2-Methyl-5-nitro-1H-indole → 5-Amino-2-methylindole

HRID 454200

反応式

HRID 454200 の反応式
[CH3:1][C:2]1[NH:3][C:4]2[C:9]([CH:10]=1)=[CH:8][C:7]([N+:11]([O-])=O)=[CH:6][CH:5]=2.[H][H]>C(O)C.C1COCC1.[Pd]>[NH2:11][C:7]1[CH:8]=[C:9]2[C:4](=[CH:5][CH:6]=1)[NH:3][C:2]([CH3:1])=[CH:10]2

参加物

6

反応物 2

HCID 2803132-Methyl-5-nitro-1H-indoleHCID 178418361HCID 178418361、化合物

生成物 1

HCID 27339925-Amino-2-methylindole収率 99.6%

試薬・触媒・溶媒 3

HCID 23938Palladium触媒HCID 702Ethanol溶媒HCID 8028Tetrahydrofuran溶媒

実験手順

A solution of 2-methyl-5-nitroindole (1 g, 5.7 mmol) in ethanol (25 ml) and THF (25 ml) containg 10% palladium on charcoal (128 mg) was hydrogenated until uptake of hydrogen ceased. The mixture was filtered and the filtrate was evaporated to give 5-amino-2-methylindole (830 mg, quant.).

後処理

  1. filtrationThe mixture was filtered
  2. customthe filtrate was evaporated

出典と根拠

ORDレコード
ord-fa041f888df349298ff5b641bf002f5e
出典データセット
uspto-grants-2013_07
特許番号
US08492560B2

関連ノート

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