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Water → 5-(Aminomethyl)-1H-indazole

HRID 1269734
ノート
印刷プレビュー

反応式

HRID 1269734 の反応式
[NH:1]1[C:9]2[C:4](=[CH:5][C:6]([C:10]#[N:11])=[CH:7][CH:8]=2)[CH:3]=[N:2]1.[H-].[Al+3].[Li+].[H-].[H-].[H-].O.[OH-].[Li+]>O1CCCC1>[NH:1]1[C:9]2[C:4](=[CH:5][C:6]([CH2:10][NH2:11])=[CH:7][CH:8]=2)[CH:3]=[N:2]1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 962Water2 回HCID 3939Lithium HydroxideHCID 111263841H-Indazole-5-carbonitrileHCID 21226445Aluminium lithium hydride

生成物 1

HCID 120962235-(Aminomethyl)-1H-indazole収率 94.3%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

実験手順

A solution of 1H-indazole-5-carbonitrile (100 mg, 0.699 mmol) in tetrahydrofuran (4 ml) was added to a solution of lithium aluminum hydride (53 mg, 1.40 mmol) in tetrahydrofuran (4 ml) at room temperature, and the resulting mixture was refluxed for 2 hours. Subsequently, water (0.053 ml), a 2N-aqueous lithium hydroxide solution (0.106 ml) and water (0.212 ml) were added in that order to the reaction solution and stirred, followed by filtration. The solvent was distilled off under reduced pressure and the residue was dried under reduced pressure to obtain 1-(1H-indazol-5-yl)methanamine (97 mg, 94%).

後処理

  1. temperaturethe resulting mixture was refluxed for 2 hours
  2. filtrationfollowed by filtration
  3. distillationThe solvent was distilled off under reduced pressure
  4. customthe residue was dried under reduced pressure

出典と根拠

ORDレコード
ord-68d13fd7f8224947a4bbf1878f118c03
出典データセット
uspto-grants-2007_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07199147B2

反応ノート

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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