تفاعل #55037

ord-808cb0a0266748a798ce898cc0ed978c

معادلة التفاعل

CCCI
1-iodopropane
O=C(Cc1ccccc1)N(c1ccc(Cl)cc1)C1CCNCC1
N-(4-chlorophenyl)-N-(4-piperidinyl)benzeneacetamide
CCN(C)C
N,N-dimethylethanamine
CCCI
1-iodopropane
CCCN1CCC(N(C(=O)Cc2ccccc2)c2ccc(Cl)cc2)CC1.Cl
N-(4-chlorophenyl)-N-(1-propyl-4-piperidinyl)benzeneacetamide hydrochloride

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةrefluxed for 47 hours
  2. 2
    workup.STIRRINGstirring
  3. 3
    درجة الحرارةrefluxing
  4. 4
    درجة الحرارةThe reaction mixture is cooled
  5. 5
    ترشيحfiltered
  6. 6
    غسيلThe filtrate is washed with water
  7. 7
    أخرىdried
  8. 8
    أخرىevaporated in vacuo
  9. 9
    ترشيحThe precipitated solid salt is filtered off
  10. 10
    أخرىdried

الإجراء التجريبي

To a stirred solution of 4 parts of N-(4-chlorophenyl)-N-(4-piperidinyl)benzeneacetamide and 3 parts of N,N-dimethylethanamine in 200 parts of benzene are added portionwise 4 parts of 1-iodopropane and the whole is stirred and refluxed for 47 hours. Then the second portion of 4 parts of 1-iodopropane is added and stirring and refluxing is continued for another 20h.20. The reaction mixture is cooled and filtered. The filtrate is washed with water, dried and evaporated in vacuo. From the oily free base, the hydrochloride salt is prepared in the conventional manner in 1,1'-oxybisethane. The precipitated solid salt is filtered off and dried, yielding 3.5 parts of N-(4-chlorophenyl)-N-(1-propyl-4-piperidinyl)benzeneacetamide hydrochloride; mp. 235.5° C.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US04151286uspto-grants-1979_04