87604-94-2Relevant academic research and scientific papers
Open-chain nitrogen compounds. Part VIII. 1-(2'-Acetylphenyl)-3-alkyltriazenes with reactive substituents in the alkyl group: synthons for five- and six-membered nitrogen heterocycles
Vaughan, Keith,LaFrance, Ronald J.,Tang, York,Hooper, Donald L.
, p. 2455 - 2461 (2007/10/02)
The synthesis of a series of 1-(2'-acetylphenyl)-3-alkyltriazenes, with electron-withdrawing α-substituents in the alkyl moiety, is described.The structure of the products from the reaction of 2-acetylbenzenediazonium ion (1) with methylamine has been reinvestigated using high field (360 MHz) nmr spectroscopy.The 2-acetylphenyltriazenes undergo cyclization to five- or six-membered heterocycles, depending on the substituent present in the alkyl group.Attack by N-3 of the triazene on the ortho-acetyl group leads to a 4-methylenetriazine, which can undergo oxidation to a benzotriazinone or acid-catalysed rearrangement to a 4-alkylaminocinnoline.The reaction of 1 with alkylamines also affords red products, which have been identified as 4-arylazomethylenetriazines and fully characterized by 1H and 13C nmr spectroscopy.The formation of these azo compounds is consistent with the enamine character of the 4-methylenetriazines.The introduction of a CO2Et group at the α-position of the alkyl moiety provides a competing cyclization pathway to give a five-membered heterocycle, a 5-hydroxytriazole.In this case the cyclization pathway to the six-membered heterocycle is favoured, whereas the introduction of a CN group can lead to exclusive triazole formation.The reaction of the nitrile (2c) with alumina in chloroform leads to a new heterocycle, a quinazolinotriazole; in DMSO solution, 2c prefers the alternative pathway and gives only the 3-cyanomethyl-4-methylenetriazine.Introduction of a benzoyl group in the alkyl moiety gives an unstable triazene; it reacts with alumina in chloroform to give a triazole, which in turn rearranges to a novel diazoalkane.
Open-chain nitrogen compounds. Part IV. Synthesis of 5-hydroxy-1,2,3-triazoles from 1-aryl-3-(ethoxycarbonylmethyl)triazenes: a new route to α-diazo-N-arylacetamides
Baines, Kim M.,Vaughan, Keith,Hooper, Donald R.,Leveck, Lorne F.
, p. 1549 - 1556 (2007/10/02)
A series of triazenes of type ArN=N-NH-CH2CO2Et, N-arylazoglycine ethyl esters, have been prepared by coupling the arene diazonium salt, ArN2+*X-, with ethyl glycinate, NH2CH2CO2Et; an electron-withdrawing substituent, e.g.NO2, CN, CO2R, and Cl, in the ortho or para position of the aryl group is essential for efficient coupling.The p-substituted arylazoglycine ethyl esters cyclize when treated with alcoholic potassium hydroxide to afford the potassium salts of the 1-aryl-5-hydroxy-1,2,3-triazoles, which can be obtained free by acidification of the potassium salt solution with acetic acid.Reaction of the potassium salts with acetic anhydride yields the 1-aryl-5-acetoxy-1,2,3-triazoles.The 5-hydroxytriazoles, when heated in ethanol, rearrange to α-diazoacetanilides, ArNH*COCHN2.The diazoamides can be obtained in low yield directly from the triazenes by prolonged refluxing in ethanol. o-Substituted aryltriazenes do not cyclize under the same conditions but fragment to the arylamine.
