A Chiral Amine Transfer Approach to the Photocatalytic Asymmetric Synthesis of α-Trialkyl-α-tertiary Amines

A long-standing challenge within radical chemistry is that of controlling the absolute stereochemistry of the products. Here, we report the stereocontrolled addition of α-amino radicals reductively generated from imines via visible-light-mediated photoredox-catalysis to alkenes, giving rise to enantioenriched α-trialkyl-α-tertiary amines. This process exploits a commercially available phenylglycinol derivative as a source of both nitrogen and chiral information. DFT studies support a stereochemical model whereby an intramolecular H-bond rigidifies the transition state of the enantiodetermining step.

* sı Supporting Information ABSTRACT: A long-standing challenge within radical chemistry is that of controlling the absolute stereochemistry of the products. Here, we report the stereocontrolled addition of α-amino radicals reductively generated from imines via visible-light-mediated photoredox-catalysis to alkenes, giving rise to enantioenriched α-trialkyl-αtertiary amines. This process exploits a commercially available phenylglycinol derivative as a source of both nitrogen and chiral information. DFT studies support a stereochemical model whereby an intramolecular H-bond rigidifies the transition state of the enantiodetermining step. C hiral alkylamines are important features in biologically active small molecules due to their high density of structural information, hydrogen-bonding capabilities, and tunable physical properties. 1 In particular, alkylamines displaying a stereodefined fully substituted carbon center adjacent to the nitrogen atom, α-trialkyl-α-tertiary amines (αtrialkyl-ATAs), are an important variant of this class of functional molecule and feature in a wide range of pharmaceuticals, agrochemicals, and natural products ( Figure  1A). 2 However, the asymmetric construction of these molecules remains a significant synthetic challenge, 3 principally due to the steric demands associated with forging fully substituted centers and poor stereodifferentiation between similar alkyl substituents. 4 Consequently, existing strategies often rely on the relay of chiral information to the fully substituted carbon center via molecular rearrangements, 5 or by remote functionalization, 6 where the prochiral fully-substituted center is preformed and subsequently desymmetrized. A more direct approach via the 1,2-addition of organometallics to ketimines has been successful in some cases, with asymmetric induction achieved either through addition to a chiral auxiliaryderived sulfinimine or via catalyst-controlled delivery of the nucleophile to activated imine derivatives, but remains limited in terms of functional group tolerance. 7 Over the past decade, photoredox catalysis has become a powerful tool for the synthesis of complex amines through the intermediacy of nucleophilic α-amino radicals that can be generated via a range of activation modes. 8 In particular, these methods have been utilized for the synthesis of α-trialkyl-ATAs. 9 Controlling the stereochemistry in reactions with these open shell species, however, remains a significant goal in the field with few examples of transformations that address this problem. Notable cases of the successful enantiocontrol of αamino radicals include work by Ooi, who demonstrated that chiral phosphoniums can control asymmetric radical−radical coupling reactions. 10 Phipps has also developed an enantioselective Minisci-type reaction enabled by a chiral BINOL phosphoric acid that binds to both the α-amino radical and heteroarene, 11,12 while Jiang has reported that chiral BINOL phosphoric acids can mediate enantioselective 1,2-additions of α-amino radicals to vinylpyridines. 13 Our group recently reported a visible light-mediated catalytic synthesis of α-trialkyl-ATAs from primary benzylic amines, dialkyl ketones, and alkenes ( Figure 1B). 14 Single electron reduction of in situ formed imines gave α-amino radicals that could engage alkenes in a 1,2-addition to forge the desired α-trialkyl-ATA products. Crucial to the success of the reaction was the use of benzylic amines, which are thought to drive the redox neutral process by translocating the radicals formed after alkene addition to stabilized aminobenzyl radicals via 1,5-hydrogen atom transfer (HAT).
We envisioned that deployment of an enantiopure chiral benzylamine could mediate a chiral amine transfer process, whereby the stereochemical information and the nitrogen atom are relayed, through reaction of the α-amino radical, to the newly forming fully-substituted center ( Figure 1C). The development of such a chiral amine transfer (CAT) reagent would enable the delivery of enantioenriched α-trialkyl-ATA products from simple starting materials. We began by investigating the effect of α-methylbenzylamine, an abundant chiral benzylic amine feedstock, in the photocatalytic hydroaminoalkylation reaction ( Figure S1). Unfortunately, low enantiomeric ratios were obtained for the α-trialkyl ATAs derived from several nonsymmetrical ketones and α-methylbenzylamine. These results are, perhaps, unsurprising, given the low barrier of rotation around the C−N axis of the αamino radical (calc. ΔG ‡ rot = 9.8 kcal mol −1 ), 15 the flexibility of the pendent chiral amine, and the early transition states often associated with radical transformations. 16 Furthermore, while α-methylbenzylamine has been shown to govern stereochemical outcomes in polar reactions, 17 diastereoselectivity is typically low in the reactions of α-amino radicals (containing an acyclic chiral amine motif) with alkenes. 18 In order to overcome these obstacles, we proposed that rigidifying the conformation of the chiral amine fragment, relative to the reacting α-amino radical, would allow for a more efficient transfer of chirality. To this end, we recognized that the N−H bond in an α-amino radical is more acidic than the corresponding amine N−H motif. The ground state hydrogen bonding interaction between alkylamine N−H bonds and ether-type oxygens is considered weak (ca. 2−3 kcal mol −1 ), while the increased acidity of the N−H bond in the corresponding α-amino radical should lead to a stronger Hbonding interaction. 19 Therefore, we questioned whether the N−H bond in an α-amino radical could be capable of forming an intramolecular hydrogen bond to a pendent Lewis basic atom within the stereodefined chiral amine architecture ( Figure 1D). Based on this premise, we considered chiral amines based on the phenylglycinol scaffold, not only because they display a proximal oxygen atom that could fulfill our rigidifying hydrogen bond hypothesis, but also because they are readily accessible, low-cost chiral building blocks.
Concurrent with this, we initiated preliminary computational modeling to provide a theoretical basis for our experimentation. Using the addition of the α-amino radical derived from (S)-phenylglycinol methyl ether and cyclohexyl methyl ketone into phenyl vinyl sulfone as a model system, density functional theory (DFT) calculations were performed at wB97XD/6-311′++(d,p) level of theory (see SI for full details). Analysis of the transition states revealed that the lowest energy pathway

