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Mild and efficient synthesis and base-promoted rearrangement of novel isoxazolo[4,5-b]pyridines

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N.D. Zelinsky Institute of Organic Chemistry RAS, Leninsky prosp. 47, 119991 Moscow, Russia
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Associate Editor: I. Baxendale
Beilstein J. Org. Chem. 2024, 20, 1069–1075. https://doi.org/10.3762/bjoc.20.94
Received 26 Feb 2024, Accepted 03 May 2024, Published 14 May 2024
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Abstract

An efficient method for the synthesis of isoxazolo[4,5-b]pyridines has been developed on the basis of readily available 2-chloro-3-nitropyridines via the intramolecular nucleophilic substitution of the nitro group as a key step. The previously unknown base-promoted Boulton–Katritzky rearrangement of isoxazolo[4,5-b]pyridine-3-carbaldehyde arylhydrazones into 3-hydroxy-2-(2-aryl[1,2,3]triazol-4-yl)pyridines was observed.

Keywords: aromatic nitro compounds; Boulton–Katritzky rearrangement; isoxazolo[4,5-b]pyridines; nucleophilic substitution; 1,2,3-triazoles

Introduction

Nitrogen heterocycles represent a very important class of organic compounds that has found application in various fields of chemistry and materials science. These compounds are widespread in medicinal chemistry [1-3], production of high-energy-density compounds [4-7], and many others. In particular, isoxazolo[4,5-b]pyridines are of considerable interest due to their remarkable variety of biological activity, such as antibacterial [8], anticancer [9] or antiproliferative [10]. In addition, isoxazolo[4,5-b]pyridines were found to inhibit cytochrome P450 CYP17 responsible for the biosynthesis of androgens and estrogen precursors [11]. Some biologically active isoxazolo[4,5-b]pyridines are shown on Figure 1.

[1860-5397-20-94-1]

Figure 1: Some examples of biologically active isoxazolo[4,5-b]pyridines with antibacterial [8], anticancer [12] and cytotoxic [10,13] acitivities.

A number of isoxazolo[4,5-b]pyridines has been described in patents, however, there are only a few methods for their synthesis reported in the literature. First representatives of this heterocyclic system were described by Gewald et al. in 1980 [14]. The known methods are usually based on either annulation of an isoxazole fragment to a pyridine cycle or vice versa formation of a pyridine ring based on appropriately substituted isoxazoles. In the first case (Scheme 1A) 3-halo- [11,15-19] or 3-hydroxypyridines [8,20] bearing a suitable functionality in position 2 were used for the cyclization. Alternatively (Scheme 1B), isoxazolo[4,5-b]pyridines can be constructed via intramolecular cyclization of 4-(propargylamino)isoxazoles [21] or through reactions of 4-amino-5-benzoylisoxazoles with ketones or 1,3-dicarbonyl compounds [10,13]. These and some additional examples of isoxazolo[4,5-b]pyridine core synthesis have been summarized in a microreview [22].

[1860-5397-20-94-i1]

Scheme 1: Methods for the synthesis of isoxazolo[4,5-b]pyridines: (A) annulation of an isoxazole fragment to a pyridine ring; (B) annulation of a pyridine ring to a functionalized isoxazole core; (C) synthesis from available 3-nitropyridines.

Here, we wish to report an efficient method for the synthesis of isoxazolo[4,5-b]pyridines bearing electron-withdrawing groups (EWG) at positions 3 and 6 starting from readily available 2-chloro-3-nitro-6-R-pyridines as shown in Scheme 1C. Since the key step of the synthesis is the intramolecular nucleophilic substitution of the aromatic nitro group, we assumed that the presence of an electron-withdrawing substituent at the pyridine ring would facilitate this transformation.

Results and Discussion

According to the general synthetic scheme (Scheme 1C), commercially available 2-chloro-3-nitropyridines 1a–c were reacted with ethyl acetoacetate in the presence of NaH to give compounds 2a–c which were not isolated and directly subjected to an in situ nitrosation affording isonitroso compounds 3a–c in good yields. Cyclization of the latter under the action of K2CO3 in MeCN at room temperature gave previously unknown ethyl isoxazolo[4,5-b]pyridine-3-carboxylates 4a–c (Scheme 2).

[1860-5397-20-94-i2]

Scheme 2: Synthesis of ethyl 6-R-isoxazolo[4,5-b]pyridine-3-carboxylates 4a–c.

To the best of our knowledge only one compound (ethyl 5,7-dimethylisoxazolo[4,5-b]pyridine-3-carboxylate) has been synthesized using a similar method, however, the cyclization occurred under drastic conditions (NaH, DMF, 130 °C) as it was reported in patent literature [23].

We assumed that a similar synthetic route (nitrosation/SNAr) would be applicable for the synthesis of isoxazolo[4,5-b]pyridine derivatives bearing other EWG in position 3, for example a formyl group. Thus, the key isonitroso compounds 7 were synthesized from chlorides 1a–c via in situ formation of pyridylacetoacetic esters 2a–c followed by decarbonylation to give 2-methyl-3-nitropyridines 5a–c [24] which were used in the next step without purification. Their reactions with DMF-DMA afforded enamines 6 which, upon nitrosation, were converted into oximes 7a–c in moderate yields (Scheme 3).

[1860-5397-20-94-i3]

Scheme 3: Synthesis of isonitroso compounds 7.

