Cesium carbonate → HCID 46831477, compound
Reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]([C:8]2[N:9]=[C:10]([N:16]3[C:20]4[CH:21]=[C:22]([OH:25])[CH:23]=[CH:24][C:19]=4[N:18]=[CH:17]3)[S:11][C:12]=2[C:13]([NH2:15])=[O:14])[CH:5]=[CH:6][CH:7]=1.Br[CH2:27][CH2:28][N:29]1[CH2:34][CH2:33][O:32][CH2:31][CH2:30]1.C(=O)([O-])[O-].[Cs+].[Cs+]>CN(C)C=O>[Cl:1][C:2]1[CH:3]=[C:4]([C:8]2[N:9]=[C:10]([N:16]3[C:20]4[CH:21]=[C:22]([O:25][CH2:27][CH2:28][N:29]5[CH2:34][CH2:33][O:32][CH2:31][CH2:30]5)[CH:23]=[CH:24][C:19]=4[N:18]=[CH:17]3)[S:11][C:12]=2[C:13]([NH2:15])=[O:14])[CH:5]=[CH:6][CH:7]=1Participants
5
Procedure
To a mixture of 0.037 (0.1 mmole) of 4-(3-chloro-phenyl)-2-(6-hydroxy-benzoimidazol-1-yl)-thiazole-5-carboxylic acid amide (I.25d), 0.039 g (0.2 mmole) of 4-(2-bromo-ethyl)-morpholine and 1 mL of dimethylformamide was added 0.16 g (0.5 mmole) of cesium carbonate. The mixture was heated at 100 degrees for 3 hours. The mixture was cooled, the solid was removed by filtration and the filtrate purified by reverse phase silica gel chromatography, eluting with acetonitrile-water (gradient 30:70-100:0) to give 0.014 g of 4-(3-chloro-phenyl)-2-[6-(2-morpholin-4-yl-ethoxy)-benzoimidazol-1-yl]-thiazole-5-carboxylic acid amide (I.26) as a white powder. MH+/Z=484
Workup
- temperatureThe mixture was heated at 100 degrees for 3 hours
- temperatureThe mixture was cooled
- customthe solid was removed by filtration
- customthe filtrate purified by reverse phase silica gel chromatography
- washeluting with acetonitrile-water (gradient 30:70-100:0)
Sources & evidence
- ORD record
- ord-e4215b152e794ad5812f6c7a8fd0c54b
- Source dataset
- uspto-grants-2011_10
- Patent number
- US08044213B2
Reaction notes
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