Next Article in Journal
Anti-Melanogenic Potential of Natural and Synthetic Substances: Application in Zebrafish Model
Previous Article in Journal
Pigments and Techniques of Hellenistic Apulian Tomb Painting
 
 
Search for Articles:
Title / Keyword
Author / Affiliation / Email
Journal
Article Type
 
 
Advanced Search
 
Section
Special Issue
Volume
Issue
Number
Page
 
Journals
Molecules
Volume 28
Issue 3
10.3390/molecules28031052
molecules-logo
Submit to this Journal Review for this Journal Propose a Special Issue
► Article Menu

Article Menu

share Share announcement Help format_quote Cite question_answer Discuss in SciProfiles thumb_up
...
Endorse textsms
...
Comment
first_page
settings
Order Article Reprints
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Development of a New Methodology for Dearomative Borylation of Coumarins and Chromenes and Its Applications to Synthesize Boron-Containing Retinoids

by
Bhaskar C. Das
1,2,3,*,
Pratik Yadav
1,
Sasmita Das
1,
Mariko Saito
3 and
Todd Evans
4,*
1
Arnold and Marie Schwartz College of Pharmacy and Health Sciences, Long Island University, Brooklyn, NY 11201, USA
2
Division of Nephrology, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA
3
Nathan S. Kline Institute for Psychiatric Research, Orangeburg, NY 10962, USA
4
Department of Surgery, Weill Cornell Medical College of Cornell University, New York, NY 10065, USA
*
Authors to whom correspondence should be addressed.
Molecules 2023, 28(3), 1052; https://doi.org/10.3390/molecules28031052
Submission received: 23 December 2022 / Revised: 13 January 2023 / Accepted: 16 January 2023 / Published: 20 January 2023
(This article belongs to the Section Chemical Biology)
Browse Figures
Review Reports Versions Notes

Abstract

:
Dearomative borylation of coumarins and chromenes via conjugate addition represents a relatively unexplored and challenging task. To address this issue, herein, we report a new and general copper (I) catalyzed dearomative borylation process to synthesize boron-containing oxacycles. In this report, the borylation of coumarins, chromones, and chromenes comprising functional groups, such as esters, nitriles, carbonyls, and amides, has been achieved. In addition, the method generates different classes of potential boron-based retinoids, including the ones with oxadiazole and anthocyanin motifs. The borylated oxacycles can serve as suitable intermediates to generate a library of compounds.

