5-Methyl-2-(1-methyl-1H-pyrazol-4-yl)benzoic acid → (1-(Aminomethyl)hexahydrocyclopenta[c]pyrrol-2(1H)-yl)(5-methyl-2-(1-methyl-1H-pyrazol-4-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]1[C:11]([C:13]1[CH:18]=[C:17]([CH3:19])[CH:16]=[CH:15][C:14]=1N1N=CC=N1)=[O:12].CC1C=CC([C:35]2[CH:36]=[N:37][N:38]([CH3:40])[CH:39]=2)=C(C=1)C(O)=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:11]([C:13]1[CH:18]=[C:17]([CH3:19])[CH:16]=[CH:15][C:14]=1[C:35]1[CH:36]=[N:37][N:38]([CH3:40])[CH:39]=1)=[O:12]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-(1-methyl-1H-pyrazol-4-yl)benzoic acid. MS (ESI) 339 (M+H).
Sources & evidence
- ORD record
- ord-c64162cb637b42268288bb892df549cc
- Source dataset
- uspto-grants-2016_09
- Patent number
- US09440982B2
Reaction notes
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