66291-33-6Relevant academic research and scientific papers
Method for synthesizing 6-methyl phenanthridine compound
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Paragraph 0061; 0062; 0063; 0065-0067; 0069-0071, (2019/03/26)
The present invention provides a method for synthesizing a 6-methyl phenanthridine compound. The method is as below: using a substituted azide terminal alkene compound represented by a formula I as astarting material, conducting a reaction in an organic solvent under the action of a copper catalyst and an oxidizing agent at 60 to 100 DEG C for 8 to 16 hours, and conducting post-treatment on the obtained reaction solution to obtain 6-methyl phenanthridine represented by a formula II and derivatives thereof, wherein the mass ratio of the substituted azide terminal alkene compound represented bythe formula I, the copper catalyst and the oxidizing agent is 1:(0.11-0.3):(1-3). The method of the present invention is safe and environmentally friendly, and does not generate waste water; the substrate has good adaptability and various substituents can be aromatized/methylated; the reaction conditions are mild, and the reaction can be carried out at a lower temperature; the raw materials do not need to be aromatized or methylated in advance; the reaction steps are simple; therefore, the method is a new route for synthesis of various 6-methyl phenanthridines containing substituents.
Dihydroaromatic boronic esters as building blocks for the synthesis of phenanthrenes and phenanthridines
Hilt, Gerhard,Hess, Wilfried,Schmidt, Frank
, p. 2526 - 2533 (2007/10/03)
Alkenyl-substituted dihydroaromatic boronic esters, generated by neutral cobalt(I)-catalysed Diels-Alder reactions, reacted under palladium catalysis conditions with diiodobenzene, bromoiodobenzene and iodoaniline derivatives for the synthesis of regioselectively substituted phenanthrene and phenanthridine derivatives. Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2005.
