تفاعل #2565

ord-7e6ae5c11c3c403ba17edba9a968e45c

معادلة التفاعل

O=C(c1ccc(F)cc1)C1CCN(CCCl)CC1
1-(2-chloroethyl)-4-(4-fluorobenzoyl)piperidine
COc1ccccc1NS(=O)(=O)c1ccc(C)cc1
N-(2-methoxyphenyl)-p-toluenesulfonamide
[I-].[Na+]
sodium iodide
[H-].[Na+]
sodium hydride
COc1ccccc1N(CCN1CCC(C(=O)c2ccc(F)cc2)CC1)S(=O)(=O)c1ccc(C)cc1
title compound
المردود 91.5%
COc1ccccc1N(CCN1CCC(C(=O)c2ccc(F)cc2)CC1)S(=O)(=O)c1ccc(C)cc1
N-{2-[4-(4-Fluorobenzoyl)piperidino]ethyl}-N-(2-methoxyphenyl)-p-toluenesulfonamide
المردود 91.5%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىat room temperature
  2. 2
    workup.WAITat 60° C. for 10 minutes
  3. 3
    workup.ADDITIONwas added to the reaction solution at 1 hour intervals at 60° C
  4. 4
    أخرىwas removed by evaporation
  5. 5
    workup.ADDITIONThe thus obtained residue was diluted with water (10 ml)
  6. 6
    استخلاصextracted with ether
  7. 7
    غسيلThe resulting organic layer was washed with water and saturated brine
  8. 8
    تجفيفdried on anhydrous sodium carbonate
  9. 9
    أخرىThereafter, the solvent was removed by evaporation
  10. 10
    أخرىthe resulting residue was purified by a silica gel column chromatography (ether:hexane=2:1)

الإجراء التجريبي

In an atmosphere of argon, N-(2-methoxyphenyl)-p-toluenesulfonamide (277 mg, 1.0 mmol) and a catalytically effective amount of sodium iodide were dissolved in DMF (3 ml) to which was subsequently added sodium hydride (44 mg, 60%, 1.1 mmol) at room temperature. After stirring at the same temperature for 30 minutes and then at 60° C. for 10 minutes, 1-(2-chloroethyl)-4-(4-fluorobenzoyl)piperidine (324 mg, 1.2 mmol) which has been divided into 3 portions, each being dissolved in DMF (1 ml), was added to the reaction solution at 1 hour intervals at 60° C. After 1.5 hours of additional stirring at the same temperature, DMF was removed by evaporation. The thus obtained residue was diluted with water (10 ml) and extracted with ether. The resulting organic layer was washed with water and saturated brine, and dried on anhydrous sodium carbonate. Thereafter, the solvent was removed by evaporation, and the resulting residue was purified by a silica gel column chromatography (ether:hexane=2:1) to obtain 467 mg (91.5%) of the title compound in the form of colorless oil.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05728835uspto-grants-1998_03