تفاعل #5825

ord-9210acb815974a8380d54b730e8abe69

معادلة التفاعل

CN(C)C=O
dimethylformamide
C1CNCCNC1
homopiperazine
O=C([O-])O.[Na+]
sodium bicarbonate
O=C(Cl)OCc1ccccc1
benzyloxycarbonyl chloride
O=C(OCc1ccccc1)N1CCCNCC1
title compound
المردود 65.5%
O=C(OCc1ccccc1)N1CCCNCC1
N-Benzyloxycarbonylhomopiperazine
المردود 65.5%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.STIRRINGthe mixture was stirred at a room temperature overnight
  2. 2
    أخرىAfter evaporating off dimethylformamide under a reduced pressure
  3. 3
    استخلاصthe reaction mixture was extracted three times with 100 ml of chloroform
  4. 4
    تجفيفthe extract was dried over magnesium sulfate
  5. 5
    أخرىevaporated
  6. 6
    أخرىto remove the solvent under a reduced pressure
  7. 7
    غسيلeluted with chloroform/methanol (9:1)

الإجراء التجريبي

To 230 ml of dimethylformamide were added 25 g of homopiperazine and 5.4 g of sodium bicarbonate and then 25 ml of water followed by dropwise addition of 10 g of benzyloxycarbonyl chloride with stirring under ice cooling, and the mixture was stirred at a room temperature overnight. After evaporating off dimethylformamide under a reduced pressure, the reaction mixture was extracted three times with 100 ml of chloroform, and the extract was dried over magnesium sulfate and evaporated to remove the solvent under a reduced pressure. The resulting residue was applied to a silica gel column and eluted with chloroform/methanol (9:1), to obtain 9 g of the title compound as a light yellow liquor liquid.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05245034uspto-grants-1993_09