Reaction equation
[C:1]([O:5][C:6](=[O:23])[NH:7][CH:8]([C:15]1[CH:20]=[CH:19][C:18]([Cl:21])=[C:17]([Cl:22])[CH:16]=1)[C:9](=[O:14])N(OC)C)([CH3:4])([CH3:3])[CH3:2].[Br:24][C:25]1[CH:30]=[CH:29][C:28](I)=[CH:27][C:26]=1[O:32][CH3:33]>>[C:1]([O:5][C:6](=[O:23])[NH:7][CH:8]([C:15]1[CH:20]=[CH:19][C:18]([Cl:21])=[C:17]([Cl:22])[CH:16]=1)[C:9]([C:28]1[CH:29]=[CH:30][C:25]([Br:24])=[C:26]([O:32][CH3:33])[CH:27]=1)=[O:14])([CH3:2])([CH3:3])[CH3:4]Participants
3
Procedure
The title compound was prepared from rac-[(3,4-dichloro-phenyl)-(methoxy-methyl-carbamoyl)-methyl]-carbamic acid tert-butyl ester (Intermediate 9) and 2-bromo-5-iodoanisole in analogy to Example 1a): MS (ISN): 488.1 (M−H)−.
Sources & evidence
- ORD record
- ord-b82d96b4df8741b98e3225e63a1cd522
- Source dataset
- uspto-grants-2013_02
- Patent number
- US08367838B2
Linked notes
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