Introduction

Synthesis of nitrogen-containing molecules is of significant importance because of their occurrence in a myriad of chemicals, materials, natural products, pharmaceuticals, etc. [¹-³]. Nitrogen-atoms present in organic compounds can be arranged in many different ways. These combinations and/or permutations of nitrogen-atoms give rise to many different functional groups, such as: amines, guanidines, ureas, lactams, amides, azides, amino acids, nucleic acids, pyridines, triazenes, etc. [⁴,⁵]. In 2014, our laboratory reported a straightforward method for the synthesis of nitrogen-enriched π-conjugated triazenes [⁶,⁷], (Fig.1). Due to the current scientific interest and known applications of π-conjugated triazenes, a review on the subject appeared in the literature in 2015 [⁸]. Figure 1 also shows two molecules with similar chemical structures that were reported last year and voted as top molecules of the year, due to their unique electronic and structure properties [⁹,¹⁰]. The chemical structure of these molecules includes three continuous nitrogen-atoms, one of the compounds serves as frustrated Lewis acid pair (Triazolium) [9], while the other molecule was the first stabilized radical using an N-heterocyclic carbene (NHC) [¹⁰], (Fig, 1). Herein, we report the synthesis and characterization of two aromatic iminium salts linked by methylene derivated from dichloromethane (Fig. 1). This due to our interest in increasing molecular complexity and to further evaluate the chemical reactivity of π-conjugated triazenes [¹¹,¹²].

Fig. 1 Examples of nitrogen-containing molecules with unique structure and electronic properties. Mes = Mesityl. 

The activation of chloroalkanes represents a considerable challenge in synthetic chemistry since the C-Cl bond is relatively inert compared with its congeners C-Br and C-I bonds [¹³]. It is of additional difficulty to activate both C-Cl bonds of a gem-dichloroalkane, for example dichloromethane [¹⁴]. Dibromomethane and diiodomethane have been used as alkylating agents (e.g., Simmons-Smith cyclopropanation), [¹⁵]. However, dichloromethane a substantially cheaper compound is considerably less exploited, because of its much lower reactivity as described above [¹⁶]. Therefore, we aimed to evaluate the nucleophilic power of our π-conjugated triazene toward alkylation with the less reactive methylene chloride. Because our π-conjugated triazene has several nucleophilic nitrogens (Fig. 1), we also investigated the regioselectivity of this alkylation reaction and the results are presented below in this manuscript.

Experimental

Synthesis of (E)-1,3-di-tert-butyl-2-(mesityltriaz-2-en-1-ylidene)-2,3-dihydro-1H-imidazole (3):

2-Azido-1,3,5-trimethyl benzene 2 (161 mg, 1.0 mmol) was added in one portion to a stirred suspension of 1,3-di-tert-butylimidazolium tetrafluoroborate 1 (224 mg, 1.0 mmol) in dry THF (5 mL). After stirring the reaction mixture for 5 minutes, NaH (40 mg, 1.5 mmol, 1.5 equiv, 60% in mineral oil) was added in one portion and the resulting mixture was stirred for 12 h at room temperature under argon. Hexanes (5 mL) were added to the reaction and this mixture was filtered through Celite. The filtrate was concentrated using a rotary evaporator and further dried using high vacuum, affording the pure triazene 3 as a yellow solid (297 mg, 87%).¹H NMR (DMSO-d ₆, 500 MHz): δ 7.12 (s, 2H), 6.75 (s, 2H), 2.18 (s, 3H), 2.05 (s, 6H), 1.50 (s, 18H); ¹³C NMR (DMSO-d ₆, 125 MHz): δ 154.0, 148.7, 131.4, 128.8, 128.6, 113.1, 58.2, 29.3, 20.4, 18.6. IR (neat) ν 3490, 1609, 1392, 1249 cm^-1. Melting point = 104-106 ºC. HRMS (ESI, N₂): m/z calcd for C₂₀H₃₂N₅ [M+H]⁺ 342.2652, found 342.2649.

