Acetyl chloride, 2-(2-chlorophenyl)- → Methyl 5-bromo-2-(2-(2-chlorophenyl)acetamido)benzoate
Reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[CH2:8][C:9](Cl)=[O:10].[Br:12][C:13]1[CH:14]=[CH:15][C:16]([NH:23]C(=O)CC2C=CC=C(C(F)(F)F)C=2)=[C:17]([CH:22]=1)[C:18]([O:20][CH3:21])=[O:19]>>[Br:12][C:13]1[CH:14]=[CH:15][C:16]([NH:23][C:9](=[O:10])[CH2:8][C:3]2[CH:4]=[CH:5][CH:6]=[CH:7][C:2]=2[Cl:1])=[C:17]([CH:22]=1)[C:18]([O:20][CH3:21])=[O:19]Participants
3
Procedure
The title compound was prepared using 2-chlorophenylacetyl chloride in place of 2-phenylacetyl chloride using the procedure described for Intermediate 7: step a.
Sources & evidence
- ORD record
- ord-b8cd742fa9cc4104bc2c41c451f9ee75
- Source dataset
- uspto-grants-2016_08
- Patent number
- US09403816B2
Reaction notes
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