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Chemical Structure| 1202759-89-4 Chemical Structure| 1202759-89-4

Structure of 1202759-89-4

Chemical Structure| 1202759-89-4

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Product Details of [ 1202759-89-4 ]

CAS No. :1202759-89-4
Formula : C15H16ClFN4O2
M.W : 338.77
SMILES Code : O=C(OC(C)(C)C)NC1=CC=CC(NC2=NC(Cl)=NC=C2F)=C1
MDL No. :MFCD28128976

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Application In Synthesis of [ 1202759-89-4 ]

* 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 [ 1202759-89-4 ]

[ 1202759-89-4 ] Synthesis Path-Downstream   1~3

  • 3
  • [ 1202759-89-4 ]
  • [ 33311-29-4 ]
  • [ 1202759-91-8 ]
  • [ 1202759-90-7 ]
YieldReaction ConditionsOperation in experiment
150 mg; 0.55 g With acetic acid; In tert-Amyl alcohol; for 4h;Reflux; tert-Butyl (3-((2-chloro-5-fluoropyrimidin-4-yl)amino)phenyl)carbamate (800 mg, 2.37 mmoL) and 4-(2-methoxyethoxy)aniline (576 mg, 2.84 mmoL) were suspended in tert-amyl alcohol (14 mL) and acetic acid (5 drops). Heated to reflux for 4 h. After cooling, solvent was removed via rotary evaporation. The dark oil was partitioned between water/brine and THF (10 mL each), agitated, and separated layers and dried organic phase over sodium sulfate. The solvent was removed via rotary evaporation to afford a purple solid, 0.55 g. LC/MS (RT=2.997/(M+1)) 470.2. Additional 150 mg of product minus the (BOC) protecting group crystallized from the aqueous layer
 

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