Organic Letters pubs.acs.org/OrgLett
Letter was consistent with the presence of a hydrogen bond between the N−H of the α-amino radical and the oxygen atom of the ether linkage within the CAT reagent, at the point of radical addition. 20 Having confirmed the viability of our proposed intramolecular hydrogen bond locked chiral amine transfer reagent, we tested our hypothesis experimentally. The condensation of acyclic ketones with sterically encumbered benzylamines is challenging, often resulting in low conversion to the corresponding imine. 14 However, we found that stirring the CAT reagent 4a (1 equiv) and ketone 1c (2 equiv) at 80°C in the presence of 20 mol % tris(2,2,2-trifluoroethyl)borate and 4 Å molecular sieves (MS) in CH 2 Cl 2 for 24 h gave optimal assay yield of the imine (87% by 1 H NMR, Table S2). Irradiation of the imine and phenyl vinyl sulfone (2b, 1.5 equiv) in the presence of 1 mol % Ir(dMeppy) 3 and 4 Å MS in CH 2 Cl 2 for 24 h at room temperature resulted in the formation of the α-trialkyl-ATA derived imine (5) in 70% yield with an enantiomeric ratio (e.r.) of 81:19. At this stage (S)-phenylglycine methyl ester was also tested as a CAT reagent to examine the effect of a carbonyl group as an alternative hydrogen bond acceptor. However, none of the desired product was observed in this case.
With these initial results in hand, we next assessed a range of phenylglycinol derivatives 4a−h, which were prepared using standard literature procedures and displayed a variety of substituents on both the oxygen and the aromatic ring. Beyond the initial reaction (Table 1, entry 1), we found the corresponding O-Bn protected phenylglycinol 4b to be equally effective compared to 4a (entry 2). The corresponding O-PMB ether 4c resulted in a decrease in yield (entry 3); however, a comparable enantiomeric ratio suggested that the group appended to the oxygen had little effect on the stereochemical outcome. Next, we turned our attention to the aryl group of the CAT reagent. While 4-MeO-substituted 4d gave poor conversion to product (entry 4), albeit with good e.r., substitution at the meta-positions (4e) afforded the desired product in good e.r. and modest yield (entry 5). This can be rationalized by considering the increase in bulk of the aryl group that results from its functionalization along nonlinear exit vectors, which in turn increases the stereodifferentiation between the aryl group and hydrogen atom emanating from the chiral center of the CAT reagent. Moreover, electronwithdrawing substituents on the aromatic ring may serve to further increase H-bond strength through inductive stabilization of the nitrogen anion. No reaction was observed when using the corresponding chiral 1,2-diamine 4f (entry 6), and αphenylglycinol derivative 4g afforded the desired α-trialkyl-ATA in diminished yield and lower e.r. (entry 7). Finally, (R)α-ethylbenzylamine 4h, where the OMe motif of 4a is replaced with a methyl group, afforded the α-trialkyl-ATA product in low e.r., consistent with our model requiring an intramolecular hydrogen bond (entry 8). As a result of these observations, we selected (R)-phenylglycinol methyl ether 4a as the optimal CAT reagent based upon its conversion to the desired chiral αtrialkyl-ATA and its availability (as well as being commercial, it can be prepared on a multigram scale from readily available N-Boc-(R)-phenylglycinol).
Having identified an optimal stereocontrolled multicomponent system, we next investigated the scope of this asymmetric hydroaminoalkylation reaction. We generally found that the redox-neutral photocatalytic cycle generated the α-trialkyl-ATA products (5) as enamines, from which the primary amine could be liberated (Figure 2). While steric challenges associated with the initial imine condensation restricted the ketone alkyl groups, methyl ketones possessing a range of structurally varied α-substituents were found to perform well ( Figure 2A). Pleasingly, both cyclohexyl methyl ketone 1c and isopropyl methyl ketone 1d gave rise to good levels of stereoselectivity in the α-trialkyl-ATAs products 3c and 3d. These results offer a strong indication of the robustness of the transformation as stereodifferentiation between aliphatic substituents is typically regarded as more challenging than distinguishing an aryl ring from an alkyl substituent. Although increasing from 6-to 7-membered cyclic ketone 1e saw selectivity maintained in ATA 3e, a slight drop off was observed on reducing to a 4-membered ring 3b. Saturated heterocycle-methyl ketones, displaying tetrahydrothiopyran and 4-(N-Boc)-piperidine motifs, generated the desired products (3g and h) with the expected selectivity. Ketal protected cyclohexanone 1i delivered the corresponding ATA 3i in good yield. Acetyl indane 1j also formed the desired ATA product 3j with good selectivity, and X-ray crystallography of 4-nitrbenzoyl protected 3j confirmed the absolute stereochemistry of the major enantiomer of the product, which was in agreement with the stereochemical model.
