An efficient and facile access to highly functionalized pyrrole derivatives

A straightforward and one-pot synthesis of pyrrolo[3,4-c]pyrrole-1,3-diones via Ag(I)-catalyzed 1,3-dipolar cycloaddition of azomethine ylides with N-alkyl maleimide, followed by readily complete oxidation with DDQ, has been successfully developed. Further transformation with alkylamine/sodium alkoxide alcohol solution conveniently afforded novel polysubstituted pyrroles in good to excellent yields. This methodology for highly functionalized pyrroles performed well over a broad scope of substrates. It is conceivable that this efficient construction method for privileged pyrrole scaffolds could deliver more active compounds for medicinal chemistry research.

A number of methods have been reported till now to synthesize pyrroles and pyrrole containing analogs [6].In the past decade, 1,3-dipolar cycloaddition has become a fundamental synthetic method for the construction of nitrogen-containing five-membered heterocycles including pyrroles.It is worth to note that considerable efforts have been expended to build stereogenic centers of pyrrolidine derivatives using chiral catalysts [7].
As our aim was to construct a small library of polysubstituted pyrroles for antibacterial screening, it prompted us to develop a concise and efficient synthesis of pyrrolo [3,4-c]pyrrole-1,3-diones [8][9][10] via 1,3-dipolar cycloaddition without any chiral catalysts/ligands and a facile access to highly substituted pyrroles with amide groups or ester groups.Herein, we propose a straightforward and one-pot synthesis of pyrrolo [3,4-c]pyrrole-1,3-diones via Ag(I)-catalyzed 1,3-dipolar cycloaddition of azomethine ylides with N-alkyl maleimide, followed by a facile oxidation using DDQ as oxidant.Further manipulation with alkylamine/sodium alkoxide alcohol solution conveniently led to novel polysubstituted pyrroles in good to excellent yields (Scheme 1).

