p-Diiodobenzene → HCID 68409931, compound
Reaction equation
[C:1]([O:5][C:6](=[O:25])[NH:7][CH:8]([C:19](=[O:24])N(OC)C)[C:9]1[CH:14]=[CH:13][C:12]([C:15]([F:18])([F:17])[F:16])=[CH:11][CH:10]=1)([CH3:4])([CH3:3])[CH3:2].[I:26][C:27]1[CH:32]=[CH:31][C:30](I)=[CH:29][CH:28]=1>>[C:1]([O:5][C:6](=[O:25])[NH:7][CH:8]([C:9]1[CH:10]=[CH:11][C:12]([C:15]([F:17])([F:16])[F:18])=[CH:13][CH:14]=1)[C:19]([C:30]1[CH:31]=[CH:32][C:27]([I:26])=[CH:28][CH:29]=1)=[O:24])([CH3:4])([CH3:2])[CH3:3]Participants
3
Procedure
The title compound was prepared from rac-[(methoxy-methyl-carbamoyl)-(4-trifluoromethyl-phenyl)-methyl]-carbamic acid tert-butyl ester (Intermediate 10) and 1,4-di-iodobenzene in analogy to Example 1a): MS (ISN): 504.0 (M−H)−.
Sources & evidence
- ORD record
- ord-0aafa4a8d01e4a4ca10a7cabff38be61
- Source dataset
- uspto-grants-2013_02
- Patent number
- US08367838B2
Reaction notes
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