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Chemical Structure| 1070870-39-1 Chemical Structure| 1070870-39-1

Structure of 1070870-39-1

Chemical Structure| 1070870-39-1

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Product Details of [ 1070870-39-1 ]

CAS No. :1070870-39-1
Formula : C5H2BrClIN
M.W : 318.34
SMILES Code : IC1=C(Br)C=NC=C1Cl
MDL No. :MFCD28128014

Safety of [ 1070870-39-1 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H312-H315-H319-H332-H335
Precautionary Statements:P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P330-P332+P313-P337+P313-P362-P403+P233-P405-P501

Application In Synthesis of [ 1070870-39-1 ]

* 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 [ 1070870-39-1 ]

[ 1070870-39-1 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1070870-39-1 ]
  • [ 216019-28-2 ]
  • [ 1070870-40-4 ]
YieldReaction ConditionsOperation in experiment
50% With sodium carbonate;bis-triphenylphosphine-palladium(II) chloride; In 1,4-dioxane; water; at 85℃; for 18h; -Bromo-5-chloro-4-iodopyridine (1.6 g, 5.0 mmol), (3- isopropylphenyl)boronic acid (0.99 g, 6.0 mmol), Na2CO3 (1.1 g, 10 mmol) and Pd(PPh3)2Cl2 (0.50 g, 0.50 mmol) were added to a flask with 1,4-dioxane / water (2:1) (15 mL). The reaction mixture was immersed into a preheated oil bath (85 0C) and stirred overnight (18 hours). The reaction mixture was allowed to cool to room temperature and then diluted with EtOAc and water. The phases were separated and the aqueous phase was extracted with EtOAc (2x). The combined organics were washed with brine, dried over MgSO4, filtered and concentrated to give 2 g of a brown oil. The crude residue was purified by flash chromatography on silica gel and isolated 0.78 g (50% yield) of 3-bromo-5-chloro-4-(3-isopropylphenyl)pyridine as a clear oil.
50% With sodium carbonate;bis-triphenylphosphine-palladium(II) chloride; In 1,4-dioxane; water; for 18h;Heating; Step 2: 3 -bromo-5 -chloro-4-(3-isopropylphenyl)pyridine3 -Bromo-5 -chloro-4-iodopyridine (1.6 g, 5.0 mmol), (3- isopropylphenyl)boronic acid (0.99 g, 6.0 mmol), Na2CO3 (1.1 g, 10 mmol) andPd(PPh3)2Cl2 (0.50 g, 0.50 mmol) were added to a flask with 1,4-dioxane / water (2:1) (15 mL). The reaction mixture was immersed into a preheated oil bath (85 0C) and stirred overnight (18 hours). The reaction mixture was allowed to cool to room temperature and then diluted with EtOAc and water. The phases were separated and the aqueous phase was extracted with EtOAc (2x). The combined organics were washed with brine, dried over MgSO4, filtered and concentrated to give 2 g of a brown oil. The crude residue was purified by flash chromatography on silica gel and isolated 0.78 g (50% yield) of 3 -bromo-5 -chloro-4-(3-isopropylphenyl)pyridine as a clear oil.
 

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