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Chemical Structure| 1402738-51-5 Chemical Structure| 1402738-51-5

Structure of 1402738-51-5

Chemical Structure| 1402738-51-5

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Product Details of [ 1402738-51-5 ]

CAS No. :1402738-51-5
Formula : C8H10ClNO2
M.W : 187.62
SMILES Code : COCC1=CC(Cl)=NC(OC)=C1

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Application In Synthesis of [ 1402738-51-5 ]

* 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 [ 1402738-51-5 ]

[ 1402738-51-5 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 193001-91-1 ]
  • [ 74-88-4 ]
  • [ 1402738-51-5 ]
YieldReaction ConditionsOperation in experiment
73% Step 3 To 34 (3.43 g, 19.8 mmol) in DMF (30 mL) at room temperature was added sodium hydride (60% dispersion in mineral oil, 1.19 g, 29.6 mmol). The solution was stirred at room temperature for 30 minutes and iodomethane (6.1 mL, 98.8 mmol) was added. The reaction vvas stirred at room temperature for 18 h. Water was added and the mixture was extracted with EtOAc. The organic layers were combined, washed with water and brine, dried ( gS04), filtered, and concentrated in vacuo to provide 35 (2.71 g, 73%).
0.112 g With potassium carbonate; In N,N-dimethyl-formamide; at 20℃; To a solution of <strong>[193001-91-1](2-chloro-6-methoxypyridin-4-yl)methanol</strong> (0.25 g) in dry DMF (1.25 ml) at room temperature was added potassium carbonate (0.6 g) and methyl iodide (0.18 ml) and the reaction mixture stirred overnight. The reaction mixture was diluted with ethyl acetate (25 ml) and washed with water (3 x 10 ml) then dried (Na2SC"4) and evaporated. The residue was purified by silica gel column chromatography (gradient from 0 to 20% ethyl acetate / hexane) to afford the title compound (0.112 g) as a colourless oil. LCMS: Rt 1.52 min, m/z 188/190 [M+H]+.
  • 2
  • [ 15855-06-8 ]
  • [ 1402738-51-5 ]
 

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