تفاعل #214471

ord-79759314c32d460ea16ec8d0fa971d1c

معادلة التفاعل

O=C1CC2(CCCC2)CC(=O)N1C1CCCNC1
8-(3-piperidinyl)-8-azaspiro [4,5]decan-7,9 -dione
COc1cc2nc(Cl)nc(N)c2cc1OC
4-amino-2-chloro-6,7-dimethoxyquinazoline
COc1cc2nc(N3CCCC(N4C(=O)CC5(CCCC5)CC4=O)C3)nc(N)c2cc1OC.Cl
8-[1-(4-amino-6,7-dimethoxy-2-quinazolinyl)-3-piperidinyl]-8-azaspiro[4,5]decan-7,9-dione hydrochloride

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةrefluxed under nitrogen for 24 hours
  2. 2
    درجة الحرارةIt is cooled to 20°
  3. 3
    ترشيحthe solids filtered off
  4. 4
    غسيلwashed with isoamyl alcohol and diethyl ether
  5. 5
    أخرىrecrystallized from the mixture of 160 ml of methanol and 110 ml of water

الإجراء التجريبي

The mixture of 3.75 g of 8-(3-piperidinyl)-8-azaspiro [4,5]decan-7,9 -dione, 3.59 g of 4-amino-2-chloro-6,7-dimethoxyquinazoline and 100 ml of isoamyl alcohol is stirred and refluxed under nitrogen for 24 hours. It is cooled to 20°, the solids filtered off, washed with isoamyl alcohol and diethyl ether and recrystallized from the mixture of 160 ml of methanol and 110 ml of water, to yield the 8-[1-(4-amino-6,7-dimethoxy-2-quinazolinyl)-3-piperidinyl]-8-azaspiro[4,5]decan-7,9-dione hydrochloride melting at 311°-312° with decomposition.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US04255429uspto-grants-1981_03