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Chemical Structure| 1154030-58-6 Chemical Structure| 1154030-58-6

Structure of 1154030-58-6

Chemical Structure| 1154030-58-6

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Product Details of [ 1154030-58-6 ]

CAS No. :1154030-58-6
Formula : C8H9N3O2
M.W : 179.18
SMILES Code : O=C(OCC)CN1C=C(C#N)N=C1
MDL No. :MFCD21336506

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Application In Synthesis of [ 1154030-58-6 ]

* 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 [ 1154030-58-6 ]

[ 1154030-58-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 105-36-2 ]
  • [ 57090-88-7 ]
  • [ 1154030-58-6 ]
YieldReaction ConditionsOperation in experiment
60% With sodium ethanolate; In ethanol; at 20℃; for 16h; 3.3 g (35.3 mmol) <strong>[57090-88-7]1H-<strong>[57090-88-7]imidazole-4-carbonitrile</strong></strong> [Matthews et al., J. Org. Chem. 1986, 51, 3228-3231] are initially introduced into 13.2 ml (11.5 g, 35.3 mmol) 21percent strength sodium ethylate solution in ethanol and 4.3 ml (6.5 g, 38.9 mmol) ethyl bromoacetate are added. The reaction mixture is stirred at RT for 16 h. For working up, the solid which has precipitated out is filtered off, the residue on the filter is washed with ethanol and the filtrate is concentrated in vacuo. Diisopropyl ether is added to the residue, the mixture is filtered again, the filtrate is concentrated again on a rotary evaporator and the residue is dried in vacuo.Yield: 3.8 g (60percent of th.)LC-MS (Method 1): Rt=1.17 min; MS (ESIpos): m/z=180 [M+H]+;1H-NMR (400 MHz, DMSO-d6): delta=8.12 (s, 1H), 7.88 (s, 1H), 5.06 (s, 2H), 4.18 (q, 2H), 1.22 (t, 3H).
In ethanol; sodium ethanolate; Example 1A Ethyl (4-cyano-1H-imidazol-1-yl)acetate 3.3 g (35.3 mmol) of <strong>[57090-88-7]1H-<strong>[57090-88-7]imidazole-4-carbonitrile</strong></strong> [Matthews et al., J. Org. Chem. 1986, 51, 3228-3231] are initially charged in 13.2 ml (11.5 g, 35.3 mmol) of 21percent strength sodium ethoxide solution in ethanol, and 4.3 ml (6.5 g, 38.9 mmol) of ethyl bromoacetate are added. The reaction mixture is stirred at RT for 16 h. For work-up, the precipitated solid is filtered off, the filter residue is washed with ethanol and the filtrate is concentrated under reduced pressure. Diisopropyl ether is added to the residue, the mixture is filtered again, the filtrate is once more concentrated on a rotary evaporator and the residue is dried under reduced pressure. Yield: 3.8 g (60percent of theory) LC-MS (Method 1): Rt=1.17 min; MS (ESIpos): m/z=180 [M+H]+; 1H-NMR (400 MHz, DMSO-d6): delta=8.12 (s, 1H), 7.88 (s, 1H), 5.06 (s, 2H), 4.18 (q, 2H), 1.22 (t, 3H).
 

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