Graphical Abstract

1. Introduction

Retinoic acid (RA) signaling is among the most significant biological pathways facilitated at its core by the interaction of RA and nuclear receptors that control gene expression [1]. Retinoic acid derivatives (Retinoids) govern numerous cellular phenomena, including inhibition of proliferation, induction of cell differentiation, regulation of apoptosis, and inhibition of inflammation [2,3,4]. However, due to the complexity of ligands and receptors and involvement in several biological processes, RA can cause side effects. Moreover, RA suffers from poor solubility, photosensitivity, and increased catabolism during intravenous administration. All these limitations encourage the development of novel and better-tolerated synthetic retinoids. Previously, our group discovered that the toxicity of retinoids might be significantly suppressed by the incorporation of an oxygen-heterocyclic ring in the hydrophobic part of RA [5].
Oxygen-heterocycles are integral parts of various natural products and bioactive molecules [6]. Among them, coumarins and chromenes belong to a privileged class of heterocycles due to their inherent biological as well as photo-physical properties [7]. Natural as well as synthetic coumarins are well known for their broad spectrum of pharmacological activities, including acting as anti-microbials [8], antioxidants, anti-inflammatory agents [9], anti-depressants [10], anti-tumor agents [11], anti-asthmatics [12], antivirals (with anti-HIV) [13], anti-nociceptives [9], and anti-coagulants [14]. Similarly, chromenes are widespread in nature and have displayed excellent biological activities [7].
Meanwhile, boron-based molecular architects have recently emerged as potential pharmaceutical agents and probes due to their interesting and broad range of activities [15]. In addition, organoboron reagents are suitable for various organic transformations [16,17,18]. Several boron-based scaffolds are under clinical trials [19], and Bortezomib (Velcade), Tavaborole (Kerydin), Crisaborole (Eurisa), Vabomere, and Epetraborole are FDA-approved boron-based marketed drugs [20,21,22]. Vacant p-orbitals of boron make boron-based scaffolds prone to accepting electrons from electron-donating atoms as well as functional groups. This governs the strong interaction of boron chemicals at the active sites of receptors. The boron-based molecular architects also possess a tendency to form hydrogen bond networks to govern several biological processes and play a major role in drug–receptor interaction. The unique nature of boron-based compounds makes them potential therapeutic agents for the development of new drug candidates [15]. Therefore, we rationalized that the amalgamation of boron and coumarins/chromenes could lead to a new class of therapeutic agents with enhanced pharmaceutical properties, wherein boron-based heterocyclics could be potential hydrophobic substitutes for RA [5,23]. In addition, boron-containing oxacycles can be efficiently used for various synthetic transformations to generate a library of biologically active compounds. Based on these concepts, we previously synthesized a novel RARα agonist [5], BD4 (Scheme 1), which reduces proteinuria and recovers kidney injury, and mice administrated with BD4 did not develop any obvious toxicity or side effect. Therefore, BD4 appeared to be a new proof-of-concept RARα agonist, which could be used as a potential therapy for patients with kidney diseases, such as HIV-associated nephropathy (HIVAN). However, BD4 has low solubility and relatively low affinity. Therefore, we planned to use BD4 as our starting point to develop better compounds for lead optimization.
Based on our study, we realized that boron could be directly added to the endo/exo-cyclic double bond of a chromene motif (Scheme 1) to generate BD4a or BD4b. The literature revealed that initially, Blum and co-workers synthesized borylated isocoumarins from esters via electrophilic oxyboration [24]. Later, Yudin et al. achieved the synthesis of boryliminocoumarin from borylketenimines [25], although these methods were limited to certain building blocks. On the other hand, the metal-catalyzed conjugate addition of diboranes remained a valuable tool for inserting boron into unsaturated molecular motifs [26,27,28,29,30,31,32]. In recent years, copper-catalyzed conjugate addition reactions [32] of boron have emerged as a viable method to construct borylated heterocycles [33,34]. Among them, the dearomative borylation strategy of indoles [35,36,37], pyrroles [37,38], pyridines [39], and 4-quinolinols [40] have been efficiently utilized to construct borylated analogs of these biologically significant frameworks. Conjugate borylation of substituted esters and ketones has also been studied, which has demonstrated various challenges in the efficient conversion into corresponding borylated products [41,42]. However, to the best of our knowledge, dearomative borylation of coumarins and chromenes bearing various pharmaceutically relevant functional groups, including esters, amides, nitriles, carbonyls, and nitrogen heterocycles, has not yet been achieved. In addition, the application of these reported conjugate borylation strategies on medicinally important scaffolds has remained an unexplored task.
As a part of our ongoing effort on the development of boron-based therapeutic agents [43,44,45,46], we envisioned that under suitable reaction conditions, copper-catalyzed conjugate addition onto coumarins/chromones could result in borylated coumarins/chromones via a dearomative mechanism and that we could introduce these compounds to our RA backbone to substitute the hydrophobic part. To explore and expand our hypothesis, we herein report a conjugate addition of diboranes onto coumarins and chromones under simple and efficient conditions. The strategy was further utilized for the synthesis of biologically relevant novel boron-based retinoids. In addition, these borylated scaffolds were also used as synthetic precursors for diversified biological active compounds.

2. Results and Discussion

2.1. Reaction Optimization

To initiate an investigation for the dearomative borylation of coumarins, ethyl coumarin-3-carboxylate and Bis(pinacolato)diboron [B2(pin)2] were chosen as model substrates. To carry out the transformation, various reaction conditions were screened (Table 1). The planned reaction was realized very challenging due to the following: 1. the presence of a highly crowded tri-substituted alkene reaction site; 2. a competitive deconstruction of coumarins under copper (I) catalyzed conditions [47]. Our initial efforts yielded the conversion of coumarins into salicylaldehyde 2a′ under various conditions (Table 1). After screening numerous reaction conditions, we successfully suppressed the formation of salicylaldehyde. Initial results showed that copper (I) in combination with phosphine ligand and NaOtBu with methanol in THF could furnish product Ethyl 2-oxo-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)chromane-3-carboxylate (2a). Copper (I) chloride (CuCl) was found to be a better copper (I) source (Table 1, entries 1, 2) in comparison to Copper (I) iodide (CuI). In search of better reaction conditions for this transformation, we screened various phosphines (Table 1, entries 1–7). Different biphenyl derived phosphine served the desired product 2a, but ligands, such as triphenylphsphine (PPh3), tricyclohexylphosphine (PCy3), and tributylphosphine (PnBu3), were found better with respective yields of 60%, 82% and 75% for 2a. Having a suitable phosphine source, we screened various bases and additives to compare their effect on the outcome of the reaction, and the results are summarized in Table 1, entries 8–12. Based on the optimization of the reaction, CuCl was found as an efficient copper (I) source, in combination with PCy3, NaOtBu, and MeOH in THF at room temperature.

