Methyl 2-amino-5-(trifluoromethoxy)benzoate → Methyl 2-amino-3-iodo-5-(trifluoromethoxy)benzoate
Reaction equation
[NH2:1][C:2]1[C:11]([I:12])=[CH:10][C:9](C(F)(F)F)=[CH:8][C:3]=1[C:4]([O:6][CH3:7])=[O:5].NC1C=CC([O:28][C:29]([F:32])([F:31])[F:30])=CC=1C(OC)=O>>[NH2:1][C:2]1[C:11]([I:12])=[CH:10][C:9]([O:28][C:29]([F:32])([F:31])[F:30])=[CH:8][C:3]=1[C:4]([O:6][CH3:7])=[O:5]Participants
3
Procedure
The title compound was prepared as in the method of compound 2 from methyl 2-amino-5-(trifluoromethoxy)benzoate to give a white solid (0.67 g, 82%).
Sources & evidence
- ORD record
- ord-10edfa2e8f0c41928c1d1ffa96e595ac
- Source dataset
- uspto-grants-2016_06
- Patent number
- US09365569B2
Reaction notes
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