Pyridine (5-methyl-2-nitrophenyl)nitride → 2-amino-5-methyl-N-(2-pyridyl)aniline

HRID 382569Notes

Reaction equation

HRID 382569 reaction equation
[CH3:1][C:2]1[CH:3]=[CH:4][C:5]([N+:15]([O-])=O)=[C:6]([CH:14]=1)[NH:7][C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][N:9]=1>[Pd].C(O)C>[NH2:15][C:5]1[CH:4]=[CH:3][C:2]([CH3:1])=[CH:14][C:6]=1[NH:7][C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][N:9]=1

Participants

4

Procedure

A mixture of 5-methyl-2-nitro-N-(2-pyridyl)aniline (3.8 g, 16.6 mmol), 5% palladium on carbon (500 mg) in ethanol (100 ml) was stirred under a hydrogen atmosphere for 3 h. The mixture was filtered through a pad of celite and the filtrate was concentrated to dryness to give 3.3 g (quant.) of the titled compound as gray solids.

Workup

  1. filtrationThe mixture was filtered through a pad of celite
  2. concentrationthe filtrate was concentrated to dryness

Sources & evidence

ORD record
ord-d1b7aa8f409d4e7aab12e97449f7e59c
Source dataset
uspto-grants-2001_10
Patent number
US06310079B1

Reaction notes

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