Imidazole → HCID 20735492, compound
Reaction equation
[NH2:1][C:2]1[N:6]([CH2:7][CH2:8][OH:9])[N:5]=[C:4]([CH2:10][CH3:11])[C:3]=1[CH2:12][C:13]1[CH:18]=[C:17]([Cl:19])[CH:16]=[C:15]([Cl:20])[CH:14]=1.N1C=CN=C1.[C:26]([Si:30]([CH3:33])([CH3:32])Cl)([CH3:29])([CH3:28])[CH3:27]>CN(C)C=O>[Si:30]([O:9][CH2:8][CH2:7][N:6]1[C:2]([NH2:1])=[C:3]([CH2:12][C:13]2[CH:14]=[C:15]([Cl:20])[CH:16]=[C:17]([Cl:19])[CH:18]=2)[C:4]([CH2:10][CH3:11])=[N:5]1)([C:26]([CH3:29])([CH3:28])[CH3:27])([CH3:33])[CH3:32]Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of the pyrazole of Example 89 (3.0 g, 9.6 mmol) in dimethylformamide (20 ml) was added imidazole (850 mg, 12.5 mmol), followed by tert-butyldimethylchlorosilane (1.58 g, 10.6 mmol). The solution was stirred at room temperature for 20 hours. The reaction mixture was partitioned between diethyl ether and aqueous sodium carbonate and the aqueous phase was separated and further extracted with diethyl ether. The combined organic phases were washed with water, washed with brine, dried over anhydrous magnesium sulphate, filtered and evaporated under reduced pressure. The crude product was purified by flash chromatography on silica gel eluting with dichloromethane:methanol:ammonia (95:5:0.5, by volume) to afford the title compound (4.0 g) as a colourless oil.
Workup
- customThe reaction mixture was partitioned between diethyl ether and aqueous sodium carbonate
- customthe aqueous phase was separated
- extractionfurther extracted with diethyl ether
- washThe combined organic phases were washed with water
- washwashed with brine
- dry with materialdried over anhydrous magnesium sulphate
- filtrationfiltered
- customevaporated under reduced pressure
- customThe crude product was purified by flash chromatography on silica gel eluting with dichloromethane:methanol:ammonia (95:5:0.5, by volume)
Sources & evidence
- ORD record
- ord-0271e7d8cecd4a0788e5afe8779b58c3
- Source dataset
- uspto-grants-2004_06
- Patent number
- US06750230B2
Reaction notes
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