Misplaced Pages

Cinnoline

Article snapshot taken from Wikipedia with creative commons attribution-sharealike license. Give it a read and then ask your questions in the chat. We can research this topic together.

This is an old revision of this page, as edited by DavidBrooks-AWB (talk | contribs) at 15:42, 17 March 2022 (EB1911 attribution). The present address (URL) is a permanent link to this revision, which may differ significantly from the current revision.

Revision as of 15:42, 17 March 2022 by DavidBrooks-AWB (talk | contribs) (EB1911 attribution)(diff) ← Previous revision | Latest revision (diff) | Newer revision → (diff) Chemical compound
Cinnoline
Cinnoline molecule
C=black, H=white, N=blue
Cinnoline molecule
C=black, H=white, N=blue
Names
Preferred IUPAC name Cinnoline
Other names Benzopyridazine
Identifiers
CAS Number
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard 100.005.423 Edit this at Wikidata
PubChem CID
UNII
CompTox Dashboard (EPA)
InChI
  • InChI=1S/C8H6N2/c1-2-4-8-7(3-1)5-6-9-10-8/h1-6HKey: WCZVZNOTHYJIEI-UHFFFAOYSA-N
  • InChI=1/C8H6N2/c1-2-4-8-7(3-1)5-6-9-10-8/h1-6HKey: WCZVZNOTHYJIEI-UHFFFAOYAA
SMILES
  • n1nccc2ccccc12
Properties
Chemical formula C8H6N2
Molar mass 130.150 g·mol
Melting point 39 °C (102 °F; 312 K)
Acidity (pKa) 2.64
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). checkY verify (what is  ?) Infobox references
Chemical compound

Cinnoline is an aromatic heterocyclic compound with the formula C8H6N2. It is isomeric with other naphthyridines including quinoxaline, phthalazine and quinazoline.

Properties

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 ethereal 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 oxycinnoline carboxylic acid, which is formed by digesting orthophenyl propiolic acid diazo chloride with water. Oxycinnoline carboxylic acid on heating gives oxycinnoline, melting at 225 °C, which with phosphorus pentachloride gives chlorcinnoline. This substance is reduced by iron filings and sulfuric acid to dihydrocinnoline.

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. This reaction is called the Richter cinnoline synthesis. 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:

Widman–Stoermer reaction
Widman–Stoermer reaction

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.

Another cinnoline method is the Borsche cinnoline synthesis.

Safety

Cinnoline is toxic.

See also

References

  1. International Union of Pure and Applied Chemistry (2014). Nomenclature of Organic Chemistry: IUPAC Recommendations and Preferred Names 2013. The Royal Society of Chemistry. p. 212. doi:10.1039/9781849733069. ISBN 978-0-85404-182-4.
  2. Brown, H.C., et al., in Baude, E.A. and Nachod, F.C., Determination of Organic Structures by Physical Methods, Academic Press, New York, 1955.
  3.  One or more of the preceding sentences incorporates text from a publication now in the public domain: Chisholm, Hugh, ed. (1911). "Cinnolin". Encyclopædia Britannica. Vol. 6 (11th ed.). Cambridge University Press. p. 377.
  4. Victor von Richter (1883). "Über Cinnolinderivate". Chemische Berichte. 16: 677–683. doi:10.1002/cber.188301601154.
  5. Parrick, J.; Shaw, C. J. G.; Mehta, L. K. (2000). "Pyridazines, cinnolines, benzocinnolines and phthalazines". Rodd's Chemistry of Carbon Compounds. Vol. 4 (2nd ed.). pp. 1–69.
  6. Bradford P. Mundy; Michael G. Ellerd; Frank G. Jr. Favaloro (2005). Name Reactions and Reagents in Organic Synthesis. ISBN 0-471-22854-0.
Categories:
Cinnoline Add topic