4-Fluoro-N-methylaniline → (4-Fluorophenyl)-methyl-(3-nitropyridin-2-ylmethyl)-amine
Reaction equation
Br[CH2:2][C:3]1[C:8]([N+:9]([O-:11])=[O:10])=[CH:7][CH:6]=[CH:5][N:4]=1.[F:12][C:13]1[CH:18]=[CH:17][C:16]([NH:19][CH3:20])=[CH:15][CH:14]=1>>[F:12][C:13]1[CH:18]=[CH:17][C:16]([N:19]([CH3:20])[CH2:2][C:3]2[C:8]([N+:9]([O-:11])=[O:10])=[CH:7][CH:6]=[CH:5][N:4]=2)=[CH:15][CH:14]=1Participants
3
Procedure
In accordance with the same procedures as in Step 1 of Preparation 2, except for using 2-bromomethyl-3-nitropyridine prepared in Step 2 of Preparation 1 and (4-fluorophenyl)-methylamine, the titled compound was obtained as yellow solid. (Yield: 80%)
Workup
- customIn accordance with the same procedures as in Step 1 of Preparation 2
Sources & evidence
- ORD record
- ord-b6ea144c535a40659c4a51d37a54c6f8
- Source dataset
- uspto-grants-2012_05
- Patent number
- US08188114B2
Reaction notes
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