Results and Discussion
As shown in Scheme 1, one advantage of this 1,3-dipolar cycloaddition for constructing privileged pyrrole scaffolds is the broad scope of azomethine ylides as substrates.To our surprise, although there were many reports [11][12][13][14][15][16] about the synthesis of ethyl N-(phenylmethylidene)glycinate (9a, azomethine ylide) as the key substrate for 1,3-dipolar cycloadditions, the reaction conditions were very different exemplified by the wide range of reaction times from 0.3 h to 120 h, and the variable yields from 68% to 100% in different solvents.In order to establish the optimal experimental conditions suitable for the one-pot synthesis of pyrrolo [3,4-c]pyrrole-1,3-diones 12a-k, we investigated the reaction conditions step by step.
Initially, benzaldehyde (7a) and ethyl glycinate hydrochloride (8a) were chosen as the model substrates for obtaining azomethine ylide 9a, and the results are summarized in Table 1.Based on reported methods, Et 3 N as base, MgSO 4 as desiccant and CH 2 Cl 2 as solvent were used for the synthesis of the azomethine ylide [13,14,[17][18][19][20][21][22][23][24].Because 9a easily decomposed to benzaldehyde on silica gel when monitored by TLC, we used 1 H NMR to monitor the reaction process.Table 1 shows that the reaction time was crucial to the extent of the reaction.9a could be obtained in excellent yield (94% total yield of 7a and 9a, of which 98% was 9a) without any further purification when the reaction time was prolonged to 8 h.The outcome of a 8 h reaction is favorable compared to the results of 2 h and 4 h reaction time (Table 1, entry 3 vs entries 1 and 2).Encouraged by the achievements on catalytic asymmetric 1,3dipolar cycloaddition to build octahydropyrrolo [3,4-c]pyrrole frameworks [7,9], we screened the optimal reaction conditions for preparing the racemic pyrrolidine 11a using N-methylmaleimide (10a) as the simple dipolarophile without any chiral catalysts/ligands.To our delight, in the presence of 10 mol % of AgOAc, the reaction reached almost completion in CH 2 Cl 2 within 1 h at room temperature and afforded the desired cycloadduct in moderate yield (64%, Table 2, entry 1).The annulation process did not occur without the catalyst (Table 2, entry 2).Since most of the 1,3-dipolar cycloadditions are known to work best in nonpolar solvents, toluene instead of CH 2 Cl 2 was selected as the reaction solvent.Unfortunately, toluene was not a good choice even the reaction time was prolonged to 2 h (36% yield, Table 2, entry 3).Switching the base Et 3 N to DBU resulted in a significant decrease of product yield (Table 2, entry 4).Given that the crude azomethine ylide 9a was used without any purification, and 9a might be sensitive to other decomposition pathways, we increased the amount of 9a up to 1.5 equivalents, which delivered the bicyclic pyrrolidine 11a in excellent yield (82%, Table 2, entry 5).Prolonging the reaction time from 3 h to 6 h had no influence on the yield (Table 2, entry 6), which demonstrated that appropriate increase on the ratio of 9a/10a was beneficial to the completion of this cycload- dition.Finally, the use of Et 3 N as the base and CH 2 Cl 2 as the solvent, and the suitable ratio of 9a/10a at 1.5:1 catalyzed by 10 mol % of AgOAc were identified as the optimal reaction conditions.Finally, the of the cycloadduct 11a to pyrrolo[3, 4-c]pyrrole-1,3-dione 12a was investigated (Table 3).For the operational simplicity and continuity of this one-pot condensation-cycloaddition-aromatization reaction, CH 2 Cl 2 was firstly selected as solvent instead of the generally used toluene [10,25,26] for this oxidation step.Unfortunately, the desired pyrrole product 12a was obtained only in 41% yield with DDQ Scheme 2: Scope of one-pot synthesis of pyrrolo [3,4-c] (4 equiv) as oxidant at room temperature for 48 h (Table 3, entry 1).As expected, toluene as solvent improved the reaction outcome to afford 12a in a good yield up to 71% (Table 3, entry 2).Subsequently, reducing the amount of DDQ (2 equiv) led to a significantly decreased yield (Table 3, entry 3), and also the addition of silica gel [9] as an additive had no considerable effect on the yield (Table 3, entry 4 vs entry 2).The results demonstrated that using 4 equiv DDQ in toluene were the best conditions for this oxidation protocol.
With the optimized reaction conditions for each step in hand, we prepared 12a starting from benzaldehyde and ethyl glycinate hydrochloride through three steps but via a one-pot process without any purification for intermediates 9a and 11a (see Supporting Information File 1).To our delight, the reaction outcome was satisfactory with a total yield of 47% for threesteps which was equivalent to the stepwise reactions (Scheme 2, 12a).In order to evaluate the generality of this process, we explored a variety of aldehydes 7b-j, and the results are shown in Scheme 2. All tested benzaldehydes bearing electron-withdrawing or electron-donating substituents on the phenyl ring reacted smoothly via condensation-cycloaddition-oxidation in the one-pot process, delivering the corresponding pyrrolo-[3,4-c]pyrrole-1,3-diones in moderate to good yields (53-77%).Heteroaromatic aldehydes 7i and 7j afforded the products 12i and 12j in excellent total yields of 81%.Additionally, cinnamaldehyde (7h) was also well tolerated, giving the product 12h in moderate yield (40%).Finally, to further explore the scope and generality of this protocol, N-ethylmaleimide (10b) instead of N-methylmaleimide (10a) as another simple dipolarophile was also examined; the target product 12k was prepared smoothly in high yield (74%).This concise and efficient protocol displays the potentiality for scale-up synthesis of pyrrolo [3,4-c]pyrrole-1,3-diones.
Having the pyrrolo [3,4-c]pyrrole-1,3-diones with diversified substituents in hand, polysubstituted pyrrole derivatives with three amide groups 13a-l were prepared smoothly by treating 12a-k with methylamine or ethylamine in EtOH at 80 °C in good to excellent yields (72-96%, Scheme 3).The structures of highly substituted pyrrole derivatives prompted us to envisage the reasonable mechanism for the formation of 3,4-diamide groups, besides the amidation of ethyl ester group on the 2-position to give one amide group on the pyrrole ring.Due to the electron-withdrawing effect of the ester group at the 2-position in 12a-k, the carbonyl group at the 3-position of the pyrrole was easily attacked by the nucleophilic amine (compared with the carbonyl at the 4-position, shown in Scheme 4) exemplified by the reaction of 12d with ethylamine to afford 13k.NOESY analysis of 13k was used to confirm the relative positions of 3,4-diamide groups formed.NOE correlations between an H of the methylamide at the 4-position and H2 or H6 of the 4-chlorophenyl moiety supported the reaction result (see Supporting Information File 1).Additionally, the corresponding pyrroles with more functionalized substituents with both amide and ester group 13m,n could also be readily achieved by treatment of 12a with MeONa in MeOH or EtONa in EtOH at room temperature in moderate to good yields (40-66%, Scheme 3).It was noted that the ethyl ester in 12a was replaced by methyl ester through transesterification when 12a was treated with MeONa in MeOH to afford 13m.Therefore, this efficient protocol developed could meet our requirement to basically construct a small library of highly functionalized pyrrole derivatives for antibacterial screening or for further chemical manipulations to get more promising compounds.

Conclusion
In summary, we have developed an efficient, operationally simple protocol to afford pyrrolo [3,4-c]pyrrole-1,3-diones via 1,3-dipolar cycloaddition of azomethine ylides from diverse commercially available aldehydes in good to excellent yields and a facile access to highly functionalized pyrroles.Notably, the versatile conversion of the cycloaddition adducts leads to fascinating polysubstituted pyrrole compounds, which can deliver potentially valuable building blocks serving as precursors for drug discovery.Further research on the development of more diversified pyrrolo [3,4-c]pyrrole-1,3-diones and more complicated polysubstituted pyrroles is currently underway in our laboratory.

Table 1 :
Optimization of the reaction conditions for the synthesis of the azomethine ylide a .

Table 3 :
Optimization of the reaction conditions of the oxidation reaction.
a Isolated yield.b 10% Amount of 11a.

Table 2 :
Optimization of the reaction conditions of the cycloaddition reaction a .