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Chemical Structure| 490030-16-5 Chemical Structure| 490030-16-5

Structure of 490030-16-5

Chemical Structure| 490030-16-5

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Product Details of [ 490030-16-5 ]

CAS No. :490030-16-5
Formula : C26H24ClN3O3
M.W : 461.95
SMILES Code : ClC1=C2C(N(C(CC3)CCC43OCCO4)C=C2C5=CC=C(OC6=CC=CC=C6)C=C5)=NC=N1
MDL No. :N/A

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Application In Synthesis of [ 490030-16-5 ]

* 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 [ 490030-16-5 ]

[ 490030-16-5 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 269410-26-6 ]
  • [ 262444-48-4 ]
  • [ 490030-16-5 ]
YieldReaction ConditionsOperation in experiment
5.22 g With tetrakis(triphenylphosphine) palladium(0); sodium carbonate; In 1,2-dimethoxyethane; water; at 80℃; for 3.5h; 4-Phenoxyphenylboronic acid pinacol ester (8.44 g) was dissolved in ethylene glycol dimethyl ether (300 mL), and 4-chloro-7-(1,4-dioxaspiro[4.5]decan-8-yl)-5-iodo-7H-pyrrolo[2,3-d]pyrimidine (7.97 g), sodium carbonate (6.02 g), water (200 mL) and tetrakis(triphenylphosphine)palladium (1.32 g) were sequentially added to the solution. The mixture was stirred at 80C for 3.5 hours. The mixture was left to cool naturally, subsequently ethyl acetate (400 mL) was added thereto, and the mixture was partitioned. The organic layer was washed with water (250 mL) and saturated brine (250 mL) and dried over anhydrous sodium sulfate, and then the solvent was distilled off under reduced pressure. A pale brown oily substance (13.8 g) was obtained, and hexane/ethyl acetate (5 : 1, 40 mL) and dichloromethane (15 mL) were added thereto. A white solid precipitated therefrom was collected by filtration and dried, and thus 4-chloro-5-(4-phenoxyphenyl)-7-(1,4-dioxaspiro[4.5]decan-8-yl)-7H-pyrrolo[2,3-d]pyrimidin e (5.22 g) was obtained.
 

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