Synthesis of (E)-1,3-di-tert-butyl-2-(3-mesityl-3-methyltriaz-1-en-1-yl)-1H-imidazol-3-ium iodide (4):

In a 10 mL round bottom flask equipped with a magnetic stir bar, (E)-1,3-di-tert-butyl-2-(mesityltriaz-2-en-1-ylidene)-2,3-dihydro-1H-imidazole 3 (50 mg, 0.3 mmol, 1 equiv) was dissolved in 5 mL of dichloromethane, then MeI (0.4 mL, 0.6 mmol, 2.0 equiv) was added to the reaction mixture and stirred at room temperature for 4 h. After this time, all the volatiles were removed under reduced pressure, yielding pure product as a pale orange solid (122 mg, >99%). ¹H NMR (DMSO-d ₆, 500 MHz): δ 7.81 (s, 2H), 7.08 (s, 2H), 3.73 (s, 3H), 2.28 (s, 3H), 2.18 (s, 6H), 1.57 (s, 18H); ¹³C NMR (DMSO-d ₆, 125 MHz): δ 146.38, 139.16, 139.02, 134.22, 129.51, 117.60, 66.98, 61.42, 29.48, 20.52, 17.56. IR (neat) ν 3158, 2972, 2119, 1563, 1447 cm^-1. Melting point = 164-166 ºC. HRMS (ESI, N₂): m/z calcd for C₂₁H₃₄N₅ [M - I]⁺ 356.2809, found 356.2810.

Synthesis of 2,2'-((1E,1'E)-methylenebis(3-mesityltriaz-1-ene-3,1-diyl))bis(1,3-di-tert-butyl-1H-imidazol-3-ium) chloride (5):

To a 5 mL round bottom flask was added (E)-1,3-di-tert-butyl-2-(mesityltriaz-2-en-1-ylidene)-2,3-dihydro-1H-imidazole 3 (200 mg, 1.2 mmol) and methylene chloride (1 mL) at room temperature and the round bottom flask was capped with a red-rubber septum. Then, a needle was pierced into the septa to allow slow evaporation of the solvent. The reaction mixture was left undisturbed for 3 days, away from light. After this period of time, colorless crystals were formed, collected (41%), and fully characterized. ¹H NMR (DMSO-d ₆, 500 MHz): δ 7.73 (d, J=1.0 Hz, 4H), 7.11 (s, 4H), 6.69 (s, 2H, -CH₂-), 2.30 (s, 6H), 2.08 (s, 12H), 1.28 (s, 36H); ¹³C NMR (DMSO-d ₆, 125 MHz): δ 144.1, 140.2, 135.1, 134.3, 129.9, 118.7, 76.5 (-CH₂-), 62.3, 29.1, 20.7, 19.1. IR (neat) ν 3377, 1606, 1368, 1232 cm^-1. Melting point = 144-147 ºC. HRMS (ESI, N₂): m/z calcd for C₄₁H₆₄N₁₀ [M - 2Cl]²⁺ 348.2652, found 348.2650.

Results and Discussion

Chemistry

The N-heterocyclic carbene (NHC) precursor 1,3-di-tert-butyl-1H-imidazol-3-ium tetrafluoroborate 1 and 2-azido-1,3,5-trimethylbenzene 2 were prepared according to known literature procedures [¹⁷,¹⁸]. It is worth noting that NHC precursor 1 is also commercially available. With both starting materials on hand, we proceeded to suspend the insoluble NHC precursor 1 in dry tetrahydrofuran (THF), followed by addition of 1.5 equivalents of sodium hydride (NaH). The reaction mixture was stirred at room temperature for 20 minutes, to allow formation of the carbene intermediate, which is soluble in THF. Then, organic azide 2 was slowly added to the reaction mixture and stirred at room temperature for 12 h. The stirring was stopped and to the reaction mixture was added hexanes to precipitate the sodium tetrafluoroborate byproduct and was eliminated by vacuum filtration. Lastly, the yellow liquid filtrate was concentrated under reduced pressure to afford the desired (E)-1,3-di-tert-butyl-2-(mesityltriaz-2-en-1-ylidene)-2,3-dihydro-1H-imidazole (π-conjugated triazene 3), as a yellow solid in 89% yield (Scheme 1).

