Abstract
Organic compounds that contain nitrogen are very important intermediates in pharmaceutical and chemical industry. Hydroamination is the reaction that can form C–N bond with high atom economy. The research progress in metals catalyzed hydroamination of alkenes and alkynes from the perspective of reaction mechanism is categorized and summarized.
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Introduction
More and more attention are attracted in hydroamination reaction as a tool for N–H synthesis, plenty of complementary synthetic methods have come to the fore for the development of intensified and industrially relevant C–N forming processes [1, 2]. According to our statistics, synthesizing C–N via hydroamination reaction has become a promising area of research, experiencing growing diversification [3, 4]. Since the first publications on this hydroamination reaction over past years, close to 450 research papers have been published on this topic [5, 6]. Further statistics indicate 78% of the published research can be classified as substrates which work under mild conditions as follows [7, 8]. At the same time, with the development of hydroamination, various catalytic systems have been gradually systematized, and many breakthrough progresses have been made [9, 10].
The attractive and challenging methods for the formation of C–N bonds are hydroamination reactions. In this review, we will mostly focus on recent developments in the effects of different substrates containing N–H. In the meantime, usage of the term hydroamidation is not only including the substrate classes of saturated fat primary amine, saturated fatty secondary amine and unsaturated fatty amine, but extended to structurally related compounds with selective, reactivity and productive yield. Moreover, intra- and inter-molecular hydroamination reactions will be mentioned as well if they are necessary for the discussion or might act as springboard for future research.
The effects of different compounds containing N–H
Saturated fatty primary amine
Fatty primary amines (C1 to C12) are essential intermediates for the chemical and pharmaceutical industries. A large amount of fatty primary amine and the corresponding derivatives are according to their cationic surface activity.
In 2007, Barry et al [11] introduce organolithium into the hydroamination reaction between the molecules of cinnamyl alcohol and primary amine 1 (Scheme 1). In the presence of metallic lithium, the nonterminal olefin and primary amine compounds were acquired, such as methylamine, benzyl amine butyl amine, but the yield is only about 50%. On the one hand, it can undergo a favorable proton transfer process to give the more stable amido-alkoxide, thus shifting the equilibrium in the desired sense. It is found that they do not introduce carbonyl and halogenated compounds to saturated fats. Besides, the reaction conditions are very hard, and the reaction temperature needs to drop to − 78 °C.
Addition of primary amines to cinnamyl alcohol
[Rh(CH3CN)2COD]BF4 possesses a great deal of benefits, including high activity and effective. In 2010, Julian et al [12] use this compound to catalyze the intramolecular hydroamination reaction (Scheme 2). The catalyst has strong applicability, and it can achieve very high catalytic effect, whether it has chlorine atom (Cl), ester base (COO), ketone (CO), nitrile (CN), or hydroxyl (OH) without protection. Meanwhile, this rhodium ligand is undefined from the ligand, which is formed by the late transition metal such as palladium (Pd), platinum (Pt), iridium (Ir), after the rhodium ligand and the carbon-carbon double bond on the bottom of primary amine substrate 2 formed complexes, it will not reverse, as a result of competitive catalyst decomposition, forming a non-cyclic precursor, and greatly improving the efficiency of molecular hydrogen amination. Besides, the forming Rh complex of hydroamination reaction was given in the Scheme 3.
Rh-catalyzed hydroamination of primary aminoalkenes
The forming Rh complex intermediate state of hydroamination reaction
In 2010, Xu group [13] firstly take advantage of Ln(CH2SiMe3)3(THF)2 and Indenyl with half-Sandwich η5 ligands, separating the catalyst and determine its structure via crystal diffraction. The experiment demonstrates that the catalyst is very effective for the intramolecular hydroamination synthesis of nitrogen heterocyclic compounds. As for the C6D6 solvent, the intramolecular hydroamination reaction was found in saturated fatty primary amine substrate 3 (Scheme 4). Consequently, these ligands containing yttrium and dysprosium, are highly active in a series of saturated fatty primary amine substrates, and are relatively easy to form nitrogen heterocyclic compounds (yielding 98%).
