Boron tribromide → HCID 53245809, compound
Reaction equation
C[O:2][C:3]1[C:12]2[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=2)[CH:6]=[C:5]([NH:13][C:14]([C:16]2[C:25](=[O:26])[C:24]3[C:19](=[CH:20][CH:21]=[CH:22][CH:23]=3)[NH:18][CH:17]=2)=[O:15])[CH:4]=1.B(Br)(Br)Br>C(Cl)Cl>[OH:2][C:3]1[C:12]2[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=2)[CH:6]=[C:5]([NH:13][C:14]([C:16]2[C:25](=[O:26])[C:24]3[C:19](=[CH:20][CH:21]=[CH:22][CH:23]=3)[NH:18][CH:17]=2)=[O:15])[CH:4]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of N-(4-methoxy-2-naphthyl)-4-oxo-1H-quinoline-3-carboxamide (73 mg, 0.21 mmol) in DCM (4 mL) was added BBr3 (1.1 mL, 11.64 mmol) dropwise at −78° C. After the addition was complete the cooling bath was removed and the resulting reaction mixture was warmed to room temperature and then was heated to 50° C. for 2 h, cooled to −10° C. and quenched with saturated solution of NaHCO3. The aqueous layer was extracted with DCM and the combined organic layer was dried over MgSO4, filtered and concentrated in vacuo. The residue was purified via reverse phase HPLC to get N-(4-hydroxy-2-naphthyl)-4-oxo-1H-quinoline-3-carboxamide. LC/MS: m/z 331 (M+H)+ at 1.47 min (10%-99% CH3CN (0.035% TFA)/H2O (0.05% TFA)).
Workup
- additionAfter the addition
- customwas removed
- customthe resulting reaction mixture
- temperaturewas heated to 50° C. for 2 h
- temperaturecooled to −10° C.
- customquenched with saturated solution of NaHCO3
- extractionThe aqueous layer was extracted with DCM
- dry with materialthe combined organic layer was dried over MgSO4
- filtrationfiltered
- concentrationconcentrated in vacuo
- customThe residue was purified via reverse phase HPLC
Sources & evidence
- ORD record
- ord-cc6fc92130de4308ad75434772d36e1f
- Source dataset
- uspto-grants-2014_08
- Patent number
- US08802700B2
Reaction notes
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