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Chemical Structure| 824390-04-7 Chemical Structure| 824390-04-7

Structure of 824390-04-7

Chemical Structure| 824390-04-7

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Product Details of [ 824390-04-7 ]

CAS No. :824390-04-7
Formula : C12H14F3NO
M.W : 245.24
SMILES Code : FC(F)(F)C1=C(OC2CCNCC2)C=CC=C1
MDL No. :MFCD06248881
InChI Key :MBZJEIRMMYDAFD-UHFFFAOYSA-N
Pubchem ID :5018790

Safety of [ 824390-04-7 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319-H335
Precautionary Statements:P261-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P362-P403+P233-P501

Application In Synthesis of [ 824390-04-7 ]

* 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.

  • Downstream synthetic route of [ 824390-04-7 ]

[ 824390-04-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 824390-04-7 ]
  • [ 65202-50-8 ]
  • methyl 6-{4-[2-(trifluoromethyl)phenoxy]piperidin-1-yl}pyridazine-3-carboxylate [ No CAS ]
YieldReaction ConditionsOperation in experiment
With tetra-(n-butyl)ammonium iodide; potassium carbonate; In 1,4-dioxane;Heating / reflux; Step 3; Methyl 6- (4-[2-(trifluoromethvDrhohenoxy]piperidin- 1 -yl ) pyridazine-3 -carboxylate; To a mixture of <strong>[65202-50-8]methyl 6-chloropyridazine-3-carboxylate</strong> (345 mg, 2.0 mmol), 4-[2- (trifluoromethyl)phenoxy]piperidine (588 mg, 2.4 mmol), tetrabutylammonium iodide (16 mg, 0.043 mmol) and potassium carbonate (573 mg, 4.1 mmol) was added 100 mL of dioxane and the mixture was heated to reflux overnight. The mixture was cooled and partitioned between ethyl acetate and water. The organic phase was dried over Na2SO4 and concentrated. Purification by silica gel chromatography (gradient 50percent to 90percent ethyl acetate: hexanes) provided the title compound.
With potassium carbonate;tetra-(n-butyl)ammonium iodide; In 1,4-dioxane; for 24h;Heating / reflux; Step 2: Methyl 6- {4-r2-(trifluoromethyl')phenoxy1piperidin- 1 -vUpyridazine-3 - carboxylateA mixture of <strong>[65202-50-8]methyl 6-chloropyridazine-3-carboxylate</strong> (500 mg, 0.2.9 mmol), 4-[2- (trifluoromethyl)phenoxy]piperidme (851 mg, 0.3.5 mmol), potassium carbonate (802 mg, 5.8 mmol) and tetrabutylammonium iodide (20 mg, 0.06 mmol) in dioxane (30 mL) was refluxed for 24 h. After cooling, the mixture was filtered through celite, washed with EtOAc and concentrated. CombiFlash chromatography (40 g, 60-90percent EtOAc in hexanes in 20 min, 35 mL/min, 18 mL/fraction) gave the title compound as a white solid. 1H NMR (400 MHz, acetone-d6): delta 1.93-1.99 (m, 2 H), 2.14-2.20 (m, 2 H),3.93 (s, 3 H), 3.97-4.09 (m, 4 H), 5.03-5.07 (m, 1 H), 7.13 (t, 1 H), 7.31 (d, 1 H), 7.40 (d, 1 H), 7.65 (dd, 2 H), 7.89 (d, 1 H).
 

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