Hydrochloric Acid → HCID 178439405, compound
Reaction equation
[F:1][C:2]([F:12])([F:11])[C:3]([CH3:10])([CH3:9])[C:4](=O)[CH2:5][C:6]#[N:7].[NH2:13][NH2:14].Cl.C(Cl)Cl>CCO.O>[F:1][C:2]([F:11])([F:12])[C:3]([C:4]1[CH:5]=[C:6]([NH2:7])[NH:14][N:13]=1)([CH3:10])[CH3:9]Participants
Conditions
- Temperature
- 100 °C
Procedure
To a mixture of 5,5,5-trifluoro-4,4-dimethyl-3-oxopentanenitrile (2 g, 11.16 mmol) in EtOH (10 mL) was added hydrazine (1.263 g, 33.5 mmol) and concentrated HCl (0.5 mL). Then the mixture was stirred at 100° C. for 18 h. Then the mixture was concentrated to give the residue which was distributed between DCM (20 mL) and H2O (10 mL), and extracted with DCM (20 mL×2). The combined organic extracts were washed with brine (20 mL), dried over Na2SO4, filtered and concentrated. The crude product was purified by silica column chromatography (100% EA, 12 g silica column). All fractions found to contain product by TLC (EA, Rf=0.3) were combined and concentrated to yield an off-white oil of 3-(1,1,1-trifluoro-2-methylpropan-2-yl)-1H-pyrazol-5-amine (500 mg, 2.459 mmol, 22.03% yield): 1H NMR (400 MHz, CD3OD) δ 5.58 (s, 1H), 1.47 (s, 6H). ES-LCMS m/z 194 (M+H).
Workup
- concentrationThen the mixture was concentrated
- customto give the residue which
- extractionextracted with DCM (20 mL×2)
- washThe combined organic extracts were washed with brine (20 mL)
- dry with materialdried over Na2SO4
- filtrationfiltered
- concentrationconcentrated
- customThe crude product was purified by silica column chromatography (100% EA, 12 g silica column)
- concentrationconcentrated
Sources & evidence
- ORD record
- ord-5dcb5d253ba84808b070460192a35d1d
- Source dataset
- uspto-grants-2016_07
- Patent number
- US09382238B2
Reaction notes
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