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Chemical Structure| 1034467-82-7 Chemical Structure| 1034467-82-7

Structure of 1034467-82-7

Chemical Structure| 1034467-82-7

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Product Details of [ 1034467-82-7 ]

CAS No. :1034467-82-7
Formula : C8H7FIN
M.W : 263.05
SMILES Code : IC1=CC(C2CC2)=CN=C1F
MDL No. :MFCD28154564

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Application In Synthesis of [ 1034467-82-7 ]

* 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 [ 1034467-82-7 ]

[ 1034467-82-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1034467-80-5 ]
  • [ 1034467-82-7 ]
YieldReaction ConditionsOperation in experiment
68% Preparation 47; S-Cyclopropyl^-fluoro-S-iodo-pyridine; Cool a solution of 5-cyclopropyl-2-fluoro-pyridine (1.3 g, 9.5 mmol) in THF (20 mL) to -75 0C in a dry ice-acetone bath under nitrogen. Add lithium diisopropylamide (2 M in THF, 6 mL, 12 mmol) over a period of 30 min. Stir the mixture for an additional 3 hours. Add iodine (2.9 g, 11.4 mmol, dissolved in 50 mL of THF) and stir the mixture for 2 hours. Add water (100 mL) and allow the temperature to rise to room temperature over 1 hour while stirring. Treat the mixture with saturated aqueous sodium thiosulfate solution (50 mL). Extract the solution with ether. Concentrate the solution in vacuo to brown oil. Purify by column chromatography (hexane to 20 % ethyl acetate in hexane) to afford the title compound (1.7 g, 68 %) as a yellow oil. 1H NMR (40OMHz-CDCl3) δ 8.03 (dd, J= 3, 8 Hz, IH), 7.99 (s, IH), 0.91-1.00 (m, 2H), 0.71-0.78 (m, 2H).
68% Preparation 155-Cyclopropyl-2-fluoro-3-iodo-pyridineCool a solution of 5-cyclopropyl-2-fluoro-pyridine (1.3 g, 9.5 mmol) in THF (20 mL) to -75 0C in a dry ice-acetone bath under nitrogen. Add lithium diisopropylamide (2 M in THF, 6 mL, 12 mmol) during a period of 30 min. Stir the mixture for another 3 h before adding iodine (2.9 g, 11.4 mmol, dissolved in 50 mL of THF). Keep stirring for 2 more hours before adding water (100 mL) to the mixture. Then allow to warm to RT during 1 h under stirring. Treat the mixture with a saturated sodium thiosulfate solution (50 mL). Extract the solution with ether. Concentrate the solution in vacuo. Purify by column chromatography (hexane-^ 20% ethyl acetate in <n="15"/>hexane) to afford the title compound as a yellow oil (1.7 g, 68 %). 1H NMR (400 MHz- CDCl3) δ 7.99 (d, J= 3 Hz, IH), 7.39 (td, J= 3, 5 Hz, IH), 6.79 (dd, J= 3, 8 Hz, IH), 0.96-1.02 (m, 2H), 0.63-0.69 (m, 2H).
 

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