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Article

The Synthesis of 2-Aminobenzoxazoles Using Reusable Ionic Liquid as a Green Catalyst under Mild Conditions

by
Ya Zhou
1,†,
Zhiqing Liu
1,†,
Tingting Yuan
1,
Jianbin Huang
1 and
Chenjiang Liu
1,2,*
1
School of Chemistry and Chemical Engineering, Xinjiang University and Key Laboratory of Oil and Gas Fine Chemicals, Ministry of Education, Urumqi 830046, China
2
Physics and Chemistry Detecting Center, Xinjiang University, Urumqi 830046, China
*
Author to whom correspondence should be addressed.
†
The two authors contributed equally to this paper.
Molecules 2017, 22(4), 576; https://doi.org/10.3390/molecules22040576
Submission received: 9 March 2017 / Revised: 27 March 2017 / Accepted: 28 March 2017 / Published: 2 April 2017
(This article belongs to the Section Green Chemistry)
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Abstract

:
A facile, green, and efficient method for the direct oxidative amination of benzoxazoles using heterocyclic ionic liquid as catalyst has been developed. The reaction proceeded smoothly at room temperature and gave the desirable 2-aminobenzoxazoles with good to excellent yields (up to 97%). The catalyst 1-butylpyridinium iodide can be easily recycled and reused with similar efficacies for at least four cycles.

Graphical Abstract

1. Introduction

Amino-substituted azoles and their derivatives are ubiquitous in functional materials, pharmaceuticals, and natural products [1,2,3]. Among them, the 2-aminobenzoxazoles have already been described as potent 5-HT3-receptor antagonists [4,5], which are promising targets for the treatment of Alzheimer’s disease and schizophrenia. Furthermore, abundant other drug targets have been addressed by 2-aminobenzoxazoles, such as α7 nicotinic acetylcholine receptor (nAchR) agonist, 5-HT6-receptor antagonist, and MK-4305 in clinical trials against insomnia [6,7]. Hence, the development of effective methods to synthesize these compounds has attracted great attention. In this regard, direct C–H amination reaction displaying an advantage in atom efficiency has been pioneered by Cho (Scheme 1a), Monguchi, Wang, Kawano, Miyasaka, Xie and others in the past decade [8,9,10,11,12,13,14,15,16,17,18,19,20]. However, most of these methods could be realized only in the presence of copper, silver, manganese, iron, cobalt. The toxicity and expense of transition metals might limit practical applications.
Recently, metal-free-catalyzed oxidative coupling reactions have undergone rapid advances in order to solve drawbacks of transition metal catalysis [21,22,23,24,25]. Thus, the discovery of green and sustainable oxidative C–H amination of benzoxazoles under metal-free conditions will be of great value. Hypervalent iodine compounds have gained much attention in organic synthesis as versatile and powerful oxidants [26,27,28,29]. For example, Chang and co-workers [30] employed stoichiometric amounts of PhI(OAc)2, and Bhanage et al. [31]. used 2-iodoxybenzoic acid (IBX) to get direct oxidative C–H bond amination of benzoxazoles. Moreover, much progress in the direct oxidative amination of benzoxazoles has been achieved through the use of a combination of an iodine source and oxidant [32,33,34,35,36,37,38]. For instance, a metal-free approach for the oxidative amination of benzoxazoles using molecular iodine as a catalyst and tert-butyl hydroperoxide (TBHP) as an oxidant was reported by Lamani and Prabhu [32]. At the same time, another report was presented by Nachtsheim’s group on the oxidative C–H amination of benzoxazoles under metal-free conditions using tetrabutylammonium iodide (TBAI) as catalyst and aqueous solutions of H2O2 or TBHP as co-oxidant at 80 °C (Scheme 1b) [33]. These catalytic systems effectively overcome some drawbacks of using stoichiometric amounts of hypervalent iodine compounds. Nevertheless, these approaches still suffer from minor drawbacks, such as high temperature, long reaction time, and low yields. Therefore, designing a highly mild, efficient, green, and recyclable catalyst system for the oxidative C–H amination of benzoxazoles under metal-free conditions at room temperature is desperately needed.
Ionic liquids (ILs) have attracted continuing interest from the majority of chemists. ILs were usually used as green reaction media because of their unique chemical and physical properties, such as high thermal stabilities, negligible vapor pressures, and nonflammability [39,40,41,42,43,44]. Recently, ILs have been employed as solvents in transition-metal-catalyzed C–H activation reactions [45,46,47,48,49]. However, it is important to note that there are few examples of the C–H bond activation reaction using classical heterocyclic ionic liquids as promoters or catalysts. We recently developed the first oxidative cross-coupling reaction for C–C bond formation promoted by ionic liquid 1,3-dibutyl-1H-benzo[d][1,2,3]triazol-3-ium bromide [50]. Soon after, the first study using IL-catalyzed C–H activation reaction for C–N bond formation has been disclosed [51]. Inspired by these works, we herein report a mild, efficient, and metal-free strategy for C–H oxidative amination of benzoxazoles by using heterocyclic ionic liquid 1-butylpyridinium iodide ([BPy]I) as catalyst, TBHP as oxidant, and acetic acid as an additive at room temperature (Scheme 1c).

