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Chemical Structure| 1350653-30-3 Chemical Structure| 1350653-30-3

Structure of 1350653-30-3

Chemical Structure| 1350653-30-3

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Product Details of [ 1350653-30-3 ]

CAS No. :1350653-30-3
Formula : C17H14F2N8
M.W : 368.34
SMILES Code : NC1=NC(C2=NN(CC3=CC=CC=C3F)C4=NC=C(F)C=C42)=NC(N)=C1N
MDL No. :MFCD26517131

Safety of [ 1350653-30-3 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H318-H410
Precautionary Statements:P273-P280-P305+P351+P338-P501
Class:9
UN#:3077
Packing Group:

Application In Synthesis of [ 1350653-30-3 ]

* 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 [ 1350653-30-3 ]

[ 1350653-30-3 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 22929-52-8 ]
  • [ 1350653-30-3 ]
  • 2-(5-fluoro-1-(2-fluorobenzyl)-1H-pyrazolo[3,4-b]pyridin-3-yl)-N5-(tetrahydrofuran-3-yl)pyrimidine-4,5,6-triamine [ No CAS ]
YieldReaction ConditionsOperation in experiment
57% Add 2-(5-fluoro-1-(2-fluorobenzyl)-1H-pyrazolo[3,4-b]pyridin-3-yl)pyrimidine to a 50 mL two-necked vialPyridine-4,5,6-triamine (0.10 g, 0.27 mmol),Dihydro-3(2H)-furanone (0.035 g, 0.41 mmol) and methanol (10 mL),Additional acetic acid (0.16 mL, 2.8 mmol) was added.After stirring at room temperature for 1 hour, sodium cyanoborohydride (0.085 g, 1.4 mmol) was added.Continue to stir at room temperature overnight.The solvent was evaporated, a saturated aqueous solution of sodium hydrogencarbonate and ethyl acetate (30 mL×2)The organic phase was washed with water (30 mL×2) and brine (30 mL×2), dried over anhydrous sodium sulfate and filtered.The residue was purified by silica gel column chromatography (dichlorobenzene / methanol (v/v) = 100/1).A pale yellow solid (0.068 g, 57percent).
 

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