبي

A solution is prepared from 410 mg of 3-(13-nitro-6-methyl-8α-ergolinyl)-1,1-diethylurea in 10 ml of methylene chloride, 40 mg of tetrabutylammonium hydrogen sulfate and 0.8 ml of acetyl chloride are added, and this mixture is poured on 1 g of pulverized potassium hydroxide. After 1.5 hours of agitation at room temperature, the mixture is diluted with sodium bicarbonate solution, the organic phase is separated and dried with sodium sulfate. After evaporation and chromatography as indicated in Example 9, 375 mg of 3-(1-acetyl-6-methyl-13-nitro-8α-ergolinyl)-1,1-diethylurea is obtained.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US04766128uspto-grants-1988_08