3,5-Bis(trifluoromethyl)benzoyl chloride → N-(4-iodopyridin-3-yl)-N-methyl-3,5-bis(trifluoromethyl)benzamide
Reaction equation
[I:1][C:2]1[CH:7]=[CH:6][N:5]=[CH:4][C:3]=1[NH:8][CH3:9].[F:10][C:11]([F:26])([F:25])[C:12]1[CH:13]=[C:14]([CH:18]=[C:19]([C:21]([F:24])([F:23])[F:22])[CH:20]=1)[C:15](Cl)=[O:16]>>[I:1][C:2]1[CH:7]=[CH:6][N:5]=[CH:4][C:3]=1[N:8]([CH3:9])[C:15](=[O:16])[C:14]1[CH:13]=[C:12]([C:11]([F:26])([F:25])[F:10])[CH:20]=[C:19]([C:21]([F:24])([F:23])[F:22])[CH:18]=1Participants
3
Procedure
The title compound was prepared in analogy to example 25, intermediate a, from (4-iodo-pyridin-3-yl)-methyl-amine and 3,5-bis-trifluoromethyl-benzoyl chloride (CAS RN 785-56-8). Pale yellow liquid (15%). MS (ESI): m/z=475 [M+H]+.
Sources & evidence
- ORD record
- ord-72175faff12546bb875e7bc25a427cfc
- Source dataset
- uspto-grants-2015_03
- Patent number
- US08987307B2
Reaction notes
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