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Chemical Structure| 1567360-55-7 Chemical Structure| 1567360-55-7

Structure of 1567360-55-7

Chemical Structure| 1567360-55-7

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Product Details of [ 1567360-55-7 ]

CAS No. :1567360-55-7
Formula : C13H14N2O5
M.W : 278.27
SMILES Code : O=C(OCC)CC(C#N)C1=CC=C(OC)C=C1[N+]([O-])=O

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Application In Synthesis of [ 1567360-55-7 ]

* 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 [ 1567360-55-7 ]

[ 1567360-55-7 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 1567360-55-7 ]
  • [ 144-55-8 ]
  • [ 1567360-56-8 ]
YieldReaction ConditionsOperation in experiment
With hydrogenchloride; In methanol; ethyl acetate; Step D 7-methoxy-2-oxo-1,2,3,4-tetrahydroquinoline-4-carbonitrile To a solution of ethyl 3-cyano-3-(4-methoxy-2-nitrophenyl)propanoate, prepared as described in Step C, (9.0 g, 0.032 mol) in MeOH (100 mL), Sn (19.3 g, 0.162 mol) was added, followed by hydrochloric acid/MeOH (40 ml, 1:1) all at once. The reaction was stirred at room temperature for 2 h. The solvent was removed in vacuo. Then ethyl acetate was added, and aqueous NaHCO3 solution was added to neutralize the solution. The organic phase was concentrated to get crude product which was used for next step without further purification.
  • 2
  • [ 1567360-55-7 ]
  • [ 1567360-56-8 ]
YieldReaction ConditionsOperation in experiment
With hydrogenchloride; tin; In methanol; water; at 20.0℃; for 2.0h; Step D 7-methoxy-2-oxo-1,2,3,4-tetrahydroquinoline-4-carbonitrile To a solution of ethyl 3-cyano-3-(4-methoxy-2-nitrophenyl)propanoate, prepared as described in Step C, (9.0 g, 0.032 mol) in MeOH (100 mL), Sn (19.3 g, 0.162 mol) was added, followed by hydrochloric acid/MeOH (40 ml, 1 : 1) all at once. The reaction was stirred at room temperature for 2 h. The solvent was removed in vacuo. Then ethyl acetate was added, and aqueous NaHCO3 solution was added to neutralize the solution. The organic phase was concentrated to get crude product which was used for next step without further purification.
With hydrogenchloride; tin; In methanol; at 20.0℃; for 2.0h; Step D 7-methoxy-2-oxo-1,2,3,4-tetrahydroquinoline-4-carbonitrile (0203) (0204) To a solution of ethyl 3-cyano-3-(4-methoxy-2-nitrophenyl)propanoate, prepared as described in Step C, (9.0 g, 0.032 mol) in MeOH (100 mL), Sn (19.3 g, 0.162 mol) was added, followed by hydrochloric acid/MeOH (40 ml, 1:1) all at once. The reaction was stirred at room temperature for 2 h. The solvent was removed in vacuo. Then ethyl acetate was added, and aqueous NaHCO3 solution was added to neutralize the solution. The organic phase was concentrated to get crude product which was used for next step without further purification.
 

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