Azirine

Azirine
Names
	IUPAC name 2H-Azirine
Identifiers
CAS Number	157-16-4;
3D model (JSmol)	Interactive image;
Beilstein Reference	1633516
ChEBI	CHEBI:30971;
ChemSpider	119750;
PubChem CID	135972;
	InChI InChI=1S/C2H3N/c1-2-3-1/h1H,2H2 Key: NTJMGOWFGQXUDY-UHFFFAOYSA-N;
	SMILES C1C=N1;
Properties
Chemical formula	C2H3N
Molar mass	41.053 g·mol−1
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
	Infobox references

Azirines are three-membered heterocyclic unsaturated (i.e. they contain a double bond) compounds containing a nitrogen atom and related to the saturated analogue aziridine.^[1] They are highly reactive yet have been reported in a few natural products such as Dysidazirine. There are two isomers of azirine: 1H-Azirines with a carbon-carbon double bond are not stable and rearrange to the tautomeric 2H-azirine, a compound with a carbon-nitrogen double bond. 2H-Azirines can be considered strained imines and are isolable.

Preparation

2H-Azirine is most often obtained by the thermolysis of vinyl azides.^[2] During this reaction, a nitrene is formed as an intermediate. Alternatively, they can be obtained by oxidation of the corresponding aziridine. Azirine can be generated during photolysis of isoxazole.^[3] Due to the weak N-O bond, the isoxazole ring tends to collapse under UV irradiation, rearranging to azirine. ^[4]

Substituted azirines can be produced via the Neber rearrangement.

Reactions

Photolysis of azirines (under 300 nm) is a very efficient way to generate nitrile ylides. These nitrile ylides are dipolar compounds and can be trapped by a variety of dipolarophiles to yield heterocyclic compounds, e.g. pyrrolines.

The strained ring system also undergoes reactions that favor ring opening and can act as a nucleophile or an electrophile.

Azirines readily hydrolyse to give aminoketones which are themselves susceptible to self-condensation.

References

↑ Teresa M. V. D. Pinho e Melo and Antonio M. d’A. Rocha Gonsalves (2004). "Exploiting 2-Halo-2H-Azirine Chemistry". Current Organic Synthesis 1 (3): 275–292. doi:10.2174/1570179043366729. http://www.bentham.org/cos/contabs/cos1-3.htm#5.
↑ "2H-Azirines as synthetic tools in organic chemistry". Eur. J. Org. Chem. 2001 (13): 2401–2414. 2001. doi:3.0.CO;2-U">10.1002/1099-0690(200107)2001:13<2401::AID-EJOC2401>3.0.CO;2-U.
↑ Edwin F. Ullman (1966). "Photochemical Transposition of Ring Atoms in Five-Membered Heterocycles. The Photorearrangement of 3,5-Diphenylisoxazole". J. Am. Chem. Soc. 88 (8): 1844–1845. doi:10.1021/ja00960a066.
↑ Cheng, K.; Qi, J.; Ren, X.; Zhang, J.; Li, H.; Xiao, H.; Wang, R.; Liu, Z. et al. (2022). "Developing Isoxazole as a Native Photo-Cross-Linker for Photoaffinity Labeling and Chemoproteomics.". Angew. Chem. Int. Ed. 61 (47): e202209947. doi:10.1002/anie.202209947.

0.00

(0 votes)

Original source: https://en.wikipedia.org/wiki/Azirine. Read more

[1] Teresa M. V. D. Pinho e Melo and Antonio M. d’A. Rocha Gonsalves (2004). "Exploiting 2-Halo-2H-Azirine Chemistry". Current Organic Synthesis 1 (3): 275–292. doi:10.2174/1570179043366729. http://www.bentham.org/cos/contabs/cos1-3.htm#5.

[2] "2H-Azirines as synthetic tools in organic chemistry". Eur. J. Org. Chem. 2001 (13): 2401–2414. 2001. doi:3.0.CO;2-U">10.1002/1099-0690(200107)2001:13<2401::AID-EJOC2401>3.0.CO;2-U.

[3] Edwin F. Ullman (1966). "Photochemical Transposition of Ring Atoms in Five-Membered Heterocycles. The Photorearrangement of 3,5-Diphenylisoxazole". J. Am. Chem. Soc. 88 (8): 1844–1845. doi:10.1021/ja00960a066.

[4] Cheng, K.; Qi, J.; Ren, X.; Zhang, J.; Li, H.; Xiao, H.; Wang, R.; Liu, Z. et al. (2022). "Developing Isoxazole as a Native Photo-Cross-Linker for Photoaffinity Labeling and Chemoproteomics.". Angew. Chem. Int. Ed. 61 (47): e202209947. doi:10.1002/anie.202209947.

Azirine

Contents

Preparation

Reactions

See also

References