تفاعل #56422

ord-47a9a65bc5684325ad2f968231dfc43c

معادلة التفاعل

[H][H]
hydrogen
c1ccsc1
thiophene
O=C1CCCC1
cyclopentanone
c1cnc(NC2CCNCC2)nc1
N-(4-piperidinyl)-2-pyrimidinamine
c1cnc(NC2CCN(C3CCCC3)CC2)nc1
N-(1-cyclopentyl-4-piperidinyl)-2-pyrimidinamine

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    ترشيحthe catalyst is filtered off
  2. 2
    أخرىthe filtrate is evaporated
  3. 3
    غسيلThe whole is washed twice with a diluted sodium hydroxide solution
  4. 4
    أخرىdried
  5. 5
    ترشيحfiltered
  6. 6
    أخرىevaporated
  7. 7
    أخرىThe residue is crystallized from 2,2'-oxybispropane
  8. 8
    ترشيحThe product is filtered off
  9. 9
    أخرىdried

الإجراء التجريبي

To 0.5 parts of a solution of 2 parts of thiophene in 40 parts of ethanol, are added 2 parts of cyclopentanone, 5.5 parts of N-(4-piperidinyl)-2-pyrimidinamine and 120 parts of methanol. The whole is hydrogenated at normal pressure and at room temperature with 2 parts of palladium-on-charcoal 10%. After the calculated amount of hydrogen is taken up, the catalyst is filtered off and the filtrate is evaporated. The residue is taken up in 4-methyl-2-pentanone and a small amount of trichloromethane. The whole is washed twice with a diluted sodium hydroxide solution, dried, filtered and evaporated. The residue is crystallized from 2,2'-oxybispropane. The product is filtered off and dried, yielding 2.3 parts of N-(1-cyclopentyl-4-piperidinyl)-2-pyrimidinamine; mp. 118° C.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US04225606uspto-grants-1980_09