HCID 22030186, compound → HCID 22030009, compound
Reaction equation
C[O:2][C:3]1[N:8]=[CH:7][C:6]([C:9]2[C:14]([C:15]([F:18])([F:17])[F:16])=[CH:13][CH:12]=[CH:11][N:10]=2)=[CH:5][CH:4]=1>Br.CC(O)=O>[F:17][C:15]([F:16])([F:18])[C:14]1[C:9]([C:6]2[CH:5]=[CH:4][C:3](=[O:2])[NH:8][CH:7]=2)=[N:10][CH:11]=[CH:12][CH:13]=1Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
Heat 6′-Methoxy-3-trifluoromethyl-[2,3′]bipyridinyl (41 g, 0.16 mol) in 30% HBr/AcOH (100 mL) to reflux for 1 hour. Cool the mixture, filter and wash the precipitate with ether (100 mL). Transfer the precipitate into 10M sodium hydroxide (500 mL) and stir for 1 hour. Treat the solution with hydrochloric acid until the solution is pH 7. Collect the white solid by filtration and air dry to give the title compound (36 g, 93%) as a white solid.
Workup
- temperatureto reflux for 1 hour
- temperatureCool the mixture
- filtrationfilter
- washwash the precipitate with ether (100 mL)
- additionTreat the solution with hydrochloric acid until the solution
- customCollect the white solid
- filtrationby filtration and air
- customdry
Sources & evidence
- ORD record
- ord-e1147c9a8cf4459c81bf288ebaa2aeeb
- Source dataset
- uspto-grants-2007_12
- Patent number
- US07304059B2
Reaction notes
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