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Chemical Structure| 133261-10-6 Chemical Structure| 133261-10-6

Structure of 133261-10-6

Chemical Structure| 133261-10-6

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Product Details of [ 133261-10-6 ]

CAS No. :133261-10-6
Formula : C11H18N2O2
M.W : 210.27
SMILES Code : O=C(C1=CC(C(C)(C)C)=NN1C)OCC
MDL No. :MFCD00085059

Safety of [ 133261-10-6 ]

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

Application In Synthesis of [ 133261-10-6 ]

* 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 [ 133261-10-6 ]

[ 133261-10-6 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 13395-36-3 ]
  • [ 60-34-4 ]
  • [ 133261-10-6 ]
  • [ 194289-30-0 ]
  • 2
  • [ 13395-36-3 ]
  • [ 60-34-4 ]
  • [ 133261-10-6 ]
YieldReaction ConditionsOperation in experiment
In ethanol; at 20 - 80℃; Step A: 5-tert-Butyl-2-methyl-2H-pyrazole-3-carboxylic acid ethyl ester Ethyl 5,5-dimethyl-2,4-dioxo-hexanoate (1.02 g, 5.09 mmol) was dissolved in absolute EtOH (20 mL). CH3NHNH2 (0.270 mL, 5.09 mmol) was added dropwise and the resulting mixture was stirred at room temperature for 2 h. The resulting mixture was warmed to 80 C. for 4 h, and then cooled to room temperature. The solvent was removed under reduced pressure, and the resulting residue was chromatographed using a 70-g pre-packed SiO2 column eluting with 1:19 EtOAc-hexanes to yield the title compound as a colorless oil. 1H-NMR (400 MHz, CDCl3) delta: 6.68 (s, 1H), 4.33 (q, J=7.2 Hz, 2H), 4.12 (s, 3H), 1.38 (t, J=7.1 Hz, 3H), 1.30 (s, 9H).
In ethanol; at 20 - 80℃; Ethyl 5,5-dimethyl-2,4-dioxo-hexanoate (1.02 g, 5.09 mmol) was dissolved in absolute EtOH (20 mL). CH3NHNH2 (0.270 mL, 5.09 mmol) was added dropwise and the resulting mixture was stirred at room temperature for 2 h. The resulting mixture was warmed to 80 C. for 4 h, and then cooled to room temperature. The solvent was removed under reduced pressure, and the resulting residue was chromatographed using a 70-g pre-packed SiO2 column eluting with 1:19 EtOAc-hexanes to yield a residue. 1H-NMR (400 MHz, CDCl3) delta: 6.68 (s, 1H), 4.33 (q, J=7.2 Hz, 2H), 4.12 (s, 3H), 1.38 (t, J=7.1 Hz, 3H), 1.30 (s, 9H).
 

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