|Jmol 3D model||Interactive image|
|Molar mass||70.10 g·mol−1|
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
|what is ?)(|
2-Imidazoline (dihydroimidazoles) is one of three isomers of the nitrogen-containing heterocycle with formula C3H6N2, derived from imidazole. 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.
Many imidazolines are biologically active. 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.
Synthesis of Imidazoline
A variety of routes exist for the synthesis of imidazolines, with the most common methods involving the condensation of 1,2-diamines with nitriles or esters. The nitrile based route is effective for both alkyl and aryl nitriles and requires high temperatures or acid catalysis.
Imidazoline in Natural Products
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.
2-imidazolines have been investigated as antihyperglycemic, anti-inflammatory, antihypertensive, antihypercholesterolemic, and antidepressant reagents. 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).
Second generation Grubbs' catalyst
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.
Imidazoline derivatives have extensive applications in surfactant in small proportions for improving detergent qualities for various purposes (fabric softeners, hair and fabric conditioning).
Imidazolines as Precursors of Imidazoles
Imidazoles can be prepared from dehydrogenation of imidazolines.
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