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

HRID 365285
ノート
印刷プレビュー

反応式

HRID 365285 の反応式
[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]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 3

HCID 4281,3-PropanediamineHCID 1049PyridineHCID 8028Tetrahydrofuran

生成物 1

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

実験手順

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.

後処理

  1. additionwas added
このページの内容参加物実験手順後処理出典と根拠反応ノート
  • 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.
  • 出典と根拠

    ORDレコード
    ord-8d6f890a37c14fd4a642ba4963973dd0
    出典データセット
    uspto-grants-2000_10
    DOI
    10.6084/m9.figshare.5104873.v1
    特許番号
    US06127343

    反応ノート

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