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The free base can be obtained as an oil by treatment of the hydrochloride with base. It co-crystallizes with one molecule of ether as white silky needles, (m.p. 24-25 °C) upon cooling etherial solutions. The free base melts at 39°C. It has a taste resembling that of chloral hydrate and leaves a sharp irritation for some time. Cinnoline derivatives are obtained from oxycinnolin carboxylic acid, which is formed by digesting orthophenyl propiolic acid diazo chloride with water. Oxycinnolin carboxylic acid on heating gives oxycinnoline, melting at 225 °C, which with phosphorus pentachloride gives chlorcinnolin. This substance is reduced by iron filings and sulfuric acid to dihydrocinnolin.
Discovery and synthesis
The compound was first obtained in impure form by cyclization of the alkyne o-C6H4(NH2)C≡CCO2H in water to give 4-hydroxycinnoline-3-carboxylic acid. This material could be decarboxylated and the hydroxyl group reductively removed to give the parent heterocycle. Improved methods exist for its synthesis. It can be prepared by dehydrogenation of dihydrocinnoline with freshly precipitated mercuric oxide. It can be isolated as the hydrochloride. 
Cinnolines are cinnoline derivatives. A classic organic reaction for synthesizing cinnolines is the Widman-Stoermer synthesis , a ring-closing reaction of an α-vinyl- aniline with hydrochloric acid and sodium nitrite:
The sodium nitrite is first converted to nitrous acid which then forms the electrophilic intermediate dinitrogen trioxide. The next intermediate is the stable Nitrosamine with goes on to lose water forming the diazonium salt which then reacts with the vinyl group in the ring-closing step. A conceptually related reaction is the Bamberger triazine synthesis towards triazines.
Other cinnoline methods are the Borsche cinnoline synthesis and the Richter cinnoline synthesis.
Cinnoline is toxic.
|This article is licensed under the GNU Free Documentation License. It uses material from the Wikipedia article "Cinnoline". A list of authors is available in Wikipedia.|