N-(2-Amino-5-chloro-phenyl)-5-bromo-2-fluoro-benzamide → HCID 178505483, compound
Reaction equation
[NH2:1][C:2]1[CH:7]=[CH:6][C:5]([Cl:8])=[CH:4][C:3]=1[NH:9][C:10](=O)[C:11]1[CH:16]=[C:15]([Br:17])[CH:14]=[CH:13][C:12]=1[F:18]>C(O)(=O)C>[Br:17][C:15]1[CH:14]=[CH:13][C:12]([F:18])=[C:11]([C:10]2[NH:1][C:2]3[CH:7]=[CH:6][C:5]([Cl:8])=[CH:4][C:3]=3[N:9]=2)[CH:16]=1Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 85 °C
Procedure
Method 7—Step b A mixture of N-(2-Amino-5-chloro-phenyl)-5-bromo-2-fluoro-benzamide (1.60 g, 4.67 mmol) in acetic acid (10 mL) was heated at 85° C. overnight. Solvent was removed under reduced pressure and the solid obtained was washed with dichloromethane and dried to obtain 1.40 g of the title compound (93%).
Workup
- customSolvent was removed under reduced pressure
- customthe solid obtained
- washwas washed with dichloromethane
- customdried
Sources & evidence
- ORD record
- ord-3c482643c6b54f34b682f4dfcc5ca817
- Source dataset
- uspto-grants-2014_09
- Patent number
- US08835648B2
Reaction notes
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