Imidazoline functions

A rather simpler compound includes both a benzodioxan nucleus and the imidazoline function associated with a-adrenergic agonists such as clonidine. As in the standard approach for preparing imidazolines, the treatment of nitrile (60-1) with alcoholic hydrogen chloride leads to the iminoether (60-2). Reaction of that intermediate with ethylenediamine then affords idazoxin (60-3) [70], a compound that interacts with a-adrenergic receptors. 

Imidazoline-functional polymers are most often prepared by modification of acrylonitrile-containing polymers (see Section 1.11.4.2.2). However, isomeric polymers (72) are obtainable via polymerization of 1-vinylimidazolinium salts (71 Scheme 18) (B-74MI11100). 

Many of the surfactants made from ethyleneamines contain the imidazoline stmcture or are prepared through an imidazoline intermediate. Various 2-alkyl-imidazolines and their salts prepared mainly from EDA or monoethoxylated EDA are reported to have good foaming properties (292—295). Ethyleneamine-based imida zolines are also important intermediates for surfactants used in shampoos by virtue of their mildness and good foaming characteristics. 2- Alkyl imidazolines made from DETA or monoethoxylated EDA and fatty acids or their methyl esters are the principal commercial intermediates (296—298). They are converted into shampoo surfactants commonly by reaction with one or two moles of sodium chloroacetate to yield amphoteric surfactants (299—301). The ease with which the imidazoline intermediates are hydrolyzed leads to arnidoamine-type stmctures when these derivatives are prepared under aqueous alkaline conditions. However, reaction of the imidazoline under anhydrous conditions with acryflc acid [79-10-7] to make salt-free, amphoteric products, leaves the imidazoline stmcture essentially intact. Certain polyamine derivatives also function as water-in-oil or od-in-water emulsifiers. These include the products of a reaction between DETA, TETA, or TEPA and fatty acids (302) or oxidized hydrocarbon wax (303). The amidoamine made from lauric acid [143-07-7] and DETA mono- and bis(2-ethylhexyl) phosphate is a very effective water-in-od emulsifier (304). 

Therapeutic Function Vasoconstrictive agent (nasal spray) Chemical Name 2-(4-lndanylamino)-2-imidazoline Common Name —... 

Therapeutic Function Peripheral vasodilator Chemical Name 4,5-dihydro-2-(phenylmethyl)-1H-imidazole Common Name Benzazoline 2-benzyl-4,5-imidazoline Structural Formula r... 

From l,l,-/)i.v-(3-methyl-4-imidazoline-2-selone)methane with iodine bromide, a solid compound containing disordered molecules with T-shaped CSeI2 and Br-Se(C)-I functions in the same crystal was isolated from 1,2-fe-(3-methyl-4-imidazoline-2-selone)ethane with iodine bromide, a solid... 

From a comparative analysis of H NMR spectra of structurally similar pairs of nitroxyl radicals of 3-imidazoline and 3-imidazoline-3-oxide, it was concluded that the nitrone group contributes to a more efficient long-range spin density delocalization in the conjugated n -system of functional groups bonded with atom C-4 (404). 

The development of chiral hydrogenation catalysts for unfunctionalized alkenes also allows enantioselective hydrogenation of functionalized olefins where the functionality in the molecule is remote from the double bond. A series of oxazoline-, imidazoline- and pyridine-derived catalysts have been screened for the hydrogenation of unsaturated derivatives of vitamin E (Scheme 30.3). Hy-... 

MCR also tolerates the aliphatic isocyanide functionality [150], thus allowing the union with various IMCRs. Finally, we developed the first example of a triple MCR process (SCR toward 83) based on our 2//-2-imidazoline (65) and W-(cyano-methyl)amide (32) MCRs united with the Ugi-4CR (Fig. 25). 

A compound that includes a carbonyl group on the imidazoline ring is described as sedative. Treatment of the guanidyl substituted amino acid creatine (87-1) with hydrochloric acid results in cyclization to the iminoimidazolinone creatinine (87-2). Condensation of that intermediate with meta-chlorophenylisocyanate (87-3) leads to the formation of a urea by condensation of the reactive function with the imidazole as its amino tautomer. There is thus obtained fenobam (87-4) [92]. 

Compositions and functions of typical commercial products in the 2-alkyl-l-(2-hydroxyethyl)-2-imidazolines series are given in Table 29. 2-Alkyl-l-(2-hydroxyethyl)-2-imidazolines are used in hydrocarbon and aqueous systems as antistatic agents, corrosion inhibitors, detergents, emulsifiers, softeners, and viscosity builders. They are prepared by heating the salt of a carboxylic acid with (2-hydroxyethyl)ethylenediamine at 150—160°C to form a substituted amide 1 mol water is eliminated to form the substituted imidazoline with further heating at 180—200°C. Substituted imidazolines yield three series of cationic surfactants by ethoxylation to form more hydrophilic products quatemization with benzyl chloride, dimethyl sulfate, and other alkyl halides and oxidation with hydrogen peroxide to amine oxides. 

The peripheral receptors activated by noradrenaline fall into at least two classes, a-receptors and /3-receptors, which differ in their function and in their response to drugs. The a-receptors cause constriction of blood vessels and compounds used to block them include indoramin (216), prazosin (217) and phentolamine (218). Another imidazoline, tolazoline (2-benzyl-2-imidazoline), is a useful vasodilator but is unsuitable for the treatment of hypertension since it stimulates the heart. Other drugs described as peripheral vasodilators are diazoxide (219), which is related to the thiazide diuretics, hydralazine (220) which also depresses the CNS, hydracarbazine (221) and minoxidil (222). The /3-receptors control the action of adrenaline on the heart (among other effects) and the agents that block them are mostly nonheterocyclic aromatic compounds with aminoethanol or 3-amino-2-hydroxypropoxy side-chains. They have proved effective in the treatment of hypertension. One heterocyclic compound of this class, timolol (223), is in use. 

An earlier series of experiments established useful synthetic transformations involving carboxylation of ketones and nitroalkanes to yield P-keto acids and a-nitro acids respectively (Scheme 94).362 363 The reagent is methylmagnesium carbonate and the intermediate (130) can be alkylated with concomitant decarboxylation to provide greater versatility. These reactions can also be extended to ketone functions in imidazoline- and oxazolidine-diones (Scheme 95).364,365... 

Similar to M11O2, BaMn04 is able to oxidize functional groups other than alcohols, including primary amines,76b anilines,76b,83a imidazolines,90 saturated hemiacetals91 and thiols.84a,88b... 

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