Abstract
Chiral α-aminoboronic acids and their derivatives are generally useful as bioactive compounds and some have been approved as therapeutic agents. Here we report a NiH-catalysed asymmetric hydroamidation process that with a simple amino alcohol ligand can easily produce a wide range of highly enantioenriched α-aminoboronates from alkenyl boronates and dioxazolones under mild conditions. The reaction is proposed to proceed by an enantioselective hydrometallation followed by an inner-sphere nitrenoid transfer and C–N bond forming sequence. The synthetic utility of this transformation was demonstrated by the efficient synthesis of a current pharmaceutical agent, Vaborbactam.
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Introduction
Enantioenriched α-aminoboronic acids and their derivatives are privileged structural elements commonly encountered in materials science and drug discovery (Fig. 1a)1,2,3. They have also been used as synthetically useful chiral building blocks in cross-coupling chemistry4,5. As a result, the development of catalytic synthetic methods to efficiently and selectively prepare molecules containing such high-value motifs from simple starting materials, has been the subject of intense research. In addition to traditional chiral auxiliary approaches6,7,8, a number of catalytic asymmetric methods have been developed for the synthesis of α-aminoboronic acids, including borylation of aromatic aldimines9,10,11, hydroboration of enamides12,13 and hydrogenation14,15,16,17 (Fig. 1b). As an alternative, a robust CuH-catalysed hydroamination18,19,20,21,22,23,24,25,26,27,28,29,30,31 of easily available alkenylBdan (dan, naphthalene-1,8-diaminato) substrates was recently disclosed by Hirano and Miura29. Subsequently, a more efficient CuH-cascade hydroboration/hydroamination catalysis using readily available alkynes as starting materials was reported by Liu and Engle31. Despite the elegant nature of hydroamination reactions, a further four step sequence is needed to convert the obtained tertiary amines bearing an adjacent Bdan substituent to the desired α-aminoboronic acid pharmacophores and this has dramatically reduced the synthetic efficiency of the process. Consequently, the development of a complementary hydroamidation approach which could directly produce the pharmacophores - enantioenriched amides with an adjacent Bpin or B(OH)2 group, is highly desirable.
Recently, our group and others have disclosed an asymmetric hydrofunctionalization platform that uses olefins directly as nucleophiles and is enabled by a highly reactive chiral NiH catalyst32,33,34,35. This strategy is general and reliable and a large variety of electrophiles can be employed as coupling partners, which allows the stereochemically controlled formation of a variety of carbon–carbon36,37,38,39,40,41,42,43,44,45,46,47,48,49,50,51,52,53,54,55 and carbon–heteroatom56,57,58,59,60,61,62,63,64,65 bonds. Very recently, Seo and Chang60,64, Yu63, and our group61 have demonstrated that dioxazolones are suitable electrophilic amidating reagents in NiH-catalysed reductive hydroamidation reactions. We envisioned that NiH-catalysed asymmetric hydrofunctionalization could be expanded to the asymmetric hydroamidation of alkenyl boronates with dioxazolones30,60,61,62,63,64, thus enabling the direct synthesis of a variety of enantioenriched α-aminoboronates which have high potential in medicinal chemistry. As shown in Fig. 1c, with a structurally simple chiral amino alcohol ligand as a chiral source, an enantioenriched alkylnickel nucleophile would be formed through an enantiodifferentiating syn-hydronickellation reaction with an alkenylBpin substrate. Subsequent inner-sphere nitrenoid transfer with an amidating reagent66,67,68,69 followed by a C–N bond formation would lead to the final chiral α-aminoboronate product.
In this work, we describe a highly enantioselective Ni-catalysed hydroamidation process enabled by a simple chiral amino alcohol ligand under exceptionally mild conditions. A wide variety of enantioenriched α-aminoboronates, a biologically active pharmacophore, were directly obtained in high yields with excellent enantioselectivities. The utility of this protocol is illustrated by the synthesis of Vaborbactam in three steps.
