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Chemical Structure| 123792-59-6 Chemical Structure| 123792-59-6

Structure of 123792-59-6

Chemical Structure| 123792-59-6

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Product Details of [ 123792-59-6 ]

CAS No. :123792-59-6
Formula : C10H12N2O2
M.W : 192.21
SMILES Code : O=[N+](C1=CN=C2C(CCCCC2)=C1)[O-]
MDL No. :MFCD12405714

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Application In Synthesis of [ 123792-59-6 ]

* 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 [ 123792-59-6 ]

[ 123792-59-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 14150-94-8 ]
  • [ 502-42-1 ]
  • [ 123792-59-6 ]
YieldReaction ConditionsOperation in experiment
94% With ammonium acetate; In ethanol; at 65℃; for 24h; General procedure: To a solution of the dinitropyridone 1 (50 mg, 0.25 mmol) in EtOH (5 mL), cyclohexanone 4a (26 muL, 0.25 mmol) and NH4OAc (289 mg, 3.75 mmol) were added, and the resultant mixture was heated at 65 C on an oil bath for 24 h. After removal of the solvent, the residue was washed with benzene (3 × 10 mL) to afford 5,6,7,8-tetrahydro-3-nitroquinoline (5a; 42 mg, 0.24 mmol, 95%) as a yellow powder. The reactions of dinitropyridone 1 with other ketones 4b-g were performed in a similar way. When the reaction was conducted using microwave heating, the procedure was analogous.
91% With ammonia; In methanol;Heating / reflux; A mixture of 1-METHYL-3, 5-DINITRO-LH-PYRIDIN-2-ONE (16. 00 g, 80 mmol), cycloheptanone (9.95 mL, 84 mmol) and 20% ammonia solution in methanol (300 mL) was refluxed overnight. The solvent was evaporated, and the residue was dissolved in ethyl acetate. The soluble portion was concentrated and purified by flash chromatography (Hexane/Ethyl acetate 3: 1, silica gel) to yield the title compound (Yield: 14.00 g, 91%). 1H NMR (400 MHZ, CDCl3) : 8 9.05 (dd, 1H), 8.08 (dd, 1H), 3.10 (M, 2H), 2.90 (M, 2H), 1.90 (M, 2H), 1.70 (m, 4H).
 

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