methyl 4-nitro-1H-indazole-1-carboxylate → methyl 4-amino-1H-indazole-1-carboxylate

HRID 586065

反応式

HRID 586065 の反応式
[N+:1]([C:4]1[CH:12]=[CH:11][CH:10]=[C:9]2[C:5]=1[CH:6]=[N:7][N:8]2[C:13]([O:15][CH3:16])=[O:14])([O-])=O.[H][H]>C(O)C.[Pd]>[NH2:1][C:4]1[CH:12]=[CH:11][CH:10]=[C:9]2[C:5]=1[CH:6]=[N:7][N:8]2[C:13]([O:15][CH3:16])=[O:14]

参加物

5

反応物 2

HCID 22032604methyl 4-nitro-1H-indazole-1-carboxylateHCID 178418361HCID 178418361、化合物

生成物 1

HCID 22032652methyl 4-amino-1H-indazole-1-carboxylate

試薬・触媒・溶媒 2

HCID 23938Palladium触媒HCID 702Ethanol溶媒

反応条件

温度
80 °C

実験手順

Methyl 4-nitro-1H-indazole-1-carboxylate 1.66 g, 7.5 mmol) and 10% Pd/C were combined in ethanol (20 mL) and exposed to a hydrogen atmosphere. The reaction mixture was heated at 80° C. for 20 minutes, allowed to cool to room temperature, and filtered through Celite. The filtrate was evaporated to provide title compound. 1H NMR (300 MHz, DMSO-d6) δ 6.1 (s, 2H), 6.41 (dd, 1H), 7.21 (m, 2H), 8.42 (s, 1H).

後処理

  1. temperatureto cool to room temperature
  2. filtrationfiltered through Celite
  3. customThe filtrate was evaporated

出典と根拠

ORDレコード
ord-5eb543c2e4c544bfa039b02fd409d3d5
出典データセット
uspto-grants-2005_08
特許番号
US06933311B2

関連ノート

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