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Chemical Structure| 86945-25-7 Chemical Structure| 86945-25-7

Structure of 86945-25-7

Chemical Structure| 86945-25-7

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CAS No.: 86945-25-7

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Product Details of [ 86945-25-7 ]

CAS No. :86945-25-7
Formula : C14H22N2
M.W : 218.34
SMILES Code : NCCC1CCN(CC2=CC=CC=C2)CC1
MDL No. :MFCD02093423
InChI Key :OUYRPOHWEJUTCQ-UHFFFAOYSA-N
Pubchem ID :1867002

Safety of [ 86945-25-7 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H332-H335
Precautionary Statements:P280-P305+P351+P338-P310

Application In Synthesis of [ 86945-25-7 ]

* 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 [ 86945-25-7 ]

[ 86945-25-7 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 1120-95-2 ]
  • [ 86945-25-7 ]
  • [2-(1-benzyl-piperidin-4-yl)-ethyl]-pyridazin-3-yl-amine [ No CAS ]
  • 2
  • [ 86945-25-7 ]
  • [ 151229-84-4 ]
  • [ 1335032-55-7 ]
YieldReaction ConditionsOperation in experiment
70% With triethylamine; In tetrahydrofuran; ethanol; at 20℃;Reflux; General procedure: The <strong>[151229-84-4]2,6-dichloropyridine-3,5-dicarbonitrile</strong>s 14 [27]-15 [28] were suspended in a mixture of THF/EtOH (2:1, v:v). Then, amine 22 or 24 [41] followed by triethylamine, were added. The mixture was then heated under reflux. After cooling, the solvent was removed in vacuo and the resulting crude submitted to flash column chromatography.
70% With triethylamine; In tetrahydrofuran; ethanol; for 1.0h;Reflux; General procedure: 2,6-Dichloro-4-phenylpyridine-3,5-dicarbonitrile 13 or <strong>[151229-84-4]2,6-dichloropyridine-3,5-dicarbonitrile</strong> 14 was suspended in a mixture of THF/EtOH (2:1, v:v). The corresponding amines 9-12, followed by triethylamine, were then added. The mixture was then heated under reflux. After cooling, the solvent was removed in vacuum and the resulting crude submitted to flash column chromatography, to give compounds 1-8.
 

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