2.2. Substrate Scope of Dearomative Borylation

With the optimized reaction conditions in hand, we evaluated the substrate scope of this transformation (Scheme 2). Substrate, methyl coumarin-3-carboxylate with B2(pin)2 under the developed reaction condition gave the desired product 2b in 80% yield. Encouraged by these results, we next turned our focus to gauging the effect of an ester group on the C-3 position of coumarins with this protocol. Therefore, a reaction of coumarin was performed under the above reaction conditions for 2a synthesis. We were able to obtain the desired product 2c with unsubstituted coumarin as well in 78%. Next, the outcome of this dearomative borylation process was investigated with differently substituted C-3 positions. The reaction was also found efficient for the synthesis of reactants bearing nitriles and carbonyl functional groups to provide compounds 2d and 2e in good yields. Due to the excellent biological activities of chlorochromenes [43,44,45,46] and to evaluate the effect of substituents, we drew our attention toward the synthesis of 2f and 2g. Halogen-bearing substrates are usually found interfering and intolerant of Miyaura borylation reactions. However, in contrast, under these dearomative borylation conditions, these groups were well tolerated to yield 2f and 2g. To check the outcome of the reaction with an amide containing coumarins, a reaction of 3-acetamidocoumarin was treated with B2(pin)2 under the developed conditions, which resulted in the formation of 2h in moderate yield (53%) via in-situ deacetylation-borylation sequence. Our efforts to convert coumarin-3-carboxylic acid into corresponding borylated product 2i did not succeed.
We next explored the scope of this dearomative borylation strategy with other classes of oxacycles. We treated various chromenes with B2(pin)2 and bis(neopentyl glycolato)diboron [B2(neo)2] under the same catalytic conditions (Scheme 3). Initially, chromenes were investigated to synthesize compound 4a. Indeed, we successfully converted into 4a with a good yield. We were also interested to see the effect of another boron source on the transformation. To investigate this, a reaction was performed with B2(neo)2 under similar reaction conditions. The reaction proceeded well to yield 74% of the desired compound 4b. However, our attempt to construct compound 4c did not result in the desired product, and the starting material remained unreacted.

2.3. Synthetic Applications of Borylated Coumarins

Organoboron compounds have been found as excellent reagents for numerous synthetic transformations [16]. Furthermore, their trifluroborate salts and oxaboroles have been realized to possess excellent pharmacological properties [15]. Therefore, we became interested in the synthesis of coumarin-based trifluroborate salts and oxaboroles. After the successful borylation of various functionalized coumarins and chromenes, we also wished to demonstrate that the borylated coumarins could serve as useful intermediates, including ethyl 4-hydroxy-2-oxochromane-3-carboxylate (5b) (Scheme 4). To evaluate our hypothesis, 2a was first converted into potassium ethyl 2-oxo-4-(trifluoro-l4-boranyl)chromane-3-carboxylate (5a). The reaction proceeded smoothly to provide 5a (80% yield). In the second transformation, oxidation of 2a in the presence of NaBO3 was attempted, which provided compound 5b an 85% yield. In contrast, our attempt to prepare oxaborole (5c) in the presence of NaBH4 in MeOH at room temperature failed to give the desired product, and we could only get a starting material. Further attempts to explore the synthetic utilities of these borylated oxacycles are ongoing currently.

2.4. Application of Dearomative Borylation Strategy

The long-term goal of our research group is to design and synthesize boron-based biologically important scaffolds for various biological targets [48,49]. Among them, suitably functionalized oxadiazoles and chromenes were explored as potential pharmacophores. Chromene 6a, an analog of naturally occurring anthocyanins, has been used as a novel retinoic acid receptor alpha agonist for the treatment of kidney disease [5,49]. In addition, oxadiazoles were also explored as pan-RAR inverse agonists [48]. Moreover, anthocyanins derived from conjugated boron-based scaffolds were also found as active retinoids [5,49]. We were, therefore, interested to utilize this protocol to generate a library of boron-based pharmacophores as part of our ongoing chemical biology program. To achieve the goal, we further extended the scope of this reaction for the synthesis of compounds 7a–c.
A new chromene-based compound 6,8-dichloro-2-phenyl-2H-chromene-3-carbonitrile 6a was prepared in good yields for the first time, starting from corresponding aldehyde 5d. A 6a was then treated with B2(pin)2 under the developed conditions to yield borylated compound 7a with 55% yield. It was noteworthy that compounds 6b and 6c can also be converted into desired novel boron-based retinoids 7b and 7c in decent yields without any modification in the reaction conditions (Scheme 5). From the initial hit BD4 (BT75) as a novel RARα agonist, we can now access the new BD4b (7c) analog regioselectively. Further development of this strategy is under investigation to generate a library of these scaffolds. The methodology provides access to the differently functionalized borylated chromenes and coumarins. We note that the synthesized borylated oxacycles were observed to be prone to decomposition, making their purification a challenging task. The method also provides diastereomeric mixtures in many cases. Therefore, our group is currently working toward a suitable chiral approach to this process.

