Hydrolysis hydroxamates

This reaction, conducted in alkaline solution, also produces carboxyl groups by hydrolysis of the amide (54). Recent work on the reaction of polyacrylamide with hydroxylamine indicates that maximum conversion to the hydroxamate fiinctionahty (—CONHOH) takes place at a pH > 12 (57). Apparendy, this reaction of hydroxylamine at high pH, where it is a free base, is faster than the hydrolysis of the amide by hydroxide ion. Previous studies on the reaction of hydroxylamine with low molecular weight amides indicated that a pH about 6.5 was optimum (55). 

Fig. 2. Functional groups on modified polyacrylamides (a) formed by reaction with dimethylamine and formaldehyde (Mannich reaction) (b), quatemized Mannich amine (c), carboxylate formed by acid or base-cataly2ed hydrolysis or copolymerization with sodium acrylate and (d), hydroxamate formed by...

Acid Hydrolysis. With hot concentrated mineral acids, primary nitroparaffins yield a fatty acid and a hydroxylamine salt. If anhydrous acid and lower temperatures are used, the intermediate hydroxamic acid can be recovered. 

R = CH3 and AR = C6H4NO2.) Actually Scheme XXV and Eq. (3-176) both take place, with some of the hydroxamic acid being formed directly and some via the intermediate. (Note that each of these reactions is itself complex, presumably occurring via a tetrahedral intermediate as shown in Scheme XXII for ester hydrolysis.)... 

When the compound for identification fails to respond to test 4 (aldehyde or ketone), the next class reactions to apply are the hydroxamic acid test and saponification, i.e., hydrolysis in alkaline solution. These are the class reactions for esters and anhydrides the rarely-encountered lactones react similarly. 

British Biotech has described co-crystal structures of both BB-3497 and actinonin bound in the active site of E. coli PDF [24]. The metal centre (Ni ) in both complexes adopts a pentacoordinate geometry, bound by the two oxygen atoms of the hydroxamate along with Cys-90, His-132 and His-136. This coordination pattern is consistent with the mechanism of de-formylation proposed by Becker et al. [56] and Jain et al. [67], in which a pentacoordinated metal centre stabilises the transition state during hydrolysis of the formamide bond. When compared to the co-crystal structure of a substrate hydrolysis product, Met-Ala-Ser, it is clear that the side chains of these two inhibitors bind into the active site pockets similarly to the substrate [56]. 

As early as 1899, 8tieglitz proposed a tetrahedral intermediate for the hydrolysis of an imino ether to an amide. Thns it was clear qnite early that a complicated overall transformation, imino ether to amide, would make more sense as the result of a series of simple steps. The detailed mechanism proposed, althongh reasonable in terms of what was known and believed at the time, wonld no longer be accepted, but the idea of tetrahedral intermediates was clearly in the air. 8tieglitz stated of the aminolysis of an ester that it is now commonly snpposed that the reaction takes place with the formation of an intermediate prodnct as follows referring to work of Lossen. (Note that the favored tautomer of a hydroxamic acid was as yet unknown.)... 

Although kinetic evidence for prior equilibrium inclusion was not obtained, competitive inhibition by cyclohexanol and apparent substrate specificity once again provide strong support for this mechanism. Since the rate of the catalytic reaction is strictly proportional to the concentration of the ionized hydroxamate function (kinetic and spectrophotometric p/Cas are identical within experimental error and are equal to 8.5), the reaction probably proceeds by a nucleophilic mechanism to produce an acyl intermediate. Although acyl derivatives of N-alkylhydroxamic acids are exceptionally labile in aqueous solution, deacylation is nevertheless the ratedetermining step of the overall hydrolysis (Gruhn and Bender, 1969). 

However, the switchover from an A2 to an A1 hydrolysis is a very common mechanistic pathway in strong acid media, probably more common than the pure A2 mechanism. Excess acidity analyses have shown that thioacetic acid, several thiobenzoic acids, and many thiolbenzoate and thionbenzoate esters show this sort of mechanism switch.179 Acylals and thioacylals also show this behavior,116 with thioacylals using two water molecules and acylals one. Many hydroxamic acids react this way,127,216 as do esters of various types,41,217,218 episulfoxides219 and aryloxatriazoles.220 Acylhydrazines can also show a mechanism switch of this sort, although with these substrates the situation is somewhat more complex.221... 

Synthesis of acid 129 starts from the commercially available 6-heptenoic acid (122), which upon reaction with (4S)-benzyloxazolidin-2-one (123) as the chiral auxiliary group yields the intermediate 124, hydroxymethylation of which affords compound 125. Hydrolysis of compound 125 followed by condensation with O-benzylhydroxylamine gives rise to the hydroxamate (126), which is then converted into (Claclam 127 via an intramolecular Mitsunobu reaction. Hydrolysis of the (Claclam 127 affords acid 128, which is subsequently formylated at the benzyloxyamine moiety to give the required intermediate acid (129) in quantitative yield, as depicted in Scheme 26. 

Other workers4 have recently shown that hydroxamic acid,. R-CONHOH, at pH 7-7 accelerates the hydrolysis of D.F.P. and sarin. They envisage the following reaction, although compound (I) has not been isolated. 

Surfactant molecules [32] and [33] which contain the hydroxamate and imidazole functions were synthesized by Kunitake et al. (1976c), and their catalytic action in aqueous CTAB micelles was examined for the hydrolysis of PNPA. 

The hydrolysis of sulfate monoesters has been studied increasingly in relation to sulfate group transfer in vivo. In general, the rate-enhancing effect on the sulfate cleavage is small even with hydroxamate- or imidazole-functionalized cationic micelles which are extremely effective for the hydrolysis of phenyl esters. Recently, Kunitake and Sakamoto (1979a) found that zwitterionic hydroxamate [47] cleaved 2,4-dinitrophenyl sulfate effectively in cationic and... 

Gruhn and Bender (2P) attached a hydroxamate group (8) to a secondary hydroxyl in an attempt to attain rapid turnover of catalyst in phenyl ester hydrolysis. The catalytic rate of the cycloamylose-hydroxamate adduct was compared to the rates brought about by (9) free in solution. Relative to the... 

Manecke and his collaborators have synthesized polymers of vinylimid-azole hydroxamic acid (75) (22, 23, 24). Hydrolysis of p-nitrophenyl acetate... 

In an attempt to move away from the hydroxamic acid zinc binding group, which is known to causes poor pharmacokinetics as a result of hydrolysis or glucuronidation, the group at Abbott searched for alternative zinc chelators culminating in the development of a series of electrophilic ketone HDACis (Figure 9.12) [64—66]. Subsequently, a group at IRBM developed a related series of thiophene trifluor-omethyl ketones and showed these to be selective class II HDACis [12]. 

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