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Chemical Structure| 1267316-28-8 Chemical Structure| 1267316-28-8

Structure of 1267316-28-8

Chemical Structure| 1267316-28-8

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Product Details of [ 1267316-28-8 ]

CAS No. :1267316-28-8
Formula : C11H14N2O2
M.W : 206.24
SMILES Code : O=C1NC2=C(C=CC(OC)=C2)C(CN)C1
MDL No. :MFCD19370292

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Application In Synthesis of [ 1267316-28-8 ]

* 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 [ 1267316-28-8 ]

[ 1267316-28-8 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1567360-56-8 ]
  • [ 1267316-28-8 ]
YieldReaction ConditionsOperation in experiment
With hydrogen; triethylamine; In methanol; at 20.0℃; for 4.0h; Step E 4-(aminomethyl)-7-methoxy-3,4-dihydroquinolin-2(1H)-one 4-(aminomethyl)-7-methoxy-3,4-dihydroquinolin-2(1H)-one Crude 7-methoxy-2-oxo-l,2,3,4-tetraliydroquinoline-4-earbonitrile, prepared as described in Step D, (6 g, 0,03 mol) and Raney Ni (10 g) was suspended in a mixture of MeOH (100 mL) and 3 mL of triethylamine. The reaction mixture was stirred under H2 (50 Psi) atmosphere at room temperature for 4 h. After the reaction was completed by monitoring by TLC, the catalyst was filtered off, and then the solvent was removed in vacuo to afford the crude product which was used for next step without further purification.
With hydrogen; triethylamine; In methanol; at 20.0℃; under 2585.81 Torr; for 4.0h; Step E 4-(aminomethyl)-7-methoxy-3,4-dihydroquinolin-2(1H)-one (0205) (0206) Crude <strong>[1567360-56-8]7-methoxy-2-oxo-1,2,3,4-tetrahydroquinoline-4-carbonitrile</strong>, prepared as described in Step D, (6 g, 0.03 mol) and Raney Ni (10 g) was suspended in a mixture of MeOH (100 mL) and 3 mL of triethylamine. The reaction mixture was stirred under H2 (50 Psi) atmosphere at room temperature for 4 h. After the reaction was completed by monitoring by TLC, the catalyst was filtered off, and then the solvent was removed in vacuo to afford the crude product which was used for next step without further purification.
 

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