2. Results and Discussion

The investigation started with the reaction of benzoxazole (1a) and morpholine (2a) as model substrates (Table 1). In the presence of 5 mol% [BPy]I, 1.5 equiv. of TBHP, and 3 equiv. of acetic acid, the reaction of 1a and 2a was proceeded at room temperature for 7 h to give 2-morpholinobenzo[d]oxazole (3a) in 94% yield (Table 1, entry 1). Encouraged by the result, further optimization of the reaction conditions was carried out. Unfortunately, when other ionic liquids (e.g., 1-butylpyridinium chloride ([BPy]Cl) and 1-butylpyridinium bromide ([BPy]Br)) were in this reaction system or the system was run in the absence of catalyst, the response almost did not give satisfactory results (Table 1, entries 2–4). Considering that ionic liquids have the advantage of being reusable, the dosage of the [BPy]I was studied in an effort to reduce the reaction time. Gratifyingly, when the amount of the [BPy]I was increased from 5 mol% to 15 mol% (Table 1, entries 1, 6), the reaction time decreased from 7 h to 3.5 h. However, when the dosage of the [BPy]I was increased to 20 mol% (Table 1, entry 7), the reaction time did not reduce. Thus, 15 mol% of [BPy]I was an adequate choice of catalyst for the reaction to achieve high yields with less reaction time. Furthermore, four kinds of organic solvents were investigated, and acetonitrile was found to be the optimal solvent (Table 1, entries 6, 8–10). In water and under solvent-free condition, product 3a was obtained in lower yields of 57% and 51%, respectively (Table 1, entries 11–12). Other oxidants, such as benzoyl peroxide (BPO), m-chloroperoxybenzoic acid (m-CPBA), di-tert-butyl peroxide (DTBP), and H2O2 were used instead of TBHP (Table 1, entries 13–16), the effect of reactions decreased dramatically and TBHP was proven to be the best oxidant.
Under optimized reaction conditions, benzoxazole (1a) and various cyclic or acyclic secondary amines (2) were investigated to examine the scope of the process. The results are listed in Scheme 2. Piperidine, thiomorpholine, 3-methylpiperidine, and 1-methylpiperazine reacted smoothly with benzoxazole to form the corresponding amination products 3b, 3c, 3d, and 3e in good to excellent yields (Scheme 2). The introduction of heteroatom and substituent on piperidine had no impact on the reaction system. Subsequently, it was found that both electron-donating and electron-withdrawing groups on the piperazine—such as methyl, phenyl, acetyl, ethoxycarbonyl, and tert-butoxycarbonyl—reacted effectively with benzoxazole (1a) to provide the respective aminobenzoxazoles (Scheme 2, 3e: 90%, 3f: 97%, 3g: 91%, 3h: 82%, 3i: 95%). As is well known, 2-(N-alkylpiperazyl)benzoxazoles of this type were already described as potent 5-HT3-receptor antagonists [2]. The coupling of benzoxazole proceeded successfully with 1,2,3,4-tetrahydroisoquinoline to give the desired aminated product 3j in 93% yield (Scheme 2). In addition to cyclic amines, acyclic secondary amines such as diethylamine, dibenzylamine, and diallylamine reacted well with benzoxazole to produce the desired products 3k–3m in good to excellent yields (Scheme 2). To our delight, oxidations or halogenations of the methylene units, the aromatic ring, or the double bonds did not occur. It should be mentioned that N,N-diallylbenzoxazol-2-amine (3m) was regarded as one of the useful organic synthetic intermediates.
To further study the potential of our method, we turned our attention to the amination reaction between various benzoxazoles and morpholine. The results are summarized in Scheme 3. Methyl- and halogen-substituted benzoxazoles could be easily aminated to generate the desired products 4a–4d in up to 97% yield with perfect regioselectivity. To expand the potential of the present synthetic methodology, a diversity of benzoxazoles including 5-methylbenzoxazole, 6-methylbenzoxazole, and 5-chlorobenzoxazole reacted satisfactorily with various linear and cyclic secondary amines such as diallylamine, dibenzylamine, and tert-butyl piperazine-1-carboxylate to furnish the corresponding 2-aminobenzothiazole derivatives 4e–4i in good to excellent yields (84%–94%).
To demonstrate the potential industrial utility of our protocol, the [BPy]I-catalyzed scale-up reaction was performed. The direct oxidative amination of benzoxazole (1a) with morpholine was easily carried out under the standard reaction conditions to generate the desired product 3a in 93% isolated yield (Scheme 4).
Ionic liquids have several advantages compared with other catalysts; for example, they are recyclable and environmentally friendly. The coupling reaction of 5-methylbenzoxazole and morpholine was chosen as a model system to study the reusability of the [BPy]I as catalyst under the standard reaction conditions. After the reaction was finished, ethyl acetate and water were added, and then the [BPy]I was recovered from the water layer and reused after drying in vacuo. The [BPy]I was utilized repeatedly at least four times without any significant loss of activity (Figure 1).
In order to elucidate the reaction mechanism, control experiments were carried out. When the radical scavenger BHT (2,6-di-tert-butyl-4-methylphenol, 3 equiv.), ethene-1,1-diyldibenzene (3 equiv.), or TEMPO (2,2,6,6-tetramethylpiperidine-N-oxyl, 3 equiv.) were added to the reaction mixture under the optimal conditions, the yield of 3a was not decreased. Thus, the reaction may not be a radical reaction. Subsequently, N-iodomorpholine hydroiodide was prepared. Then, the reaction of benzoxazole (0.672 mmol, 1 equiv.) and N-iodomorpholine hydroiodide (0.672 mmol, 1 equiv.) with acetic acid (2.016 mmol, 3 equiv.) as an additive in 2 mL CH3CN at room temperature for 3.5 h afforded the desired product 3a in 25% yield (Table 2, entry 1). When the dosage of N-iodomorpholine hydroiodide was increased from 1 equiv. to 2 equiv., the desired amination product was obtained in 53% yield (Table 2, entry 2). It is worth noting that the reaction of 1a and 2a underwent smoothly in the presence of 15 mol% N-iodomorpholine hydroiodide, 1.5 equiv. TBHP, and 3 equiv. acetic acid to give 2-morpholinobenzo[d]oxazole (3a) in 95% yield (Table 2, entry 3). All of the above results indicate that the activation of the morpholine (2a) via in situ preparation of a highly reactive N-I bond from [BPy]I and TBHP seems plausible.
Based on the above results and existing literature [33], a plausible mechanism is proposed as shown in Scheme 5. Initially, [BPy]I is oxidized by TBHP to form [BPy]+[I(OAc)2]− (A) in the presence of acetic acid, and then releases acetylhypoiodite B. Subsequently, C is generated by combining morpholine with highly potent I+ source B. Immediately following, the reaction of C and benzoxazole affords D. Finally, the desired amination reaction product 3a can be obtained after the elimination of hydrogen iodide.

