92437-12-2Relevant academic research and scientific papers
Studies with enaminonitriles: Synthesis and chemical reactivity of 2-phenyl-3-piperidin-1-yl acrylonitrile under microwave heating
Salaheldin, Abdellatif M.,Alphy, Maryana K.
, p. 307 - 310 (2008/09/20)
(Chemical Equation Presented) Benzyl cyanide reacts with triethylorthoformate and piperidine in DMF solution to yield the title compound 2. This reacted with aromatic amines to yield either aminoacrylonitriles orquinoline depending on reaction conditions and substitution pattern on the aromatic amine. The reaction of compound 2 with hydrazine hydrate could only be effected in the microwave oven and resulted in the formation of aminopyrazole 7. Diazotization of 7 and coupling with an active methylene reagent afforded pyrazolo[5,1-c]-[1,2,4]triazine derivatives.
Synthetic Routes to Arylpyrido-azepines and -azepines.
Schofield, Joseph,Smalley, Robert K.,Scopes, David I. C.,Patel, Dalpat I.
, p. 1401 - 1426 (2007/10/02)
9-Phenyl-6-methoxy-5H-pyridoazepine and 9-phenyl-7-methoxy-5H-pyridoazepine have been obtained by arylation (PhLi) of 6,9-dimethoxy-5H-pyridoazepine and by photolysis of 6-azido-9-phenylquinoline in potassium methoxide-methanol-dioxan
