Assembly of Tetrahydroquinolines and 2-Benzazepines by Pd-Catalyzed Cycloadditions Involving the Activation of C(sp3)–H Bonds

Cycloaddition reactions are among the most practical strategies to assemble cyclic products; however, they usually require the presence of reactive functional groups in the reactants. Here, we report a palladium-catalyzed formal (4 + 2) cycloaddition that involves the activation of C(sp3)–H bonds and provides a direct, unconventional entry to tetrahydroquinoline skeletons. The reaction utilizes amidotolyl precursors and allenes as annulation partners, and is catalyzed by Pd(II) precursors in combination with specific N-acetylated amino acid ligands. The reactivity can be extended to ortho-methyl benzylamides, which provide for the assembly of appealing tetrahydro-2-benzazepines in a formal (5 + 2) annulation process.

A zaheterocycles form the scaffold of many drugs, agrochemicals, dyes, and fragrances and can be found in many natural products. Therefore, the assembly of these skeletons in a sustainable and atom economical fashion remains a primary goal in modern organic synthesis. In this context, one of the more appealing synthetic strategies to build these type of rings consists of the use of metal-catalyzed cycloadditions involving the direct activation of C−H bonds. 1,2 This is exemplified by the synthesis of indoles from anilides through a formal (3 + 2) oxidative cycloaddition (Scheme 1A). 3 The reaction involves an initial C(sp 2 )−H activation to form metallacycle A, followed by migratory insertion of the unsaturated partner and reductive elimination (Scheme 1A). One could envision a similar annulation to build tetrahydroquinolines (THQs) instead of indoles, which is a central scaffold in many bioactive alkaloids; however this would require the use of 3-carbon cycloaddition partners, which are not obvious to identify (Scheme 1B, lef t arrow). 4 An alternative, more attractive disconnection for THQ skeletons could be based on a (4 + 2) instead a (3 + 3) disconnection, like that shown in Scheme 1B (right arrow), as this would entail the use of common 2-carbon unsaturated partners. Moreover, as 4-atom components, orthomethylanilines are very appealing because of their availability.
However, synthetic reactions that fulfill this retrosynthetic analysis, enabling a formal (4 + 2) cycloaddition between ortho methylanilides and unsaturated partners, are unknown. Performing this transformation using transition metal catalysis is challenging, not only because of the well-known difficulties associated with the activation of sp 3 C−H bonds 5 but also because the subsequent steps (migratory insertion into the C(sp 3 )−metal bond and reductive elimination) are also more problematic than in the case of substrates with sp 2 reacting carbons. Indeed, while a vast array of different types of annulations (especially formal cycloadditions) involving the activation of aromatic C(sp 2 )−H bonds have been described, mechanistically related processes based on the activation of sp 3 C−H bonds are very scarce. 6 Herein, we report the first examples of transition metal formal (4 + 2) annulations involving ortho-methylanilides, using allenes as two-carbon partners (Scheme 1C). Importantly, we also demonstrate that the reaction, which is catalyzed by Pd(II) species, can be extended to benzylamides, providing for the direct assembly of azepines in a formal (5 + 2) cycloaddition approach.
As previously established, 7 the presence of strong electronwithdrawing groups at the nitrogen is key for successful C−H functionalization reactions in amino aromatic substrates. Therefore, we started our investigation by examining the reactivity of 1,1,1-trifluoro-N-(o-tolyl)methanesulfonamide (1a, Table 1). As partners we paid attention to allenes, owing to their successful performance in previous cycloadditions involving the activation of C(sp 2 )−H bonds. 8 Using commercially available allene 5-vinylidenenonane (2a), we observed no reaction in the presence of 10 mol % of palladium acetate, and copper acetate as oxidant (in toluene at 105°C). In line with previous reports on the role of monoprotected amino acids accelerating the rate of Pdmediated C−H activations, 9 we found that using 40 mol % of Boc-protected valine as ligand promotes the formation of the desired tetrahydroquinoline product 3aa in a promising 25% yield (based on allene), as a single regioisomer (entries 1 and 2). We tested other amino acid ligands, bearing different amino-protecting groups, discovering that N-acetyl-L-valine (Ac-Val-OH) produces the best results (3aa formed in 60% yield, entry 8). Other oxidants, including benzoquinone or silver carbonate, are clearly inferior to copper acetate (26% and 20% yield respectively). It is possible to use substrates with other electron-withdrawing groups at the nitrogen than triflyl, such as mesyl and nosyl, albeit the reactions are less efficient (entries 9−10). Interestingly, the reaction also works using the environmentally friendly solvent methyl-THF (54% yield), which even allowed it to proceed at lower temperature (85°C ). Decreasing the amount of Cu(OAc) 2 and Cs 2 CO 3 to 1 equiv resulted in the product being obtained in 61% yield (entry 14), while with a lesser amount of palladium salt, conversions were not complete. Finally, we found that a slow addition of allene over a 4 h period led to an increase in yield up to 71% (entry 16).
