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Chemical Structure| 82153-68-2 Chemical Structure| 82153-68-2

Structure of 82153-68-2

Chemical Structure| 82153-68-2

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Product Details of [ 82153-68-2 ]

CAS No. :82153-68-2
Formula : C6H7ClN2O
M.W : 158.59
SMILES Code : CCOC1=CN=C(Cl)N=C1
MDL No. :MFCD10697651
InChI Key :QFRSOKNULFUQDS-UHFFFAOYSA-N
Pubchem ID :15565267

Safety of [ 82153-68-2 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of [ 82153-68-2 ]

* 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 [ 82153-68-2 ]

[ 82153-68-2 ] Synthesis Path-Downstream   1~3

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  • [ 280582-25-4 ]
  • [ 82153-68-2 ]
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  • [ 75-03-6 ]
  • [ 4983-28-2 ]
  • [ 82153-68-2 ]
YieldReaction ConditionsOperation in experiment
88% With potassium carbonate; In N,N-dimethyl-formamide; at 50℃; for 1h; To a solution of <strong>[4983-28-2]2-chloro-5-hydroxypyrimidine</strong> (1.00 g) in dimethylformamide (15 mL) were added potassium carbonate (1.59 g) and ethyl iodide (1.84 mL), and the mixture was stirred at 50°C for 1 hour. To the reaction mixture was added water, and then the mixture was extracted with ethyl acetate. The organic layer was washed with water and brine, and then dried over magnesium sulfate and filtered. The filtrate was concentrated under reduced pressure, and the resulting residue was purified by column chromatography on silica gel (solvent; hexane/ethyl acetate = 99/1 to 78/22) to give the titled compound (1.07 g) as a colorless solid (yield: 88percent). MS(APCI)m/z; 159/161[M+H]+.
With potassium carbonate; In N,N-dimethyl-formamide; at 50℃; for 4h; 2-Chloropyrimidin-5-ol (13.0 g, 100 mmol) was dissolved in DMF (130 mL) (solution) and K2C03 (27.5 g, 199 mmol) was added (suspension), followed by iodoethane (16.1 mL, 199 mmol). The reaction mixture was stirred at 50°C for 4 hr and subsequently cooled to ambient temperature and stirred overnight. The reaction mixture was partitioned between EtOAc (650 mL) and 10percent aqueous NaCl (650 mL). The organic layer was washed with 10percent aqueous NaCl (650 mL). The first aqueous layer was extracted with EtOAc (325 mL). The combined organic layers-were driedOver Na2S0 , filtered, and concentrated in vacuo. The crude mixture was diluted with D'CM-to a final volume of 40 mL and purified by flash chromatography (MPLC, 5-4percent EtOAc-Hexanes) to provide 2-chloro-5-ethoxypyrimidine as a white solid.LRMS (EST) calc'd fbr C6K8C1N02 [M+H]+: 159; Found: 159
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  • [ 280582-25-4 ]
  • zinc dust [ No CAS ]
  • [ 82153-68-2 ]
 

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Related Functional Groups of
[ 82153-68-2 ]

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Related Parent Nucleus of
[ 82153-68-2 ]

Pyrimidines

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