Hydroamination of 2,2-dimethylpent-4-enylamine catalyzed by (1,3-(SiMe3)2C9H5)Sc(CH2SiMe3)2(THF)
2005, Collin et al [14] reported the lanthanide compounds catalyst intramolecular asymmetric hydroamination reaction of saturated fatty primary amine 4 (Scheme 5), which has undergone the activation of isopropyl group, and further obtained spiral pyrrolidine. The selectivity of the reaction is good, and the e.e. value reaches 70%.
Hydroamination/cyclization of 1-(aminomethyl)-1-allylcyclohexane by Li2[(R)-C20H12N2-(C10H22)]
While Collin group [15] designed a kind of highly active lanthanide to catalyze intramolecular asymmetric hydroamination reaction of saturated fatty primary amine 5 (Scheme 6), introducing the tertiary butyl group into the catalyst, it can get high yield of secondary amine derivatives, the maximum yield can reach 94%, and it has the very good stereoselectivity, the e.e. value reaches 40%.
Hydroamination-cyclization of 1-(aminomethyl)-1-allylcyclohexane by {Li(THF)4}{Ln[(R)-C20H12N2(C10H22)]2}
In 2003, Kim et al [16] formed a bident ligand through lanthanide and triphenylphosphine, which catalyzed intramolecular hydroamination reaction of saturated fatty primary amine 6 (Scheme 7), and synthesized a variety of secondary amines. But the selectivity of this reaction is not so good, vice product was generated. In addition, the study found that compared with the covalent radius of neodymium and yttrium, the covalent radius of dysprosium is small. Therefore, when it catalyzes intramolecular hydroamination reaction, it can make the product do not change the configuration in a short time, and further raise the antipodal selectivity.
Catalyzed cyclization of 2-aminohex-5-ene
In 2008, aiming to synthesizing a novel kind of ligand, Tamm group [17] select rare earth metals and alkali metal as the hydroamination reaction catalyst, limiting the geometry of that catalyst. And then its structure was determined by single crystal diffraction. Maybe due to the catalyst is meso-structure, consist of two cyclopentadiene group, exhibiting strong ability of electron-donating. It also greatly enhances the activity of intramolecular hydroamination reaction of saturated fatty primary amine 7 (Scheme 8), beneficial for shifting from trans to cis.
Hydroamination reaction of terminal aminoalkenes and alkynes catalyzed by Ca catalyst
Saturated fatty secondary amine
Nitrogen compounds are widespread in many natural organic compounds and possess a series of physiological activity [18, 19]. After pharmacology studies, these compounds have good anti-inflammatory effects such as antiseptic, antifungal and other aspects [20]. Therefore, the reaction of hydroamination has been one of the hotspots in the research of organic synthesis [21]. In order to further enrich the kinds of nitrogenous compounds, chemists synthesized a variety of multifunctional nitrogen compounds [22]. Based on saturated fatty secondary amine, it will show more complex molecular structure as well, meeting the needs of pharmaceutical industry [23].
In 2010, Randive et al [24] found that it is good for the intermolecular hydroamination reaction in water phase. As for propiolic acid ethyl ester and saturated fat secondary amine 8 (Scheme 9), including dimethylamine, diisopropyl amine and piperidine, sequentially beta amino ester compounds were acquired. This reaction not only has high regio-selectivity and stereo-selectivity, using the green and inexpensive solvent, providing a pioneering research method for studying the hydroamination reaction.
Reactions of thiols and amines with ethyl propiolate
In 2010, Toups and Widenhoefer [25] co-found a new intramolecular palladium catalyzed hydroamination reaction with substrate 9 (Scheme 10) and divinyl. It is involved that this reaction is initiated by the oxidation reaction between allyl group of propadiene and the silver trifluoromethane. palladium ion (Pd2+) attack from the back of the propadiene, forming the π propadiene ligand of cationic palladium, and generating the trans product at last, and the corresponding reaction mechanism was displayed (Scheme 11).
