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Chemical Structure| 499193-57-6

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Product Details of [ 499193-57-6 ]

CAS No. :499193-57-6
Formula : C10H12ClNSi
M.W : 209.75
SMILES Code : C[Si](C#CC1=CC(Cl)=NC=C1)(C)C
MDL No. :MFCD20488864

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Application In Synthesis of [ 499193-57-6 ]

* 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.

  • Upstream synthesis route of [ 499193-57-6 ]

[ 499193-57-6 ] Synthesis Path-Upstream   1~1

  • 1
  • [ 499193-57-6 ]
  • [ 945717-09-9 ]
YieldReaction ConditionsOperation in experiment
91% With tetrabutyl ammonium fluoride In tetrahydrofuran at -78 - 0℃; for 0.75 h; To a solution of 2.389 g of 2-chloro-4-trimethylsilanylethynyl-pyridine (11.39 mmol) in THF (90 ml) were added 11.39 ml of a 1 M TBAF solution in THF at -78° C. and the reaction mixture was stirred for 45 min at 0° C.
Then saturated NH4Cl solution was added and the THF was removed under reduced pressure.
The aqueous mixture was extracted with diethylether and the combined organic extracts were washed with water and brine, dried (Na2SO4), filtered and concentrated in vacuo.
The remaining residue was purified by column chromatography (pentane/diethylether 100:0 to 4:1) to give 2-chloro-4-ethynyl-pyridine (1.427 g, 91percent) as an off-white solid. 1H-NMR (CDCl3, 300 MHz: δ 3.36 (s, 1H), 7.27 (dd, J=5 and 1 Hz, 2H), 7.40 (br s, 1H), 8.37 (d, J=8 Hz, 2H).
91%
Stage #1: With tetrabutyl ammonium fluoride In tetrahydrofuran at -78 - 0℃; for 0.75 h;
Stage #2: With water; ammonium chloride In tetrahydrofuran
b) Preparation of 2-chloro-4-ethynyl-pyridine:; To a solution of 2.389 g of 2-chloro-4-trimethylsilanylethynyl-pyridine (11.39 mmol) in THF (90 ml) were added 11.39 ml of a IM TBAF solution in THF at -780C and the reaction mixture was stirred for 45 min at O0C. Then saturated NH4Cl solution was added and the THF was removed under reduced pressure. The aqueous mixture was extracted with di- ethylether and the combined organic extracts were washed with water and brine, dried (Na2SO4), filtered and concentrated in vacuo. The remaining residue was purified by column chromatography (pentane/diethylether 100:0 to 4:1) to give 2-chloro-4-ethynyl- pyridine (1.427 g, 91percent) as an off-white solid. m-NMR (CDCl3, 300 MHz): δ 3.36 (s, IH), 7.27 (dd, J=5 and 1 Hz, 2H), 7.40 (br s, IH), 8.37 (d, J=8 Hz, 2H).
57.2% With tetrabutyl ammonium fluoride In tetrahydrofuran for 0.05 h; To a solution of 6(0.4g, I 9iminoi) in 10 mL THF was added IM TBAF over 3 minutes, TLC showed the starting material was consumed. The reaction mixture was then concentrated in vacuo. The crude product was purified by silica gel column chromatography to give product 7(0.15g. yield: 57.2 percent).LCMS: m/ i38(M+Hi.
References: [1] Patent: US2007/185058, 2007, A1, . Location in patent: Page/Page column 12.
[2] Patent: WO2007/90752, 2007, A1, . Location in patent: Page/Page column 30.
[3] Journal of Medicinal Chemistry, 2012, vol. 55, # 11, p. 5270 - 5290.
[4] Patent: WO2017/117708, 2017, A1, . Location in patent: Page/Page column 18.
[5] Chemical Communications, 2013, vol. 49, # 20, p. 2037 - 2039.
 

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