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Water → 5-(Aminomethyl)-1H-indazole

HRID 1269734
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HRID 1269734 반응식
[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
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참가 물질

6

반응물 4

HCID 962Water2회HCID 3939Lithium HydroxideHCID 111263841H-Indazole-5-carbonitrileHCID 21226445Aluminium lithium hydride

생성물 1

HCID 120962235-(Aminomethyl)-1H-indazole수율 94.3%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

실험 절차

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%).

후처리

  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

출처 및 근거

ORD 기록
ord-68d13fd7f8224947a4bbf1878f118c03
출처 데이터셋
uspto-grants-2007_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07199147B2

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