Water → HCID 9885393, compound
Reaction equation
Cl.[Br:2][C:3]1[N:7]([CH2:8][CH3:9])[C:6]([CH2:10]Cl)=[N:5][C:4]=1[CH3:12].C([O-])([O-])=O.[K+].[K+].[F:19][C:20]1[CH:25]=[CH:24][CH:23]=[C:22]([C:26]2[NH:27][CH:28]=[CH:29][N:30]=2)[N:21]=1.O>CN(C=O)C>[Br:2][C:3]1[N:7]([CH2:8][CH3:9])[C:6]([CH2:10][N:30]2[CH:29]=[CH:28][N:27]=[C:26]2[C:22]2[CH:23]=[CH:24][CH:25]=[C:20]([F:19])[N:21]=2)=[N:5][C:4]=1[CH3:12]Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of 74 mg (0.27 mmol) of 5-bromo-2-chloromethyl-1-ethyl-4-methyl-1H-imidazole hydrochloride in 1.5 ml of DMF is added 224 mg (1.62 mmol) of K2CO3 and 45 mg (0.27 mmol) of 2-fluoro-6-(1H-imidazol-2-yl)-pyridine. The mixture is stirred at room temperature for 24 hours. 5 ml water is added and the mixture was extracted with EtOAc (3×15 ml). The combined extracts are washed with 15 ml brine, dried (Na2SO4), filtered and evaporated in vacuo. The residue is purified by preparative TLC, developing with 10:0.4:0.05 CH2Cl2—MeOH—NH4OH solution. The purified compound is then dissolved in 3 ml of EtOAc and to it is added 2 ml of 2N HCl in ether. The resulting suspension is stirred at room temperature for 15 minutes. Evaporation of the solvent provided the title compound as a white powder. LC-MS (M+1) 364.
Workup
- extractionthe mixture was extracted with EtOAc (3×15 ml)
- washThe combined extracts are washed with 15 ml brine
- dry with materialdried (Na2SO4)
- filtrationfiltered
- customevaporated in vacuo
- customThe residue is purified by preparative TLC
- dissolutionThe purified compound is then dissolved in 3 ml of EtOAc and to it
- additionis added 2 ml of 2N HCl in ether
- stirringThe resulting suspension is stirred at room temperature for 15 minutes
- customEvaporation of the solvent
Sources & evidence
- ORD record
- ord-0972a2998b234963a9a8848af7b204e4
- Source dataset
- uspto-grants-2006_04
- Patent number
- US07030144B2
Reaction notes
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