Scheme 1: Synthesis of π-conjugated triazene 3. 

The freshly prepared π-conjugated triazene 3 was reacted with 2.0 equivalents of iodomethane at room temperature, using dichloromethane as a solvent. After 12 h of stirring, all volatiles were removed under reduced pressure to afford pure (E)-1,3-di-tert-butyl-2-(3-mesityl-3-methyltriaz-1-en-1-yl)-1H-imidazol-3-ium iodide 4, as a pale orange solid in quantitative yield (Scheme 2). It was exciting to observe a single regioisomer, where the methyl group was added to the nitrogen-atom next to the mesityl group. This outcome represents a highly regioselective example of an extremely efficient and mild alkylation of π-conjugated triazenes, even in the presence of two ortho methyl groups from the mesityl moiety (Scheme 2).

Scheme 2: Regioselective alkylation of π-conjugated triazene 3, with iodomethane. 

In addition, using the same freshly prepared π-conjugated triazene 3 and to further demonstrate the nucleophilic ability of the nitrogen-atom proximal to mesityl group. π-conjugated triazene 3 was dissolved in dichloromethane and allowed to precipitate, for 3 days. This time, dichloromethane was used as the solvent and the reagent (Scheme 3). To our delight, quantitative conversion was observed, and excellent crystals were formed, isolated, and fully characterized. The chemical structure of these crystals was confirmed to be 2,2’-((1E,1’E)-methylenebis(3-mesityltriaz-1-ene-3,1-diyl))bis(1,3-di-tert-butyl-1H-imidazol-3-ium) chloride 5 (Scheme 3). Again, it was breathtaking to discover a single regioisomer, where the methylene group was added to the same nitrogen-atom of both molecules. Additionally, these results indicate that carbon-chloride bond activation is highly favored using π-conjugated triazenes, such as 3 (Scheme 3). It is also important to note that both carbon-chlorine bonds were activated/substituted. To further understand the carbon-halide activation and to obtain additional insight into the reaction mechanism, a small set of experiments employing dichloromethane (CH₂Cl₂), dibromomethane (CH₂Br₂), and diiodomethane (CH₂I₂) were conducted. Starting material (3) was consumed after 1 day using CH₂I₂, 2 days with CH₂Br₂, and 3 days with CH₂Cl₂, which is in agreement with the known properties of halides as leaving groups. Although, diiodomethane reacted relatively faster compared with its counterparts, it was difficult to dissolve the triazene in this solvent, and additional heating was required, before stirring the reaction at room temperature for 1 d. It is worth noting that the dimeric adduct 5 was obtained even in the presence of excess dihalomethanes, thus indicating that the initial monoalkylated intermediate undergoes a halide elimination, driven by the adjacent nitrogen lone pair, to form an iminium ion (Eschenmoser’s salt). This iminium ion (observed by ¹H NMR) is trapped by another triazene molecule, delivering the final dimeric compound 5. This mechanistic sequence favors the formation of dimeric compound versus monomer since the iminium ion is considerably more electrophilic than the dihalomethanes present in the reaction mixture. Furthermore, during our efforts to obtain good quality crystals, for solid state studies, we found that the aromatic iminium salt derivated from CH₂Cl₂ (i.e., 5) formed better crystals, whereas diiodo- and dibromomethane showed higher product decomposition, we believe this is due to the nucleophilicity of both bromine and iodine ions, which could react with the adduct. Therefore, dichloromethane was our preferred choice due to its lower boiling point (easier to remove from the reaction mixture) and of course its considerable lowest price. Finally, the observed double regioselective alkylation of an already highly hindered intermediate to afford compound 5 is potentially due to the electron-density on the NHC moiety, while maintaining π-conjugation with the aromatic imidazolium salt.

