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5-chloro-4-nitro-1H-indazole → 5-Chloro-1H-indazol-4-amine

HRID 1869402
ノート
印刷プレビュー

反応式

HRID 1869402 の反応式
[Cl:1][C:2]1[C:3]([N+:11]([O-])=O)=[C:4]2[C:8](=[CH:9][CH:10]=1)[NH:7][N:6]=[CH:5]2>[Pd]>[Cl:1][C:2]1[C:3]([NH2:11])=[C:4]2[C:8](=[CH:9][CH:10]=1)[NH:7][N:6]=[CH:5]2
参加物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 179892685-chloro-4-nitro-1H-indazole

生成物 1

HCID 179892615-Chloro-1H-indazol-4-amine

試薬・触媒・溶媒 1

HCID 23938Palladium触媒

実験手順

A solution that consists of 5-chloro-4-nitro-1H-indazole (872 mg, 4.41 mmol) is mixed with 150 mg of palladium on carbon (10%) and stirred under hydrogen atmosphere at room temperature. After 45 minutes, the catalyst is suctioned off on one frit and washed with methanol. The filtrate is concentrated by evaporation, and the residue is taken up in 200 ml of ethyl acetate and heated. After renewed suctioning-off and concentration by evaporation of the filtrate, the purification on silica gel is carried out with hexane/ethyl acetate (100-33% hexane). 296 mg (40% of theory) of the product is obtained.

後処理

  1. washwashed with methanol
  2. concentrationThe filtrate is concentrated by evaporation
  3. temperatureheated
  4. concentrationconcentration
  5. customby evaporation of the filtrate
  6. customthe purification on silica gel
  7. custom296 mg (40% of theory) of the product is obtained

出典と根拠

ORDレコード
ord-8ec87901cb0c4796b9a0c1d7c65f51b7
出典データセット
uspto-grants-2009_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07638515B2

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