Triarylmethanes and their Medium‐Ring Analogues by Unactivated Truce–Smiles Rearrangement of Benzanilides

Abstract Intramolecular nucleophilic aromatic substitution (Truce–Smiles rearrangement) of the anions of 2‐benzyl benzanilides leads to triarylmethanes in an operationally simple manner. The reaction succeeds even without electronic activation of the ring that plays the role of electrophile in the SNAr reaction, being accelerated instead by the preferred conformation imposed by the tertiary amide tether. The amide substituent of the product may be removed or transformed into alternative functional groups. A ring‐expanding variant (n to n+4) of the reaction provided a route to doubly benzo‐fused medium ring lactams of 10 or 11 members. Hammett analysis returned a ρ value consistent with the operation of a partially concerted reaction mechanism.

Abstract: Intramolecular nucleophilic aromatic substitution (Truce-Smiles rearrangement) of the anions of 2-benzyl benzanilides leads to triarylmethanes in an operationally simple manner. The reaction succeeds even without electronic activation of the ring that plays the role of electrophile in the S N Ar reaction, being accelerated instead by the preferred conformation imposed by the tertiary amide tether. The amide substituent of the product may be removed or transformed into alternative functional groups. A ring-expanding variant (n to n + 4) of the reaction provided a route to doubly benzo-fused medium ring lactams of 10 or 11 members. Hammett analysis returned a 1 value consistent with the operation of a partially concerted reaction mechanism.
Triarylmethanes are privileged molecular structures finding application in numerous aspects of chemical science. [1][2][3][4][5][6][7][8] The triarylmethane scaffold occurs in natural products, [1] medicinal agents, [2] building blocks in materials chemistry, [3] and ligand scaffolds. [4] Additionally, triarylmethanes are commonly used as dyes [5] and fluorescent probes, [6] culminating in their recent use as red light-absorbing photoredox catalysts [7] and red light-fluorescing OLEDs. [8] Owing to the diverse utility of triarylmethanes, various synthetic methods have been developed for their preparation. [9] Common approaches include Lewis and Brønsted acidmediated Friedel-Crafts alkylations, [10] and transition metalcatalysed C(sp 3 ) À C(sp 2 ) Suzuki or Kumada cross-couplings (Scheme 1 a). [11] They may also be made by the CÀH arylation of diarylmethanes that results from deprotonative transition metal-catalysed cross-coupling processes (Scheme 1 b), [12] or by Lewis or Brønsted acid-promoted arylations of quinone methides (Scheme 1 c). [13] Nucleophilic aromatic substitution (S N Ar) reactions have been used as a valuable way of making Ar À heteroatom and ArÀC bonds, but as a reaction class they have recently undergone an academic resurgence, as a result of several related discoveries in the field of concerted S N Ar mechanisms. [14][15][16][17][18] Jacobsen and co-workers [14] showed that concerted S N Ar reactions are far from a mechanistic rarity, paving the way for their broader application in synthesis as they provide a transition metal-free route to arylation reactions. [15] S N Ar reactions of diarylmethane carbanions conceptually offer a simple method for triarylmethane construction, but reports are surprisingly sparse and restricted to highly activated nitrocontaining aryl electrophiles (Scheme 1 d). [19] Here we describe a much more general and operationally simple approach to triarylmethanes by the use of a conformationally enhanced intramolecular S N Ar reaction, or Truce-Smiles rearrangement (Scheme 1 e). Classical Truce-Smiles rearrangements proceed by 1,4-or 1,5-N or O to C intramolecular S N Ar of electron-deficient aryl rings, but in our conformationally accelerated variant, much greater substrate generality is possible because no electronic activation is required. [20,21] N-Methylated benzanilides such as 1 prefer to adopt E conformations in which the N-aryl ring lies trans to the carbonyl group, [22] and with the amide carbonyl group twisted more or less perpendicular to the benzamide ring. [23] This conformational bias can be used to promote intramolecular S N Ar for unactivated and even moderately electron-rich aryl rings, by pre-organisation of the nucleophilic and electrophilic components for reaction. [18] With the aim of exploiting such a reaction for the synthesis of triarylmethanes, 2-benzylbenzamide 1 was treated with base with the aim of generating a nucleophilic benzylic anion (Table 1).
