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CAS No. : | 351003-49-1 | MDL No. : | MFCD03094221 |
Formula : | C6H3Cl2FO2S | Boiling Point : | - |
Linear Structure Formula : | - | InChI Key : | OZKAHSNNKADHTK-UHFFFAOYSA-N |
M.W : | 229.06 | Pubchem ID : | 2778273 |
Synonyms : |
|
Signal Word: | Danger | Class: | 8 |
Precautionary Statements: | P260-P280-P303+P361+P353-P301+P330+P331-P304+P340+P310-P305+P351+P338+P310 | UN#: | 3261 |
Hazard Statements: | H314 | Packing Group: | Ⅱ |
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 |
---|---|---|
The following sulfonyl chlorides may be substituted for benzenesulfonyl chloride of Step One: ... 2-Cyanobenzenesulfonyl chloride 3-(Chlorosulfonyl)benzoic acid 5-Chloro-2-fluorobenzenesulfonyl chloride 4-Chloro-2,5-dimethylbenzenesulfonyl chloride ... |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
With triethylamine; In dichloromethane; at 20℃;Cooling; | Example 10 5-Chloro-N-[(3R)-1-cyano-3-pyrrolidinyl]-2-fluorobenzenesulfonamide To a chilled solution of <strong>[351003-49-1]5-chloro-2-fluorobenzenesulfonyl chloride</strong> (0.125 g, 0.546 mmol) and triethylamine (0.3 ml, 2.15 mmol) in DCM (2 mL) was added 1,1-dimethylethyl (3R)-3-amino-1-pyrrolidinecarboxylate (0.080 ml, 0.471 mmol). The reaction mixture was stirred at room temperature overnight. Water (1.5 ml) was added to the reaction mixture with stirring. The mixture was diluted with DCM (2 ml) and water (1.5 ml) and put through a phase separator to dry. Then 4N HCl in 1,4-dioxane (2.0 ml) was added. After 1.5 hours, the reaction was blown down to dryness. The dry material was then diluted with DCM (8 ml), and mixed with DIEA (0.45 mL, 2.58 mmol) and BrCN (0.40 mL, 1.2 mmol). The resultant mixture was stirred at room temperature overnight. The solvent was evaporated under vacuum and the solid purified by preparatory HPLC (without TFA) to afford the title compound (0.0671 g). LC-MS: m/z, 304 (M+H), rt 1.6 min. |
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