3. Experimental Section

A reaction vessel was charged with acetic acid (2.016 mmol) and TBHP (70% in water, 1.008 mmol) in acetonitrile (2 mL). After the addition of [BPy]I (0.1008 mmol), benzoxazole (0.672 mmol) and secondary amines (1.344 mmol) were added. Then, the reaction mixture was stirred at room temperature for 3.5 h. After the reaction finished, the mixture was extracted with dichloromethane (5 × 10 mL), and the combined organic phases were dried over anhydrous Na2SO4. The solvent was evaporated under vacuum, and the crude residue was purified by column chromatography on silica gel. Aqueous phase was dried in a vacuum evaporator to recover the ionic liquid and directly reused in subsequent runs.

4. Conclusions

In summary, we have found an IL-catalyzed direct oxidative amination of benzoxazoles under metal-free conditions at room temperature. This mild catalytic system is suitable for the oxidative amination reactions between a wide range of secondary amines and benzoxazoles. In addition, the inexpensive and environmentally friendly ionic liquid [BPy]I can be easily recycled and reused for four runs without any obvious loss of catalytic activity. ILs-catalyzed C–H bond activation is ongoing in our group.

Supplementary Files

Supplementary File 1

Acknowledgments

This work was supported by Grants from the Key Laboratory of Xinjiang Uyghur Autonomous Region (2015KL014), NSFC (21572195, 21502162, and 21262035), and Xinjiang University students innovative training program (201510755012).

