Methyl 3-{[3-(4-chlorophenyl)-5-oxo-4-(3,3,3-trifluoro-2-hydroxypropyl)-4,5-dihydro-1H-1,2,4-triazol-1-yl]methyl}benzoate → 3-{[3-(4-Chlorophenyl)-5-oxo-4-(3,3,3-trifluoro-2-hydroxypropyl)-4,5-dihydro-1H-1,2,4-triazol-1-yl]methyl}benzoic acid
Reaction equation
ClC1C=CC(C2N(CC(O)C(F)(F)F)C(=O)N(CC3C=CC(C(O)=O)=CC=3)N=2)=CC=1.[Cl:31][C:32]1[CH:37]=[CH:36][C:35]([C:38]2[N:42]([CH2:43][CH:44]([OH:49])[C:45]([F:48])([F:47])[F:46])[C:41](=[O:50])[N:40]([CH2:51][C:52]3[CH:53]=[C:54]([CH:59]=[CH:60][CH:61]=3)[C:55]([O:57]C)=[O:56])[N:39]=2)=[CH:34][CH:33]=1>>[Cl:31][C:32]1[CH:33]=[CH:34][C:35]([C:38]2[N:42]([CH2:43][CH:44]([OH:49])[C:45]([F:47])([F:46])[F:48])[C:41](=[O:50])[N:40]([CH2:51][C:52]3[CH:53]=[C:54]([CH:59]=[CH:60][CH:61]=3)[C:55]([OH:57])=[O:56])[N:39]=2)=[CH:36][CH:37]=1Participants
3
Reactant 2
Product 1
Procedure
In the same way as for the compound from Example 28A, 265 mg (0.58 mmol) of the compound from Example 25A were reacted. This gave 250 mg (97% of theory) of the target compound.
Sources & evidence
- ORD record
- ord-f2bec4f82e354756bbac638f69bb724d
- Source dataset
- uspto-grants-2014_10
- Patent number
- US08859601B2
Reaction notes
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