Acetonitrile → HCID 86607977, compound
Reaction equation
[F:1][C:2]([F:22])([F:21])[C:3]1[CH:4]=[C:5]([N:13]2[C:17]([CH3:18])=[C:16]([CH2:19]Cl)[CH:15]=[N:14]2)[CH:6]=[C:7]([C:9]([F:12])([F:11])[F:10])[CH:8]=1.[OH:23][C:24]1[CH:25]=[C:26]2[C:30](=[CH:31][CH:32]=1)[N:29]([C:33]([CH3:38])([CH3:37])[C:34]([OH:36])=[O:35])[CH:28]=[CH:27]2.C([O-])([O-])=O.[Cs+].[Cs+].[C:45](#N)[CH3:46]>>[CH2:45]([O:35][C:34](=[O:36])[C:33]([N:29]1[C:30]2[C:26](=[CH:25][C:24]([O:23][CH2:19][C:16]3[CH:15]=[N:14][N:13]([C:5]4[CH:4]=[C:3]([C:2]([F:22])([F:21])[F:1])[CH:8]=[C:7]([C:9]([F:12])([F:11])[F:10])[CH:6]=4)[C:17]=3[CH3:18])=[CH:32][CH:31]=2)[CH:27]=[CH:28]1)([CH3:38])[CH3:37])[CH3:46]Participants
5
Procedure
To a solution of 1-(3,5-bis-trifluoromethyl-phenyl)-4-chloromethyl-5-methyl-1H-pyrazole (170 mg, 0.5 mmol) and (2-(5-hydroxy-indol-1-yl)-2-methyl-propionic acid (150 mg) in acetonitrile (3 mL) is added Cs2CO3 (325 mg, 1 mmol). The mixture is stirred at room temperature over night, quenched by water, extracted with ethyl acetate, dried over sodium sulfate. Concentration yields the crude product.
Workup
- customquenched by water
- extractionextracted with ethyl acetate
- dry with materialdried over sodium sulfate
- concentrationConcentration
Sources & evidence
- ORD record
- ord-0c68c61bb9094bc1852362df48d0a7a5
- Source dataset
- uspto-grants-2009_05
- Patent number
- US07528160B2
Reaction notes
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