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Chemical Structure| 1005788-29-3 Chemical Structure| 1005788-29-3

Structure of 1005788-29-3

Chemical Structure| 1005788-29-3

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Product Details of [ 1005788-29-3 ]

CAS No. :1005788-29-3
Formula : C8H12N2O3
M.W : 184.19
SMILES Code : O=C(C1=CC(OCC)=NN1C)OC

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Application In Synthesis of [ 1005788-29-3 ]

* 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 [ 1005788-29-3 ]

[ 1005788-29-3 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 75-03-6 ]
  • [ 52867-42-2 ]
  • [ 1005788-29-3 ]
YieldReaction ConditionsOperation in experiment
94% With potassium carbonate; In N,N-dimethyl-formamide; Reference Example 59 Production of methyl 3-ethoxy-1-methyl-1H-pyrazole-5-carboxylate Using <strong>[52867-42-2]methyl 3-hydroxy-1-methyl-1H-pyrazole-5-carboxylate</strong> (2.34 g, 15.0 mmol), iodoethane (3.51 g, 22.5 mmol), potassium carbonate (4.15 g, 30.0 mmol) and N,N-dimethylformamide (15 mL), and in the same manner as in Reference Example 57, the title compound (2.59 g, yield 94%) was obtained. 1H-NMR (DMSO-d6, 300 MHz) delta 1.28 (3H, t, J=7.0 Hz), 3.81 (3H, s), 3.93 (3H, s), 4.10 (2H, q, J=7.0 Hz), 6.25 (1H, s).
94% With potassium carbonate; In N,N-dimethyl-formamide; at 50℃; for 16h; To a stirred suspension of methyl 5-hydroxy-2-methyl-pyrazole-3-carboxylate (3.00 g, 19.0 mmol) and K2CO3 (2.90 g, 21.0 mmol) in DMF (19 mL) at room temperature was added iodoethane (1.71 mL, 21.0 mmol) and the reaction mixture stirred at 50 C for 16 h. The reaction mixture was diluted with water (190 mL) and the aqueous layer extracted with ethyl acetate (3 x 100 mL). The combined organic layers were washed with water (2 x 100 mL), passed through a phase separator and concentrated in vacuo. The crude material was purified by flash chromatography [EtOAc/isohexanes (0-50%)] to afford the title compound (3.33 g, 94% Yield) as a colourless oil. 6H (300 MHz, d-Chloroform) 6.17 (s, 1H), 4.16 (q, J = 7.1 Hz, 2H), 4.03 (s, 3H), 3.86 (s, 3H), 1.38 (t, J = 7.1 Hz, 3H).
 

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