Results and discussions
Reaction design and optimisation
Our initial studies focused on the enantioselective hydro-amidation of a pinacol-protected alkenylboronate (1a) using 3-phenyl-1,4,2-dioxazol-5-one (2a) as an amidating reagent (Fig. 2). We found that NiCl2∙6H2O and the chiral amino alcohol ligand (L*) with triethoxysilane could afford the desired hydroamidation product (3a) in 71% isolated yield with 95% ee (entry 1). Other nickel sources such as NiCl2∙dme (dme = dimethoxyethane) led to lower yields and ee (entry 2). Other ligands (L1–L6) also gave significantly lower yields and ee (entries 3–8). Dimethoxy(methyl)silane was shown to be a less effective silane (entry 9). Addition of a catalytic amount of an iodide salt was found to improve the yield (entry 10) and LiI was proved to be the best additive (entry 11). Currently, the exact role of LiI is still under investigation. Inclusion of an extra proton source improved both the yield and the ee (entry 12), but alcohol was less effective than H2O (entry 13). Through DFT calculation, Chang, Seo and coworkers have demonstrated that the transmetalation between Ni-enamido complex and hydrosilane is thermodynamically unfavorable, and the addition of H2O could provide thermodynamic driving force for this step by an irreversible Si–O bond formation60. Similarly, with other solvents, the reaction proceeded less efficiently (entry 14). Notably, the E,Z-configuration of alkenyl boronates has a significant effect on the ee of the products. For example, a diminished ee was observed when (Z)-1a was used (entry 15). Notably, the reaction is insensitive to air (entry 16) and moisture (entry 17).
Substrate scope
Under the optimal conditions, the scope of the alkenyl boronate partner is fairly broad (Fig. 3). Substrates containing a variety of functional groups, including an alkyl chloride (3f, 3g), a variety of ethers (3h, 3i, 3l, 3o and 3p), esters (3j, 3l–3p), as well as sulfonamides (3k, 3m), were shown to be competent. Notably, the reaction is orthogonal to alkyl chlorides (3f, 3g), a potential coupling handle for further derivatization. The generality of this protocol was further highlighted by the successful introduction of several core structures of bioactive and pharmaceutical molecules, including gemfibrozil (3l), probenecid (3m), menthol (3n), glucose (3o), and vitamin E (3p), which afforded molecules with two bioactive fragments that are useful in pharmaceutical research. High levels of diastereoselectivity were achieved in the hydroamidation of substrates (3n, 3n’, 3o, 3o’, 3p, 3p’) derived from a series of chiral molecules. Unfortunately, β,β-disubstituted and α,β-disubstituted alkenyl boronates, which are less reactive towards hydronickellation, produced the desired products (3q, 3r) with low yields under these conditions. When β-aryl substituted alkenyl boronate (3s) was used, amidation happened at both the α-carbon atom of the boronate and the benzylic position as a 2.3:1 mixture.
A subsequent survey of possible dioxazolone components revealed a wide range of aromatic (4a–4h), alkenyl (4i) and aliphatic (4j–4v) amide electrophiles as competent substrates (Fig. 4)66,67,68,69. For aromatic amide electrophiles, both electron-donating (4b–4d) and electron-withdrawing (4f, 4g) substituents on the benzene ring of the electrophile, as well as a heterocyclic electrophile (4h) underwent asymmetric hydroamidation smoothly. For alkyl amide electrophiles, a various primary (4j–4n, 4t–4v), secondary (4o–4q), and tertiary (4r, 4s) aliphatic amide electrophiles all were efficiently converted into the corresponding amide products. Functional groups, including a variety of ethers (4b, 4c, 4j, 4k, 4q, 4r, 4t, 4v), carbamates (4d, 4p), aryl chlorides (4f, 4v), esters (4g, 4s), a nitrile (4m) and an easily reduced ketone (4t), were left intact. Heterocycles such as thiophene (4h), furan (4n), oxazole (4u), and indole (4v) were also accommodated. Successful functionalization of a series of biologically important compounds such as isoxepac (4t), oxaprozin (4u), and indomethacin (4v) was achieved, demonstrating the potential utility of this protocol in the late-stage functionalization of complex molecules.
Application
The preparative utility of this process was highlighted by a 5 mmol scale experiment (Fig. 5a). Product 3a was obtained without notable erosion of the yield or the enantioselectivity (cf. Fig. 2, entry 1, 71% yield, 95% ee). As shown in Fig. 5b, the desired hydroamidation product (3a) could also be obtained directly from alkyne through a one-pot reaction sequence without isolating the hydroboration intermediate (1a). The synthetic utility was further demonstrated by a three-step synthesis of Vaborbactam, a β-lactamase inhibitor (Fig. 5c)70. The key hydroamidation of the alkenyl boronate (6), obtained through Zr-catalysed hydroboration, generated the α-aminoboronate product (7) in moderate yield (50%) with high diastereoselectivity (97:3 dr). The synthesis of target compound, Vaborbactam was completed by HCl-mediated deprotection.