Author Contributions

Chenjiang Liu conceived the idea of this piece of research; Zhiqing Liu, Ya Zhou and Chenjiang Liu designed the experiments; Ya Zhou, Zhiqing Liu and Tingting Yuan performed the chemical experiments; Ya Zhou and Zhiqing Liu performed the spectra analyses; Ya Zhou, Zhiqing Liu, Jianbin Huang and Chenjiang Liu wrote the paper.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Kablaoui, N.; Patel, S.; Shao, J.; Demian, D.; Hoffmaster, K.; Berlioz, F.; Vazquez, M.L.; Moore, W.M.; Nugent, R.A. Novel benzoxazole inhibitors of mPGES-1. Bioorg. Med. Chem. Lett. 2013, 23, 907–911. [Google Scholar] [CrossRef] [PubMed]
  2. Liu, K.G.; Lo, J.R.; Comery, T.A.; Zhang, G.M.; Zhang, J.Y.; Kowal, D.M.; Smith, D.L.; Di, L.; Kerns, E.H.; Schechter, L.E.; et al. Identification of a series of benzoxazoles as potent 5-HT6 ligands. Bioorg. Med. Chem. Lett. 2009, 19, 1115–1117. [Google Scholar] [CrossRef] [PubMed]
  3. Ningaiah, S.; Bhadraiah, U.K.; Keshavamurthy, S.; Javarasetty, C. Novel pyrazoline amidoxime and their 1,2,4-oxadiazole analogues: Synthesis and pharmacological screening. Bioorg. Med. Chem. Lett. 2013, 23, 4532–4539. [Google Scholar] [CrossRef] [PubMed]
  4. Gao, M.Z.; Wang, M.; Hutchins, G.D.; Zheng, Q.H. Synthesis of new carbon-11 labeled benzoxazole derivatives for PET imaging of 5-HT3 receptor. Eur. J. Med. Chem. 2008, 43, 1570–1574. [Google Scholar] [CrossRef] [PubMed]
  5. Yoshida, S.; Shiokawa, S.; Kawano, K.I.; Ito, T.; Murakami, H.; Suzuki, H.; Sato, Y. Orally Active Benzoxazole Derivative as 5-HT3 Receptor Partial Agonist for Treatment of Diarrhea-Predominant Irritable Bowel Syndrome. J. Med. Chem. 2005, 48, 7075–7079. [Google Scholar] [CrossRef] [PubMed]
  6. O’Donnell, C.J.; Rogers, B.N.; Bronk, B.S.; Bryce, D.K.; Coe, J.W.; Cook, K.K.; Duplantier, A.J.; Evrard, E.; Hajós, M.; Hoffmann, W.E.; et al. Discovery of 4-(5-Methyloxazolo[4,5-b]pyridin-2-yl)-1,4-diazabicyclo [3.2.2]nonane (CP-810,123), a Novel α7 Nicotinic Acetylcholine Receptor Agonist for the Treatment of Cognitive Disorders in Schizophrenia: Synthesis, SAR Development, and in Vivo Efficacy in Cognition Models. J. Med. Chem. 2010, 53, 1222–1237. [Google Scholar] [PubMed]
  7. Cox, C.D.; Breslin, M.J.; Whitman, D.B.; Schreier, J.D.; McGaughey, G.B.; Bogusky, M.J.; Roecker, A.J.; Mercer, S.P.; Bednar, R.A.; Lemaire, W.; et al. Discovery of the Dual Orexin Receptor Antagonist [(7R)-4-(5-Chloro-1,3-benzoxazol-2-yl)-7-methyl-1,4-diazepan-1-yl] [5-methyl-2-(2H -1,2,3-triazol-2-yl)phenyl] methanone (MK-4305) for the Treatment of Insomnia. J. Med. Chem. 2010, 53, 5320–5332. [Google Scholar] [CrossRef] [PubMed]
  8. Cho, S.H.; Kim, J.Y.; Lee, S.Y.; Chang, S. Silver-Mediated Direct Amination of Benzoxazoles: Tuning the Amino Group Source from Formamides to Parent Amines. Angew. Chem. Int. Ed. 2009, 48, 9127–9130. [Google Scholar] [CrossRef] [PubMed]
  9. Kim, J.Y.; Cho, S.H.; Joseph, J.; Chang, S. Cobalt- and Manganese-Catalyzed Direct Amination of Azoles under Mild Reaction Conditions and the Mechanistic Details. Angew. Chem. Int. Ed. 2010, 122, 10095–10099. [Google Scholar] [CrossRef]
  10. Monguchi, D.; Fujiwara, T.; Furukawa, H.; Mori, A. Direct Amination of Azoles via Catalytic C–H, N–H Coupling. Org. Lett. 2009, 11, 1607–1610. [Google Scholar] [CrossRef] [PubMed]
  11. Wang, Q.; Schreiber, S.L. Copper-Mediated Amidation of Heterocyclic and Aromatic C–H Bonds. Org. Lett. 2009, 11, 5178–5180. [Google Scholar] [CrossRef] [PubMed]
