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Cu-catalyzed transannulation reaction of pyridotriazoles with terminal alkynes under aerobic conditions: efficient synthesis of indolizines

V. Helan , A. V. Gulevich and V. Gevorgyan *
Department of Chemistry, University of Illinois at Chicago, 845 W Taylor St., Room 4500, Chicago, Illinois 60607, USA. E-mail: vlad@uic.edu

Received 1st November 2014 , Accepted 3rd January 2015

First published on 5th January 2015


Abstract

A Cu(I)-catalyzed denitrogenative transannulation reaction of pyridotriazoles with terminal alkynes en route to indolizines was developed. Compared to the previously reported Rh-catalyzed transannulation reaction, this Cu-catalyzed method features aerobic conditions and a much broader scope of pyridotriazoles and alkynes.


The transition-metal-catalyzed denitrogenative transannulation of pyridotriazoles represents an efficient method for the synthesis of fused nitrogen-containing heterocycles.1 This method is based on the ability of pyridotriazole to exist in an equilibrium with diazo-form A,2,3 which can be trapped with Rh(II) to form the reactive pyridyl carbene intermediate B, capable of reacting with terminal alkynes1a to produce valuable indolizines 3 (Scheme 1).4,5 However, this transannulation reaction has several shortcomings.
image file: c4sc03358b-s1.tif
Scheme 1 Metal-catalyzed transannulation reactions of pyridotriazoles with terminal alkynes.

Thus, a Cl substituent at the C-7 position (AG, activating group) and an electron withdrawing ester group (EWG) at the C-3 position of the pyridotriazoles were requisite to facilitate the formation of a sufficient amount of the open form of triazole A even at room temperature and subsequently generate indolizines 3.2,3,6 In addition, the reaction was limited to aryl alkynes only (eqn (1)).1a Herein, we report the first general and efficient Cu-catalyzed transannulation of pyridotriazoles 1 with terminal alkynes 2 to form indolizines 3 (eqn (2)). This newly developed method features several important advantages over the previously reported Rh-catalyzed protocol.1a Thus, it is highly practical as it employs a cheap Cu-catalyst and efficiently operates under aerobic conditions. It is also more general demonstrating a much broader reaction scope, as unactivated pyridotriazoles 1 and aliphatic alkynes 2 now become competent reaction partners (eqn (2)).

The above-mentioned transannulation reaction of pyridotriazoles 1 (eqn (1)),1 as well as the further developed and widely used transannulation reactions of N-sulfonyl 1,2,3-triazoles,7 require the use of a Rh-catalyst,8 which is one of the most expensive and rare metals used in catalysis. Naturally, the development of alternative catalysts for transannulation reactions of triazoles would dramatically increase the synthetic applicability of this methodology.9 Accordingly, aiming at the discovery of a cheaper catalyst and at expanding the scope of transannulation reactions of pyridotriazoles, we turned our attention to the potential employment of copper catalysts.10 To ensure sufficient amounts of the open form A of the unactivated pyridotriazole, we tested the potential transannulation reaction at elevated temperatures.3 Thus, we tested various copper catalysts in the reaction of unactivated pyridotriazole 1a with phenylacetylene 2a (Table 1). While CuCl was found to be inefficient (entry 1), the use of Cu(I) and Cu(II) triflates led to the formation of the corresponding indolizine 3a in moderate yields (entries 2 and 3).11 Delightfully, the more electrophilic Cu(MeCN)4PF6 catalyst turned out to be even more efficient in the formation of 3a (entry 4). Finally, after optimization of the temperature (entries 5, 6), a virtually quantitative yield of 3a was achieved (entry 6). Moreover, we were pleased to find that this reaction works equally efficiently under aerobic conditions (entry 7). As expected, under thermal conditions no reaction occurred (entry 8). Moreover, it was found that Rh2(hfb)4 is not a capable catalyst for this reaction (entry 9).

Table 1 Optimization of the Cu-transannulation reaction conditionsa

image file: c4sc03358b-u1.tif

Entry Catalyst, mol% T (°C) Yieldb
a Triazole (1 equiv.), alkyne (3 equiv.), Cu cat. (15 mol%), toluene (1 M) in a Wheaton V-vial capped with a Mininert syringe valve. b GC/MS yields are given. c 1.2 equiv. of alkyne was used. d In air with 1.2 equiv. of alkyne. e Lower catalyst loading led to decreased reaction yields.11 f Polymerization of the alkyne was observed; hfb = heptafluorobutyrate.
1 CuCl, 15% 100 N.R.
2 CuOTf·0.5C6H6, 15% 100 38%
3 Cu(OTf)2, 15% 100 25%
4 Cu(MeCN)4PF6, 15% 100 50%
5c Cu(MeCN)4PF6, 15% 120 96%
6c Cu(MeCN)4PF6, 15% 130 99%
7d,e Cu(MeCN)4PF6, 15% 130 99%
8 No catalyst 100 N.R.
9 Rh2(hfb)4, 1% 100 N.R.f


