Center for Drug Design and Development, The University of Toledo, Toledo, Ohio 43606-3390, USA.
J Phys Chem B. 2010 Jan 14;114(1):349-60. doi: 10.1021/jp9082085.
Theoretical calculations were carried out for studying the tautomeric protonation of N-methylpiperazine as a prototype six-member aliphatic ring containing a secondary and a tertiary nitrogen atom. The protonation was investigated in three solvents, water, acetonitrile, and dichloromethane. Calculations were performed up to the B3LYP/aug-cc-pvtz and QCISD(T)/CBS levels by applying the IEF-PCM polarizable continuum dielectric solvent model. Relative solvation free energies also were calculated upon explicit solvent models by utilizing the free-energy perturbation theory as implemented in Monte Carlo simulations. The relative free energy for the N-methylpiperazine tautomer protonated at the secondary (NMps) rather than at the tertiary (NMpt) nitrogen was calculated at a ratio of 47/53 in infinitely dilute aqueous solution. The ratio further decreased in lower-polarity solvents. In contrast, NMR experiments suggested that the protonation takes place primarily at the secondary nitrogen in 0.37 molar aqueous solution with NMps/NMpt = 80/20. The NMps tautomer was exclusive in dichloromethane at the same concentration. The discrepancy between theory and experiment was resolved by considering association equilibria in parallel with the protonation for the solute. As a result, the theoretically predicted tautomer ratios were obtained in close agreement with the experimental values. The NMps tautomer could form a preferable dimeric structure, where one or two chloride anion(s) was/were in hydrogen bonds with protons of the associating monomers. The calculations suggest that the proton relocation may take place by solvent assistance in water or along an intramolecular proton jump in the twist-boat conformation. The predicted activation free energy was about 10 kcal/mol on the basis of variable-temperature NMR experiments in DCM.
理论计算用于研究 N-甲基哌嗪作为含有仲氮和叔氮的原型六元脂环的质子化的互变异构质子化。在水、乙腈和二氯甲烷三种溶剂中研究了质子化。通过应用 IEF-PCM 极化连续介电溶剂模型,在 B3LYP/aug-cc-pvtz 和 QCISD(T)/CBS 水平上进行了计算。还通过在蒙特卡罗模拟中实施自由能微扰理论,利用显式溶剂模型计算了相对溶剂化自由能。在无限稀水溶液中,N-甲基哌嗪互变异构质子化在仲氮(NMps)而不是叔氮(NMpt)上的相对自由能比计算为 47/53。在极性较低的溶剂中,该比例进一步降低。相比之下,NMR 实验表明,在 0.37 摩尔的水溶液中,质子化主要发生在仲氮上,NMps/NMpt = 80/20。在相同浓度的二氯甲烷中,NMps 互变异构体是唯一的。通过考虑溶质与质子化平行的缔合平衡,解决了理论与实验之间的差异。因此,理论预测的互变异构体比例与实验值非常吻合。NMps 互变异构体可以形成更优的二聚体结构,其中一个或两个氯离子与缔合单体的质子形成氢键。计算表明,质子迁移可能通过水的溶剂协助或在扭曲船构象中的分子内质子跳跃来发生。根据 DCM 中的变温 NMR 实验,预测的活化自由能约为 10 kcal/mol。