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Chemical Structure| 117423-41-3 Chemical Structure| 117423-41-3

Structure of 117423-41-3

Chemical Structure| 117423-41-3

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Product Details of [ 117423-41-3 ]

CAS No. :117423-41-3
Formula : C12H21NOSi
M.W : 223.39
SMILES Code : C[Si](OCC1=CC=NC=C1)(C(C)(C)C)C
MDL No. :MFCD07368892

Safety of [ 117423-41-3 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H227-H302-H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of [ 117423-41-3 ]

* 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 [ 117423-41-3 ]

[ 117423-41-3 ] Synthesis Path-Downstream   1~5

  • 1
  • [ 116332-54-8 ]
  • [ 117423-41-3 ]
  • [ 152122-41-3 ]
YieldReaction ConditionsOperation in experiment
Step 1-A 1-(4-Fluorophenyl)-2-hydroxy-2-pyridin-4-yl-ethanone tert-butyldimethylsilyl ether To a stirring solution of diisopropyl amine (0.42 mol, 42.5 g) in THF (400 mL) cooled to -78C was added n-butyl lithium (0.42 mol, 263 mL of a 1.6M solution in hexanes). The reaction was warmed to -20C and 4-pyridyl carbinol tert-butyldimethylsilyl ether (0.32 mol, 67.0 g) was added in THF (100 mL). The reaction was stirred at -20C for 0.5 h. and the 4-fluorophenyl-N,O-dimethyl benzhydroxamide was added and the solution was stirred at -20C for 0.5 h. The reaction was diluted with I L saturated aqueous sodium hydrogen carbonate, the phases were separated and the aqueous layer was extracted with ethyl acetate (2x200mL). The combined organic layers were washed with brine, dried over anhydrous sodium sulfate and evaporated under reduced pressure. The residue was chromatographed over silica, eluding with 20% EtOAc:Hexanes. The pure fractions were combined and evaporated under reduced pressure to give 74.65 g of a pale orange oil. 1H NMR (CDCl3) d 8.59 (d,J=6.1Hz,2H), 8.03 (dd,J=8.8 and 5.5Hz,2H), 7.45 (d,J=5.6Hz,2H), 7.00 (t,J=8.8Hz,1H), 5.60 (s,1H), 0.899 (s,9H), 0.112 (s,3H), -0.011 (s,3H)
  • 4
  • [ 116332-54-8 ]
  • [ 117423-41-3 ]
  • 6‑amino‑2‑(4‑fluorophenyl)‑4‑benzyloxy‑3‑(4‑pyridyl)‑1H-pyrrolo[2,3‑b]pyridine [ No CAS ]
  • 5
  • [ 117423-41-3 ]
  • [ 923169-37-3 ]
 

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