2.5. Proposed Mechanism of Dearomative Borylation of Oxacycles

On the basis of the literature, a mechanism was also proposed for this copper(I)-catalyzed dearomative borylation of oxacycles (Scheme 6) [33,34,35,36,37]. In the first step, Cu(I)Cl would react with base (NaOtBu) and ligand (L) to generate the active catalyst A, which subsequently would transfer B2pin2 onto the Cu(I) center to form intermediate B. In the next step, copper would coordinate with unsaturated oxacycles (1) to generate intermediate C. Subsequently, 3,4-addition of boron would result in a copper(I)-enolate and the formation of a C –B bond. After the formation of intermediate D, the proton donor (MeOH) would furnish the synthesis of desired product 2 and regenerate the active catalyst A.

3. Conclusions

In conclusion, we report here for the first time the dearomative synthesis of newboron-based oxygen heterocycles. The reaction works efficiently with various coumarin and chromenes, while functional groups, such as ester, nitrile, carbonyl amide, and chloro, were well tolerated. The developed methodology was also used for the development of boron-based new retinoids and biologically relevant scaffolds. These boron-based coumarins also serve as potential intermediates. This process provides a useful alternative to generate a library of coumarin/chromene-based molecular architects for future drug and molecular probe development. Further development of this approach and biological activities of synthesized oxacycles are currently under investigation at our laboratory.

Supplementary Materials

The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/molecules28031052/s1. Supplementary material contains procedures, experimental and spectral data.

Author Contributions

Conceptualization, B.C.D.; methodology, B.C.D. and P.Y.; validation, B.C.D. and P.Y.; formal analysis B.C.D. and P.Y.; investigation, B.C.D. and P.Y.; data curation, B.C.D. and P.Y.; writing—original draft preparation, B.C.D., P.Y. and S.D.; writing—review and editing, B.C.D., P.Y., S.D., M.S. and T.E.; supervision, B.C.D.; project administration, B.C.D. and T.E.; funding acquisition, B.C.D. All authors have read and agreed to the published version of the manuscript.

Funding

NIH for support R01AI132614-01A1, R21 AA027374-01, 1R01NS109423-01A.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

All the supporting data has been provided in Supplementary Materials.