Intermolecular hydroamination of monosubstituted allenes with secondary alkylamines catalyzed by a mixture of (dppf)PtCl2 and AgOTf in toluene at 80 °C
A mechanism for the platinum catalyzed hydroamination of allenes with secondary alkylamines
In 2010, Jimenez et al [26] reported the hydroamination based on the N-substrate 10 (Scheme 12) with intermolecular regio-selectivity catalyzed by Rh+ salt, producing anti-Markovnikov products. In addition, the structure of the catalyst was confirmed by single crystal diffraction. It was found that Rh+ and diphenylphosphine can generate trans chelate, greatly promoting the formation of anti-Markovnikov products. However, this reaction has some limitations. This reaction limited to saturated fatty secondary amine and produced a large number of by-products.
Rh-catalyzed hydroamination of styrene with piperidine
In 2009, Leitch et al [27] reported intramolecular hydroamination reaction of saturated fatty secondary amine catalyzed by Zr(NMe2)4 proligand. This method is used to synthesize six nitrogen heterocyclic synthesis of various kinds of activity in different substituted allyl amines 11 (Scheme 13), but also are applied for synthesizing natural product intermediates. More importantly, Zr(NMe2)4 have high chemical selectivity for saturated fatty secondary amines. It is unnecessary for shape didentate ligands in the process of ring forming.
In situ catalyst screening of both primary and secondary aminoalkene substrates
Exploiting more practical, less limitations of catalyst are used for intramolecular hydroamination, in favor of seeking another new scheme. With the direction of Komeyam et al [28] they studied a simple and effective method for hydroamination with 12 (Scheme 14), and synthesized pyrrole derivatives under the catalysis of ferric chloride through intramolecular hydrogenation amination. The reaction conditions are moderate, regardless of any ligands.
Intramolecular hydroamination of amino olefins by FeCl3·6H2O
In 2005, Bender and Widenhoefer [29] jointly designed the intramolecular amination of saturated fatty secondary amine 13 (Scheme 15). The substrate, such as gamma aminolefine, was induced by the Pt-based catalytic system, and the corresponding five membered nitrogen heterocyclic compounds were obtained. The author speculated that the formation of trans Pt-C bond by platinum hydride, is conducive to the deprotonation and get good yield.
Hydroamination of amino olefins catalyzed by a mixture of [PtCl2(H2CdCH2)]2 and PPh3 in Dioxane at 120 °C
Fukumoto research group [30] in 2007 designed and synthesized organic rhodium catalyst to catalyze the hydroamination between the alkyne and saturated fatty secondary amine 14 (Scheme 16). For the intermolecular alkynes hydroamination synthesis of the corresponding anti-Markovnikov enamines and imines, the organic rhodium metal catalyst has good regio-selectivity. The author also explains the result of this specificity, because the metal rhodium complex can not turn over after its coordination with the unsaturated bond.
TpRh(C2H4)2/PPh3-catalyzed hydroamination of 1-octyne with amines
In 2009, Ohmiya et al [31] reported the synthesis of pyrrolidine and piperidine derivatives by intramolecular hydroamination of terminal olefin catalyzed by copper. The experiment showed that the Cu complex could effectively catalyze the hydroamination reaction of saturated fatty secondary amine 15 (Scheme 17). After introducing methoxy group (–CH3), fluorine atom (F), nitrile group (–CN) and ester group (–COO) on the amine group, the cyclization process was not affected, and the yield was very high at the same time. It is worth noticing that the mechanism of the phenomenon is explained by the authors. The carbon carbon double bonds on olefin and alkyl copper formed copper olefin-π ligands. Because of the protonation effect, the copper ligand on the five membered rings eliminated faster than the beta hydrogen, and finally formed the enamine and hydrides of copper.
