Hydrogen Bonding Phase-Transfer Catalysis with Ionic Reactants: Enantioselective Synthesis of γ-Fluoroamines

Ammonium salts are used as phase-transfer catalysts for fluorination with alkali metal fluorides. We now demonstrate that these organic salts, specifically azetidinium triflates, are suitable substrates for enantioselective ring opening with CsF and a chiral bis-urea catalyst. This process, which highlights the ability of hydrogen bonding phase-transfer catalysts to couple two ionic reactants, affords enantioenriched γ-fluoroamines in high yields. Mechanistic studies underline the role of the catalyst for phase-transfer, and computed transition state structures account for the enantioconvergence observed for mixtures of achiral azetidinium diastereomers. The N-substituents in the electrophile influence the reactivity, but the configuration at nitrogen is unimportant for the enantioselectivity.

A symmetric phase-transfer catalysis (PTC) is one of the most practical methods for enantioselective synthesis. 1 For many years, PTC approaches to asymmetric fluorinations have used F 2 -derived electrophilic reagents and cationic or anionic chiral species for effective phase-transfer. 2 Inspired by nature's fluorinase, 3 we reported a complementary hydrogen bonding phase-transfer catalysis (HB-PTC) manifold that employed alkali metal fluorides for asymmetric nucleophilic fluorinations. 4 Specifically, a chiral N-alkylated bis-urea served as the hydrogen bond donor (HBD) catalyst to bring KF or CsF in solution. The process involves a chiral urea−fluoride complex that is capable of ion-pairing with in situ-formed mesoepisulfonium or -aziridinium ions. The ensuing enantioselective desymmetrization afforded enantioenriched β-fluorosulfides and β-fluoroamines. To date, all enantioselective fluorinations carried out under PTC use nonionic substrates, including β-keto esters, alkenes, β-bromosulfides or β-chloroamines. An unexplored scenario in asymmetric C−F bond construction under PTC is the use of two ionic reactants. We became interested in this challenge as we envisioned that enantioselective desymmetrization of achiral azetidinium salts with fluoride would afford γ-fluoroamines of high value for medicinal chemistry. 5 Azetidinium salts 6 with non-nucleophilic counteranions are bench-stable solids 7a and can be prepared from commercially available 7b or readily synthesized 7c azetidines. Few methods are available to access enantioenriched γ-fluoroamines, 8 and strategies for the enantioselective installation of CH 2 F are scarce. 9 In 2018, Sun and co-workers reported the desymmetrization of azetidinium salts with mercaptobenzothiazoles and a chiral phosphate catalyst (Scheme 1A, left). 10 This pioneering study encouraged experimentation applying this anionic PTC approach (CAPT) with TBAF or CsF; none of our attempts yielded γ-fluoroamines (Scheme S6). This result prompted the Scheme 1. (A) Desymmetrization of Azetidinium Salts; (B) R 4 N + X − as a Catalyst (CPTC) versus R 4 N + X − as a Substrate (HB-PTC); (C) Computational Binding Studies (R 4 N + X − Treated as a Dissociated Species) use of HB-PTC as an alternative manifold. Mechanistically, achiral azetidinium salts could themselves act as phase-transfer agents enabling solubilization of solid alkali metal fluorides as azetidinium fluorides. Indeed, ammonium salts, 11a−c pyridinium salts, 11d and imidazolium-based ionic liquids 11e have been used as phase-transfer catalysts for non-enantioselective fluorination reactions with KF or CsF (Scheme 1B, left). 11f,g Such a cationic phase-transfer catalysis (CPTC) scenario would transform in situ-formed azetidinium fluoride into racemic γ-fluoroamine. We envisioned that HB-PTC using a chiral bis-urea catalyst could offer a viable approach for the desymmetrization of achiral azetidinium salts with alkali metal fluorides (Scheme 1A,B, right). This scenario is not without challenges because the use of two preformed ionic reactants implies a high concentration of ions in solution, a drastic change compared with transformations featuring transiently formed ion pairs. 4a,b Significant variation in the fluorination kinetics and competitive binding events (e.g. azetidinium counteranion X − vs F − ) can be expected. 12 Computational studies indicated that a neutral chiral N-methyl-bis(urea) 4a binds a CsF unit more strongly than 1,1-dimethylazetidinium ion in 1,2-dichloroethane (1,2-DCE) (ΔG urea = −69 kJ/mol, ΔG azet = −14 kJ/mol; Scheme 1C). 13a Encouraged by these findings, 13b we surmised that azetidinium salts (R 4 N + X − ) could undergo enantioselective fluorination with an alkali metal fluoride (M + F − ) in the presence of a chiral HBD catalyst (urea*) if orchestrated hydrogen bonding and ion metathesis generate the soluble chiral ion pair [R 4 N] + [F·urea*] − . This species could undergo C−F bond formation with release of the enantioenriched γfluoroamine and the catalyst. Herein we describe the development of this unusual PTC process featuring two ionic reactants and demonstrate that achiral azetidinium salts are amenable to desymmetrization with CsF and a chiral BINAM-derived bis-urea catalyst.
The benefit of the N-benzhydryl group on reactivity prompted further investigation. 14 Fluorination reactions performed on differently N,N-disubstituted azetidinium salts under homogeneous conditions (TBAF·3H 2 O, 1,2-DCE, no catalyst) showed benzhydryl to be superior to all other Nsubstituents (Scheme S4). The increased reactivity of Nbenzhydrylazetidinium salts is therefore unconnected with phase-transfer. Computed transition state (TS) structures for the fluorination of seven azetidinium ions by free fluoride (homogeneous conditions) showed that the increased experimental yields are consistent with smaller computed activation barriers. N-Benzhydrylazetidinium ions have barriers to fluorination that are ∼6 kJ/mol lower than those for the corresponding N-benzyl substrates. This can be traced to increased reactant strain: N-benzhydrylazetidinium ions have more elongated C−N bonds and earlier fluoride delivery TS positions compared with the methyl or benzyl substrates (Figure 1).
