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Aluminium lithium hydride → HCID 67335147、化合物

HRID 1672157
ノート
印刷プレビュー

反応式

HRID 1672157 の反応式
[NH:1]1[C:9]2[C:4](=[CH:5][C:6]([NH:10][C:11]3([C:17]#[N:18])[CH2:16][CH2:15][CH2:14][CH2:13][CH2:12]3)=[CH:7][CH:8]=2)[CH:3]=[N:2]1.[H-].[H-].[H-].[H-].[Li+].[Al+3]>C1COCC1>[NH2:18][CH2:17][C:11]1([NH:10][C:6]2[CH:5]=[C:4]3[C:9](=[CH:8][CH:7]=2)[NH:1][N:2]=[CH:3]3)[CH2:12][CH2:13][CH2:14][CH2:15][CH2:16]1
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

4

反応物 2

HCID 21226445Aluminium lithium hydrideHCID 67336325HCID 67336325、化合物

生成物 1

HCID 67335147HCID 67335147、化合物収率 31%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

反応条件

温度
70 °C

実験手順

To a stirred solution of 1-(1H-indazol-5-ylamino)-cyclohexanecarbonitrile (2.53 g, 10.5 mmol) in THF (40 mL) at room temperature and under nitrogen was added LiAlH4 (21.0 mL of a 1.0 M solution in THF, 21.0 mmol) dropwise over 3 minutes. After 30 minutes the reaction mixture was warmed to 70° C. After 2 hours the reaction mixture was cooled and stirred at ambient temperature for 14 hours, then quenched by the addition of sodium sulfate decahydrate (3 g). The reaction mixture was diluted with DCM:MeOH:NH4OH (90:9:1, 200 mL) then filtered and concentrated in vacuo. Purification by chromatography (silica, 3 to 20% of a 9:1 MeOH:NH4OH solution in DCM) gave (1-aminomethyl-cyclohexyl)-(1H-indazol-5-yl)-amine (0.785 g, 3.22 mmol, 31 %) as a solid.

後処理

  1. temperatureAfter 2 hours the reaction mixture was cooled
  2. customquenched by the addition of sodium sulfate decahydrate (3 g)
  3. additionThe reaction mixture was diluted with DCM:MeOH:NH4OH (90:9:1, 200 mL)
  4. filtrationthen filtered
  5. concentrationconcentrated in vacuo
  6. customPurification by chromatography (silica, 3 to 20% of a 9:1 MeOH:NH4OH solution in DCM)

出典と根拠

ORDレコード
ord-9a08f65eeb664d419e1cf3a00c399db4
出典データセット
uspto-grants-2011_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07998963B2

反応ノート

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