Reaction equation
Br[C:2]1[C:7]([N+:8]([O-:10])=[O:9])=[CH:6][C:5]([F:11])=[CH:4][N:3]=1.[NH3:12]>CO>[F:11][C:5]1[CH:6]=[C:7]([N+:8]([O-:10])=[O:9])[C:2]([NH2:12])=[N:3][CH:4]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 75 °C
Procedure
A solution of 2-bromo-5-fluoro-3-nitropyridine (1.176 g, 5.321 mmol) in 2M NH3 in MeOH (20 ml) was sealed in an autoclave and then heated at 75° C. for 6 h and then at 90° C. for a further 18 h. The reaction mixture was then cooled and evaporated, treated with sat. aq. NaHCO3 (100 ml) and then extracted with 5% MeOH/DCM (3×200 ml). The combined organic phases were dried and the solvent was removed. The residue was subjected to column chromatography on silica gel using a 0-5% MeOH in DCM gradient to provide the desired compound as a yellow solid (561 mg, 67%).
Workup
- temperatureThe reaction mixture was then cooled
- customevaporated
- additiontreated with sat. aq. NaHCO3 (100 ml)
- extractionextracted with 5% MeOH/DCM (3×200 ml)
- customThe combined organic phases were dried
- customthe solvent was removed
Sources & evidence
- ORD record
- ord-1b5765252d184358ababd3851fe7a8f5
- Source dataset
- uspto-grants-2011_12
- Patent number
- US08071592B2
Linked notes
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