Acknowledgments

BD acknowledges NIH for support R01AI132614-01A1, R21 AA027374-01, 1R01NS109423-01A1. TE is a co-founder of OncoBeat, LLC.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Das, B.C.; Thapa, P.; Karki, R.; Das, S.; Mahapatra, S.; Liu, T.-C.; Torregroza, I.; Wallace, D.P.; Kambhampati, S.; Van Veldhuizen, P. Retinoic acid signaling pathways in development and diseases. Bioorg. Med. Chem. 2014, 22, 673–683. [Google Scholar] [CrossRef] [Green Version]
  2. Evans, T.; Kaye, S. Retinoids: Present role and future potential. Br. J. Cancer 1999, 80, 1–8. [Google Scholar] [CrossRef]
  3. Merlet-Bénichou, C.; Vilar, J.; Lelièvre-Pégorier, M.; Gilbert, T. Role of retinoids in renal development: Pathophysiological implication. Curr. Opin. Nephrol. Hypertens. 1999, 8, 39–43. [Google Scholar] [CrossRef]
  4. Xu, Q.; Lucio-Cazana, J.; Kitamura, M.; Ruan, X.; Fine, L.G.; Norman, J.T. Retinoids in nephrology: Promises and pitfalls. Kidney Int. 2004, 66, 2119–2131. [Google Scholar] [CrossRef] [Green Version]
  5. Zhong, Y.; Wu, Y.; Liu, R.; Li, Z.; Chen, Y.; Evans, T.; Chuang, P.; Das, B.; He, J.C. Novel Retinoic Acid Receptor Alpha Agonists for Treatment of Kidney Disease. PLoS ONE 2011, 6, e27945. [Google Scholar] [CrossRef] [Green Version]
  6. Ram, V.J.; Sethi, A.; Nath, M.; Pratap, R. The Chemistry of Heterocycles: Chemistry of Six to Eight Membered N, O, S, P and Se Heterocycles; Elsevier: Amsterdam, The Netherlands, 2019. [Google Scholar]
  7. Pratap, R.; Ram, V.J. Natural and Synthetic Chromenes, fused Chromenes, and versatility of dihydrobenzo[h]chromenes in organic synthesis. Chem. Rev. 2014, 114, 10476–10526. [Google Scholar] [CrossRef]
  8. Smyth, T.; Ramachandran, V.; Smyth, W. A study of the antimicrobial activity of selected naturally occurring and synthetic coumarins. Int. J. Antimicrob. Agents 2009, 33, 421–426. [Google Scholar] [CrossRef]
  9. Fylaktakidou, K.C.; Hadjipavlou-Litina, D.J.; Litinas, K.E.; Nicolaides, D.N. Natural and synthetic coumarin derivatives with anti-inflammatory/antioxidant activities. Curr. Pharm. Des. 2004, 10, 3813–3833. [Google Scholar] [CrossRef]
  10. Skalicka-Woźniak, K.; Orhan, I.E.; Cordell, G.A.; Nabavi, S.M.; Budzyńska, B. Implication of coumarins towards central nervous system disorders. Pharmacol. Res. 2016, 103, 188–203. [Google Scholar] [CrossRef]
  11. Kostova, I. Synthetic and natural coumarins as cytotoxic agents. Curr. Med. Chem.-Anti-Cancer Agents 2005, 5, 29–46. [Google Scholar] [CrossRef]
  12. Kirsch, G.; Abdelwahab, A.B.; Chaimbault, P. Natural and Synthetic Coumarins with Effects on Inflammation. Molecules 2016, 21, 1322. [Google Scholar] [CrossRef]
  13. Hassan, M.Z.; Osman, H.; Ali, M.A.; Ahsan, M.J. Therapeutic potential of coumarins as antiviral agents. Eur. J. Med. Chem. 2016, 123, 236–255. [Google Scholar] [CrossRef]
  14. Riveiro, M.E.; De Kimpe, N.; Moglioni, A.; Vazquez, R.; Monczor, F.; Shayo, C.; Davio, C. Coumarins: Old compounds with novel promising therapeutic perspectives. Curr. Med. Chem. 2010, 17, 1325–1338. [Google Scholar] [CrossRef]
  15. Das, B.C.; Shareef, M.A.; Das, S.; Nandwana, N.K.; Das, Y.; Saito, M.; Weiss, L.M. Boron-Containing heterocycles as promising pharmacological agents. Bioorg. Med. Chem. 2022, 63, 116748. [Google Scholar] [CrossRef]
  16. DeFrancesco, H.; Dudley, J.; Coca, A. Boron Reagents in Synthesis; American Chemical Society: Washington, DC, USA, 2016. [Google Scholar] [CrossRef]
  17. Yao, W.; Wang, J.; Zhong, A.; Wang, S.; Shao, Y. Transition-metal-free catalytic hydroboration reduction of amides to amines. Org. Chem. Front. 2020, 7, 3515–3520. [Google Scholar] [CrossRef]
