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CAS No. : | 121643-44-5 | MDL No. : | MFCD00153202 |
Formula : | C7H6F3NO | Boiling Point : | - |
Linear Structure Formula : | - | InChI Key : | SSAZZVQVJJXPMB-UHFFFAOYSA-N |
M.W : | 177.12 | Pubchem ID : | 2775309 |
Synonyms : |
|
Signal Word: | Danger | Class: | 3 |
Precautionary Statements: | P210-P233-P240-P241+P242+P243-P264-P280-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313-P403+P235-P501 | UN#: | 1993 |
Hazard Statements: | H225-H315-H319 | Packing Group: | Ⅲ |
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 |
---|---|---|
for 18h;Heating / reflux; | EXAMPLE 2Synthesis of Additional Representative Substituted Biaryl Ouinolin-4-ylamine AnaloguesA. 5-Trifluoromethyl-6-[8-('5-trifluoromethyl-pyridm-2-ylammo)-pyrido[2,3-&lpyrazin-3-yll- nicotinamide (compound 4) 1. 2-Methoxy-3-trifluoromethyl-pyridine Heat a mixture of 2-chloro-3-trifluoromethyl-pyridine (1.8 g, 10 mmol) and sodium methoxide (4M, 5 mL, 20 mmol) in MeOH (20 mL) at reflux for 18 hours. Cool the mixture and remove the volatiles by rotary evaporation. Dissolve the residue in EtOAc (50 mL) and wash with water (50 mL), saturated NaHCO3(aq) (50 mL) and brine (50 mL). Dry the organic extract overMgSO4 and remove the solvent under reduced pressure to yield the title compound. |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
With water; hydrogen bromide; acetic acid; for 1h;Heating / reflux; | 2. 3-Trifluoromethyl-pyridin-2-ol EPO <DP n="53"/>Heat a mixture of <strong>[121643-44-5]2-methoxy-3-trifluoromethyl-pyridine</strong> (1.0 g, 5.6 mmol) and 30% HBr in acetic acid (5 mL) at reflux for 1 hour. Cool the mixture and remove the volatiles by rotary evaporation. Add ether and collect the precipitate by filtration. Air-dry to give the title compound as the hydrogen bromide salt. |
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