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Hydrazine hydrate (1:1) → 3-Amino-1H-indazole-4-carbonitrile

HRID 1892932
ノート
印刷プレビュー

反応式

HRID 1892932 の反応式
F[C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([C:8]#[N:9])[C:3]=1[C:10]#[N:11].O.[NH2:13][NH2:14]>C(O)C>[NH2:11][C:10]1[C:3]2[C:4]([C:8]#[N:9])=[CH:5][CH:6]=[CH:7][C:2]=2[NH:14][N:13]=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 24654Hydrazine hydrate (1:1)HCID 119609643-fluorophthalonitrile

生成物 1

HCID 540163943-Amino-1H-indazole-4-carbonitrile収率 87%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

反応条件

温度
70 °C

実験手順

3-Fluoro-1,2-benzenedicarbonitrile (APIN) (5 g, 34.2 mmol) was dissolved in ethanol (80 mL) and hydrazine monohydrate (4.98 mL, 103 mmol) was added to the solution. The reaction was heated at 70° C. overnight. The reaction mixture was concentrated in vacuo and the residue was partitioned between ethyl acetate (200 mL) and water (200 mL). The organic layer was washed with water (100 mL). The aqueous layers were extracted with ethyl acetate (200 mL). Organic layers were combined, dried over anhydrous magnesium sulfate and evaporated in vacuo to give the title compound (4.7 g, 87%) as a yellow solid. LCMS (System A) RT=0.53 min, ES+ve m/z 159 (M+H)+.

後処理

  1. concentrationThe reaction mixture was concentrated in vacuo
  2. customthe residue was partitioned between ethyl acetate (200 mL) and water (200 mL)
  3. washThe organic layer was washed with water (100 mL)
  4. extractionThe aqueous layers were extracted with ethyl acetate (200 mL)
  5. dry with materialdried over anhydrous magnesium sulfate
  6. customevaporated in vacuo

出典と根拠

ORDレコード
ord-00e0ae83330b4f73bd4c8984b7a72125
出典データセット
uspto-grants-2013_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08507543B2

反応ノート

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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