4-(5-Methyl-1H-1,2,4-triazol-1-yl)benzoic acid → N-Cyclopropyl-N-(3'-fluoro-5'-trifluoromethyl-3,4,5,6-tetrahydro-2H-[1,2']bipyridinyl-4-yl)-4-(5-methyl-[1,2,4]triazol-1-yl)-benzamide
Reaction equation
[CH:1]1([NH:4][CH:5]2[CH2:10][CH2:9][N:8]([C:11]3[C:16]([F:17])=[CH:15][C:14]([C:18]([F:21])([F:20])[F:19])=[CH:13][N:12]=3)[CH2:7][CH2:6]2)[CH2:3][CH2:2]1.[CH3:22][C:23]1[N:27]([C:28]2[CH:36]=[CH:35][C:31]([C:32](O)=[O:33])=[CH:30][CH:29]=2)[N:26]=[CH:25][N:24]=1>>[CH:1]1([N:4]([CH:5]2[CH2:10][CH2:9][N:8]([C:11]3[C:16]([F:17])=[CH:15][C:14]([C:18]([F:20])([F:19])[F:21])=[CH:13][N:12]=3)[CH2:7][CH2:6]2)[C:32](=[O:33])[C:31]2[CH:30]=[CH:29][C:28]([N:27]3[C:23]([CH3:22])=[N:24][CH:25]=[N:26]3)=[CH:36][CH:35]=2)[CH2:2][CH2:3]1Participants
3
Reactant 2
Product 1
Procedure
The title compound is prepared from cyclopropyl-(3′-fluoro-5′-trifluoromethyl-3,4,5,6-tetrahydro-2H-[1,2′]bipyridinyl-4-yl)-amine and 4-(5-methyl-[1,2,4]triazol-1-yl)-benzoic acid following a procedure analogous to that described in Example 90. LC (method 19): tR=4.54 min; Mass spectrum (ESI+): m/z=489 [M+H]+.
Sources & evidence
- ORD record
- ord-8c5c929414c14ada85acc3ba12dbd14a
- Source dataset
- uspto-grants-2014_09
- Patent number
- US08822471B2
Reaction notes
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