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Chemical Structure| 209003-46-3 Chemical Structure| 209003-46-3

Structure of 209003-46-3

Chemical Structure| 209003-46-3

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Product Details of [ 209003-46-3 ]

CAS No. :209003-46-3
Formula : C10H6BrNO2
M.W : 252.06
SMILES Code : OC(=O)C1=NC2=C(C=CC=C2)C(Br)=C1
MDL No. :MFCD08705670
InChI Key :DLAHQKXVDUYPHR-UHFFFAOYSA-N
Pubchem ID :15530812

Safety of [ 209003-46-3 ]

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

Application In Synthesis of [ 209003-46-3 ]

* 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 [ 209003-46-3 ]

[ 209003-46-3 ] Synthesis Path-Downstream   1~2

  • 2
  • [ 209003-46-3 ]
  • [ 1240390-32-2 ]
  • [ 1314141-44-0 ]
YieldReaction ConditionsOperation in experiment
With (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; triethylamine; In dichloromethane; at 20℃; for 16h; 4-Bromoquinoline-2-carboxylic acid (A3) was prepared as described in Example 1.To a solution of A3 (0.35 g, 1.4 mmol) in 6.0 mL CH2C12 was added (3S,4S)-3-aminotetrahydro- 2H-pyran-4-ol (0.20 g, 1.7 mmol). BOP reagent (0.74 g, 1.7 mmol), and triethylamine (0.58 mL, 4.2 mmol). The reaction mixture was stirred at room temperature for 16 h, diluted with CH2CI2, washed with water, dried over sodium sulfate, filtered, and concentrated. The resultant residue was subjected to silica gel chromatography eluting with 25-100% ethyl acetate in hexanes to afford 4-bromo-N-[(35,4S,)-4-hydroxytetrahydro-2H-pyran-3-yl]quinoline-2-carboxamide that gave a mass ion (ES+) of 353.1 (81Br) for M+H+.
 

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[ 209003-46-3 ]

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