Benzimidazoles basicity

These data seemed to suggest that the electronic effects of benzimidazole substituents had little effect on primary potency (NO2 versus Me), although disubstituted exemplars were generally more potent, perhaps suggesting a preference for greater steric bulk. Substituents that increased the benzimidazole basicity demonstrated improved solubility, but also an increased hERG activity as expected. The OCE3 substituent had little effect on the calculated plCa values relative to compound 123 but... 

Fu et al. [11] reported the acid-base blend membranes based on 2-amino-benzimidazole (basic polymer) and sulfonated poly(ether ether ketone) (SPEEK) (acidic polymer) for direct methanol fuel cells. A novel polymer, polysulfone-2-amide-benzimidazole (PSf-ABIm), using carboxylated polysulfone and 2-amino-benzimidazole was synthesized for this purpose. The blend membrane of SPEEK/PSf-ABIm showed high performance a s represented by Figure 1.12. The blend membrane with 3 wt% PSf-ABIm was evaluated continuously for 120 h and little or no decline in performance was found after 120 h. On the other hand, the Nafion 112 membrane standard was observed to have a decline in performance due to a much higher amount of methanol crossover. 

The piC values of polymethine dyes depend on terminal group basicity (64) thus the protonation abHity diminishes if the basic properties of the residues decrease, passing from benzimidazole, quinoline, benzothiazole, to indolenine. On the other hand, the piC of higher homologues increases with chain lengthening. The rate constant of protonation is sensitive to other features, for example, substituents and rings in the chain and steric hindrance for short-chain dyes. 

Chemical Reactions of Dyes. Decolorization is important for cyanines used ia imaging materials. Understanding decolorization provides clues to dye reactions that may cause degradation of imaging materials duting preparation and storage. For many dyes, protonation of the methine chain occurs readily and reversibly (64). Highly basic carbocyanine dyes like those from benzimidazole (eg, 36) protonate so readily that this provides a practical decolorization method. 

Not much information has been added in recent years to the earlier studies of tautomeric equilibria of benzimidazoles based on basicity measurements [76AHC(S1), p. 292]. For 5(6)- and 4(7)-substituted benzimidazoles and 2-methyl-5(6)-substituted benzimidazoles values are very close to 1, which indicates near equivalence in the stability of N1(H) and N3(H) tautomers. The tautomeric equilibria of 2-substituted (H, NH2, OMe, CN) 5-nitrobenzimidazoles and 4-nitrobenzimidazoles were analyzed with the use of semiempirical MINDO/3 and INDO methods. It was predicted that electron-releasing groups in position 2 shifted the equilibria to the 6-NO2 and 4-NO2 tautomers, respectively. 

Benzimidazole is also aromatic (65AX573, 97T13111), less acidic and more basic in the gas phase than imidazole (83AGE323), although in solution the basicity trend is reverted. This is ascribed to the polarization effects of the annulation. 

By using basicity data, Ridd and Smith- showed that 5-nitro- and 5-chloro-benzimidazole and their 2-methyl analogs exist essentially as mixtures of equivalent amounts of 29 and 30, and, in agreement with this ratio, 5-substituted benzimidazoles form comparable amounts of 1- and 3-derivatives on alkylation,- showing earlier alkylation ratios- to be erroneous. There are, however, other factors which can lead to the predominance of one tautomeric form. Basicity measurements indicate that 31 is preferred to the alternative non-hydro-... 

The Boger group [64-66] has extensively studied the use of a-ketoheterocycles as FAAH inhibitors. In their initial studies, a range of a-ketoheterocycles based on oleic acid was synthesised. A range of five- and six-membered monocyclic heterocycles and three bicyclic heterocycles (benzothiazole, benzimidazole and benzoxazole) was examined. Although many of the compounds tested were found to inhibit FAAH activity with micromolar affinities, the best results were obtained with heterocycles that incorporated a weakly basic nitrogen a - to the heterocycle (Table 6.5) [64]. 

It is convenient to define the basicity constant, K]of the indicator, BH, in the micellar pseudophase as a dimensionless quantity in terms of the mole ratio of micellar bound OH- (p. 225) using (21). The quantity [OHm] (or m oh) can be calculated from the ion-exchange relation and the experimental data fitted, usually by computer simulation, following the approach discussed for treatment of rate constants (p. 229). This treatment fits micellar effects upon the deprotonation of benzimidazole for a variety of CTAX surfactants (X = Cl, Br, N03) over a range of concentrations of NaOH and of added salts (Bunton et al., 1982a). A similar, but less general approach, was also applied to deprotonation of phenols and oximes (Bunton et al., 1980c). 

