4-Chlorobenzaldehyde → ethyl 4-((4-chlorophenyl)(hydroxy)methyl)-1-cyclopropyl-3-(trifluoromethyl)-1H-Pyrazole-5-carboxylate
Reaction equation
[CH:1]1([N:4]2[C:8]([C:9]([O:11][CH2:12][CH3:13])=[O:10])=[CH:7][C:6]([C:14]([F:17])([F:16])[F:15])=[N:5]2)[CH2:3][CH2:2]1.[Cl:18][C:19]1[CH:26]=[CH:25][C:22]([CH:23]=[O:24])=[CH:21][CH:20]=1>CCCCCC>[Cl:18][C:19]1[CH:26]=[CH:25][C:22]([CH:23]([OH:24])[C:7]2[C:6]([C:14]([F:17])([F:16])[F:15])=[N:5][N:4]([CH:1]3[CH2:3][CH2:2]3)[C:8]=2[C:9]([O:11][CH2:12][CH3:13])=[O:10])=[CH:21][CH:20]=1Participants
4
Procedure
The title compound was prepared in analogy to the procedure described in Step 40.2 using ethyl 1-cyclopropyl-3-(trifluoromethyl)-1H-pyrazole-5-carboxylate (Step 44.1) and 4-chlorobenzaldehyde. tR: 1.29 min (LC-MS 2); ESI-MS: 389 [M+H]+ (LC-MS 2); Rf=0.12 (hexane/15% EtOAc).
Sources & evidence
- ORD record
- ord-fb005f8ea2ca466cb018d10349654917
- Source dataset
- uspto-grants-2015_03
- Patent number
- US08975417B2
Reaction notes
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