(1-(Aminomethyl)hexahydrocyclopenta[c]pyrrol-2(1H)-yl)(5-methyl-2-(2H-1,2,3-triazol-2-yl)phenyl)methanone → (1-(Aminomethyl)hexahydrocyclopenta[c]pyrrol-2(1H)-yl)(5-methyl-2-(3-(trifluoromethyl)-1H-1,2,4-triazol-1-yl)phenyl)methanone
Reaction equation
[NH2:1][CH2:2][CH:3]1[CH:7]2[CH2:8][CH2:9][CH2:10][CH:6]2[CH2:5][N:4]1C(C1C=C(C)C=CC=1N1N=CC=N1)=O.[CH3:25][C:26]1[CH:27]=[CH:28][C:29]([N:35]2[CH:39]=[N:38][C:37]([C:40]([F:43])([F:42])[F:41])=[N:36]2)=[C:30]([CH:34]=1)[C:31]([OH:33])=O>>[NH2:1][CH2:2][CH:3]1[CH:7]2[CH2:8][CH2:9][CH2:10][CH:6]2[CH2:5][N:4]1[C:31]([C:30]1[CH:34]=[C:26]([CH3:25])[CH:27]=[CH:28][C:29]=1[N:35]1[CH:39]=[N:38][C:37]([C:40]([F:43])([F:42])[F:41])=[N:36]1)=[O:33]Participants
3
Reactant 2
Product 1
Procedure
The title compound was prepared following the same general protocol as described for (1-(aminomethyl)hexahydrocyclopenta[c]pyrrol-2(1H)-yl)(5-methyl-2-(2H-1,2,3-triazol-2-yl)phenyl)methanone in Example A68 using 5-methyl-2-(3-(trifluoromethyl)-1H-1,2,4-triazol-1-yl)benzoic acid. MS (ESI) 394 (M+H).
Sources & evidence
- ORD record
- ord-395396ab93cb46348a4ec0f01947f9d7
- Source dataset
- uspto-grants-2016_09
- Patent number
- US09440982B2
Reaction notes
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