Methylamine → N-methyl-5-nitropyridin-2-amine

HRID 1992550Notes

Reaction equation

HRID 1992550 reaction equation
[CH3:1][NH2:2].Cl[C:4]1[CH:9]=[CH:8][C:7]([N+:10]([O-:12])=[O:11])=[CH:6][N:5]=1>ClCCl>[CH3:1][NH:2][C:4]1[CH:9]=[CH:8][C:7]([N+:10]([O-:12])=[O:11])=[CH:6][N:5]=1

Participants

4

Procedure

Methylamine gas was bubbled through a stirred solution of 2-chloro-5-nitropyridine (4 g, 25.2 mmol) in dichloromethane (60 mL), at room temperature, until saturation had occurred. The resulting yellow precipitate was then filtered off, washed with dichloromethane and dried under vacuum to afford the title compound as a yellow solid in 80% yield, 3.07 g.

Workup

  1. filtrationThe resulting yellow precipitate was then filtered off
  2. washwashed with dichloromethane
  3. customdried under vacuum

Sources & evidence

ORD record
ord-7934b30d52ef432cbe6c9a0dcc5a3a9b
Source dataset
uspto-grants-2010_01
Patent number
US07649003B2

Reaction notes

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