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2-Imidazoline
Skeletal formula of imidazoline
Ball-and-stick model of the imidazoline molecule
Names
Preferred IUPAC name
4,5-Dihydro-1H-imidazole
Systematic IUPAC name
1,3-Diazacyclopent-2-ene
Other names
2-Imidazoline
4,5-Dihydro-1,3-diazole
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
ECHA InfoCard 100.007.273 Edit this at Wikidata
UNII
  • InChI=1S/C3H6N2/c1-2-5-3-4-1/h3H,1-2H2,(H,4,5) checkY
    Key: MTNDZQHUAFNZQY-UHFFFAOYSA-N checkY
  • InChI=1/C3H6N2/c1-2-5-3-4-1/h3H,1-2H2,(H,4,5)
    Key: MTNDZQHUAFNZQY-UHFFFAOYAB
  • N\1=C\NCC/1
Properties
C3H6N2
Molar mass 70.095 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
checkY verify (what is checkY☒N ?)

2-Imidazoline (Preferred IUPAC name: 4,5-dihydro-1H-imidazole) is one of three isomers of the nitrogen-containing heterocycle imidazoline, with the formula C3H6N2. The 2-imidazolines are the most common imidazolines commercially, as the ring exists in some natural products and some pharmaceuticals. They also have been examined in the context of organic synthesis, coordination chemistry, and homogeneous catalysis.[1]

Synthesis[edit]

Synthesis of imidazolines from nitrile and from ester precursors.

A variety of routes exist for the synthesis of imidazolines,[1][2] with the most common methods involving the condensation of 1,2-diamines (e.g. ethylenediamine) with nitriles or esters. The nitrile based route is essentially a cyclic Pinner reaction; it requires high temperatures and acid catalysis and is effective for both alkyl and aryl nitriles.

As natural products[edit]

Imidazoline has been found in various natural products. Natural molecules topsentin D and spongotine B were discovered in several marine sponges. These metabolites have received considerable attention because of their potent properties such as antitumor, antiviral, and anti-inflammatory activities.[3]

Biological role[edit]

Many imidazolines are biologically active.[4] Most bio-active derivatives bear a substituent (aryl or alkyl group) on the carbon between the nitrogen centers. Some generic names include oxymetazoline, xylometazoline, tetrahydrozoline, and naphazoline.

Applications[edit]

Pharmaceutical[edit]

2-imidazolines have been investigated as antihyperglycemic, anti-inflammatory, antihypertensive, antihypercholesterolemic, and antidepressant reagents.[1][5] The imidazoline-containing drug clonidine is used alone or in combination with other medications to treat high blood pressure. It is also used in the treatment of dysmenorrhea, hypertensive crisis, Tourette's syndrome and attention deficit hyperactivity disorder (ADHD).[6]

  • 2-Imidazolines
  • Clonidine
    Clonidine
  • Biimidazoline ligands and a complex.
    Biimidazoline ligands and a complex.
  • Second generation Grubbs' catalyst
    Second generation Grubbs' catalyst
  • Spongotine B
    Spongotine B

As p53 activators[edit]

Cis-imidazolines act as small-molecule antagonists of MDM2. These compounds bind MDM2/X in the p53-binding pocket and activate the p53 pathway in cancer cells, leading to cell cycle arrest, apoptosis, and growth inhibition of human tumor xenografts in nude mice. The most active compounds are nutlin-3a[7] and rg-7112,[8] but some other analogs also activate p53.[9][10][11]

Surfactants[edit]

Surfactants based around 2-imidazoline, such as sodium lauroamphoacetate, are used in personal care products where mildness and non-irritancy are particularly important (e.g. baby products, "no more tears" shampoos etc.).[12]

As precursors of imidazoles[edit]

Imidazoles can be prepared from dehydrogenation of imidazolines.[13]

Homogeneous catalysis[edit]

As a structural analogue of 2-oxazolines, 2-imidazolines have been developed as ligands in coordination chemistry. The substitutions on the nitrogen atom in the imidazoline ring provide opportunities for fine-tuning the electronic and steric properties. Some of the complexes function as catalysts for Suzuki–Miyaura couplings, Mizoroki–Heck reactions, Diels–Alder reactions, asymmetric allylic substitution, [3,3] sigmatropic rearrangement, Henry reactions, etc.[1]

See also[edit]

