Heterocyclic compounds imidazole

K. Hofmann, in A. Weissberger, The Chemistry of Heterocyclic Compounds, Imidazole and Derivatives, Intersciencc Publishers, New York, 1. Auflage, 1953. 

Selective C-2(H)deuteriation of a number of heterocyclic compounds (imidazole,... 

K. Hofmann, Chemistry of heterocyclic compounds imidazole and its derivatives (A. Weissberger, Ed.). Interscience, New York, 1953, Part I, Vol. 6. 

Details of bond lengths and bond angles for all the X-ray structures of heterocyclic compounds through 1970 are listed in Physical Methods in Heterocyclic Chemistry , volume 5. This compilation contains many examples for five-membered rings containing two heteroatoms, particularly pyrazoles, imidazoles, Isoxazoles, oxazoles, isothlazoles, thlazoles, 1,2-dlthloles and 1,3-dlthloles. Further examples of more recent measurements on these heterocyclic compounds can be found in the monograph chapters. 

The electrolysis of asymmetric ketones 43 led to the formation of isomers and stereoisomers. Kinetic measurements for the formation of ketimine 43 in saturated ammoniacal methanol indicated that at least 12 h of the reaction time were required to reach the equilibrium in which approximately 40% of 42 was converted into the ketimine 43. However, the electrolysis was completed within 2.5 h and the products 44 were isolated in 50-76% yields. It seems that the sluggish equilibrium gives a significant concentration of ketimine 43 which is oxidized by the 1 generated at the anode, and the equilibrium is shifted towards formation of the product 44. 2,5-Dihydro-IH-imidazols of type 44, which were unsubstituted on nitrogen, are rare compounds. They can be hydrolyzed with hydrochloric acid to afford the corresponding a-amino ketones as versatile synthetic intermediates for a wide variety of heterocyclic compounds, that are otherwise difficult to prepare. 

Aromatic N-containing heterocycles (pyridine, imidazole etc.,) and their alkyl derivatives represent an important group of products and they have received considerable attention because of their various applications. For instance, methyl pyridines (picolines) and dimethyl pyridines (lutidines) are a class of industrially valuable compounds for the production of dyes and fine chemicals [108]. Sreekumar et al [109] reported pyridine methylation to 3-picolines over Zni xCoxFe204 spinel systems at reaction temperature between 325 and 425°C. The... 

Many of the simple heterocycles occur naturally within human biochemistry. For example, the amino acids proline, histidine, and tryptophan contain, respectively, a pyrrolidine, an imidazole, and an indole ring. The nucleic acids contain purine and pyrimidine rings. Vitamins are heterocyclic compounds vitamin Bg (8.8) is a substituted pyridine vitamin Bj (8.9) contains a pyrimidine ring. Simple heterocycles are therefore important to human biochemistry and thus to drug design. 

As previously indicated (see pp. 88-91), formation of heterocyclic compounds, mainly pyrazines, was found only in the ammonolysis of some aldose nicotinates33 35 and acetates and benzoates of ketoses.39 37 For ketose esters, whose behavior differed from that of the aldose esters, the formation of imidazole derivatives was also observed these heterocyclic compounds also result from the direct action of ammonia upon the corresponding free sugars, but the presence of the esterifying acyl groups evidently increases their ease of formation and raises their yields. 

The high reactivity of the dinitrate may be used to obtain heterocyclic compounds. An ingenious method of forming imidazol derivatives was developed by Payman and Fargher [102] ... 

