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Chemical Structure| 169335-50-6 Chemical Structure| 169335-50-6

Structure of 169335-50-6

Chemical Structure| 169335-50-6

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Product Details of [ 169335-50-6 ]

CAS No. :169335-50-6
Formula : C9H11ClN2O2
M.W : 214.65
SMILES Code : O=C(C1=NC=C(Cl)N=C1)OC(C)(C)C
MDL No. :MFCD18070852

Safety of [ 169335-50-6 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P330-P332+P313-P337+P313-P362-P403+P233-P405-P501

Application In Synthesis of [ 169335-50-6 ]

* 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.

  • Downstream synthetic route of [ 169335-50-6 ]

[ 169335-50-6 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 1196473-37-6 ]
  • [ 169335-50-6 ]
  • C16H17BN2O5 [ No CAS ]
  • 2
  • [ 2914-69-4 ]
  • [ 169335-50-6 ]
  • C13H16N2O3 [ No CAS ]
  • C13H12N2O3 [ No CAS ]
YieldReaction ConditionsOperation in experiment
To a solution of <strong>[2914-69-4](S)-(-)-3-butyn-2-ol</strong> (Alfa Aesar, 0,91 mL, 11.46 mmol) in THF (15 mL) was added potassium tert-butoxide (1.36 g, 12.11 mmol). The resulting solution was stirred at RT for 15 min and then a solution of tert-butyl 5-chloropyrazine-2- carboxylate (272A, 2.00 g, 9.32 mmol) in THF (20 mL) was added at 0 C. The mixture was gradually warmed to RT and stirred for 5 h. The reaction was quenched with sat. NH4Cl, and the mixture was then extracted with EtOAc. The organic layer was dried over Na2SO4 and concentrated in vacuo. The material thus obtained was purified by silica gel chromatography (0-50% EtOAc in heptane) to provide a mixture of the desired product 290A and trans-esterification product 290B as a colorless oil (1.35 g).
 

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