| Popis: |
The introduction reviews the Michael addition, and shows how the addition of dimethyl acetylenedicarboxylate to heterocycles can be explained if initial attack gives a zwitterion, = +N-Co = −Co, which can then react further in several ways. A summary of how the acetylenic ester combines with various heterocycles is given, and brief mention is made of the related Diels-Alder and 1, 3-dipolar additions. Chapter One discusses the reaction of 2-phenylpyridine with dimethyl acetylenedicarboxylate. The initial product has structure [1], which,on heating above its melting point, isomerises to [2], these structures being assigned by consideration of the spectral properties. Heating [1] with excess acetylenic ester gives the 9a-vinyl-9aH-quinolizine, [3], whose spectra resemble those of [1] rather than those of [2]. The 9a-vinyl- 9aH-quinolizines, [4] and [5], are obtained from the acetylenic ester and 2-vinyl- and 2-methyl-6-vinylpyridine, respectively. A minor product from 2-vinylpyridine is [6], and a possible mode of formation is proposed. In Chapter Two, the addition of dimethyl acetylenedicarboxylate to azoles is discussed. Thiazole and 4-methylthiazole give the adducts [7] and [8], while a minor product of the thiazole reaction is [9]. Objections to alternative structures1 for [7] and some analogues are put forward. Benzoxazole forms the adduct [10] which can be reduced to the dihydroderivative [ll]. 2-Methylbenzoxazole and the acetylenic ester give the compound [12], a possible reaction scheme being postulated, and the similar compounds [13] and [14] are obtained from l-alkyl-2-methyl-benziminazoles. The nuclear magnetic resonance spectra of these adducts are discussed, and compared with those of [15] and [16], previously prepared.2 1, 2-Dimethylbenziminazole gives a second adduct which has been shown to be [l7]. The sole adduct from 2-ethyl-1-methylbenziminazole and the acetylenic ester is the analogous compound [18]. Comparison of the nuclear magnetic resonance and ultraviolet absorption spectra of these compounds with those of a minor product from the reaction of 1-methylbenziminazole and dimethyl acetylenedicarboxylate, indicate it has the structure [19], but the major product of the reaction is [20]. A similar compound [21] is obtained from benziminazole. Attempts to convert [19] into [20], or both into the same perchlorate, were unsuccessful. Two adducts [22] and [23] are obtained from 1-methylpyrazole, while 1-methylindazole and the acetylenic ester give [24]. These structures are based mainly on spectral evidence. 1-Methyl- and 1-benzylbenzotriazole react with dimethyl acetylene-dicarboxylate to give 1:2 molar adducts, which are formulated as [25] and [26], on the basis of their reduction and oxidation products, and their respective spectra. Structure [25] is preferred to [27], which might be expected by analogy with earlier results, because of its ready loss of CH2, characteristic of vinyl ethers. A method of formation of [25] and related compounds is suggested. l-Methyl-l,2,4-triazole and the acetylenic ester form the compound [28], but the N-methyl derivative of 3-methyl-l,2,4-triazole gives three 1:2 molar adducts, for which no definite structures could be proposed. The reactions between some diazines and dimethyl acetylenedicarboxylate are considered in Chapter Three. In acetonitrile, the sole products from 2-methyl- and 2,6-dimethylpyrazine and the ester are [29] and [3O], while the similar compounds [31], [32], and [33] are minor products when pyridazine, 3-methylpyridazine, and 1-methylphthalazine are used. The structures [31] and [32], previously described, are confirmed by nuclear magnetic resonance spectroscopy, which was also used to assign structures to the major products of the reactions of the acetylenic ester with pyridazine and its 3-methyl derivative, [34] and [35] respectively. [36], the analogue of [35] is obtained from 3,6-dimethylpyridazine and the ester, but the major product of this reaction is [37], identified by its proton resonance spectrum, which is similar to those of the compounds [12]-[16]. Unlike 3-methylpyridazine, 1-methylphthalazine gives a 1:2 molar adduct with a hydrogen at the bridgehead, [38], and this is isomerised to [39] in acid solution. In aprotic solvents, phthalazine, quinazoline, and quinoxaline give no crystalline products with dimethyl acetylenedicarboxylate, but, in methanol, phthalazine gives [40]. Phenazine and the acetylenic ester in methanol form the adduct [4l], the structure being supported by the proton resonance spectrum, consistent with a symmetrical molecule, and derivatives obtained on reduction and bromination. Chapter four is concerned with alkylquinoxalines and methyl- substituted diazines, whose methyl groups take part in the reactions with acetylenic esters. Thus, 2-methylquinoxaline and dimethyl acetylene dicarboxylate give two isomeric 1:2 molar adducts, [42] and [43]. These structures are based partly on analogy with the "red adduct" from quinaldine4, and partly on the chemistry and spectra of the compounds. The nuclear magnetic resonance spectrum of [42] is discussed in detail, and a theoretical spectrum of the CH2-CH system has been calculated5, excellent agreement being found between calculated and observed spectra for both methyl and ethyl esters. Reduction of [42] gives [45], and again agreement between observed and calculated proton resonance spectra is found. 2,3~Dimethylquinoxaline forms the methyl analogue of [43] i.e. [44], and the differences in the CH2-CHCOOMe systems of [42] and [44] are used to justify the differences in the respective proton resonance spectra. Attempts to degrade these adducts were unsuccessful. Reduction of [44] gives the 5,6-dihydro derivative, while bromination of [42] gives the 2,3-dibromo derivative, and bromination of [44] gives bromo-compounds, substituted in the benzene ring and/or the methyl side chain. An interesting reaction is the conversion of [44] to [43] by selenium dioxide. Possible ways in which these adducts could be formed are discussed. 4,6-Dimethyl- and 2,4,6-trimethylpyrimidine and 4-methylquinazoline form 1:2 molar adducts with dimethyl acetylenedicarboxylate, whose nuclear magnetic resonance spectra show the presence of CH2-CH groupings. Structures [46], [47], and [48] are proposed for these compounds, although, the CH2-CH systems may be reversed. A 1:3 molar adduct from 2,4-dimethyl-quinazoline and the acetylenic ester is formulated as [49], on the basis of its nuclear magnetic resonance spectrum. 2,3,5,6-Tetramethylpyrazine and the acetylenic ester give a compound, whose structure is considered to be [50], although alternatives are discussed. The similar compound [51] is obtained in small yield from 2,3-dimethylquinoxaline, while 2,5-dimethylpyrazine and dimethyl acetylene-dioarboxylate give an adduct, whose properties support the structure [52]. A scheme is suggested for the formation of this compound. In Chapter Five, adducts from the acetylenic ester and some heterocyoles containing a free amino group are shown to be one of two types. 4-Methyliminazole and indazole form adducts like [53], while indazole, 3-methylindazole, 1,2,3-triazole, benzotriazole, 1,2,4-triazole, and 3-methyl-1,2,4-triazole give adducts of the type [54]. The position of attachment of the side chain cannot be decided, except in the adducts of indazole and 3-methylindazole, [55] and [56] respectively. Unlike the other succinates, [55] and [56] show two sets of peaks in their nuclear magnetic resonance spectra, indicating the asymmetry of the molecules. Diazoaminobenzene and dimethyl acetylenedicarboxylate give three adducts, two of which correspond to [53] and [54], while the structure [57] is suggested for the third adduct. |
