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Chemical Structure| 71083-71-1 Chemical Structure| 71083-71-1

Structure of 71083-71-1

Chemical Structure| 71083-71-1

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Product Details of [ 71083-71-1 ]

CAS No. :71083-71-1
Formula : C11H8N2O2
M.W : 200.19
SMILES Code : N#CC1C(=O)C2C=CC=C(OC)C=2NC=1
MDL No. :N/A

Safety of [ 71083-71-1 ]

Application In Synthesis of [ 71083-71-1 ]

* 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 [ 71083-71-1 ]

[ 71083-71-1 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 71083-71-1 ]
  • [ 214476-78-5 ]
YieldReaction ConditionsOperation in experiment
91% With trichlorophosphate;N,N-dimethyl-formamide; for 0.5h;Heating / reflux; A mixture of 3.8 g (19 mmol) of 1,4-dihydro-8-methoxy-4-oxo-3-quinolinecarbonitrile and 40 mL of phosphorous oxochloride and 5 drops of DMF was refluxed for 0.5 hours. The mixture was evaporated to dryness and diluted with hexanes. The solid was collected and mixed with cold dilute sodium carbonate solution and extracted several times with ethyl acetate. The organic layer was dried over sodium sulfate and filtered through a pad of silica gel. Removal of the solvent gave 3.8 g of 4-chloro-8-methoxy-3-quinolinecarbonitrile as an off white solid in 91 % yield, mass spectrum (electrospray, m/e): M+H 219.1.
With trichlorophosphate;N,N-dimethyl-formamide; for 0.5h;Heating / reflux; A mixture of 3.8 g (19 mmol) of 1,4-dihydro-8-methoxy-4-oxo-quinoline-3-carbonitrile and 40 mL of phosphorous oxochloride and 5 drops of DMF was refluxed for 0.5 hours. The mixture was evaporated to dryness and diluted with hexanes. The solid was collected and mixed with cold dilute sodium carbonate solution and extracted several times with ethyl acetate. The organic layer was dried over sodium sulfate and filtered through a pad of silica gel. Removal of the solvent gave 3.8 g of 4-chloro-8-methoxy -quinoline-3-carbonitrile as an off white solid in 91 % yield, mass spectrum (electrospray, m/e): M+H 219.1.
  • 3
  • phosphorous oxochloride [ No CAS ]
  • [ 71083-71-1 ]
  • [ 214476-78-5 ]
YieldReaction ConditionsOperation in experiment
91% With sodium carbonate; In N,N-dimethyl-formamide; EXAMPLE 273 4-Chloro-8-methoxy -3-quinolinecarbonitrile A mixture of 3.8 g (19 mmol) of 1,4-dihydro-8-methoxy-4-oxo-3-quinolinecarbonitrile and 40 mL of phosphorous oxochloride and 5 drops of DMF was refluxed for 0.5 hours. The mixture was evaporated to dryness and diluted with hexanes. The solid was collected and mixed with cold dilute sodium carbonate solution and extracted several times with ethyl acetate. The organic layer was dried over sodium sulfate and filtered through a pad of silica gel. Removal of the solvent gave 3.8 g of 4-chloro-8-methoxy -3-quinolinecarbonitrile as an off white solid in 91% yield, mass spectrum (electrospray, m/e): M+H 219.1.
91% With sodium carbonate; In N,N-dimethyl-formamide; EXAMPLE 273 4-Chloro-8-methoxy-3-quinolinecarbonitrile A mixture of 3.8 g (19 mmol) of 1,4-dihydro-8-methoxy-4-oxo-3-quinolinecarbonitrile and 40 mL of phosphorous oxochloride and 5 drops of DMF was refluxed for 0.5 hours. The mixture was evaporated to dryness and diluted with hexanes. The solid was collected and mixed with cold dilute sodium carbonate solution and extracted several times with ethyl acetate. The organic layer was dried over sodium sulfate and filtered through a pad of silica gel. Removal of the solvent gave 3.8 g of 4-chloro-8-methoxy-3-quinolinecarbonitrile as an off white solid in 91% yield, mass spectrum (electrospray, m/e): M+H 219.1.
91% With sodium carbonate; In N,N-dimethyl-formamide; EXAMPLE 92 4-Chloro-8-methoxy-quinoline-3-carbonitrile A mixture of 3.8 g (19 mmol) of 1,4-dihydro-8-methoxy-4-oxo-quinoline-3-carbonitrile and 40 mL of phosphorous oxochloride and 5 drops of DMF was refluxed for 0.5 hours. The mixture was evaporated to dryness and diluted with hexanes. The solid was collected and mixed with cold dilute sodium carbonate solution and extracted several times with ethyl acetate. The organic layer was dried over sodium sulfate and filtered through a pad of silica gel. Removal of the solvent gave 3.8 g of 4-chloro-8-methoxy-quinoline-3-carbonitrile as an off white solid in 91% yield, mass spectrum (electrospray, m/e): M+H 219.1.
91% With sodium carbonate; In N,N-dimethyl-formamide; Example 273 4-Chloro-8-methoxy-3-quinolinecarbonitrile A mixture of 3.8 g (19 mmol) of 1,4-dihydro-8-methoxy-4-oxo-3-quinolinecarbonitrile and 40 mL of phosphorous oxochloride and 5 drops of DMF was refluxed for 0.5 hours. The mixture was evaporated to dryness and diluted with hexanes. The solid was collected and mixed with cold dilute sodium carbonate solution and extracted several times with ethyl acetate. The organic layer was dried over sodium sulfate and filtered through a pad of silica gel. Removal of the solvent gave 3.8 g of 4-chloro-8-methoxy-3-quinolinecarbonitrile as an off white solid in 91 % yield, mass spectrum (electrospray, m/e): M+H 219.1.

 

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