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Chemical Structure| 1313408-99-9 Chemical Structure| 1313408-99-9

Structure of 1313408-99-9

Chemical Structure| 1313408-99-9

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Product Details of [ 1313408-99-9 ]

CAS No. :1313408-99-9
Formula : C10H9FN2O2
M.W : 208.19
SMILES Code : O=C(C1=CN=C2C=C(F)C=CN21)OCC
MDL No. :MFCD28368508

Safety of [ 1313408-99-9 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319
Precautionary Statements:P501-P270-P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313-P301+P312+P330

Application In Synthesis of [ 1313408-99-9 ]

* 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 [ 1313408-99-9 ]

[ 1313408-99-9 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 944401-77-8 ]
  • [ 33142-21-1 ]
  • [ 1313408-99-9 ]
YieldReaction ConditionsOperation in experiment
Fluoropyridin-2-amine (10.0 g, 48.0 mmol) was mixed with ethanol (40 mL) in a reaction flask, under an atmosphere of dry nitrogen. A solution of <strong>[33142-21-1]ethyl 2-chloro-3-oxopropanoate</strong> (5% in benzene, 178 mL, Commercial solution from Toronto Research Chemicals Inc.) was added. The mixture was heated to 60 C under nitrogen for 4 hours. After allowing the mixture to cool the solvent was removed under vacuum to give a brown solid. The solid was mixed with ethyl acetate (300 mL) and sodium bicarbonate solution (75 mL) and stirred to dissolve. The phases were separated and the bicarbonate solution was extracted further with ethyl acetate (75 mL). The combined ethyl acetate extracts were dried over sodium sulfate, filtered and concentrated under vacuum to give a solid. The crude material was dissolved in ethyl acetate and passed through a short column of silica, eluting with ethyl acetate. Fractions containing the product were concentrated to give ethyl 7-fluoroimidazo[l,2-a]pyridine-3- carboxylate as a white solid (13 g).
4-Fluoropyridin-2-amine (10.0 g, 48.0 mmol) was mixed with ethanol (40 mL) in a reaction flask, under an atmosphere of dry nitrogen. A solution of <strong>[33142-21-1]ethyl 2-chloro-3-oxopropanoate</strong> (5% in benzene, 178 mL (commercial solution from Toronto Research Chemicals Inc.) was added. The mixture was heated to 60 C under nitrogen for 4 hours. After allowing the mixture to cool the solvent was removed under vacuum to give a brown solid. The solid was mixed with ethyl acetate (300 mL) and sodium bicarbonate solution (75 mL) and stirred to dissolve. The phases were separated and the bicarbonate solution was extracted further with ethyl acetate (75 mL). The combined ethyl acetate extracts were dried over sodium sulfate, filtered and concentrated under vacuum to give a solid. The crude material was dissolved in ethyl acetate and passed through a short column of silica, eluting with ethyl acetate. Factions containing the desired product were concentrated to give ethyl 7-fluoroimidazo[l,2- a]pyridine-3-carboxylate as a white solid (13 g).
 

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