Compounds with heterocyclic rings are inextricably woven into the most basic biochemical processes of life. If one were to choose a step in a biochemical pathway at random, there would be a very good chance that one of the reactants or products would be a heterocyclic compound. Even if this was not true, participation of heterocyclics in the reaction in question would almost be certain as all biochemical transformations are catalyzed by enzymes, and three of the twenty amino acids found in enzymes contain heterocyclic rings. Of these, the imidazole ring of histidine in particular would be likely to be involved histidine is present at the active sites of many enzymes and usually functions as a general acid-base or as a metal ion ligand. Furthermore, many enzymes function only in the presence of certain small non-amino acid molecules called coenzymes (or cofactors) which more often than not are heterocyclic compounds. But even if the enzyme in question contained none of these coenzymes or the three amino acids referred to above, an essential role would still be played by heterocycles as all enzymes are synthesized according to the code in DNA, which of course is defined by the sequence of the heterocyclic bases found in DNA. 

The catalytic effect has been explained in terms of the activation of the anhydride by interaction with the amine to give a zwitterionic intermediate (47 Scheme 10) (B-68MI11501). Imidazoles have also been suggested as accelerators for anhydride cures (68USP3394105). A review of the patent literature (B-77MI11502) shows that several heterocyclic compounds are of interest as curatives for epoxy resins. 

Substituted imidazoles are an example of a pharmaceutically important class of heterocyclic compounds, several of which have been incorporated in drugs that have reached the market, e.g. cimetidine, ondansetron and losartan (figure 1). 

Primary alcohols are oxidized to aldehydes, n-butanol being the substrate oxidized at the highest rate. Although secondary alcohols are oxidized to ketones, the rate is less than for primary alcohols, and tertiary alcohols are not readily oxidized. Alcohol dehydrogenase is inhibited by a number of heterocyclic compounds such as pyrazole, imidazole, and their derivatives. 

Formation mechanisms of imidazoles in the Maillard reaction are not as well understood as those of other heterocyclic compounds. The role of a-amino carbonyl fragments as intermediates in imidazole formation was suggested in the reaction of sucrose and ammonia (43). In a study of a L-rhamnose/ammonia model system, which produced fifty-two imidazoles, it was proposed that an amino-hydroxy fragment was responsible for imidazole... 

Nitrogen-containing heterocyclic compounds such as indoles and imidazoles are also formylated by the electron-rich olefin. 3-Methylimidazol-5-carboxaldehyde can be prepared from 2-methyl-imidazole (yield 83%) and 2-phenylindole-3-carboxaldehyde from 2-phenylindole (yield 64%). 

Hoffman K (1953) Imidazole and its derivatives, Part 1. In Weissberger A (ed) The chemistry of heterocyclic Compounds. Interscience, New York... 

Considerable work was done to induce chirality via chiral auxiliaries. Reac tions with aromatic a-ketoesters like phenylglyoxylates 21 and electron-rich al kenes like dioxoles 22 and furan 23 were particularly efficient (Scheme 6). Yield up to 99% and diastereoselectivities higher than 96% have been observed whet 8-phenylmenthol 21a or 2-r-butylcyclohexanol 21b were used as chiral auxiliarie [14-18]. It should be noted that only the exoisomers 24 and 25 were obtained from the reaction of dioxoles 22. Furthermore, the reaction with furan 23 wa regioselective. 24 were suitable intermediates in the synthesis of rare carbohydrate derivatives like branched chain sugars [16], Other heterocyclic compounds liki oxazole 28 [19] and imidazole 29 [20] derivatives as well as acyclic alkenes 3fl 31, and 32 [14,15,21,22] were used as olefinic partners. Numerous cyclohexane derived alcohols [18,21-24] and carbohydrate derivatives [25] were used as chiri... 

A comprehensive monograph on imidazole and its derivatives by K. Hofmann1 was published in 1953. A chapter dealing with imidazoles and condensed imidazoles by Schipper and Hay2 in Heterocyclic Compounds edited by Elderfield reviewed the literature to 1955, while a more recent review by Pozharskii et al.3 brought the chemistry of imidazole and some important condensed imidazoles up to date to 1964. A number of monographs on the chemistry of heterocyclic compounds4-10 have also dealt with aspects of imidazole chemistry in a necessarily brief manner. Specific topics in imidazole chemistry and biochemistry have been covered in further reviews.11-21 In the most... 

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