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Chemical Structure| 859174-38-2 Chemical Structure| 859174-38-2

Structure of 859174-38-2

Chemical Structure| 859174-38-2

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Product Details of [ 859174-38-2 ]

CAS No. :859174-38-2
Formula : C6H2ClF2NO
M.W : 177.54
SMILES Code : O=C(Cl)C1=CC=C(F)N=C1F

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Application In Synthesis of [ 859174-38-2 ]

* 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 [ 859174-38-2 ]

[ 859174-38-2 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 171178-50-0 ]
  • [ 859174-38-2 ]
YieldReaction ConditionsOperation in experiment
With thionyl chloride; In dichloromethane; for 3h;Heating / reflux; 2,6-Difluoro-nicotinoyl chloride. A mixture of <strong>[171178-50-0]2,6-difluoronicotinic acid</strong> (6.2 g), thionyl chloride (15 mL) and CH2Cl2 (100 mL) was heated to reflux for 3 h. The mixture was evaporated to dryness, CH2Cl2, was added and evaporated to dryness to afford 1.1 g of the <strong>[171178-50-0]2,6-difluoronicotinic acid</strong> chloride. This material used without further purification.
With thionyl chloride; In dichloromethane; for 1.5h;Heating / reflux; EXAMPLE 1 Synthesis of 2-(2-fluoro,5-chloro)phenyl-7-fluoro-pyrido-8-pyrimidone. (Entry 7, Table II) 2,6 difluoronicotinic acid, (0.479 g, 3.012 mmol) was suspended in 30 mL dry methylene chloride and treated with thionyl chloride (2.5 mL, 34.27 mmol), under reflux for 90 minutes. The reaction mixture was cooled to room temperature and the solvents removed under reduced pressure on a rotary evaporator, the residue obtained was further dried under high vacuum to give 2,6 difluoronicotinoyl chloride.
With thionyl chloride; for 2h;Inert atmosphere; Reflux; 2,6-Difluoronicotinic acid (10.6 g, 66.6 mmol) and thionyl chloride (35 mF, 480 mmol) were combined under nitrogen and heated to gentle reflux for 2 h. The solution was concentrated to dryness under reduced pressure. Toluene (100 mF) was added to the crude and it was evaporated to dryness once more. The crude acid chloride was dissolved in DCM (50 mF) under nitrogen and cooled in an ice bath. A mixture of triethylamine (25 mF, 180 mmol) and benzyl alcohol (7.25 ml, 70.1 mmol) in DCM (50 mF) was added dropwise over 10 min. 0.1 N HC1 (100 mF) was added and the phases mixed and separated. The organic was dried with magnesium sulfate and evaporated to dryness under reduced pressure to provide benzyl 2,6-difluoronicotinate (50A) which was used without purification. m/z (ESI): 250.0 (M+H)+.
With thionyl chloride; for 2h;Inert atmosphere; Reflux; 2,6-Difluoronicotinic acid (10.6 g, 66.6 mmol) and thionyl chloride (35 mL, 480 mmol) were combined under nitrogen and heated to gentle reflux for 2 h. The solution was concentrated to dryness under reduced pressure. Toluene (100 mL) was added to the crude and it was evaporated to dryness once more. The crude acid chloride was dissolved in DCM (50 mL) under nitrogen and cooled in an ice bath. A mixture of triethylamine (25 mL, 180 mmol) and benzyl alcohol (7.25 mL, 70.1 mmol) in DCM (50 mL) was added dropwise over 10 min, and the mixture was stirred at rt for 30 min. Then, 0.1 N HCl (100 mL) was added and the phases mixed and separated. The organic phase was taken, dried with magnesium sulfate, and evaporated to dryness under reduced pressure to provide benzyl 2,6-difluoronicotinate which was used without purification. m/z (ESI): 250.0 (M+H)+.

 

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