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Chemical Structure| 78301-07-2 Chemical Structure| 78301-07-2

Structure of 78301-07-2

Chemical Structure| 78301-07-2

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Product Details of [ 78301-07-2 ]

CAS No. :78301-07-2
Formula : C4H4Cl2N2O
M.W : 166.99
SMILES Code : O=C(Cl)C1=CNC=N1.[H]Cl
MDL No. :MFCD09910327

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Application In Synthesis of [ 78301-07-2 ]

* 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 [ 78301-07-2 ]

[ 78301-07-2 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1072-84-0 ]
  • [ 78301-07-2 ]
YieldReaction ConditionsOperation in experiment
100% With oxalyl dichloride;N,N-dimethyl-formamide; at 20℃; for 1.5h;Heating / reflux; Step 1: To a 10 mL solution of oxalyl chloride was added 4-imidazolecarboxylic acid (1.0 g, 8.92 mmol) at room temperature, followed by 2 drops of dimethylformamide. The mixture was heated to reflux for 90 minutes, then cooled to room temperature. Following removal of the solvent by evaporation, toluene was added and evaporated to dryness twice to provide 1.49 g of imidazole-4-carbonyl chloride hydrochloride in quantitative yield as a yellow solid. This was used in the subsequent step without purification.
94% With thionyl chloride; for 72h;Heating / reflux; 1H-Imidazole-4-carbonyl Chloride Hydrochloride As suggested by Moss, et al J. Amer. Chem. Soc., 109, 6209-6210 (1987), a suspension of 1 H-<strong>[1072-84-0]imidazole-4-carboxylic acid</strong> (575 mg, 5. 13 MMOL) in thionyl chloride (25 ml) was heated at reflux for 3 days. The solution was allowed to cool to ambient temperature and concentrated in vacuo to afford 800 mg of yellow powder in 94percent yield, which was used without further purification. H NMR (DMSO-d6) : 5 8. 86 (s, 1 H), 8. 22 (s, 1 H)
 

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