Initial attempts with NaHMDS at ambient temperature only afforded trace amounts of product (Table 1, entry 1). However, at elevated temperatures 2-benzylbenzamide 1 underwent Truce-Smiles rearrangement to give triarylmethane 2 (Table 1, entries 2, 3). A base screen identified KHMDS as the optimal choice (Table 1, entries 3-5), with THF and Et 2 O as the best performing solvents (See SI). Slightly lower yields were obtained when the KHMDS stoichiometry was reduced from 2.0 or if the reaction temperature was elevated to 120 8C (Table 1, entries 6, 7). Key indicators of the spectroscopic assignment of the structure of the product are shown in the scheme in Table 1.
With optimised conditions identified for the rearrangement of 1 we investigated the generality of the reaction. Firstly, we explored the scope of aromatic rings that undergo N to C migration (Scheme 2). As with other conformationally accelerated Truce-Smiles rearrangements, [16,17] migration even of electron-rich (4 a and 4 b) and ortho-functionalised (4 c and 4 d) aromatic rings proceeded cleanly at elevated temperatures. Fluorinated aromatic rings (4 e and 4 f) were likewise successfully incorporated into their triarylmethanes, with 4 f forming even at ambient temperature. The migrations of both chlorinated and brominated aromatics required lower reaction temperatures to avoid protodehalogenation, but were all ultimately successful (4 g-i). Heterocyclic triarylmethanes could also be formed, with 4-, 3-, and 2-substituted pyridines all migrating in excellent yield (4 j-l).
The ring coloured red in the schemes plays the role of an anion-stabilising group, and extensive variation in this ring was explored, as indicated in Scheme 3. The reaction was unaffected by variation in this position, tolerating a variety of substituents, including methoxy, methyl, phenyl, and fluoro Entry [a] Base (equiv) T [8C] [b] t groups (6 a-6 d). Substitution in the ortho position was not detrimental, with products containing more hindered orthotolyl and 1-naphthyl groups forming readily (6 e and 6 f).
Triarylmethanes containing 3,4-disubstituted phenyl rings bearing methyl, fluoro, and a dibenzothiophene heterocycle were likewise all formed in good yield (6 g-6 i). Substitution on the third ring, the benzamide ring itself (coloured black), was also possible-significantly even with the substituent ortho to the amide, a position which imposes a significant conformational restraint (6 j). [23] Alternative starting materials in which the migrating ring formed part of a heterocyclic precursor allowed the rearrangement to form products containing medium ring lactams (Scheme 4). Thus the tetrahydroquinoline 7 a was readily expanded to the 10-membered lactam 8 a upon treatment of base. Similar reactivity was shown with the tetrahydronaphthyridine 7 b, and with the benzo-fused 7-ring starting material 7 c, as well as with the dihydro dibenzazepinederived 7 d, each forming their respective 10 and 11-membered lactams (8 b-8 d). The conformational restriction characteristic of medium rings gives them particular interest in medicinal chemistry, [24] and ring expansion has proved to be a viable method for the preparation of medium-ring heterocycles, [25a] circumventing the difficulties associated with entropically and enthalpically unfavourable cyclisations. [18b, 25-27]  The rearrangement leads to products that carry a secondary amide substituent. To explore the potential broadening of this synthetic approach to a more general range of targets, the transformation of this group to other substituents (or none) was explored (Scheme 5). N-Nitrosation of triarylmethane 6 a formed N-nitrosoamide 9, [28] converting the amide to an activated acyl group. In one pot, 6 a was readily converted onwards to carboxylic acid 10 by basic hydrolysis. The carboxylic acid of 10 was removed by a copper-catalysed decarboxylation, [29] revealing the "traceless" triarylmethane product 11. Alternatively, the N-methylbenzamide of 6 a could be used as a useful synthetic handle in, for example, an unoptimised palladium-catalysed annulation to yield the Nmethyl isoquinolone 12. [30] Our proposed mechanism for the rearrangement that leads to the triarylmethane products starts with deprotonation of the 2-benzylbenzamide 1 by KHMDS (Scheme 6 a). The DMSO pK a values of HMDS (26) [31] and diarylmethane (33.5-28) [31] suggest that the equilibrium between 2-benzylbenzamide 1 and carbanion 13 may lie in favour of the protonated form, although the carbanion is additionally stabilised by the amide group. Nonetheless, enough carbanion must be formed to allow the rate of attack on the migrating ring, which initiates an intramolecular S N Ar reaction, to be sufficiently high that it is synthetically useful. Protonation of product amide anion 14 by the aqueous quench yields the desired triarylmethane product.
