Sodium borohydride → HCID 118431875, compound
Reaction equation
[F:1][C:2]1[CH:7]=[C:6]([F:8])[CH:5]=[CH:4][C:3]=1[N:9]1[CH:13]([C:14]2[CH:19]=[CH:18][CH:17]=[C:16]([C:20]3[CH:25]=[CH:24][C:23]([CH:26]=[O:27])=[CH:22][N:21]=3)[CH:15]=2)[CH2:12][C:11]([C:28]([F:34])([F:33])[C:29]([F:32])([F:31])[F:30])=[N:10]1.[BH4-].[Na+]>C(O)C>[F:1][C:2]1[CH:7]=[C:6]([F:8])[CH:5]=[CH:4][C:3]=1[N:9]1[CH:13]([C:14]2[CH:19]=[CH:18][CH:17]=[C:16]([C:20]3[CH:25]=[CH:24][C:23]([CH2:26][OH:27])=[CH:22][N:21]=3)[CH:15]=2)[CH2:12][C:11]([C:28]([F:33])([F:34])[C:29]([F:32])([F:30])[F:31])=[N:10]1Participants
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of 1-(2,4-difluoro-phenyl)-5-[3-(5-formyl-pyridin-2-yl)-phenyl]-3-pentafluoroethyl-4,5-dihydro-1H-pyrazole (20 mg, 0.04 mmol) prepared in Example 79 in ethanol (1 mL), was slowly added sodium borohydride (6.0 mg, 0.16 mmol) at 0° C. The reaction mixture was stirred at room temperature for 1 hour, quenched with a 1N hydrochloric acid solution, and then extracted with ethyl acetate three times. The combined extract was washed with brine, dried on anhydrous magnesium sulfate, and then concentrated under reduced pressure to give a residue as a pale yellow liquid. The resulting residue was purified by silica gel column chromatography (eluent: ethyl acetate/n-hexane=2/1) to give 3.0 mg of the titled compound as a white solid.
Workup
- customat 0° C
- customquenched with a 1N hydrochloric acid solution
- extractionextracted with ethyl acetate three times
- extractionThe combined extract
- washwas washed with brine
- dry with materialdried on anhydrous magnesium sulfate
- concentrationconcentrated under reduced pressure
Sources & evidence
- ORD record
- ord-9852d646b5e6404eae7036a42e11cd92
- Source dataset
- uspto-grants-2016_06
- Patent number
- US09376420B2
Reaction notes
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