References[edit]

  1. ^ a b c d Liu H, Du DM (March 2009). "Recent Advances in the Synthesis of 2-Imidazolines and Their Applications in Homogeneous Catalysis". Advanced Synthesis & Catalysis. 351 (4): 489–519. doi:10.1002/adsc.200800797.
  2. ^ Crouch RD (March 2009). "Synthetic routes toward 2-substituted 2-imidazolines". Tetrahedron. 65 (12): 2387–2397. doi:10.1016/j.tet.2008.12.022.
  3. ^ Guinchard X, Vallée Y, Denis JN (May 2007). "Total synthesis of marine sponge bis(indole) alkaloids of the topsentin class". The Journal of Organic Chemistry. 72 (10): 3972–3975. doi:10.1021/jo070286r. PMID 17444688.
  4. ^ Macinnes N, Duty S (December 2004). "Locomotor effects of imidazoline I2-site-specific ligands and monoamine oxidase inhibitors in rats with a unilateral 6-hydroxydopamine lesion of the nigrostriatal pathway". British Journal of Pharmacology. 143 (8): 952–959. doi:10.1038/sj.bjp.0706019. PMC 1575965. PMID 15545290.
  5. ^ Dardonville C, Rozas I (September 2004). "Imidazoline binding sites and their ligands: an overview of the different chemical structures". Medicinal Research Reviews. 24 (5): 639–661. doi:10.1002/med.20007. PMID 15224384. S2CID 31258438.
  6. ^ "Clonidine". Pubmed Health. October 2008. Archived from the original on 28 June 2010.
  7. ^ Vassilev LT, Vu BT, Graves B, Carvajal D, Podlaski F, Filipovic Z, et al. (February 2004). "In vivo activation of the p53 pathway by small-molecule antagonists of MDM2". Science. 303 (5659): 844–848. Bibcode:2004Sci...303..844V. doi:10.1126/science.1092472. PMID 14704432. S2CID 16132757.
  8. ^ Vu B, Wovkulich P, Pizzolato G, Lovey A, Ding Q, Jiang N, et al. (May 2013). "Discovery of RG7112: A Small-Molecule MDM2 Inhibitor in Clinical Development". ACS Medicinal Chemistry Letters. 4 (5): 466–469. doi:10.1021/ml4000657. PMC 4027145. PMID 24900694.
  9. ^ Bazanov DR, Pervushin NV, Savin EV, Tsymliakov MD, Maksutova AI, Sosonyuk SE, et al. (December 2021). "Sulfonamide derivatives of cis-imidazolines as potent p53-MDM2/MDMX protein-protein interaction inhibitors". Medicinal Chemistry Research. 30 (12): 2216–2227. doi:10.1007/s00044-021-02802-w. ISSN 1054-2523. S2CID 241788123.
  10. ^ Bazanov DR, Pervushin NV, Savitskaya VY, Anikina LV, Proskurnina MV, Lozinskaya NA, Kopeina GS (August 2019). "2,4,5-Tris(alkoxyaryl)imidazoline derivatives as potent scaffold for novel p53-MDM2 interaction inhibitors: Design, synthesis, and biological evaluation". Bioorganic & Medicinal Chemistry Letters. 29 (16): 2364–2368. doi:10.1016/j.bmcl.2019.06.007. PMID 31196710. S2CID 189815065.
  11. ^ Bazanov DR, Pervushin NV, Savin EV, Tsymliakov MD, Maksutova AI, Savitskaya VY, et al. (April 2022). "Synthetic Design and Biological Evaluation of New p53-MDM2 Interaction Inhibitors Based on Imidazoline Core". Pharmaceuticals. 15 (4): 444. doi:10.3390/ph15040444. PMC 9027661. PMID 35455441.
  12. ^ Tyagi R, Tyagi VK, Pandey SK (2007). "Imidazoline and its derivatives: an overview". Journal of Oleo Science. 56 (5): 211–222. doi:10.5650/jos.56.211. PMID 17898484.
  13. ^ Ishihara M, Togo H (2006). "An Efficient Preparation of 2-Imidazolines and Imidazoles from Aldehydes with Molecular Iodine and (Diacetoxyiodo)benzene". Synlett (2): 227–230. doi:10.1055/s-2005-923604.
source: https://en.wikipedia.org/wiki/2-Imidazoline

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