p-Diiodobenzene → HCID 68410404, compound
Reaction equation
[C:1]([O:5][C:6](=[O:26])[NH:7][CH:8]([C:15]1[CH:20]=[CH:19][C:18]([C:21]([F:24])([F:23])[F:22])=[C:17]([F:25])[CH:16]=1)[C:9](=[O:14])N(OC)C)([CH3:4])([CH3:3])[CH3:2].[I:27][C:28]1[CH:33]=[CH:32][C:31](I)=[CH:30][CH:29]=1>>[C:1]([O:5][C:6](=[O:26])[NH:7][CH:8]([C:15]1[CH:20]=[CH:19][C:18]([C:21]([F:22])([F:24])[F:23])=[C:17]([F:25])[CH:16]=1)[C:9]([C:31]1[CH:32]=[CH:33][C:28]([I:27])=[CH:29][CH:30]=1)=[O:14])([CH3:3])([CH3:2])[CH3:4]Participants
3
Procedure
The title compound was prepared from rac-[(3-fluoro-4-trifluoromethyl-phenyl)-(methoxy-methyl-carbamoyl)-methyl]-carbamic acid tert-butyl ester (Intermediate 5) and 1,4-di-iodobenzene in analogy to Example 1a): MS (ISN): 522.1 (M−H)−.
Sources & evidence
- ORD record
- ord-a99db722c2ff495cb86176a91759dc79
- Source dataset
- uspto-grants-2013_02
- Patent number
- US08367838B2
Reaction notes
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