7-methyl-6-nitro-1H-indole → 7-methyl-1H-indol-6-amine
反応式
[CH3:1][C:2]1[C:3]([N+:11]([O-])=O)=[CH:4][CH:5]=[C:6]2[C:10]=1[NH:9][CH:8]=[CH:7]2>[Pd].C(O)C>[NH2:11][C:3]1[C:2]([CH3:1])=[C:10]2[C:6]([CH:7]=[CH:8][NH:9]2)=[CH:5][CH:4]=1参加物
4
実験手順
A degassed suspension of 7-methyl-6-nitroindole (1.5 g, 8.5 mmol) and catalytic 10% palladium on carbon in ethanol (75 mL) is placed under an atmosphere of hydrogen at 50 p.s.i. for 7 hours. The reaction mixture is filtered through Celite and the mixture concentrated by rotary evaporation. The crude residue is purified via silica gel column chromatography using 20% isopropanol/hexanes as the eluting solvent. The product containing fractions are combined and the solvents removed by rotary evaporation to yield 0.95 g of 6-amino-7-methylindole as a light brown solid (76% yield).
後処理
- filtrationThe reaction mixture is filtered through Celite
- concentrationthe mixture concentrated by rotary evaporation
- customThe crude residue is purified via silica gel column chromatography
- additionThe product containing fractions
- customthe solvents removed by rotary evaporation
出典と根拠
- ORDレコード
- ord-d2a03392bdb94c01a270bc30d39bf796
- 出典データセット
- uspto-grants-2000_12
- 特許番号
- US06162818
反応ノート
読み込み中…