Potassium Carbonate → 2-(3-piperidinopropyl)-4-phenyl-1(2H)-isoquinolone

HRID 1074617노트

반응식

HRID 1074617 반응식
Cl[CH2:2][CH2:3][CH2:4][N:5]1[CH:14]=[C:13]([C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)[C:12]2[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=2)[C:6]1=[O:21].C(=O)([O-])[O-].[K+].[K+]>N1CCCCC1>[N:5]1([CH2:2][CH2:3][CH2:4][N:5]2[CH:14]=[C:13]([C:15]3[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=3)[C:12]3[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=3)[C:6]2=[O:21])[CH2:14][CH2:13][CH2:12][CH2:7][CH2:6]1

참가 물질

4

실험 절차

Then, 14.9 g of 2-(3-chloropropyl)-4-phenyl-1(2H)-isoquinolone, 7 g of anhydrous potassium carbonate and 40 ml of piperidine were mixed and heated at reflux for 5 hours. Thereafter, any excess of piperidine was distilled off and the residue was dissolved in dichloromethane. The solution was washed with water, dried and the solvent was distilled off. The resulting crystals were recrystallized from a mixture of diethyl ether and petroleum ether to obtain 15.6 g of 2-(3-piperidinopropyl)-4-phenyl-1(2H)-isoquinolone having a melting point of 117.5° C. as colorless prisms.

후처리

  1. temperatureheated
  2. temperatureat reflux for 5 hours
  3. distillationThereafter, any excess of piperidine was distilled off
  4. dissolutionthe residue was dissolved in dichloromethane
  5. washThe solution was washed with water
  6. customdried
  7. distillationthe solvent was distilled off
  8. customThe resulting crystals were recrystallized from a mixture of diethyl ether and petroleum ether

출처 및 근거

ORD 기록
ord-ca40588b2ee04409a36c6936f2d90ad6
출처 데이터셋
uspto-grants-1983_07
특허 번호
US04393210

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