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Chemical Structure| 313339-36-5 Chemical Structure| 313339-36-5

Structure of 313339-36-5

Chemical Structure| 313339-36-5

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Product Details of [ 313339-36-5 ]

CAS No. :313339-36-5
Formula : C6H5Cl2N3OS
M.W : 238.09
SMILES Code : CSC1=NC(Cl)=C(C(N)=O)C(Cl)=N1
MDL No. :MFCD15071707

Safety of [ 313339-36-5 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H317
Precautionary Statements:P280

Application In Synthesis of [ 313339-36-5 ]

* 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 [ 313339-36-5 ]

[ 313339-36-5 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 35216-39-8 ]
  • [ 313339-36-5 ]
  • [ 1254057-16-3 ]
  • 2
  • [ 35216-39-8 ]
  • [ 313339-36-5 ]
  • [ 1254057-15-2 ]
YieldReaction ConditionsOperation in experiment
To a mixture of 55% sodium hydride in oil (733 mg) and DMF (20 mL), a mixture of <strong>[35216-39-8]3-(methylsulfonyl)aniline</strong> (1.44 g) and THF (20 mL) were added under ice cooling and stirred for 30 minutes under ice cooling. After dropwise addition of a mixture of 4,6-dichloro-2-(methylsulfanyl)pyrimidine-5-carboxamide (2.0 g) and DMF (30 mL) over 15 minutes, the reaction liquid was further stirred under ice cooling for 15 minutes. After addition of 10% aqueous citric acid (300 mL) and extraction with ethyl acetate, the organic layer was washed with saturated aqueous sodium chloride. After drying over anhydrous magnesium sulfate, the solvent was concentrated, and the precipitated solid was collected by filtration and dried to give 4-chloro-2-(methylsulfanyl)-6-[3-(methylsulfonyl)phenyl]amino}pyrimidine-5-carboxamide (1.95 g) as a light yellow solid.
  • 3
  • [ 1979-98-2 ]
  • [ 313339-36-5 ]
 

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