  18. Yao, W.; Wang, J.; Lou, Y.; Wu, H.; Qi, X.; Yang, J.; Zhong, A. Chemoselective hydroborative reduction of nitro motifs using a transition-metal-free catalyst. Org. Chem. Front. 2021, 8, 4554–4559. [Google Scholar] [CrossRef]
  19. Ali, F.; Hosmane, N.; Zhu, Y. Boron chemistry for medical applications. Molecules 2020, 25, 828. [Google Scholar] [CrossRef] [Green Version]
  20. Song, S.; Gao, P.; Sun, L.; Kang, D.; Kongsted, J.; Poongavanam, V.; Zhan, P.; Liu, X. Recent developments in the medicinal chemistry of single boron atom-containing compounds. Acta Pharm. Sin. B 2021, 11, 3035–3059. [Google Scholar] [CrossRef]
  21. Hey-Hawkins, E.; Teixidor, C.V. Boron-Based Compounds: Potential and Emerging Applications in Medicine; Wiley: Hoboken, NJ, USA, 2018. [Google Scholar]
  22. Das, B.C.; Nandwana, N.K.; Das, S.; Nandwana, V.; Shareef, M.A.; Das, Y.; Saito, M.; Weiss, L.M.; Almaguel, F.; Hosmane, N.S. Boron chemicals in drug discovery and development: Synthesis and medicinal perspective. Molecules 2022, 27, 2615. [Google Scholar] [CrossRef]
  23. Torregroza, I.; Evans, T.; Das, B.C. A forward chemical screen using zebrafish embryos with novel 2-substituted 2 h-chromene derivatives. Chem. Biol. Drug Des. 2009, 73, 339–345. [Google Scholar] [CrossRef] [Green Version]
  24. Faizi, D.J.; Issaian, A.; Davis, A.J.; Blum, S.A. Catalyst-free synthesis of borylated lactones from esters via electrophilic oxyboration. J. Am. Chem. Soc. 2016, 138, 2126–2129. [Google Scholar] [CrossRef] [Green Version]
  25. Kaldas, S.J.; O’Keefe, K.T.; Mendoza-Sanchez, R.; Yudin, A.K. Amphoteric borylketenimines: Versatile intermediates in the synthesis of borylated heterocycles. Chem.-Eur. J. 2017, 23, 9711–9715. [Google Scholar] [CrossRef]
  26. Fyfe, J.W.; Watson, A.J. Recent developments in organoboron chemistry: Old dogs, new tricks. Chem 2017, 3, 31–55. [Google Scholar] [CrossRef] [Green Version]
  27. Coapes, R.B.; Souza, F.E.; Thomas, R.L.; Hall, J.J.; Marder, T.B. Rhodium catalysed dehydrogenative borylation of vinylarenes and 1,1-disubstituted alkenes without sacrificial hydrogenation—A route to 1,1-disubstituted vinylboronates. Chem. Commun. 2003, 9, 614–615. [Google Scholar] [CrossRef]
  28. Kabalka, G.W.; Das, B.C.; Das, S. Rhodium-catalyzed 1,4-addition reactions of diboron reagents to electron deficient olefins. Tetrahedron Lett. 2002, 43, 2323–2325. [Google Scholar] [CrossRef]
  29. Schiffner, J.A.; Müther, K.; Oestreich, M. Enantioselective conjugate borylation. Angew. Chem. Int. Ed. 2010, 49, 1194–1196. [Google Scholar] [CrossRef]
  30. Hartmann, E.; Vyas, D.J.; Oestreich, M. Enantioselective formal hydration of α,β-unsaturated acceptors: Asymmetric conjugate addition of silicon and boron nucleophiles. Chem. Commun. 2011, 47, 7917–7932. [Google Scholar] [CrossRef]
  31. Hemming, D.; Fritzemeier, R.; Westcott, S.A.; Santos, W.L.; Steel, P.G. Copper-boryl mediated organic synthesis. Chem. Soc. Rev. 2018, 47, 7477–7494. [Google Scholar] [CrossRef] [Green Version]
  32. Wang, Y.-F.; Wang, C.-J.; Feng, Q.-Z.; Zhai, J.-J.; Qi, S.-S.; Zhong, A.-G.; Chu, M.-M.; Xu, D.-Q. Copper-catalyzed asymmetric 1,6-conjugate addition of in situ generated para-quinone methides with β-ketoesters. Chem. Commun. 2022, 58, 6653–6656. [Google Scholar] [CrossRef]
  33. Hu, J.; Ferger, M.; Shi, Z.; Marder, T.B. Recent advances in asymmetric borylation by transition metal catalysis. Chem. Soc. Rev. 2021, 50, 13129–13188. [Google Scholar] [CrossRef]
  34. Larin, E.M.; Loup, J.; Polishchuk, I.; Ross, R.J.; Whyte, A.; Lautens, M. Enantio- and diastereoselective conjugate borylation/Mannich cyclization. Chem. Sci. 2020, 11, 5716–5723. [Google Scholar] [CrossRef]
  35. Kubota, K.; Hayama, K.; Iwamoto, H.; Ito, H. Enantioselective borylative dearomatization of indoles through copper(i) catalysis. Angew. Chem. Int. Ed. 2015, 54, 8809–8813. [Google Scholar] [CrossRef] [Green Version]
