Department of Chemistry and The Skaggs Institute for Chemical Biology, The Scripps Research Institute, 10550 N. Torrey Pines Road, La Jolla, California 92037, United States.
J Am Chem Soc. 2020 Dec 9;142(49):20778-20787. doi: 10.1021/jacs.0c09775. Epub 2020 Nov 30.
An unprecedented 1,4-cycloaddition (vs 3,6-cycloaddition) of 1,2,4,5-tetrazines is described with preformed or in situ generated aryl-conjugated enamines promoted by the solvent hydrogen bonding of hexafluoroisopropanol (HFIP) that is conducted under mild reaction conditions (0.1 M HFIP, 25 °C, 12 h). The reaction constitutes a formal [4 + 2] cycloaddition across the two nitrogen atoms (N1/N4) of the 1,2,4,5-tetrazine followed by a formal retro [4 + 2] cycloaddition loss of a nitrile and aromatization to generate a 1,2,4-triazine derivative. The factors that impact the remarkable change in the reaction mode, optimization of reaction parameters, the scope and simplification of its implementation through in situ enamine generation from aldehydes and ketones, the reaction scope for 3,6-bis(thiomethyl)-1,2,4,5-tetrazine, a survey of participating 1,2,4,5-tetrazines, and key mechanistic insights into this reaction are detailed. Given its simplicity and breath, the study establishes a novel method for the simple and efficient one-step synthesis of 1,2,4-triazines under mild conditions from readily accessible starting materials. Whereas alternative protic solvents (e.g., MeOH vs HFIP) provide products of the conventional 3,6-cycoladdition, the enhanced hydrogen bonding capability of HFIP uniquely results in promotion of the unprecedented formal 1,4-cycloaddition. As such, the studies represent an example of not just an enhancement in the rate or efficiency of a heterocyclic azadiene cycloaddition by hydrogen bonding catalysis but also the first to alter the mode (N1/N4 vs C3/C6) of cycloaddition.
描述了一种前所未有的 1,4-环加成(与 3,6-环加成相反),其中 1,2,4,5-四嗪与预先形成或原位生成的芳基共轭烯胺反应,由六氟异丙醇(HFIP)的溶剂氢键促进,反应条件温和(0.1 M HFIP,25°C,12 h)。该反应构成了 1,2,4,5-四嗪的两个氮原子(N1/N4)上的形式[4 + 2]环加成,随后通过形式的反[4 + 2]环加成失去腈并芳构化生成 1,2,4-三嗪衍生物。影响反应模式显著变化的因素、反应参数的优化、通过醛和酮原位生成烯胺简化其实施的范围和简化、3,6-双(硫甲基)-1,2,4,5-四嗪的反应范围、参与的 1,2,4,5-四嗪调查以及对该反应的关键机械见解都进行了详细说明。鉴于其简单性和通用性,该研究建立了一种从易得起始原料在温和条件下简单高效地一步合成 1,2,4-三嗪的新方法。虽然替代质子溶剂(例如 MeOH 与 HFIP)提供了常规 3,6-环加成的产物,但 HFIP 增强的氢键能力独特地促进了前所未有的形式 1,4-环加成。因此,这些研究不仅代表了通过氢键催化增强杂环氮二烯环加成的速率或效率的一个例子,而且也是第一个改变环加成模式(N1/N4 与 C3/C6)的例子。