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CAS No. : | 22236-08-4 | MDL No. : | MFCD00236221 |
Formula : | C7H7F2NO | Boiling Point : | No data available |
Linear Structure Formula : | - | InChI Key : | RSOFZRXRIPVBBM-UHFFFAOYSA-N |
M.W : | 159.13 | Pubchem ID : | 2774110 |
Synonyms : |
|
Signal Word: | Warning | Class: | |
Precautionary Statements: | P210-P261-P264-P270-P271-P280-P301+P312+P330-P302+P352+P312-P304+P340+P312-P370+P378-P403+P235-P501 | UN#: | |
Hazard Statements: | H227-H302+H312+H332 | Packing Group: | |
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 |
---|---|---|
55.9% | With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; In 1,4-dioxane; at 20 - 50℃; | General procedure: The synthesis was carried out by using the synthetic method a. To a solution of 2-picolinic acid (0.871 g,7.08 mmol), N-hydroxybenzotriazolehydrate (HOBt.H2O,1.084 g, 7.08 mmol), diisopropylethylamine(DIPEA, 1.83 g, 14.17mmol) and N-(3-methylaminopropyl)-N?-ethylcarbodiimidehydrochloride (EDCHCl, 2.036 g, 10.63mmol) in anhydrous 1,4-dioxane (60 mL) was added 3-fluoro-3-methoxyanilline (1.00 g, 7.08 mmol) at room temperature. The mixture was heated to 50 oC and stirred overnight. To the reaction mixture was added 300 mL of dichloromethane, and sequentially washed with water (3 x100 mL). After the organic layer was separated and concentrated, the reaction mixture was purified by silica-gel chromatography (hexane/ethyl acetate) to give the product as a pale-yellow solid (1.559 g, 6.33mmol, 89.4percent yield). |
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