  36. Chen, L.; Shen, J.-J.; Gao, Q.; Xu, S. Synthesis of cyclic chiral α-amino boronates by copper-catalyzed asymmetric dearomative borylation of indoles. Chem. Sci. 2018, 9, 5855–5859. [Google Scholar] [CrossRef] [Green Version]
  37. Hayama, K.; Takahashi, R.; Kubota, K.; Ito, H. Copper(i)-catalyzed stereoselective silylative dearomatization of indoles and pyrroles using silylboronates. Chem. Lett. 2021, 50, 289–292. [Google Scholar] [CrossRef]
  38. Hayama, K.; Kojima, R.; Kubota, K.; Ito, H. Synthesis of chiral n-heterocyclic allylboronates via the enantioselective borylative dearomatization of pyrroles. Org. Lett. 2020, 22, 739–744. [Google Scholar] [CrossRef]
  39. Kubota, K.; Watanabe, Y.; Hayama, K.; Ito, H. Enantioselective synthesis of chiral piperidines via the stepwise dearomatization/borylation of pyridines. J. Am. Chem. Soc. 2016, 138, 4338–4341. [Google Scholar] [CrossRef]
  40. Xu, M.; Ouyang, Y.; Wang, L.; Zhang, S.; Li, P. Enantioselective synthesis of cyclic α-aminoboronates via copper-catalyzed dearomative borylation of 4-quinolinols. Chem. Commun. 2022, 58, 3677–3680. [Google Scholar] [CrossRef]
  41. Dahiya, G.; Pappoppula, M.; Aponick, A. Configuration sampling with five-membered atropisomeric p,n-ligands. Angew. Chem. Int. Ed. 2021, 60, 19604–19608. [Google Scholar] [CrossRef]
  42. Xie, J.-B.; Lin, S.; Qiao, S.; Li, G. Asymmetric catalytic enantio- and diastereoselective boron conjugate addition reactions of α-functionalized α,β-unsaturated carbonyl substrates. Org. Lett. 2016, 18, 3926–3929. [Google Scholar] [CrossRef]
  43. Anguiano, J.; Garner, T.P.; Mahalingam, M.; Das, B.C.; Gavathiotis, E.; Cuervo, A.M. Chemical modulation of chaperone-mediated autophagy by retinoic acid derivatives. Nat. Chem. Biol. 2013, 9, 374–382. [Google Scholar] [CrossRef] [Green Version]
  44. Yang, J.; Das, B.C.; Aljitawi, O.; Kumar, A.; Das, S.; Van Veldhuizen, P. Magmas inhibition in prostate cancer: A novel target for treatment-resistant disease. Cancers 2022, 14, 2732. [Google Scholar] [CrossRef]
  45. Cook, B.; Walker, N.; Zhang, Q.; Chen, S.; Evans, T. The small molecule DIPQUO promotes osteogenic differentiation via inhibition of glycogen synthase kinase 3-beta signaling. J. Biol. Chem. 2021, 296, 100696. [Google Scholar] [CrossRef]
  46. Das, B.C.; Yadav, P.; Das, S.; He, J.C. A novel procedure for the synthesis of borylated quinolines and its application in the development of potential boron-based homeodomain interacting protein kinase 2 (HIPK2) inhibitors. RSC Adv. 2022, 12, 24187–24191. [Google Scholar] [CrossRef]
  47. Zheng, T.-Y.; Zhou, Y.-Q.; Yu, N.; Li, Y.-L.; Wei, T.; Peng, L.; Ling, Y.; Jiang, K.; Wei, Y. Deconstructive insertion of oximes into coumarins: Modular synthesis of dihydrobenzofuran-fused pyridones. Org. Lett. 2022, 24, 2282–2287. [Google Scholar] [CrossRef]
  48. Das, B.C.; Tang, X.-Y.; Evans, T. Design and synthesis of boron containing potential pan-RAR inverse agonists. Tetrahedron Lett. 2012, 53, 1316–1318. [Google Scholar] [CrossRef]
  49. Sai, K.K.S.; Das, B.C.; Sattiraju, A.; Almaguel, F.G.; Craft, S.; Mintz, A. Radiolabeling and initial biological evaluation of [18F]KBM-1 for imaging RAR-α receptors in neuroblastoma. Bioorg. Med. Chem. Lett. 2017, 27, 1425–1427. [Google Scholar]
Molecules 28 01052 sch001 550
Scheme 1. Design of new class of boron-retinoids.
Scheme 1. Design of new class of boron-retinoids.
Molecules 28 01052 sch001
Molecules 28 01052 sch002a 550Molecules 28 01052 sch002b 550
Scheme 2. Dearomative borylation reaction with various coumarins 1. 1 Reaction was performed with 1a–i (0.5 mmol), B2(pin)2 (0.6 mmol), CuCl (10 mol%), P(Cy)3 (10 mol%), NaOtBu (20 mol%), MeOH (1 mmol), and THF (2 mL) at room temperature (rt), 12–16 h.