  12. Miyasaka, M.; Hirano, K.; Satoh, T.; Kowalczyk, R.; Bolm, C.; Miura, M. Copper-Catalyzed Direct Sulfoximination of Azoles and Polyfluoroarenes under Ambient Conditions. Org. Lett. 2011, 13, 359–361. [Google Scholar] [CrossRef] [PubMed]
  13. Kawano, T.; Hirano, K.; Satoh, T.; Miura, M. A New Entry of Amination Reagents for Heteroaromatic C-H Bonds: Copper-Catalyzed Direct Amination of Azoles with Chloroamines at Room Temperature. J. Am. Chem. Soc. 2010, 132, 6900–6901. [Google Scholar] [CrossRef] [PubMed]
  14. Matsuda, N.; Hirano, K.; Satoh, T.; Miura, M. Copper-Catalyzed Direct Amination of Electron-Deficient Arenes with Hydroxylamines. Org. Lett. 2011, 13, 2860–2863. [Google Scholar] [CrossRef] [PubMed]
  15. Xie, Y.J.; Qian, B.; Xie, P.; Huang, H.M. Cooperative Catalysis with Aldehydes and Copper: Development and Application in Aerobic Oxidative CH Amination at Room Temperature. Adv. Synth. Catal. 2013, 355, 1315–1322. [Google Scholar] [CrossRef]
  16. Wertz, S.; Kodama, S.; Studer, A. Cooperative Catalysis with Aldehydes and Copper: Development and Application in Aerobic Oxidative CH Amination at Room Temperature. Angew. Chem. Int. Ed. 2011, 50, 11511–11515. [Google Scholar] [CrossRef] [PubMed]
  17. Wang, J.; Hou, J.T.; Wen, J.; Yu, X.Q. Iron-catalyzed direct amination of azoles using formamides or amines as nitrogen sources in air. Chem. Commun. 2011, 47, 3652–3654. [Google Scholar] [CrossRef] [PubMed]
  18. Xu, J.; Li, J.R.; Wei, Z.; Zhang, Q.; Shi, D.X. Direct amination of azoles using CuCl2 complexes of amines under mild conditions. RSC. Adv. 2013, 3, 9622–9624. [Google Scholar] [CrossRef]
  19. Li, Y.M.; Liu, J.; Xie, Y.S.; Zhang, R.; Jin, K.; Wang, X.N.; Duan, C.Y. Nickel-catalyzed C–H direct amination of benzoxazoles with secondary Amines. Org. Biomol. Chem. 2012, 10, 3715–3720. [Google Scholar] [CrossRef] [PubMed]
  20. Cioffi, C.L.; Lansing, J.J.; Yüksel, H. Synthesis of 2-Aminobenzoxazoles Using Tetramethyl Orthocarbonate or 1,1-Dichlorodiphenoxymethane. J. Org. Chem. 2010, 75, 7942–7945. [Google Scholar] [CrossRef] [PubMed]
  21. Parumala, S.K.R.; Peddinti, R.K. Iodine catalyzed cross-dehydrogenative C–S coupling by C(sp2)–H bond activation: Direct access to aryl sulfides from aryl thiols. Green Chem. 2015, 17, 4068–4072. [Google Scholar] [CrossRef]
  22. Yang, K.; Ke, M.L.; Lin, Y.G.; Song, Q.L. Sulfonamide formation from sodium sulfinates and amines or ammonia under metal-free conditions at ambient temperature. Green Chem. 2015, 17, 1395–1399. [Google Scholar] [CrossRef]
  23. Zhang, X.B.; Wang, L. TBHP/I2-promoted oxidative coupling of acetophenones with amines at room temperature under metal-free and solvent-free conditions for the synthesis of α-ketoamides. Green Chem. 2012, 14, 2141–2145. [Google Scholar] [CrossRef]
  24. Huang, H.; Chen, W.H.; Xu, Y.; Li, J. I−/TBHP catalyzed Csp3–N/Csp2–N bond formation via oxidative coupling with benzophenone imine in water. Green Chem. 2015, 17, 4715–4719. [Google Scholar] [CrossRef]
  25. Zeng, J.W.; Liu, Y.C.; Hsieh, P.A.; Huang, Y.T.; Yi, C.L.; Badsara, S.S.; Lee, C.F. Metal-free cross-coupling reaction of aldehydes with disulfides by using DTBP as an oxidant under solvent-free conditions. Green Chem. 2014, 16, 2644–2652. [Google Scholar] [CrossRef]
  26. Wen, J.W.; Wei, W.; Xue, S.N.; Yang, D.S.; Lou, Y.; Gao, C.Y.; Wang, H. Metal-Free Oxidative Spirocyclization of Alkynes with Sulfonylhydrazides Leading to 3-Sulfonated Azaspiro[4,5]trienones. J. Org. Chem. 2015, 80, 4966–4972. [Google Scholar] [CrossRef] [PubMed]
