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1,3-Propanediamine → N~1~-(Quinolin-2-yl)propane-1,3-diamine

HRID 365285
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HRID 365285 반응식
[CH2:1]([NH2:5])[CH2:2][CH2:3][NH2:4].O1[CH2:10][CH2:9][CH2:8][CH2:7]1.[N:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1>>[N:11]1[C:12]2[C:10](=[CH:16][CH:15]=[CH:14][CH:13]=2)[CH:9]=[CH:8][C:7]=1[NH:4][CH2:3][CH2:2][CH2:1][NH2:5]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 4281,3-PropanediamineHCID 1049PyridineHCID 8028Tetrahydrofuran

생성물 1

HCID 22118517N~1~-(Quinolin-2-yl)propane-1,3-diamine수율 82%

실험 절차

To a solution of propane-1,3-diamine (65.1 ml, 0.764 mol) in dry pyridine (25 ml) kept under an atmosphere of nitrogen 2-chloro-quinoline (25 g, 0.153 mol) was added. The reaction mixture was heated at reflux temperature for 18 h. To the cooled reaction mixture was added tetrahydrofuran (100 ml) and the precipitate was filtered off and washed with tetrahydrofuran (2×50 ml). The solvent was evaporated in vacuo and the residue purified by distillation at 154° C. and 2.5×10-2 mbar affording 25.34 g (82%) of N-(quinolin-2-yl)propane-1,3-diamine as a crystallising oil.

후처리

  1. addition
이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
was added
  • temperatureThe reaction mixture was heated
  • temperatureat reflux temperature for 18 h
  • customTo the cooled reaction mixture
  • filtrationthe precipitate was filtered off
  • washwashed with tetrahydrofuran (2×50 ml)
  • customThe solvent was evaporated in vacuo
  • distillationthe residue purified by distillation at 154° C.
  • 출처 및 근거

    ORD 기록
    ord-8d6f890a37c14fd4a642ba4963973dd0
    출처 데이터셋
    uspto-grants-2000_10
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US06127343

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