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Chemical Structure| 739366-03-1 Chemical Structure| 739366-03-1

Structure of 739366-03-1

Chemical Structure| 739366-03-1

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Product Details of [ 739366-03-1 ]

CAS No. :739366-03-1
Formula : C5H9N3O
M.W : 127.14
SMILES Code : NC1=NNC(COC)=C1
MDL No. :MFCD22576523
InChI Key :VFDNIDGPEBLDNH-UHFFFAOYSA-N
Pubchem ID :23091908

Safety of [ 739366-03-1 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H314
Precautionary Statements:P280-P305+P351+P338-P310
Class:8
UN#:3259
Packing Group:

Application In Synthesis of [ 739366-03-1 ]

* 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 [ 739366-03-1 ]

[ 739366-03-1 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 739366-03-1 ]
  • [ 80370-42-9 ]
  • [ 739366-04-2 ]
YieldReaction ConditionsOperation in experiment
69% In ethanol; Ethyl 2-formyl-3-oxopropionate (775 mg) was added to a solution of the thus obtained 5-methoxymethyl-2H-pyrazol-3-ylamine (684 mg) in ethanol (50 ml), and stirred overnight. The reaction solution was concentrated under reduced pressure, and a saturated sodium bicarbonate solution was added to the residue which were then extracted with ethyl acetate. The organic phase was washed with a saturated saline solution and dried over sodium sulfate anhydrous. The resulting product was concentrated under reduced pressure, and the residue was purified by column chromatography (eluding solvent; n-hexane: ethyl acetate 4: 1) to give ethyl 2-methoxymethylpyrazolo[1,5-a] pyrimidine-6-carboxylate (878 mg, Y.: 69%).
 

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[ 739366-03-1 ]

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