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Chemical Structure| 2415222-46-5 Chemical Structure| 2415222-46-5

Structure of 2415222-46-5

Chemical Structure| 2415222-46-5

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Product Details of [ 2415222-46-5 ]

CAS No. :2415222-46-5
Formula : C11H16N2O2
M.W : 208.26
SMILES Code : OC1=CN(C2CC2)N=C1C3CCOCC3
English Name :1-Cyclopropyl-3-(tetrahydro-2H-pyran-4-yl)-1H-pyrazol-4-ol
MDL No. :N/A

Safety of [ 2415222-46-5 ]

Application In Synthesis of [ 2415222-46-5 ]

* 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 [ 2415222-46-5 ]

[ 2415222-46-5 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 476660-71-6 ]
  • [ 2415222-46-5 ]
  • [ 2415222-47-6 ]
YieldReaction ConditionsOperation in experiment
With potassium carbonate In N,N-dimethyl-formamide at 140℃; for 2h; Inert atmosphere; 18.1 Step 1: Preparation of 6-bromo-4-((1-cyclopropyl-3-(tetrahydro-2H-pyran-4-yl)-1H-pyrazol-4-yl)oxy)-7-methoxyquinoline Weigh 6-bromo-4-chloro-7-methoxyquinoline (27mg, 0.1mmol),1-cyclopropyl-3- (tetrahydro-2H-pyran-4-yl) -1H-pyrazol-4-ol (21mg, 0.1mmol)With potassium carbonate (28mg, 0.2mmol) in a 50mL single-necked bottle, add 10mL of anhydrous N, N-dimethylformamide, under argon protection, stirring at 140°C for 2h.After the reaction was completed, 20 mL of water was added, extracted with ethyl acetate, the organic phases were combined, washed with saturated sodium chloride solution, dried over anhydrous sodium sulfate, and concentrated under reduced pressure to obtain the title compound, which was directly used in the next reaction.
 

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