3-(4-Fluoropiperidin-1-yl)-2-nitropyridine → 3-(4-Fluoropiperidin-1-yl)pyridin-2-amine
Reaction equation
[F:1][CH:2]1[CH2:7][CH2:6][N:5]([C:8]2[C:9]([N+:14]([O-])=O)=[N:10][CH:11]=[CH:12][CH:13]=2)[CH2:4][CH2:3]1>CO>[F:1][CH:2]1[CH2:7][CH2:6][N:5]([C:8]2[C:9]([NH2:14])=[N:10][CH:11]=[CH:12][CH:13]=2)[CH2:4][CH2:3]1Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of 3-(4-fluoropiperidin-1-yl)-2-nitropyridine (2.0 g, 8.9 mmol) in methanol (25 mL) was added a generous spoon of rainey-nickel and the mixture stirred under an atmosphere of hydrogen for 5 hours. The reaction was then filtered over Hyflo and the solvent was evaporated in vacuo to afford the product used without need for further purification. The title compound was obtained as a dark brown solid (1.7 g, 100%).
Workup
- filtrationThe reaction was then filtered over Hyflo
- customthe solvent was evaporated in vacuo
- customto afford the product
- customused without need for further purification
Sources & evidence
- ORD record
- ord-362c2c603be24fee991df04488b4636c
- Source dataset
- uspto-grants-2013_07
- Patent number
- US08486967B2
Reaction notes
Loading…