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1H-Indazole-5-carbonitrile → 5-(Aminomethyl)-1H-indazole

HRID 398356
ノート
印刷プレビュー

反応式

HRID 398356 の反応式
[C:1]([C:3]1[CH:4]=[C:5]2[C:9](=[CH:10][CH:11]=1)[NH:8][N:7]=[CH:6]2)#[N:2]>C1COCC1>[NH2:2][CH2:1][C:3]1[CH:4]=[C:5]2[C:9](=[CH:10][CH:11]=1)[NH:8][N:7]=[CH:6]2
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

3

反応物 1

HCID 111263841H-Indazole-5-carbonitrile

生成物 1

HCID 120962235-(Aminomethyl)-1H-indazole

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

反応条件

温度
0 °C

実験手順

To a solution of LiAl H4 (0.76 g, 20.1 mmol) in THF (10 mL) cooled to 0° C. was added a solution of 5-cyanoindazole (0.64 g, 4.47 mmol) in THF (10 mL) dropwise. After 0.5 h the reaction mixture was warmed to reflux for 2 h, then cooled to 0° C. and quenched by the careful addition of water (0.76 mL), 1.0 N sodium hydroxide (0.76 mL), and water (2.28 mL). This mixture was filtered through a pad of celite and washed with THF/MeOH (3:1, 300 mL). Removal of the solvent in vacuo provided a solid which was purified via flash column chromatography (25×150 mm column; elution with MeOH:CH2Cl2:CH2Cl2 saturated with NH3, 10:60:30). This afforded the title compound as a light yellow solid:

このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート

後処理

  1. temperatureAfter 0.5 h the reaction mixture was warmed
  2. temperatureto reflux for 2 h
  3. customquenched by the careful addition of water (0.76 mL), 1.0 N sodium hydroxide (0.76 mL), and water (2.28 mL)
  4. filtrationThis mixture was filtered through a pad of celite
  5. washwashed with THF/MeOH (3:1, 300 mL)
  6. customRemoval of the solvent in vacuo
  7. customprovided a solid which
  8. customwas purified via flash column chromatography (25×150 mm column; elution with MeOH:CH2Cl2:CH2Cl2 saturated with NH3, 10:60:30)

出典と根拠

ORDレコード
ord-5002a3a397694005bff0f67d171d89d0
出典データセット
uspto-grants-2003_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06610692B1

反応ノート

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