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Piperazine → HCID 14128502, 화합물

HRID 621574
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HRID 621574 반응식
Cl[CH2:2][CH2:3][CH2:4][O:5][C:6]1[CH:15]=[CH:14][CH:13]=[C:12]2[C:7]=1[CH2:8][CH2:9][C:10](=[O:16])[NH:11]2.[NH:17]1[CH2:22][CH2:21][NH:20][CH2:19][CH2:18]1.C([O-])(O)=O.[Na+]>>[N:17]1([CH2:2][CH2:3][CH2:4][O:5][C:6]2[CH:15]=[CH:14][CH:13]=[C:12]3[C:7]=2[CH2:8][CH2:9][C:10](=[O:16])[NH:11]3)[CH2:22][CH2:21][NH:20][CH2:19][CH2:18]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 4837PiperazineHCID 516892Sodium BicarbonateHCID 12899139HCID 12899139, 화합물

생성물 1

HCID 14128502HCID 14128502, 화합물수율 49.7%

실험 절차

(a)-1 3.0 grams of 5-(3-chloropropoxy)-3,4-dihydrocarbostyril and 10 g of piperazine are mixed with 20 ml of hexamethylphosphoryl triamide and heated at 80°-90° C. for 5 hours. The reaction mixture is distilled under a reduced pressure to remove hexamethylphosphoryl triamide and unreacted piperazine. To the residue thus obtained are added 30 ml of 5%-NaHCO3 aqueous solution, followed by extraction with chloroform. The chloroform layer is washed with water and chloroform is removed by distillation. The residue thus obtained is purified by silica-gel chromatography to obtain 1.8 g of 5-(3-piperazinylpropoxy)-3,4-dihydrocarbostyril having a melting point of 192°-195° C.

후처리

  1. temperatureheated at 80°-90° C. for 5 hours
  2. distillationThe reaction mixture is distilled under a reduced pressure
  3. customto remove hexamethylphosphoryl triamide and unreacted piperazine
  4. customTo the residue thus obtained
  5. extractionfollowed by extraction with chloroform
  6. washThe chloroform layer is washed with water and chloroform
  7. customis removed by distillation
  8. customThe residue thus obtained
  9. customis purified by silica-gel chromatography

출처 및 근거

ORD 기록
ord-43e9f53517924ca99085d57bf35da754
출처 데이터셋
uspto-grants-1989_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04824840

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