Cu(I)-catalyzed intramolecular hydroamination of aminoalkene
In 2010, Reznichenko et al [32] reported the asymmetric hydroamination reaction catalyzed by several lanthanide catalysts. Chain olefins, such as 1-heptene and benzyl amines 16 (Scheme 18), has very high and selective enantioselectivity in hydroamination, and has little by-product. This method often produces chiral amine ligands in the reaction process. Research shows that even when para benzyl amines have a methoxy, it will greatly reduce the asymmetric hydroamination activity of chain olefin.
Asymmetric intermolecular hydroamination of 1-alkenes with a primary amine
Kang et al [33] reported in 2006 that the intermolecular hydroamination between allene and saturated fatty secondary amine 17 (Scheme 19) catalyzed by Au. In the process of this reaction, Au+ substrate formed carbene ligand and produced a chiral center, ultimately contributing to the formation of a single markovnikov product. This gold complex has been proved to be a highly efficient catalyst for the hydroamination between saturated fatty secondary amine and a series of dienes, and the catalyst can be reused while maintaining its high activity and selectivity.
Hydroamination of allenes with secondary alkylamines
Piperazine derivatives have attracted much attention of chemists because of its very good pharmic and biological activity. As early as 1998, Belier and Breind [34] found that in the n-BuLi/THF system and in the absence of any catalyst and additives, they also achieved intermolecular hydroamination reaction between styrene and piperazine compound 18 (Scheme 20), and this reaction can generate a single anti-Markovnikov product with a high yield. However, n-butyl lithium has a large limitation and can be used only for piperazine compounds.
Base-catalyzed hydroamination of styrene with l-(4-fluorophenyl)piperazine
In 2003, Utsunomiya et al [35] reported the synthesis of morpholine derivatives with Tf-OH and palladium salt. From the view of thermodynamics, in the effect of palladium salt, the reaction formed η 3-styrene transition state was more easily than the η 3-alkyl transition state, then the intermediate state removed Tf-OH by hydroamination with 19 (Scheme 21), further generating markovnikov products.
Pd-catalyzed hydroamination of alkylamines with vinylarenes
In second years, Utsunomiya et al [36] improved the catalytic system and used the ruthenium complex to catalyze the synthesis of morpholine derivatives, based on the substrate 19 (Scheme 22) likewise. From the kinetic point of view, this reaction is conducive to the formation of anti-Markovnikov amine ruthenium intermediate. In the presence of trifluoromethanesulfonic acid, the rapid irreversible deprotonation reaction occurs in the middle of the anti-Markovnikov amine ruthenium, and then occurring the elimination of beta hydrogen to get the anti-Markovnikov additive product.
Ruthenium-catalyzed hydroamination of vinylarenes with alkylamines
Unsaturated fatty amine
The hydroamination of unsaturated fatty amines as substrates has been studied for decades [37]. These substrates are often concentrated in the imidazole, pyrrole and other nitrogenous heterocyclic compounds [38]. Based on our research [39,40,41,42], it is noteworthy that such substances are very important intermediates for synthetic drugs and natural products.
In 2010, the Yan project group [43] reported a new type of intermolecular hydroamination of unsaturated fat secondary amines catalyzed by copper. Among them, CuI as a key catalyst, and oxygen as an oxidant, they provide highly selective pyrrole compounds. And the author provides a preliminary mechanism to experience the catalytic cycle of Cu(I/II). The reaction activates secondary amine 20 (Scheme 23) under the action of CuI, and then isomerization occurs in the intermediate state at high temperature. After that, pyrrole compounds are produced by [3 + 3] cyclization, and hydrogen peroxide is released at the same time.
Synthesis of polysubstituted pyrroles from dialkyl ethylenecarboxylate and β-enamino ester
In 2008, Moran et al [44] reported that methyl benzoate as photosensitizer, through 254 nm ultraviolet light initiation, imidazoles unsaturated fatty secondary amine 21 (Scheme 24) and a series of olefins were photoisomerized in the process of hydroamination, obtaining complex Markovnikov products. It has been shown that the synthesized series of compounds have antifungal activity.
