105224-25-7Relevant academic research and scientific papers
Fused tricyclic compound and application in medicines
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Paragraph 0352-0357, (2020/06/17)
The invention relates to a condensed tricyclic compound and application in medicines, particularly to application of the condensed tricyclic compound as a medicine for treating and/or preventing hepatitis B. Specifically the present invention relates to a
Process for the preparation of substituted pyrimidine derivatives
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Page/Page column 21, (2010/02/16)
The present invention is directed to processes for the preparation of substituted pyrimidine derivatives, useful as intermediates in the synthesis of histamine H4 receptor modulators, and to intermediates in H4 modulator synthesis.
First synthesis of 5-cyanosalicylates by formal [3+3] Cyclocondensations of 1,3-Bis(silyloxy)-1,3-butadienes
Riahi, Abdolmajid,Fatunsin, Olumide,Shkoor, Mohanad,Dede, Ruediger,Reinke, Helmut,Fischer, Christine,Langer, Peter
experimental part, p. 1623 - 1634 (2009/12/10)
A variety of functionalized benzonitriles were regioselectively prepared by formal [3+3] cyclocondensation of 1,3-bis(silyloxy)-1,3-butadienes with 3-ethoxy- and 3-silyloxy-2-cyano-2-en-1-ones. Georg Thieme Verlag Stuttgart.
First synthesis of functionalized benzonitriles by formal [3+3] cyclocondensations of 1,3-bis(silyloxy)buta-1,3-dienes
Fatunsin, Olumide,Shkoor, Mohanad,Riahi, Abdolmajid,Dede, Rüdiger,Reinke, Helmut,Langer, Peter
body text, p. 201 - 204 (2009/06/05)
A variety of functionalized benzonitriles were regioselectively prepared by formal [3+3] cyclocondensation of 1,3-bis(silyloxy) buta-1,3-dienes with 3-ethoxy- and 3-silyloxy-2-cyano-2-en-1-ones. Georg Thieme Verlag Stuttgart.
4-AMINOETHYLENE DERIVATIVES OF 2-METHYLBENZOTRIAZOLE
Milata, Viktor,Ilavsky, Dusan,Goljer, Igor,Lesko, Jan,Chahinian, Marc,Henry-Basch, Erica
, p. 1038 - 1048 (2007/10/02)
N-Methylation of 4(7)-nitrobenzotriazole (I) afforded a mixture of three isomers; one of them, 4-nitro-2-methylbenzotriazole (II) could easily be isolated.Catalytical hydrogenation of II led to the corresponding amine which in turn, afforded products of nucleophilic substitution IVa-IVi on reaction with alkoxymethylene derivatives IIIa - IIIi.Thermal cyclocondensation of IVi yielded 7-ethoxycarbonyl-6,9-dihydro-6-oxo-2-methyl-2H-triazoloquinoline (V).The structure of all products was deduced from the IR, UV, 1H and 13C NMR spectral data.
