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CAS No. : | 103577-40-8 | MDL No. : | MFCD00834357 |
Formula : | C16H14F3N3OS | Boiling Point : | - |
Linear Structure Formula : | - | InChI Key : | CCHLMSUZHFPSFC-UHFFFAOYSA-N |
M.W : | 353.36 | Pubchem ID : | 1094080 |
Synonyms : |
|
Chemical Name : | 2-(((3-Methyl-4-(2,2,2-trifluoroethoxy)pyridin-2-yl)methyl)thio)-1H-benzo[d]imidazole |
Signal Word: | Warning | Class: | N/A |
Precautionary Statements: | P261-P280-P305+P351+P338 | UN#: | N/A |
Hazard Statements: | H302-H315-H319-H332-H335 | Packing Group: | N/A |
GHS Pictogram: |
* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
To the solution of 2-[[[3-methyl-4-(2,2,2-trifluoroethoxy)-2-pyridinyl]methyl] sulfanyl]-lH-benzimidazole (100 g) present in methylenechloride (1500 ml) added potassium carbonate (58.5g) and heated the reaction mixture to reflux temperature. Added a solution of L-(-)-camphorsulfonyl chloride (106 g) in methylenechloride (500 ml) to the reaction mixture slowly at the same temperature. Stirred the reaction mixture for 6 hrs. Cooled the reaction mixture and added water to the reaction mixture. Separated the both aqueous and organic layers. Distilled off the solvent completely under reduced pressure from the organic layer. To the reaction mixture n-heptane (400 ml) was added and stirred for 45 min. Filtered the solid precipitated and washed with n-heptane. The title compound obtained as a crystalline solid. Yield: 220 grams |
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