Having the optimized conditions in hand, we investigated the scope of this Cu-catalyzed transannulation reaction of pyridotriazoles with terminal alkynes (Table 2). A variety of aryl alkynes bearing electron-neutral, electron withdrawing and electron donating substituents at ortho-, meta- and para-positions produced the corresponding indolizines 3 in high yields upon reaction with pyridotriazole 1a (Table 2, entries 1–10).12 Heteroaromatic alkynes such as 3-thienyl acetylene and enyne led to the indolizines 3k, l in reasonable yields (entries 11 and 12). We were pleased to find that in contrast to the previously reported Rh-catalyzed reaction, aliphatic alkynes were also competent reactants. Thus, benzyl-, n-butyl, and c-hexyl acetylenes reacted smoothly to produce the corresponding indolizines in good yields (entries 13–15). To our delight, functional groups including benzyloxy- and N-phthalimido were perfectly tolerated under the reaction conditions (entries 16 and 17). Moreover, while our group previously reported the Rh-catalyzed transannulation reaction of pyridotriazoles with nitriles,1a the Cu-catalyzed transannulation showed a strong preference for the alkyne over the nitrile group. Thus, the reaction of pyridotriazole 1a with 5-hexynenitrile furnished indolizine 3r with the nitrile group staying intact (entry 18). Notably, pyridotriazoles which did not contain electron withdrawing groups at the C-3 position were found to be reactive substrates as well. Hence, the indolizines derived from 3-phenyl and 3-methyl pyridotriazoles were produced in reasonable yields (entries 19–23). Remarkably, even a non-substituted pyridotriazole (R1 = H) reacted with phenylacetylene to form indolizine 3x in a moderate yield. Noteworthily, trialkylsilyl-substituted alkynes were either unstable (TMS, TES) or stayed intact (TIPS) under the reaction conditions.

Table 2 Scope of the Cu-catalyzed transannulation reaction of pyridotriazoles with alkynesa

image file: c4sc03358b-u2.tif

Entry Product Yield, % Entry Product Yield, % Entry Product Yield, %
a Isolated yields.
1 image file: c4sc03358b-u3.tif 70 9 image file: c4sc03358b-u4.tif 78 17 image file: c4sc03358b-u5.tif 82
2 image file: c4sc03358b-u6.tif 74 10 image file: c4sc03358b-u7.tif 75 18 image file: c4sc03358b-u8.tif 66
3 image file: c4sc03358b-u9.tif 65 11 image file: c4sc03358b-u10.tif 33 19 image file: c4sc03358b-u11.tif 77
4 image file: c4sc03358b-u12.tif 70 12 image file: c4sc03358b-u13.tif 67 20 image file: c4sc03358b-u14.tif 80
5 image file: c4sc03358b-u15.tif 48 13 image file: c4sc03358b-u16.tif 68 21 image file: c4sc03358b-u17.tif 67
6 image file: c4sc03358b-u18.tif 57 14 image file: c4sc03358b-u19.tif 82 22 image file: c4sc03358b-u20.tif 50
7 image file: c4sc03358b-u21.tif 60 15 image file: c4sc03358b-u22.tif 83 23 image file: c4sc03358b-u23.tif 41
8 image file: c4sc03358b-u24.tif 94 16 image file: c4sc03358b-u25.tif 53 24 image file: c4sc03358b-u26.tif 54


We envisioned two alternative pathways for this Cu-catalyzed transannulation reaction (Scheme 2). First, the copper catalyst can react with the terminal alkyne 2 to form copper acetylide 4, which would react with the α-imino diazo compound A to generate the Cu–carbene complex C (path a). Alternatively, the copper–carbene C can be formed via the reaction of alkyne 2 with copper–carbene B, which is produced from the diazo compound A and the Cu-catalyst (path b). Next, migratory insertion of the alkynyl group at the carbene C-atom of C would form the propargyl intermediate D.13 The latter would undergo cyclization via a nucleophilic attack of the pyridine nitrogen at the triple bond activated by the electrophilic Cu-species14 to produce the triazolyl-copper intermediate G. Also, one cannot exclude the formation of propargylic (E) or allenic (F) intermediates upon protiodemetalation of D. Cycloisomerization of E and F would form intermediate G.15 A subsequent protiodemetalation of G would lead to the indolizine 3.


image file: c4sc03358b-s2.tif
Scheme 2 Proposed mechanism for the Cu-catalyzed transannulation reaction of pyridotriazoles with alkynes.

In order to verify a potential involvement of Cu-acetylide 4 in this transformation, we performed several test experiments. First, it was found that the reaction of pyridotriazole 1a with 4 did not produce indolizine 3a (Scheme 3, entry 1). However, the reaction of 1a with 4 can be catalyzed by both Cu(MeCN)4PF6 (entry 2)16 and HPF6(aq.) (entry 3). This observation suggests that the presence of an electrophilic Cu-species is required to activate the alkyne during the cyclization of D into G,17,18 and potentially to shift the equilibrium of the pyridotriazole towards the reactive α-imino diazo compound A.19 Although more detailed studies are required to elucidate the exact mechanism of this transformation, based on literature data20,21 and the above-mentioned observations, it is believed that the reaction most likely proceeds via path a (Scheme 2).


image file: c4sc03358b-s3.tif
Scheme 3 Reactions of the Cu-acetylide with triazole 1a.

Conclusions

We have developed a practical and efficient copper-catalyzed denitrogenative transannulation reaction of pyridotriazoles with terminal alkynes into indolizines. Compared to the known Rh-catalyzed transannulation reaction, this newly developed method features not only the use of a cheap Cu-catalyst and aerobic conditions, but also a much broader scope of multisubstituted indolizines that now can be accessed from unactivated pyridotriazoles and diverse terminal alkynes.

Acknowledgements

The support of the National Institutes of Health (GM 64444) and National Science Foundation (CHE-1401722) is gratefully acknowledged. We also thank Dr S. Chuprakov for initial experiments.

Notes and references

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Footnote

Electronic supplementary information (ESI) available: Experimental procedures and characterization for new compounds are provided. See DOI: 10.1039/c4sc03358b

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