  27. Panda, N.; Mattan, I.; Nayak, D.K. Synthesis of Dibenzofurans via C−H Activation of o-Iodo Diaryl Ethers. J. Org. Chem. 2015, 80, 6590–6597. [Google Scholar] [CrossRef] [PubMed]
  28. Tinnis, F.; Stridfeldt, E.; Lundberg, H.; Adolfsson, H.; Olofsson, B. Metal-Free N-Arylation of Secondary Amides at Room Temperature. Org. Lett. 2015, 17, 2688–2691. [Google Scholar] [CrossRef] [PubMed]
  29. Danneman, M.W.; Hong, K.B.; Johnston, J.N. Oxidative Inter-/Intermolecular Alkene Diamination of Hydroxy Styrenes with Electron-Rich Amines. Org. Lett. 2015, 17, 2558–2561. [Google Scholar] [CrossRef] [PubMed]
  30. Joseph, J.; Kim, J.Y.; Chang, S. A Metal-Free Route to 2-Aminooxazoles by Taking Advantage of the Unique Ring Opening of Benzoxazoles and Oxadiazoles with Secondary Amines. Chem. Eur. J. 2011, 17, 8294–8298. [Google Scholar] [CrossRef] [PubMed]
  31. Wagh, Y.S.; Tiwari, N.J.; Bhanage, B.M. Metal-free synthesis of 2-aminobenzoxazoles using hypervalent iodine reagent. Tetrahedron Lett. 2013, 54, 1290–1293. [Google Scholar] [CrossRef]
  32. Lamani, M.; Prabhu, K.R. Iodine-Catalyzed Amination of Benzoxazoles: A Metal-Free Route to 2-Aminobenzoxazoles under Mild Conditions. J. Org. Chem. 2011, 76, 7938–7944. [Google Scholar] [CrossRef] [PubMed]
  33. Froehr, T.; Sindlinger, C.P.; Kloeckner, U.; Finkbeiner, P.; Nachtsheim, B.J. A Metal-Free Amination of Benzoxazoles The First Example of an Iodide-Catalyzed Oxidative Amination of Heteroarenes. Org. Lett. 2011, 13, 3754–3757. [Google Scholar] [CrossRef] [PubMed]
  34. Gao, W.J.; Li, W.C.; Zeng, C.C.; Tian, H.Y.; Hu, L.M.; Little, R.D. Electrochemically Initiated Oxidative Amination of Benzoxazoles Using Tetraalkylammonium Halides as Redox Catalysts. J. Org. Chem. 2014, 79, 9613–9618. [Google Scholar] [CrossRef] [PubMed]
  35. Wagh, Y.S.; Sawant, D.N.; Bhanage, B.M. Metal-free N-iodosuccinimide-catalyzed mild oxidative C–H bond amination of benzoxazoles. Tetrahedron Lett. 2012, 53, 3482–3485. [Google Scholar] [CrossRef]
  36. Wang, R.; Liu, H.; Yue, L.; Zhang, X.K.; Tan, Q.Y.; Pan, R.L. Transition metal-free direct amination of benzoxazoles using formamides as nitrogen sources. Tetrahedron Lett. 2014, 55, 2233–2237. [Google Scholar] [CrossRef]
  37. Wang, X.; Xu, D.Q.; Miao, C.X.; Zhang, Q.H.; Sun, W. N-Bromosuccinimide as an oxidant for the transition-metal-free synthesis of 2-aminobenzoxazoles from benzoxazoles and secondary amines. Org. Biomol. Chem. 2014, 12, 3108–3113. [Google Scholar] [CrossRef] [PubMed]
  38. Yotphan, S.; Beukeaw, D.; Reutrakul, V. A Convenient One-Pot Synthesis of N-Substituted 2-Aminoazole Derivatives. Synthesis 2013, 45, 936–942. [Google Scholar] [CrossRef]
  39. Martins, M.P.; Frizzo, C.; Moreira, D.; Zanatta, N.; Bonacorso, H. Ionic Liquids in Heterocyclic Synthesis. Chem. Rev. 2008, 108, 2015–2050. [Google Scholar] [CrossRef] [PubMed]
  40. Zhang, Q.; Shreeve, J.M. Energetic Ionic Liquids as Explosives and Propellant Fuels: A New Journey of Ionic Liquid Chemistry. Chem. Rev. 2014, 114, 10527–10574. [Google Scholar] [CrossRef] [PubMed]
  41. Zhang, Q.; Zhang, S.; Deng, Y. Recent advances in ionic liquid catalysis. Green Chem. 2011, 13, 2619–2637. [Google Scholar] [CrossRef]
  42. Giernoth, R. Task-Specific Ionic Liquids. Angew. Chem. Int. Ed. 2010, 49, 2834–2839. [Google Scholar] [CrossRef] [PubMed]