Mechanistic investigation
A series of experiments were carried out to gain insight into the reaction mechanism. A linear correlation between the ee value of the ligand L* and that of the product 3a was observed (Fig. 6a), an observation that is consistent with the monomeric nature of the active catalyst. Since H2O38 and hydrosilane could both act as a hydride source, an isotopic labelling experiment was carried out using D2O (Fig. 6b, top). No deuterium incorporation was observed in the product (3a), eliminating the possibility of a protic reagent as the hydride source. To gain insight into the hydrometallation process, the reaction of a deuterium labeled olefin (1b-D) was evaluated (Fig. 6b, bottom). Diastereomerically pure 3b-D was obtained from this reaction, indicating that syn-hydronickellation is involved in the enantio-determining step. This conclusion is also consistent with the observation that the E,Z-configuration of alkenyl boronates has a significant effect on the ee of the products (cf. Fig. 2, entry 1 vs. entry 15).
To further understand the subsequent amidation process, we treated dioxazolone (2a) with triphenylphosphine (PPh3) under standard conditions (Fig. 6c)60. A nitrene transfer to the phosphine adduct, imidophosphorane was obtained, suggesting that the formation of a nickel-nitrenoid species could be one possible pathway for amidation process.
In conclusion, we are reporting development of a NiH-catalysed enantioselective hydroamidation procedure which enables the facile synthesis of a variety of enantioenriched α-aminoboronates with high potential in medicinal chemistry. With a simple chiral amino alcohol ligand as the source of chirality, a broad range of both alkenyl boronates and dioxazolone partners are suitable for this transformation. This mild and straightforward hydroamidation process has been applied to the efficient synthesis of a pharmaceutical agent.
Methods
General procedure (A) for NiH-catalysed asymmetric hydroamidation of alkenyl boronates
In a nitrogen-filled glove box, to an oven-dried 8 mL screw-cap vial equipped with a magnetic stir bar was added NiCl2·6H2O (4.8 mg, 10 mol%), L* (8.0 mg, 12 mol%), LiI (13.4 mg, 0.10 mmol, 0.50 equiv), 1,4,2-dioxazol-5-one (0.30 mmol, 1.5 equiv) (if the olefin is a solid, it was also added at this time), and anhydrous DMA (1.0 mL, 0.20 M). The mixture was stirred for 10 min at rt, at which time alkenyl boronate (0.20 mmol, 1.0 equiv) (if the 1,4,2-dioxazol-5-one is a liquid, it was added at this time), H2O (1.8 μL, 0.10 mmol, 0.50 equiv), and (EtO)3SiH (92 μL, 0.50 mmol, 2.5 equiv) were added to the resulting mixture in this order. The tube was sealed with a teflon-lined screw cap, removed from the glove box and the reaction was stirred at 25 °C water bath for up to 20 h (the mixture was stirred at 800 rpm). After the reaction was complete, the reaction was quenched upon the addition of H2O, and the mixture was extracted with Et2O. The organic layer was concentrated to give the crude product. n-Dodecane (20 μL) was added as an internal standard for GC analysis. The product was purified by flash column chromatography (petroleum ether/EtOAc) for each substrate. The yields reported are the average of at least two experiments, unless otherwise indicated. The enantiomeric excesses (% ee) were determined by HPLC analysis using chiral stationary phases.
Data availability
The authors declare that the main data supporting the findings of this study, including experimental procedures and compound characterization, are available within the article and its Supplementary information files, and also are available from the corresponding authors.
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Acknowledgements
Support was provided by NSFC (92156004, 22271143, 22271146), NSF of Jiangsu Province (BK20190281, BK20201245), programs for high-level entrepreneurial and innovative talents introduction of Jiangsu Province (group program), Fundamental Research Funds for the Central Universities (020514380282), and Open Research Fund of School of Chemistry and Chemical Engineering, Henan Normal University.
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S.Z. and Y.W. designed and supervised the project. Y.Z., D.Q., and M.D. performed and analysed the experiments. All authors co-wrote the manuscript, analysed the data, discussed the results, commented on the manuscript, and approved the final version of the manuscript.
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The authors declare the following competing interest(s): S.Z. and Y.Z. are inventors on a patent application number CN202210526440.5 which is based on the synthesis of Vaborbactam using this method. D.Q., M.D., and Y.W. declare no competing interests.
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Zhang, Y., Qiao, D., Duan, M. et al. Enantioselective synthesis of α-aminoboronates by NiH-catalysed asymmetric hydroamidation of alkenyl boronates. Nat Commun 13, 5630 (2022). https://doi.org/10.1038/s41467-022-33411-9
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DOI: https://doi.org/10.1038/s41467-022-33411-9
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Intramolecular hydroamidation of alkenes enabling asymmetric synthesis of β-lactams via transposed NiH catalysis
Nature Catalysis (2023)
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Recent Progress in NiH-Catalyzed Linear or Branch Hydrofunctionalization of Terminal or Internal Alkenes
Topics in Current Chemistry (2023)