1-Methyl-6-nitro-1H-indole → 1-methyl-1H-indol-6-amine

HRID 651760노트

반응식

HRID 651760 반응식
[CH3:1][N:2]1[C:10]2[C:5](=[CH:6][CH:7]=[C:8]([N+:11]([O-])=O)[CH:9]=2)[CH:4]=[CH:3]1>C(O)C.O1CCCC1.[Pd]>[CH3:1][N:2]1[C:10]2[C:5](=[CH:6][CH:7]=[C:8]([NH2:11])[CH:9]=2)[CH:4]=[CH:3]1

참가 물질

5

실험 절차

A mixture of 1-methyl-6-nitro-1H-indole (5.0 g, 28.4 mmol) and 10% Pd/C(1.0 g) in ethanol (200 ml) and tetrahydrofuran (100 ml) was hydrogenated at atmospheric pressure for 14 hours. The reaction mixture was filtered and concentrated to give 1-methyl-6-amino-1H-indole after crystallization from ether/hexane (3.8 g, 80%).

후처리

  1. filtrationThe reaction mixture was filtered
  2. concentrationconcentrated

출처 및 근거

ORD 기록
ord-43114244a0d84dc88471a1748567d7c5
출처 데이터셋
uspto-grants-2001_08
특허 번호
US06281356B1

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