  43. Taheri, A.; Liu, C.H.; Lai, B.B.; Cheng, C.; Pan, X.J.; Gu, Y.L. Brønsted acid ionic liquid catalyzed facile synthesis of 3-vinylindoles through direct C3 alkenylation of indoles with simple ketones. Green Chem. 2014, 16, 3715–3719. [Google Scholar] [CrossRef]
  44. Glasnov, T.N.; Holbrey, J.D.; Kappe, C.O.; Seddon, K.R.; Yan, T. Methylation using dimethylcarbonate catalysed by ionic liquids under continuous flow conditions. Green Chem. 2012, 14, 3071–3076. [Google Scholar] [CrossRef]
  45. Li, J.X.; Yang, W.F.; Yang, S.R.; Huang, L.B.; Wu, W.Q.; Sun, Y.D.; Jiang, H.F. Palladium-Catalyzed Cascade Annulation to Construct Functionalized β- and γ-Lactones in Ionic Liquids. Angew. Chem. Int. Ed. 2014, 53, 7219–7222. [Google Scholar] [CrossRef] [PubMed]
  46. Ehlers, P.; Petrosyan, A.; Baumgard, J.; Jopp, S.; Steinfeld, N.; Ghochikyan, T.V.; Saghyan, A.S.; Fischer, C.; Langer, P. Synthesis of 2,5-Diarylpyrroles by Ligand-Free Palladium-Catalyzed CH Activation of Pyrroles in Ionic Liquids. ChemCatChem 2013, 5, 2504–2511. [Google Scholar] [CrossRef]
  47. Baslé, O.; Borduas, N.; Dubois, P.; Chapuzet, J.M.; Chan, T.H.; Lessard, J.; Li, C.J. Aerobic and Electrochemical Oxidative Cross-Dehydrogenative-Coupling (CDC) Reaction in an Imidazolium-Based Ionic Liquid. Chem. Eur. J. 2010, 16, 8162–8166. [Google Scholar] [CrossRef] [PubMed]
  48. Biffis, A.; Gazzola, L.; Tubaro, C.; Basato, M. Alkyne Hydroarylation in Ionic Liquids Catalyzed by Palladium(II) Complexes. ChemSusChem 2010, 3, 834–839. [Google Scholar] [CrossRef] [PubMed]
  49. Li, J.X.; Yang, S.R.; Jiang, H.F.; Wu, W.Q.; Zhao, J.W. Palladium-Catalyzed Coupling of Alkynes with Unactivated Alkenes in Ionic Liquids: A Regio-and Stereoselective Synthesis of Functionalized 1,6-Dienes and Their Analogues. J. Org. Chem. 2013, 78, 12477–12486. [Google Scholar] [CrossRef] [PubMed]
  50. Li, H.; Liu, C.J.; Zhang, Y.H.; Sun, Y.D.; Wang, B.; Liu, W.B. Green Method for the Synthesis of Chromeno[2,3-c]pyrazol-4(1H)-ones through Ionic Liquid Promoted Directed Annulation of 5-(Aryloxy)-1H-pyrazole-4-carbaldehydes in Aqueous Media. Org. Lett. 2015, 17, 932–935. [Google Scholar] [CrossRef] [PubMed]
  51. Liu, W.B.; Liu, C.J.; Zhang, Y.H.; Sun, Y.D.; Abdukadera, A.; Wang, B.; Li, H.; Ma, X.C.; Zhang, Z.P. Reusable ionic liquid-catalyzed oxidative coupling of azoles and benzylic compounds via sp3 C–N bond formation under metal-free conditions. Org. Biomol. Chem. 2015, 13, 7154–7158. [Google Scholar] [CrossRef] [PubMed]
Sample Availability: All samples are available from the authors.
Molecules 22 00576 sch001 550
Scheme 1. Reported and designed routes for the oxidative amination of benzoxazoles. IL: ionic liquid; TBHP: tert-butyl hydroperoxide. Equiv: equivalent.
Scheme 1. Reported and designed routes for the oxidative amination of benzoxazoles. IL: ionic liquid; TBHP: tert-butyl hydroperoxide. Equiv: equivalent.
Molecules 22 00576 sch001
Molecules 22 00576 sch002 550
Scheme 2. Amination reaction of benzoxazole with various secondary amines. Reaction conditions: 1 (0.672 mmol), 2 (1.344 mmol), oxidant (1.008 mmol), acetic acid (2.016 mmol), [BPy]I (15 mol%), CH3CN (2 mL), at room temperature, 3.5 h. Isolated yield. [BPy]I: 1-butylpyridinium iodide.
Scheme 2. Amination reaction of benzoxazole with various secondary amines. Reaction conditions: 1 (0.672 mmol), 2 (1.344 mmol), oxidant (1.008 mmol), acetic acid (2.016 mmol), [BPy]I (15 mol%), CH3CN (2 mL), at room temperature, 3.5 h. Isolated yield. [BPy]I: 1-butylpyridinium iodide.