With S-vinylsulfilimines. A novel synthesis of the dihydro-thiazolo [3,2- ]benzimidazole 414 was achieved by the ring closure of 2-mercaptobenzoimidazole 412 using d -ethenylsulfilimine 413 and basic conditions (Equation 188)... 

The two-phase alkylation reactions have been extended to the acylation of simple heteroaromatic systems. Generally, the required conditions are milder than those employed for the alkylation reactions, but an excess of the acylating agent is usually required, owing to its facile hydrolysis in the basic media. Thus, benzimidazole and its 2-alkyl and 2-aryl derivatives have been benzoylated [46], and pyrrole and indole have been converted into a range of A-acyl [47, 48] and A-sulphonyl derivatives [48-53] (Table 5.35 and Table 5.36). 

One of the first examples of this type of blend was composed of SPEEK or SPES as the acidic component and diaminated PES, poly(4-vinylpyridine) (P4VP), poly(benzimidazole) (PBl), or poly(ethyleneimine) (PEI) as the basic component. " For blend lEC values of 1.0 meq/g, conductivity values were reported to be good, as was H2/O2 EC performance. Thermal stabilities for these blends was also demonstrated to be high (>270°C). Other examples of acid-base PEMs include blends of SPPO and PBI, sulfonated poly(phthalazinone ether ketone) and aminated SPES, SPIs and aminated Pls, and SPEEK with PES bearing benzimidazole side groups, ° as well as an unusual example in which the blend is composed of sulfonated, hyper-branched polyether and pyridine-functionalized polysulfone. ... 

Photolytic. Irradiation of trifluralin in hexane by laboratory light produced a,a,a-trifluoro-2,6-dinitro-A-propyl-jo-toluidine and a,a,a-trifluoro-2,6-dinitro-p-toluidine. The sunlight irradiation of trifluralin in water yielded a,a,a-trifluoro-A, 7 -dipropyl-5-nitrotoluene-3,4-diamine, a,a,a-trifluoro-A/ ,A/ -dipropyltoluene-3,4,5-triamine, 2-ethyl-7-nitro-5-(trifluoromethyl)benzimidazole, 2,3-dihydroxy-2-ethyl-7-nitro-l-propyl-5-(trifluoromethyl)benzimidazoline, and 2-ethyl-7-nitro-5-(trifluoromethyl)benzimidazole. 2-Amino-6-nitro-a,a,a-trifluoro-p-toluidine and 2-ethyl-5-nitro-7-(trifluoromethyl)benzimidazole also were reported as major products under acidic and basic conditions, respectively (Crosby and Leitis, 1973). In a later study, Leitis and Crosby (1974) reported that trifluralin in aqueous solutions was very unstable to sunlight, especially in the presence of methanol. The photodecomposition of trifluralin involved oxidative TV-dealkylation, nitro reduction, and reductive cyclization. The principal photodecomposition products of trifluralin were 2-amino-6-nitro-a,a,a-trifluoro-jo-toluidine, 2-ethyl-7-nitro-5-(trifluoromethyl)benzimida-zole 3-oxide, 2,3-dihydroxy-2-ethyl-7-nitro-l-propyl-5-(trifluoromethyl)benzimidazole, and two azoxybenzenes. Under alkaline conditions, the principal photodecomposition product was 2-ethyl-7-nitro-5-(trifluoromethyl)-benzimidazole (Leitis and Crosby, 1974). 

The rather high basic strength of 3,5-diazaindole [91] (p/sTa = 6T) is not due to the protonation of the imidazole ring (for benzimidazole p g = 5-53), but rather of the pyridine ring. Cation [92] is formed and this is stabilized by the same kind of resonance as... 

Pyrrolo[l,2-a]benzimidazoles [181] (R = H, Me, Ph R = Me, CH2Ph), unsubstituted at the 1- and 3-positions, protonate in trifluoroacetic acid exclusively on C-1 (Alekseeva et al., 1972b). A methyl substituent in the 1-position leads to mixtures of C-1 and C-3 protonated forms, the relative amounts depending on the presence and nature of substituents at C-3. Without a C-3 substituent, the extent of protonation at the position is 81%, but decreases to 18% in the 3-methyl- and 3-phenyl derivatives the basicity of the derivatives increases simultaneously. 

Alekseeva et al. (1972b) have carried out a comparison of calculated values of localization energies and free valency indices of pyrrolo[ 1,2-a] imidazole, pyrrolo[l,2-a] benzimidazole and indolizine. In all these molecules the a-position of the pyrrole ring is calculated to be more reactive than the / -position. The free valence indices increase in the order indolizine < pyrrolobenzimidazole < pyrroloimidazole, which is also the order of increasing basicity. 

Equation (40) further indicates that 2-X-benzimidazoles are less basic than the corresponding 2-X-imidazoles. 

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