When compounds 7 were treated with K2CO3 3-hydroxypyridine-2-carbonitriles 8 were obtained as sole products (Scheme 4). Apparently, a cyclization of oximes 7 to 3-formylisoxazolo[4,5-b]pyridine took place, followed by a base-promoted decarbonylation/isoxazole ring opening. Such transformations have been previously reported for benzo[d]isoxazoles with a carbonyl or carboxyl group in position 3 or 3-unsubstituted benzo[d]isoxazoles [25-29]. This means that the formyl group of compounds 7 should be protected prior to the attempted isoxazole ring formation. Indeed, reactions of 7a–c with ethylene glycol gave dioxolane derivatives 9a–c which were converted into isoxazolo[4,5-b]pyridines 10a–c in high yields under mild conditions (Scheme 4).

[1860-5397-20-94-i4]

Scheme 4: Base-promoted cyclization of compounds 7a–c.

The obtained result prompted us to try another protecting group for the formyl function, namely arylhydrazone. Thus, reactions of compounds 7a–c with a number of arylhydrazines afforded the corresponding hydrazones 11 which were not isolated and subjected to cyclization under the action of K2CO3 (Scheme 5). In most cases the isoxazolo[4,5-b]pyridines 12 were obtained in pure form, however, cyclization of hydrazone 11a provided an inseparable mixture of two compounds which could be attributed to the target isoxazolo[4,5-b]pyridine 12a and triazole 13a formed as a result of Boulton–Katritzky rearrangement (Scheme 5). When this mixture was treated with K2CO3 in DMF at 60 °C, compound 13a was isolated in 92% yield (from 7a) (Table 1, entry 1). Such rearrangement has been reported previously for the benzo[d]isoxazole series [30], however, it has not been observed for isoxazolo[4,5-b]pyridine derivatives. It was found that the similar rearrangement of the other arylhydrazones 12b–h strongly depends on the aryl substituent. Indeed, the 2,4-dinitrophenylhydrazones 12b,e, and h did not undergo recyclization even under drastic conditions, apparently due to a low nucleophilicity of the hydrazone anion (Table 1, entries 2, 5, and 8). All other compounds 12 bearing no electron-withdrawing groups in the aryl moiety readily afforded the corresponding triazole derivatives in high yields under relatively mild conditions (K2CO3, DMF, 60 °C, Scheme 5). Substituents in the pyridine ring did not affect this transformation thus indicating that they do not participate in the stabilization of the pyridine-3-olate anion.

[1860-5397-20-94-i5]

Scheme 5: Synthesis and rearrangement of arylhydrazones 12.

Table 1: Yields of compounds 12 and 13.

Entry R Ar Compound 12, yield (%) Compound 13, yield (%)
1 NO2 C6H5 12a, not isolated 13a, 92
2 NO2 2,4-(NO2)2C6H3 12b, 87 13b, n.r.a
3 CF3 C6H5 12c, 85 13c, 95
4 CF3 2-Cl-C6H4 12d, 82 13d, 91
5 CF3 2,4-(NO2)2C6H3 12e, 71 13e, n.r.
6 Cl C6H5 12f, 79 13f, 90
7 Cl 4-CH3-C6H4 12g, 76 13g, 95
8 Cl 2,4-(NO2)2C6H3 12h, 74 13h, n.r.

aNo reaction.

It should be noted that the 4-(2-pyridyl)[1,2,3]triazole fragment is part of some pharmaceutically oriented molecules such as tradipitant, an experimental neurokinin-1 receptor antagonist [31], MU1787, a highly selective inhibitor of homeodomain-interacting protein kinases (HIPKs) [32], and combretastatin A-4 analogs evaluated for their anticancer properties against a panel of 60 human cancer cell lines [33] (Figure 2).

[1860-5397-20-94-2]

Figure 2: Biologically active analogs of compounds 13.

The structures of all new compounds were confirmed by 1H and 13C NMR and HRMS. X-ray diffraction studies were performed for compounds 12c and 13c,d (Figure 3; see Supporting Information File 1 for details) that allowed us to unambiguously establish the structures of both the starting hydrazones and rearrangement products.

[1860-5397-20-94-3]

Figure 3: X-ray crystal structures of compounds 12c (top left; the second crystallographically unique molecule is not shown), 13c (top right), and 13d (bottom) with thermal ellipsoids set at a 50% probability level. Intermolecular hydrogen bonds are drawn with dashed lines.

Conclusion

In summary, we have developed an efficient method for the synthesis of isoxazolo[4,5-b]pyridines based on the intramolecular nucleophilic substitution of the nitro group. The method comprises readily available starting materials, mild reaction conditions, easy work-up and high product yields. It was found that isoxazolo[4,5-b]pyridine-3-carbaldehyde arylhydrazones readily undergo a base-promoted Boulton–Katritzky rearrangement to give otherwise inaccessible 3-hydroxy-2-(2-aryl[1,2,3]triazol-4-yl)pyridines in excellent yields. As a result, a wide range of polyfunctional pyridines was synthesized, which can be considered as prospective platform for the design of pharmacology-oriented heterocyclic systems.

Supporting Information

Supporting Information File 1: Experimental section, NMR spectra and X-ray analysis data.
Format: PDF Size: 6.2 MB Download

Author Contributions

Vladislav V. Nikol’skiy: data curation; investigation. Mikhail E. Minyaev: resources; writing – original draft. Maxim A. Bastrakov: investigation; resources. Alexey M. Starosotnikov: conceptualization; supervision; writing – original draft.

Data Availability Statement

All data that supports the findings of this study is available in the published article and/or the supporting information to this article.

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