Pyridine → HCID 66778593, compound
Reaction equation
[CH3:1][CH:2]([C:4]1[C:8]([C:9]([O:11][CH3:12])=[O:10])=[CH:7][NH:6][N:5]=1)[CH3:3].[CH3:13][O:14][C:15]1[CH:16]=[C:17](B(O)O)[CH:18]=[CH:19][CH:20]=1.N1C=CC=CC=1>CN(C)C(=O)C.C([O-])(=O)C.[Cu+2].C([O-])(=O)C>[CH3:13][O:14][C:15]1[CH:20]=[C:19]([N:6]2[CH:7]=[C:8]([C:9]([O:11][CH3:12])=[O:10])[C:4]([CH:2]([CH3:1])[CH3:3])=[N:5]2)[CH:18]=[CH:17][CH:16]=1Participants
6
Procedure
Methyl 3-(1-methylethyl)-1H-pyrazole-4-carboxylate (2.8 g) synthesized in Example 7(1) was dissolved in N,N-dimethylacetamide (50 mL), 3-methoxyphenylboronic acid (5.0 g), copper acetate (6.0 g) and pyridine (5.3 mL) were added, and the mixture was stirred at room temperature overnight. The reaction mixture was filtered through celite, 1N hydrochloric acid (50 mL) was added to the filtrate, and the mixture was extracted with diethyl ether. The extract was washed with brine, dried over magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate:hexane=1:2, volume ratio) to give the title object compound (3.4 g, 75%) as a pale-yellow oil.
Workup
- filtrationThe reaction mixture was filtered through celite, 1N hydrochloric acid (50 mL)
- additionwas added to the filtrate
- extractionthe mixture was extracted with diethyl ether
- washThe extract was washed with brine
- dry with materialdried over magnesium sulfate
- concentrationconcentrated under reduced pressure
- customThe residue was purified by silica gel column chromatography (ethyl acetate:hexane=1:2, volume ratio)
Sources & evidence
- ORD record
- ord-44d53630775b412a981e18a3517117a4
- Source dataset
- uspto-grants-2013_05
- Patent number
- US08436043B2
Reaction notes
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