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Chemical Structure| 1075756-93-2 Chemical Structure| 1075756-93-2

Structure of 1075756-93-2

Chemical Structure| 1075756-93-2

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Product Details of [ 1075756-93-2 ]

CAS No. :1075756-93-2
Formula : C8H7F2NO2
M.W : 187.14
SMILES Code : COCC(C1=NC=C(F)C=C1F)=O
MDL No. :MFCD20226880

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Application In Synthesis of [ 1075756-93-2 ]

* 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 [ 1075756-93-2 ]

[ 1075756-93-2 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 6290-49-9 ]
  • [ 71902-33-5 ]
  • [ 1075756-93-2 ]
YieldReaction ConditionsOperation in experiment
With chloro-trimethyl-silane; lithium diisopropyl amide; In tetrahydrofuran; 3,5-Difluoropyridine (5.0 g, 43.45 mmol) in THF was cooled to -720C (external -8O0C). LDA (23.9 mL, 1.1 eq.) was added drop-wise so that the internal temp did not increase more than 30C during addition. The reaction mixture turned into a deep brownish, thick phase and was stirred for 30 minutes at this temperature. TMS-Cl (43.4 mL, 43.45 mmol) was added drop-wise in a relatively fast fashion. The reaction became a clear and light yellow solution. LDA (23.9 mL, 1.1 eq.) was added drop-wise in a quicker version, and the reaction mixture was allowed to stir for 2h. Methyl 2-methoxyacetate (5.59 mL, 56.48 mmol) was added quickly through a syringe. The reaction mixture was quenched at -780C by adding 20 ml of saturated NH4Cl solution. Evaporation of the organic extracts under reduced pressure gave a colored residue. Purification utilizing ISCO (0-25percent EtOAc/hexanes), gave the title compound (3 g). LCMS: 188 [M+H]+.
Intermediate 30 l-(3,5-Difluoropyridin-2-yl)-2-methoxyethanone3,5-Difluoropyridine (5.0 g, 43.45 mmol) in THF was cooled to -720C (external -8O0C). LDA (23.9 mL, 1.1 eq.) was added drop-wise at such rate that the internal temp did not increase more than 30C during addition. The reaction mixture turned into a deep brownish, thick phase and was stirred for 30 minutes at this temperature. TMS-Cl (43.4 mL, 43.45 mmol) was added via syringe in a relatively fast fashion. The reaction became a clear and light yellow solution. LDA (23.9 mL, 1.1 eq.) was added drop-wise in a quicker version, and the reaction mixture was allowed to stir for 2 hours. Methyl 2-methoxyacetate (5.59 mL, 56.48 mmol) was added quickly through a syringe. The reaction mixture was quenched at -780C by adding 20 ml of saturated NH4Cl solution. Evaporation of the organic extracts under reduced pressure gave a colored residue. Purification utilizing ISCO (0-^25percent EtOAc/hexanes), gave the title product (3 g). LCMS: 188 [M+H]+.
Intermediate 49 l-(3,5-Difluoropyridin-2-yl)-2-methoxyethanone3,5-Difluoropyridine (5.0 g, 43.45 mmol) in THF was cooled to -72°C (external -800C). LDA (23.9 mL, 1.1 eq.) was added drop-wise so that the internal temp did not increase more than 3°C during addition. The reaction turned into a deep brownish, thick phase. The reaction was stirred for 30 minutes. TMS-Cl (43.4 mL, 43.45 mmol) was added drop-wise in a relatively fast fashion. The reaction became a clear and light yellow solution. LDA (23.9 mL, 1.1 eq.) was added drop- wise in a quicker version, and the reaction was allowed to stir for 2h. Methyl 2-methoxyacetate (5.59 mL, 56.48 mmol) was added quickly through a syringe. The reaction was quenched at - 78°C by adding 20 ml of saturated NH4Cl solution. Evaporation of the organic extracts under reduced pressure gave a colored residue. Purification by ISCO (0-25percent EtOAc/hexanes), gave the title compound (3 g). LCMS: 188 [M+H]+.
3,5-Difluoropyridine (5.0 g, 43.45 mmol) in THF was cooled to -72°C (external -800C). LDA (23.9 rnL, 1.1 eq.) was added drop-wise so that the internal temperature did not increase more than 3°C during addition. The reaction mixture turned into a deep brownish, thick phase. The reaction mixture was stirred for 30 mins. TMS-Cl (43.4 mL, 43.45 mmol) was added in a relatively fast fashion. The reaction became a clear and light yellow solution. LDA (23.9 mL, 1.1 eq.) was added drop-wise in a quicker version, and the reaction mixture was allowed to stir for 2 hours. Methyl 2-methoxyacetate (5.59 mL, 56.48 mmol) was added quickly through a syringe. The reaction mixture was quenched at -78°C by adding 20 ml of saturated NH4Cl solution. Evaporation of the organic extracts under reduced pressure gave a colored residue. Purification by ISCO (0- 25percent EtOAc/hexanes), gave the title product (3 g). LCMS: 188 [M+H]+.

 

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