Scheme 2. Dearomative borylation reaction with various coumarins 1. 1 Reaction was performed with 1a–i (0.5 mmol), B2(pin)2 (0.6 mmol), CuCl (10 mol%), P(Cy)3 (10 mol%), NaOtBu (20 mol%), MeOH (1 mmol), and THF (2 mL) at room temperature (rt), 12–16 h.
Molecules 28 01052 sch002aMolecules 28 01052 sch002b
Molecules 28 01052 sch003 550
Scheme 3. Dearomative borylation reaction with various chromenes 1. 1 Reaction was performed with 3a–c (0.5 mmol), B2(pin)2 (0.6 mmol), CuCl (10 mol%), P(Cy)3 (10 mol%), NaOtBu (20 mol%), MeOH (1 mmol), and THF (2mL) at room temperature (rt), 12–16 h.
Scheme 3. Dearomative borylation reaction with various chromenes 1. 1 Reaction was performed with 3a–c (0.5 mmol), B2(pin)2 (0.6 mmol), CuCl (10 mol%), P(Cy)3 (10 mol%), NaOtBu (20 mol%), MeOH (1 mmol), and THF (2mL) at room temperature (rt), 12–16 h.
Molecules 28 01052 sch003
Molecules 28 01052 sch004 550
Scheme 4. Synthetic utilities of borylated coumarins 1,2,3. 1 2a (0.5 mmol), NaBO3 (2 mmol) and 4 mL THF:H2O (1:1); 2 2a (0.5 mmol), KHF2 (2.5 mmol) and MeCN:H2O (4:1) 5 mL; 3 2a (0.5 mmol), NaBH4 (1.5 mmol), and MeOH (4 mL) at rt.
Scheme 4. Synthetic utilities of borylated coumarins 1,2,3. 1 2a (0.5 mmol), NaBO3 (2 mmol) and 4 mL THF:H2O (1:1); 2 2a (0.5 mmol), KHF2 (2.5 mmol) and MeCN:H2O (4:1) 5 mL; 3 2a (0.5 mmol), NaBH4 (1.5 mmol), and MeOH (4 mL) at rt.
Molecules 28 01052 sch004
Molecules 28 01052 sch005a 550Molecules 28 01052 sch005b 550
Scheme 5. Application of dearomative borylation strategy for the synthesis of boron-containing pharmacophores.
Scheme 5. Application of dearomative borylation strategy for the synthesis of boron-containing pharmacophores.
Molecules 28 01052 sch005aMolecules 28 01052 sch005b
Molecules 28 01052 sch006 550
Scheme 6. Proposed mechanism of dearomative borylation of oxacycles.
Scheme 6. Proposed mechanism of dearomative borylation of oxacycles.
Molecules 28 01052 sch006
Table
Table 1. Optimization of reaction conditions for 1,4 borylations of oxacycles 1.
Table 1. Optimization of reaction conditions for 1,4 borylations of oxacycles 1.
Molecules 28 01052 i001
Entry[Cu]
(10 mol%)		Ligand
(10 mol%)		BaseAdditiveConversion 2 (%)
2a2a′
1CuClXphosNaOtBuMeOH3050
2CuIXphosNaOtBuMeOH2055
3CuClXantphosNaOtBuMeOH5520
4CuClRac-BinapNaOtBuMeOH3510
5CuClPPh3NaOtBuMeOH60-
6CuClP(nBu)3NaOtBuMeOH75-
7CuClPCy3NaOtBuMeOH82-
8CuClPCy3NaOtBut-BuOH5015
9CuClPCy3NaOtBut-amyl-OH3025
10CuClPCy3NaOtBun-PrOH3815
11CuClPCy3KOtBuMeOH6010
12CuClPCy3LiOtBuMeOH55-
1 Reaction was performed with 1a (0.5 mmol), B2(pin)2 (0.6 mmol), Cu (I) (10 mol%), ligand (10 mol%), base (20 mol%), additive (1 mmol), and THF (2mL) at room temperature (rt), 12–16 h; 2 1H NMR conversion.
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

Share and Cite

MDPI and ACS Style

Das, B.C.; Yadav, P.; Das, S.; Saito, M.; Evans, T. Development of a New Methodology for Dearomative Borylation of Coumarins and Chromenes and Its Applications to Synthesize Boron-Containing Retinoids. Molecules 2023, 28, 1052. https://doi.org/10.3390/molecules28031052

AMA Style

Das BC, Yadav P, Das S, Saito M, Evans T. Development of a New Methodology for Dearomative Borylation of Coumarins and Chromenes and Its Applications to Synthesize Boron-Containing Retinoids. Molecules. 2023; 28(3):1052. https://doi.org/10.3390/molecules28031052

Chicago/Turabian Style

Das, Bhaskar C., Pratik Yadav, Sasmita Das, Mariko Saito, and Todd Evans. 2023. "Development of a New Methodology for Dearomative Borylation of Coumarins and Chromenes and Its Applications to Synthesize Boron-Containing Retinoids" Molecules 28, no. 3: 1052. https://doi.org/10.3390/molecules28031052

Article Metrics

Back to TopTop