Photoinduced additions of azoles to 1-methyl-1-cyclohexene
In 1999, the Tzalis group [45] reported that pyrrole was used as a substrate to synthesize a series of different pyrrole derivatives. The author took pyrrole 22 (Scheme 25) as starting materials, with cyclohexene, occurred hydroamination reaction catalyzed by cesium hydroxide monohydrate. This method can also be applied to the synthesis of other nitrogen heterocyclic compounds, such as indole, imidazole, etc.
The addition of alcohols and secondary amines by the cesium hydroxide and CsOH catalyzed in NMP
In 2009, Huynh et al [46] have presented a straightforward and efficient synthesis of benzannulated dicarbene complexes bearing labile acetato, fluoroacetato, and acetonitrile co-ligands, which are unusually stable in solution and resist ligand disproportionation. The molecular structure of the complexes was determined by X-ray single crystal diffraction. A preliminary catalytic study showed that the reaction between styrene and aniline 23 (Scheme 26) using hydroamination reaction showed the certain activity of complex containing trifluoro ethyl ester.
Pd-catalyzed hydroamination of styrene with aniline
In 2010, Zheng et al [47] reported a simple synthesis route of 1, 2, 5-three substituted of pyrrole. Under 100°, with CuCl as catalyst, intermolecular and intramolecular double hydroamination reaction has generated between 1,3-butadiyne and primary amine 24 (Scheme 27), 1,4-two substituted 1,3-butadiyne and alkynes through selective intermolecular hydroamination to form 1, 2, 5-three substituted pyrroles with a high yield. And it has the advantages of easy to start, mild reaction conditions, cheap catalyst, and high yield.
One-pot synthesis of 1, 2, 5-three substituted pyrrole
In 2005, Luo et al [48] reported a new synthetic method of highly selective multi substituted 1,2-two hydrogen quinoline derivatives under a series of domino 25 (Scheme 28) processes and the catalysis of silver catalyst. Hydrogenation, alkylation, intramolecular hydrogenation and hydrogenation of three molecular alkyl can be completed in the single pot process of the 100% atom economy.
A silver-catalyzed domino reaction of simple aniline and alkyne
In 2008, cheng et al [49] studied the effects of different lewis acids on intermolecular hydroamination by hydroamination of aromatic amine 26 (Scheme 29) with norbornene. The common metal halides and their catalytic properties were compared. BiCl3 is the most efficient, delivering a higher yield in a shorter response time. ZrCl4 catalytic reaction can be completed at a relatively low temperature, but requires a higher and longer reaction time. Most of the reactions catalyzed by FeCl3 have chemical selectivity. When AlCl3 is used as a catalyst, some amines can be substituted by different functional groups. The acidity of amine hydrogen atoms is an important factor for conversion benefit.
Lewis acid catalyzed hydroamination of norbornene with aromatic amine
In 2010, Demir et al [50] successfully developed a 4-amine 24 (Scheme 30) cyclochemistry catalyzed by Au(I)/Zn(II) in series as well. An effective, versatile and widely available synthetic pyrrole with multiple substituents is provided. Au (I) species combined with Zn (II) salts to catalyze hydrogenation. The reaction mechanism was further studied as shown in Scheme 31, the product distribution of the reaction was elucidated, and the range of synthesis was expanded.
Au(I)/Zn(II)-catalyzed sequential intermolecular hydroamination reaction of 4-yne-nitriles with amine
Plausible mechanism for pyrrole formation by Au(I)/Zn(II)-catalyzed
In 2009, Yin et al [51] reported that Lu(OTf)3/I2 catalytic system had better catalytic activity in the hydroamination reaction of inactive olefin and similar aniline 23 (Scheme 32). This system has the advantages of simple use, cheap catalyst, atomic economy and high yield. The proposed catalytic system provides a good strategy for hydroamination under mild conditions.
