HCID 67335196, compound → 3-morpholinopyridin-2-amine
Reaction equation
[N+:1]([C:4]1[C:9]([N:10]2[CH2:15][CH2:14][O:13][CH2:12][CH2:11]2)=[CH:8][CH:7]=[CH:6][N:5]=1)([O-])=O>C(OCC)(=O)C.[Pd]>[O:13]1[CH2:14][CH2:15][N:10]([C:9]2[C:4]([NH2:1])=[N:5][CH:6]=[CH:7][CH:8]=2)[CH2:11][CH2:12]1Participants
4
Reactant 1
Product 1
Reagents, catalysts & solvents 2
Procedure
To a solution of 4-(2-nitropyridin-3-yl)morpholine (155 mg, 741 μmol) in ethyl acetate was added Pd/C 10% (15.5 mg, 146 μmol) and the reaction was hydrogenated under an atmosphere of hydrogen for 3 hours at room temperature. The catalyst was filtered off, washed with ethyl acetate and the solvent was evaporated under reduced pressure. The title compound was obtained as a purple solid (128 mg, 96%).
Workup
- filtrationThe catalyst was filtered off
- washwashed with ethyl acetate
- customthe solvent was evaporated under reduced pressure
Sources & evidence
- ORD record
- ord-32f459d0445f420eb01e1820048b6ae1
- Source dataset
- uspto-grants-2013_07
- Patent number
- US08486967B2
Reaction notes
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