Molecules 22 00576 sch002
Molecules 22 00576 sch003 550
Scheme 3. Amination reaction of various benzoxazoles with secondary amines. a Reaction conditions: (1) (0.672 mmol); (2) (1.344 mmol), oxidant (1.008 mmol), acetic acid (2.016 mmol), [BPy]I (15 mol%), CH3CN (2 mL), at room temperature, 3.5 h. Isolated yield.
Scheme 3. Amination reaction of various benzoxazoles with secondary amines. a Reaction conditions: (1) (0.672 mmol); (2) (1.344 mmol), oxidant (1.008 mmol), acetic acid (2.016 mmol), [BPy]I (15 mol%), CH3CN (2 mL), at room temperature, 3.5 h. Isolated yield.
Molecules 22 00576 sch003
Molecules 22 00576 sch004 550
Scheme 4. Gram-scale oxidative amination of benzoxazoles and morpholine.
Scheme 4. Gram-scale oxidative amination of benzoxazoles and morpholine.
Molecules 22 00576 sch004
Molecules 22 00576 g001 550
Figure 1. Recycling reactions.
Figure 1. Recycling reactions.
Molecules 22 00576 g001
Molecules 22 00576 sch005 550
Scheme 5. The proposed mechanism. HOAc: acetic acid.
Scheme 5. The proposed mechanism. HOAc: acetic acid.
Molecules 22 00576 sch005
Table
Table 1. Optimizing the reaction conditions. a
Table 1. Optimizing the reaction conditions. a
Molecules 22 00576 i001
EntryCatalyst (mol%)Oxidant bSolventTime (h)Yield (%) c
1[BPy]I (5)TBHPCH3CN794
2[BPy]Cl (5)TBHPCH3CN7Trace
3[BPy]Br (5)TBHPCH3CN7N.R. d
4-TBHPCH3CN7N.R.
5[BPy]I (10)TBHPCH3CN591
6[BPy]I (15)TBHPCH3CN3.594
7[BPy]I (20)TBHPCH3CN3.594
8 c[BPy]I (15)TBHPCH2Cl23.588
9[BPy]I (15)TBHPTHF3.585
10[BPy]I (15)TBHPtoluene3.586
11[BPy]I (15)TBHPH2O3.557
12[BPy]I (15)TBHPNeat3.551
13[BPy]I (15)BPOCH3CN3.565
14[BPy]I (15)m-CPBACH3CN3.5N.R.
15[BPy]I (15)DTBPCH3CN3.5Trace
16[BPy]I (15)H2O2CH3CN3.579
a Reaction conditions: 1a (0.672 mmol), 2a (1.344 mmol), oxidant (1.008 mmol), acetic acid (2.016 mmol) in 2 mL solvent at room temperature. b TBHP: tert-butyl hydroperoxide 70% in water, BPO: benzoyl peroxide, m-CPBA: m-chloroperoxybenzoic acid, DTBP: di-tert-butyl peroxide, H2O2 30% in water, THF: tetrahydrofuran. c Isolated yield. d Not reaction. The optimized reaction conditions were 15 mol% [BPy]I as catalyst, 1.5 equiv. TBHP as oxidant, and 3 equiv. acetic acid as additive in 2 mL CH3CN at room temperature for 3.5 h.
Table
Table 2. Reactivity of N-Iodomorpholine Hydroiodide C.HI a.
Table 2. Reactivity of N-Iodomorpholine Hydroiodide C.HI a.
Molecules 22 00576 i002
Entry1a (Equiv.)C.HI (Equiv.)2a (Equiv.)TBHP (Equiv.)Yield (%) b
1110025
2120053
310.1521.595
a Reaction conditions: 1a (0.672 mmol), acetic acid (2.016 mmol), CH3CN (2 mL), room temperature, 3.5 h; b Isolated yield.

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Zhou, Y.; Liu, Z.; Yuan, T.; Huang, J.; Liu, C. The Synthesis of 2-Aminobenzoxazoles Using Reusable Ionic Liquid as a Green Catalyst under Mild Conditions. Molecules 2017, 22, 576. https://doi.org/10.3390/molecules22040576

AMA Style

Zhou Y, Liu Z, Yuan T, Huang J, Liu C. The Synthesis of 2-Aminobenzoxazoles Using Reusable Ionic Liquid as a Green Catalyst under Mild Conditions. Molecules. 2017; 22(4):576. https://doi.org/10.3390/molecules22040576

Chicago/Turabian Style

Zhou, Ya, Zhiqing Liu, Tingting Yuan, Jianbin Huang, and Chenjiang Liu. 2017. "The Synthesis of 2-Aminobenzoxazoles Using Reusable Ionic Liquid as a Green Catalyst under Mild Conditions" Molecules 22, no. 4: 576. https://doi.org/10.3390/molecules22040576

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