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Chemical Structure| 1453211-49-8 Chemical Structure| 1453211-49-8

Structure of 1453211-49-8

Chemical Structure| 1453211-49-8

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Product Details of [ 1453211-49-8 ]

CAS No. :1453211-49-8
Formula : C10H8F2O2
M.W : 198.17
SMILES Code : COC1=C(F)C(C#C)=C(F)C(OC)=C1
MDL No. :MFCD28365526

Safety of [ 1453211-49-8 ]

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 [ 1453211-49-8 ]

* 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 [ 1453211-49-8 ]

[ 1453211-49-8 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1445-39-2 ]
  • [ 1453211-49-8 ]
  • [ 1453211-53-4 ]
YieldReaction ConditionsOperation in experiment
1.07 g With copper(l) iodide; tetrakis(triphenylphosphine) palladium(0); N-ethyl-N,N-diisopropylamine; In N,N-dimethyl-formamide; at 80℃; for 1h;Inert atmosphere; Preparation Example 7 To a mixture of <strong>[1445-39-2]2-amino-5-iodopyrimidine</strong> (1 g), 3-ethynyl-2,4-difluoro-1,5-dimethoxybenzene (897 mg), tetrakistriphenylphosphine palladium (261 mg), copper iodide (43 mg), and N,N-dimethylformamide (20 mL), N,N-diisopropylethylamine (1.55 mL) was added under an argon atmosphere followed by stirring at 80 C. for 1 hour. The reaction mixture was concentrated under reduced pressure, and to the obtained residue were added chloroform and water, and insoluble materials were removed by filtration through celite. After the filtrate was extracted with chloroform, the organic layer was washed with saturated brine, dried over anhydrous sodium sulfate, and then filtered. After the filtrate was concentrated under reduced pressure, the resulting residue was purified by silica gel column chromatography (chloroform/methanol) to give 5-[(2,6-difluoro-3,5-dimethoxyphenyl)ethynyl]pyrimidin-2-amine (1.07 g).
 

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