Intermolecular hydroamination of unactivated alkenes and anilines catalyzed by lanthanide salts
Conclusion and outlook
In summary, the raw materials of hydroamination, whether alkyne, alkene, amine or olefin, are widely existed in various moieties, applying for high atomic economy in artificial synthesis [52,53,54]. Over the past decades, heterogeneous catalysis for a more sustainable hydroamination due to the possibility of recycling and simple isolation of the secondary amines or imines by simple centrifugation or filtration of the solid, avoiding work-up and metal contamination of the product. It is believed that in the near future, hydroamination can replace those unsustainable reactions of methodology during the industrial circles, especial for medicine and paint intermediate, such as coupling reaction and Wittig reaction. In spite of these excellent achievements, research on the use of nonprecious metals is still open for both hydroamination and C-N formations. Soon intensive work will focus not only on new metal-organic design in the solid state, i.e. metal-organic frameworks or zeolites, also allow the stability, low toxicity and reusability of such heterogeneous catalysts [55].
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Acknowledgements
The authors are thankful to Institute of Electrochemical Corrosion, College of Materials Science and Energy Engineering, Foshan University for providing necessary facilities to carry out this research work. Meanwhile, we are grateful to the High-Level Talent Start-Up Research Project of Foshan University (cgg040947), Guangdong Natural Science Foundation of China (Grant Nos. 2018A1660001, 2017A030313307), National Natural Science Foundation of China (No. 51702051), the key Project of Department of Education of Guangdong Province (2016GCZX008), the key Research Platform Project of Department of Education of Guangdong Province (cgg041002), the Project of Engineering Research Center of Foshan (20172010018), Education Department Foundation of Guangdong province (No. 2016KTSCX151) for financial support.
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JH, GH, WC, XH, QD and DC have designed and prepared the review article. All authors read and approved the final manuscript.
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Dr. Jingpei Huo was born in Chancheng district, Foshan, Guangdong China, in 1988. He received his bachelor’s degree from Foshan University in 2010, a master's degree in 2013 from South China Normal University and a Ph.D. degree in 2016 from South China Technology University, working under the direction of Prof. Heping Zeng. From 2016 to forever, he was working in the group of Prof. Dongchu Chen at Foshan University. His current research interests lie in organic synthesis, especial for N-compounds. Some articles have been published on Catal. Sci. Technol., J. Mater. Chem. A, Appl. Catal B.-Environ., Macro. Rap. Comm., Polym. Chem., RSC adv., Appl. Surf. Sci., BMC Chemistry, ACS Omega and Ind. Eng. Chem. Res.
Dr. Guozhng He was born in Dongguan, Guangdong China, in 1995. He received his bachelor’s degree from Foshan University in 2018. His research focuses on the synthesis and activity of N-H compounds.
Dr. Weilan Chen was born in Foshan, Guangdong China, in 1997. She received his bachelor’s degree from Foshan University in 2020. His current research interests lie in synthesis and activity of bithiazole.
Dr. Xiaohong Hu was born in Jingdezhen, Jiangxi China, in 1964. He received his Ph.D. degree in 2013 from the State Key Laboratory of Organic Geochemistry, Guangzhou Institute of Geochemistry, Chinese Academy of Sciences, working under the direction of Prof. Taicheng An. His current research interests lie in improving the photodegradation efficiency of dye, especially the modification of TiO2.
Dr. Qianjun Deng was born in Chengzhou, Hunan China, in 1968. He received his Ph.D. degree in 2010 from Central South University. His current research interests lie in enhancing the photocatalytic efficiency of photocatalysts, including the synthesis and modification of metal complex.
Dr. Dongchu Chen was born in Chongyi, Jiangxi China, in 1972. He earned his chemistry Ph.D. from Huazhong University of Science and Technology. He did his postdoctoral work at the South China University of Technology, and is currently professor at the Foshan University. He is a researcher of metal composite, especially the surface modification of organic material, some articles have been published on Polym. Chem., RSC adv., Appl. Surf. Sci. and ACS omega.
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Huo, J., He, G., Chen, W. et al. A minireview of hydroamination catalysis: alkene and alkyne substrate selective, metal complex design. BMC Chemistry 13, 89 (2019). https://doi.org/10.1186/s13065-019-0606-7
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DOI: https://doi.org/10.1186/s13065-019-0606-7