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Chemical Structure| 286371-49-1 Chemical Structure| 286371-49-1

Structure of 286371-49-1

Chemical Structure| 286371-49-1

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Product Details of [ 286371-49-1 ]

CAS No. :286371-49-1
Formula : C17H14ClNO2
M.W : 299.75
SMILES Code : COC1=C(OCC2=CC=CC=C2)C=C3N=CC=C(Cl)C3=C1
MDL No. :MFCD12910463
InChI Key :SYKLZPMKNBDEOF-UHFFFAOYSA-N
Pubchem ID :22646562

Safety of [ 286371-49-1 ]

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

Application In Synthesis of [ 286371-49-1 ]

* 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 [ 286371-49-1 ]

[ 286371-49-1 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 649736-31-2 ]
  • [ 286371-49-1 ]
  • [ 1210828-42-4 ]
YieldReaction ConditionsOperation in experiment
84% With 1,4-diaza-bicyclo[2.2.2]octane; In 1-methyl-pyrrolidin-2-one; at 100℃; 7-Benzyloxy-4-chloro-6-methoxyquinoline 1 (29.98 g, 100 mmol) was added to a three-neck flask.1-(2-Fluoro-3-hydroxy-6-nitrophenyl)propyl-2-one 2 (21.32 g, 100 mmol)And N-methylpyrrolidone (150 mL), DABCO (11.22 g, 100 mmol),After stirring uniformly, the mixture was heated to 100 C to react overnight.At the end of the reaction, water (600 mL) was added to precipitate a large amount of solid and filtered.The crude product was recrystallized from isopropyl alcohol and water to give Compound 3 (40.02 g, 84%).
 

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[ 286371-49-1 ]

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Related Parent Nucleus of
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