A range of electron-deficient olefins were found to be excellent coupling partners ( Figure 2B), allowing the incorporation of sulfone (3k), phosphonate (3l), nitrile (3m), and ester (3n) functionalities in good yields and with consistent levels of stereoselectivity. In addition, perfluor- Organic Letters pubs.acs.org/OrgLett Letter oalkene 2e afforded the corresponding ATA 3o with good conversion and selectivity. Vinyl sulfonamides (2f−h) were also found to be suitable acceptors, delivering a range of complex α-trialkyl-ATAs 3p−r, highlighting the tolerance of the reaction toward medicinally relevant functionality. A 1,1disubstituted acceptor, tert-butyl methacrylate 2i, generated 3s in moderate yield as a mixture of diastereomers, but with high selectivity (91:9 e.r.) in the major isomeric component. The low diastereomeric ratio seen in this example can be rationalized by considering the competing factors required in order to set the α vs γ position and the differing associated stereochemical models invoked vide infra. We propose that the reaction proceeds via a redox-neutral photocatalytic cycle, support for which was reported in our previous work on a racemic version of this reaction ( Figure  S2). 14 Under this pathway we consider the addition of the αamino radical to the alkene to be enantiodetermining. However, when unsymmetrical 1,1-disubstituted acceptors are used there is potential for a chiral center to be formed at the γ-position, with 1,5-HAT becoming the enantiodetermining step. While limited diastereoselectivity was observed when amine 4a was used as the CAT reagent, it led us to question whether further CAT reagent design could enable control of additional stereocenters.
To test this, we conducted a survey of different CAT reagents that were at our disposal (Table S4) and identified commercially available (+)-1-(1-naphthyl)ethylamine 4i as an effective CAT reagent for controlling the γ-amino center Figure 2. Scope for synthesis of enantioenriched ATAs through the combination of a simple CAT reagent derived from phenylglycinol, ketones, and olefins. Compound 3j, ellipsoid contour 50% probability level. † Reaction conducted using [Ir(4′-OMeppy) 3 Figure 2C). Employing tetrahydropyran-4-one 1l and tertbutyl methacrylate 2i gave rise to γ-chiral α-trialkyl-ATA 8 in moderate yield and high stereoselectivity (93:7 e.r.). This can be rationalized by considering the minimization of 1,3-diaxial interactions between the naphthalene and tert-butyl ester in the proposed chairlike transition state of the 1,5-HAT process. Moreover, it highlights that a different set of stereochemical control elements are operational with subtle changes to the nature of the ketone, alkene, and CAT components, providing the potential for a more general approach to the stereoselective reaction of α-amino radicals.
In conclusion, we have developed a multicomponent photoredox-mediated platform for the asymmetric construction of complex α-trialkyl ATAs from simple feedstocks. While the stereoselectivity in this process is not yet optimal, the results presented break new ground in understanding how to control diastereoselective radical reactions toward the formation of enantioenriched products, a challenge to which a general solution remains elusive. We envisage that this distinct approach toward radical selectivity, paired with the practical simplicity of our platform, will inspire further investigation into novel modes of stereocontrol in photocatalytic radical reactions.

■ ASSOCIATED CONTENT Data Availability Statement
The data underlying this study are available in the published article and its Supporting Information.
Experimental procedures, DFT calculation, and spectroscopic data for new compounds (PDF)

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