The scope of γ-fluoroamine synthesis was examined next (Scheme 2). High yields and enantioselectivities were obtained with 3-arylazetidinium triflates. Substrates bearing aromatic groups with electron-withdrawing and electron-donating substituents at the meta or para position were converted in excellent yields and enantioselectivities (2aa−2ha, up to 99% yield, 97.5:2.5 e.r.). Heteroaromatic groups such as thiophene (2pa), pyrazole (2qa), and indole (2ra) were compatible, representing pharmaceutically relevant motifs (up to 99% yield, 94:6 e.r.). Additional highlights are the suitability of Nallylazetidinium salts (2ac, 2ic), the tolerance of the reaction to 3-aryloxy (2ia−2ja, up to 99% yield, 93.5:6.5 e.r.), 3-alkoxy (2ka−2mb), and 3-phthalimido (2sa) groups, and the Journal of the American Chemical Society pubs.acs.org/JACS Communication synthesis of enantioenriched γ-fluoroamines 2oa and 2va−2ua featuring a tetrasubstituted stereogenic carbon. Furthermore, 2ta bearing an ester group stands out as an immediate precursor to enantioenriched fluorinated β-lactams and βamino acids. 16 Tertiary fluoride 2wa was accessed in good yield with moderate enantioselectivity. A single recrystallization of 2sa, 2ta and 2wa afforded these fluorinated amines in high enantioselectivity or as a single enantiomer. Substrates mono-or bis-alkylated at position 3 were less successful (Scheme S7). 13a Single-crystal X-ray diffraction analysis of 2ma·HCl and 3ab·HCl (Scheme 3A) enabled the assignment of the absolute configuration ((S)-catalyst affords (S)product). 17 This new catalytic protocol enabled the preparative-scale synthesis of γ-fluoroamines 3aa and 3ab (Scheme 3A). The reaction of 1 g of 1aa was conducted with a lower catalyst loading (3 mol%) and no compromise in e.r. relative to the smaller-scale reaction. Deprotection and a single recrystallization gave the primary γ-fluoroamine 3aa with 99:1 e.r. A similar protocol afforded enantioenriched secondary γ-fluoroamine 3ab with 98.5:1.5 e.r. The synthesis of the fluorinated analogue of lorcaserin, 18 a selective serotonin 2C receptor agonist that is FDA-approved for chronic weight management, illustrates the value of the method for accessing valuable pharmaceutical motifs (Scheme 3B).
Further experimentation was undertaken to gain more insight into this process.  (Table S5). (ii) Exchanging OTf − of 1aa with PF 6 − gave 2aa with identical e.r. (96:4) but in only 31% yield (Table S6). This observation indicates that the counteranion influences the efficacy of phasetransfer and advocates against anion-binding catalysis. This is further supported by NMR studies showing the stronger binding preference of the catalyst for fluoride compared with other anions (F − ≫ TfO − ≈ BF 4 − > PF 6 − ). 13a (iii) The linear relationship between the enantiopurities of the catalyst and product supports the involvement of a single urea catalyst in the enantiodetermining step (Table S7). (iv) When diastereomerically pure N-methyl-substituted cis-1a or trans-1a was subjected to asymmetric fluorination under the standard reaction conditions, fluoroamine (S)-2a was formed with comparable e.r. values (80.5:19.5 and 80:20, respectively; Table S4).
Finally, we turned our attention to the origin of enantioconvergence for this transformation. The TSs for fluorination of 1a mediated by catalyst (S)-D were computed using density functional theory (DFT). 19 An ensemble of TSs were optimized for both cis and trans substrates (Figure 2). With the cis substrate (major diastereomer), both TS Major -cis and TS Minor -cis feature a face-to-face π interaction between the phenyl group at the 3-position of the substrate and the catalyst (Figure 2Ai), orienting the substrate in the catalytic pocket. In contrast, the benzhydryl groups point in different directions. In TS Major -cis, the azetidinium ion adopts its favored conformation, with an intramolecular CH···π interaction worth approximately 2−5 kJ/mol (Figure 2Aii). In TS Minor -cis, this is compensated by an aromatic edge-to-face interaction of the benzhydryl group with the catalyst BINAM backbone ( Figure  2Aiii). When computed with an N-ethyl substituent (1ab), the (S)-catalyst affords the (S)-product with 91:9 e.r., consistent with the experimental enantioselectivity of 96:4 e.r. Comparison of the lowest-energy TS, TS Major -cis, to the TS for the major product with the trans substrate, TS Major -trans, shows remarkable similarity, with excellent superposition of the catalyst, fluoride, and substrate. The only exception is the reversal of the configuration at nitrogen, which causes the sterically demanding benzhydryl group to point in a different direction ( Figure 2B). The enantioconvergence of the diastereomers originates from the projection of the azetidinium N-substituents away from the catalyst and the resulting indifference to the configuration at nitrogen. 20 In conclusion, this study provides new insights into HB-PTC and its application to high-value fluorine-containing molecules. Neutral N-alkyl-bis(urea) catalysts are more effective at fluoride binding than azetidinium ions, a feature enabling efficient enantioselective ring opening with CsF for the synthesis of γ-fluoroamines. As the use of ammonium salts as substrates is uncommon in asymmetric catalysis, 21 the principles outlined here may encourage further studies to transform ionic starting materials into enantioenriched products by applying HB-PTC.