Further details of the reaction mechanism were explored by in situ infra-red spectroscopy (React-IR). Addition of KHMDS to a solution of 3 h in THF (Scheme 6 b) led to decay of the amide carbonyl stretching frequency (1652 cm À1 ) as a new absorption appeared at 1560 cm À1 (Scheme 6 c). This band was assigned to the carbonyl group of the amide anion of 4 h, confirmed by addition of KHMDS to triarylmethane 4 h Scheme 4. Scope of the ring-expanding rearrangement reaction. Reactions were carried out on a 0.80 mmol scale. Yields of product after isolation by chromatography. Scheme 5. Synthetic modifications of rearrangement product 6 a. Yields of product after isolation by chromatography.
to generate an authentic sample of its amide anion (See SI). No C=O signal corresponding to reaction intermediate 13 was seen, an observation consistent either with rate limiting Cdeprotonation, or with rate limiting rearrangement from an undetectably low concentration of the anion. These two possibilities were distinguished by carrying out the rearrangement of 3 h in the presence of deuterated HMDS, quenching the reaction before complete consumption of starting material (Scheme 6 d). Deuterium incorporation at the benzylic position of 3 h indicated that deprotonation is fast and reversible, confirming that the rearrangement (S N Ar) step is rate-determining.
Classical nucleophilic aromatic substitution reactions require electron-deficient migrating groups, yet the results presented in Schemes 2 and 4 suggest that the rate of this reaction is largely independent of the nature of the electrophilic ring. The role of electronic effects in this reaction was therefore investigated using a Hammett plot. KHMDS was added at 22 8C to a series of N-aryl 2-benzylbenzamides, with the formation of triarylmethane amide anion monitored by React-IR. Under these conditions, the formation of the triarylmethane amide anion from the 2-benzylbenzamide followed first-order kinetics, and the linear section of a plot of ln( [14] 1 À[14] t ) against time gave a rate constant k obs for each substrate (Figure 1). A Hammett plot of log (k R /k H ) versus the substituent constant s À yielded a value for 1 of + 4.0, indicating substantial build-up of negative charge on the migrating ring during the reaction. This significant dependence on s À explains why the products in Scheme 2 may be formed in good yield at much lower temperatures when the migrating ring is electron-deficient. Nonetheless, the facility with which even the p-OMe group of 4 a undergoes intramolecular S N Ar points to the importance of the conformational restriction inherent in the amide starting materials as a major factor in accelerating the absolute values of these rate constants over corresponding intermolecular variants. [22] Murphy and Tuttle [32] have shown that the 1 value is insufficient as an indicator of whether a reaction proceeds by a Meisenheimer complex or by a concerted S N Ar reaction, but given the lack of stabilisation offered to any intermediate anion in most substrates the reaction very likely falls into the latter class, along with other similar recently described reactions. [14][15][16][17][18] In summary, a base-mediated intramolecular S N Ar reaction of N-aryl 2-benzylbenzamides to form triarylmethanes of varied structure is made possible by conformationally induced rate acceleration of an otherwise apparently unfavourable intramolecular S N Ar reaction. This methodology is tolerant of a range of functional groups and aromatic rings, with the resulting triarylmethane products amenable to subsequent constructive or defunctionalising transformations. Novel medium ring-containing triarylmethane scaffolds may be prepared by an n to n + 4 ring expanding variant of the rearrangement. React-IR, deuteration, and Hammett analysis support an empirical mechanistic model in which reversible deprotonation generated a low concentration of a benzyl anion which undergoes rate-determining nucleophilic substitution on the migrating ring. Scheme 6. A) Proposed reaction pathway, with approximate C=O stretching frequencies. B) In situ infra-red trace of the reaction of Naryl 2-benzylbenzamide 3 h, showing diagnostic changes in carbonylstretching frequencies. C) Plot of absorbance against time for peaks at 1652 cm À1 (3 h, starting material) and 1560 cm À1 (4 h, product anion). D) Deuterium-exchange study with N-aryl 2-benzylbenzamide 3 h.