Scheme 3: Synthesis of the double aromatic imidazolium salt (compound 5), using methylene chloride. 

X-Ray Crystal Structure

Single crystals of compound 5 were grown by slow evaporation of a solution of 5 in dichloromethane, at room temperature. Its solid-state structure was established by single crystal X-ray diffraction analysis. The ORTEP and molecular packing diagrams are shown in Figures 2 and 3, respectively. Details of crystal structure, data collection, and structure refinement are summarized in Table 1. Likewise, the pertinent bond angles and lengths of the compound 5 are tabulated in Table 2. The molecule crystallizes in the triclinic system with the space group P-1(#2), with β = 85.554(5)°. The cell dimensions are a = 12.104(5) Å, b = 13.182(5) Å and c = 15.742(4) Å and volume = 2467.584 ų. The crystal structure of compound 5 reveals that the five and six membered rings are not in the same plane. The crystal structure consists of two cations [mesitylene triazene]⁺ and two Cl⁻ anions. Consequently, the charges on compound 5 are neutralized by the presence of two Cl anions in the crystal lattice. Furthermore, compound 5 does not contain any organic solvent molecules or lattice held water molecules in the unit cell of the determined structure. The bond lengths and angles in the five membered rings (NCNCC) compare well with similar reported compounds [1-(4-chlorophenyl-3-(1,3-dimethylimidazol-2-ylidene)triazene and 1-(3-nitrophenyl-3-(1,3-dimethylimidazol-2-ylidene)triazene] [⁶,⁷]. The C-C bond lengths in phenyl rings are in the normal range of 1.28-1.57 Å, which is characteristic of delocalized benzene rings. The C-C-C bond angles in phenyl rings are close to 120°, it suggests that carbon atoms are sp² hybridized. Furthermore, compound 5 lies in three planes with plane I [C(2), N(1), C(35), C(34), N(10), C(3), C(36), C(29), N(9), C(28), C(27), N(8), C(6) and C(5)] making a dihedral angle of 87.39° and 78.14° with plane II [C(21), C(20), C(19), C(18), C(23), C(22), C(26), C(25), C(9), C(10), C(11), C(12), C(14), C(15), C(13) and C(16)] and plane III [N(7), N(6), N(5), C(4), N(2), N(3), and N(4)], whereas plane II forms a dihedral angle of 75.25ºwith plane III. The molecular packing diagram shows two molecules, which are independently arranged in the unit cell without the involvement of intra- or intermolecular hydrogen bonds (Fig. 3). Finally, the crystallographic data with the structural analysis have been deposited in the Cambridge Crystallographic Data Centre and the CCDC 1832942 contains the supplementary crystallographic data for the present work. This data can be obtained free of charge at www.ccdc.cam.ac.uk/data_request/cif using CCDC 1832942 as the deposition number [¹⁹].

Fig. 2 ORTEP representation of the X-ray crystal structure of compound 5 showing atom labeling. 50% Probability amplitude displacement ellipsoids are shown. For clarity, all hydrogen atoms are omitted. 

Fig. 3 Molecular packing diagram of compound 5. 

Conclusion

A two-step synthesis of a couple of aromatic iminium salts has been developed, starting from readily available mesityl azide. All the experiments were conducted at room temperature, without using specialized equipment or anhydrous conditions. In addition, we observed a regioselective alkylation employing both iodomethane and methylene chloride. Therefore, we established that the nitrogen-atom next to the mesityl group is quite more nucleophilic than any other nitrogen-atoms presented in the triazene intermediate. Furthermore, isolation of a single regioisomer in high yields for each of the reported alkylation reactions supports the preceding statement.