With the optimized conditions in hand, we investigated the scope of the reaction using different types of allene partners (Scheme 2). Similar to 2a, the 1,1-disubstituted allene vinylidenecyclohexane (2b) worked in good yield (61%). Symmetrical 1,3-disubstituted allenes such nona-4,5-diene (2c) also led to the quinoline product 3ac in 61% yield. Gratifyingly nonsymmetrical 1,3-allenes 2d and 2e led to the expected products, with excellent regio-and diastereoselectivities and an up to 76% yield. Furthermore, while ethyl 2,3-butadienoate did not work, probably because of the presence of an electronwithdrawing group, electron-rich monosubstituted allenes like cyclohexylallene (2f) or the aryl-substituted derivative 2g produced the cycloadducts 3af and 3ag as mixtures of E/Z isomers. Remarkably, trisubstituted allenes are also valid Scheme 1. Metal-Catalyzed Annulations To Give Azaheterocycles Ns ( Organic Letters pubs.acs.org/OrgLett Letter cycloaddition partners, and therefore products 3ah, 3ai, and 3aj were obtained (42−73% yields). 10 The use of allenes as reaction partners is key for the success of the annulation. Alkynes, like diphenylacetylene, were essentially unreactive, while alkenes, such as ethyl acrylate, failed to give the cycloadducts, providing just traces of products resulting from addition/β-hydride elimination processes (olefination). 11 This success with allenes is likely associated with several factors: (1) they are not as coordinating as alkynes, and thereby avoid the saturation of the metal coordination sphere to give nonactive complexes; (2) they favor the migratory insertion step owing to the formation of πallyl intermediates; (3) they also facilitate the reductive elimination step because of the presence of an extra coordinating handle (double bond). 12 We then explored the scope regarding the ortho-methyl anilides, by testing substrates 1b−1n, most of which were prepared by triflation of commercially available substrates. Precursors 1b and 1c with substituents ortho to the methyl group gave the corresponding products 3ba and 3ca in 69% and 50% yield, respectively. Substrates equipped with substituents meta to the methyl group such as phenyl or methoxy, or even with halogens (chloro, bromide), also led to moderate yields (3da−3ga), exhibiting better performance for the electron-rich substrates. The reaction is also compatible with substituents para to the methyl group (chloro, methyl ester, methoxy and phenyl), to give the expected products (3ha−3ka, 50−69% yield). Aryl-disubstituted substrates such 1l and 1m, as well as naphthyl anilide 1n, also led to effective reactions (3la−3na, 52−67% yield). Finally, as expected, the reaction is general for other allenes, as demonstrated with substrate 1f and product 3fh.
Running the reaction of 1a in the presence of D 2 O or Ac(d 3 )-OD under standard conditions revealed no deuterium incorporation in neither the starting material nor the product, which suggests the C−H activation step is irreversible (eq 1).
We also measured the primary kinetic isotopic effect carrying out a competition between 1a and the deuterated analogue 1ad 3 . When the competition experiments were carried out in the same vessel, we obtained a k H /k D ≈ 7.3. Using parallel experiments, the resulting value was 2.7. From both experiments we can conclude that the C−H bond cleavage is the turnover limiting step (eq 2). 13 At this stage, we wondered whether it would be possible to use ortho-methyl benzylamides instead of anilides as annulation precursors. In these substrates the amide directing group is Organic Letters pubs.acs.org/OrgLett Letter further apart from the methyl substituent, and therefore the required C(sp 3 )−H bond activation was not warranted. The annulation is synthetically relevant, as it could allow the formation of seven-membered tetrahydro-2-benzazepines, through a novel type of formal (5 + 2) annulation. The route requires use of ortho disubstituted benzylamide precursors, to avoid the activation of the C(sp 2 )−H of the aromatic ring (see the Supporting Information). The reaction works well (Scheme 3) and even leads to better yields than that of the homologous anilides. The annulations were better performed using N-acetyl-L-valine as an amino acid ligand and toluene as solvent, at 105°C. It is also beneficial to use 2 equiv of allene and of copper acetate. Several interesting azepine products (5aa−5da) were obtained from readily available starting materials in good to excellent yields (61−90% yield). Substitution in the α-position to the amino group (5ea, 87%) are also tolerated. The reaction can also be performed with allenes other than 2a, illustrated with the formation of 5ch (61%). 14 We have also made a preliminary exploration of a kinetic resolution with substrates 4e and 4f. After a brief screening of ligands, we found out that with Boc-L-Leu-NHOMe, using standard reaction conditions at 60°C, the cycloadduct 5fa was produced with a promising 90:10 enantiomeric ratio (Scheme 4). 15,16 This result indicates that we can generate optically active tetrahydrobenzazepine skeletons in only three steps from commercially available starting materials and warrants further studies to optimize the process.
In conclusion, we have developed a palladium-catalyzed annulation between ortho-methyl anilides or benzylamides and allenes involving the activation of benzylic methyl groups. The technology represents a substantial addition to the yet very scarce arsenal of metal cycloaddition tools lying on the activation of C(sp 3 )−H bonds. The approach allows a straightforward assembly of highly substituted tetrahydroquinoline or benzazepine skeletons from inexpensive and readily available starting materials.
Experimental procedures and spectroscopic data for new compounds; X-ray data for 3fa and for 6 (PDF) ■ REFERENCES