Réaction #63596

Équation de réaction

4-(phenylmethyl)-2-piperazinecarboxamide

1,1'-(4-chlorobutylidene)bis[4-fluorobenzene]

sodium carbonate

potassium iodide

→

1-[4,4-bis(4-fluorophenyl)butyl]-4-(phenylmethyl)-2-piperazinecarboxamide

Rendement 63.6%

Solvants

water

4-methyl-2-pentanone

Conditions de réaction

Traitement

1. 1
   Températurerefluxed for 72 hours
2. 2
   Filtrationfiltered
3. 3
   Autrethe filtrate was evaporated
4. 4
   AutreThe oily residue was purified by column-chromatography over silica gel using
5. 5
   workup.ADDITIONa mixture of trichloromethane and methanol (97:3 by volume) as eluent
6. 6
   AutreThe pure fractions were collected
7. 7
   Autrethe eluent was evaporated
8. 8
   AutreThe residue was crystallized from 2,2'-oxybispropane
9. 9
   FiltrationThe product was filtered off
10. 10
    Autredried

Mode opératoire

A mixture of 13.2 parts of 4-(phenylmethyl)-2-piperazinecarboxamide, 18.5 parts of 1,1'-(4-chlorobutylidene)bis[4-fluorobenzene], 14.8 parts of sodium carbonate, 0.1 parts of potassium iodide and 200 parts of 4-methyl-2-pentanone was stirred and refluxed for 72 hours using a water-separator. The reaction mixture was cooled to room temperature, filtered and the filtrate was evaporated. The oily residue was purified by column-chromatography over silica gel using a mixture of trichloromethane and methanol (97:3 by volume) as eluent. The pure fractions were collected and the eluent was evaporated. The residue was crystallized from 2,2'-oxybispropane. The product was filtered off and dried, yielding 17.7 parts (63.6%) of 1-[4,4-bis(4-fluorophenyl)butyl]-4-(phenylmethyl)-2-piperazinecarboxamide; mp. 79.2° C. (intermediate 46).

Source