Palladium-catalyzed C–N and C–O bond formation of N-substituted 4-bromo-7-azaindoles with amides, amines, amino acid esters and phenols

Simple and efficient procedures for palladium-catalyzed cross-coupling reactions of N-substituted 4-bromo-7-azaindole (1H-pyrrole[2,3-b]pyridine), with amides, amines, amino acid esters and phenols through C–N and C–O bond formation have been developed. The C–N cross-coupling reaction of amides, amines and amino acid esters takes place rapidly by using the combination of Xantphos, Cs2CO3, dioxane and palladium catalyst precursors Pd(OAc)2/Pd2(dba)3. The combination of Pd(OAc)2, Xantphos, K2CO3 and dioxane was found to be crucial for the C–O cross-coupling reaction. This is the first report on coupling of amides, amino acid esters and phenols with N-protected 4-bromo-7-azaindole derivatives.


Introduction
Palladium-catalyzed C-N and C-O bond-forming reactions between 4-substituted 7-azaindoles and amides, amines, amino acid esters or phenols have recently gained popularity among the scientific community for different drug-discovery and -development programs.Particularly, several 7-azaindoles (1Hpyrrole [2,3-b]pyridine) [1][2][3][4], including 4-substituted compounds [5][6][7][8] have found applications in various therapeutic areas.Despite their utility in various drug-development programs in academic research and the pharmaceutical industry, methods for the synthesis of this class of compounds and functionalization of 7-azaindole scaffolds remain limited [9].Although the literature enumerates various methods for the synthesis of substituted azaindole motifs, they are limited to N-1, C-2 or C-3 functionalized structures [5][6][7][8]10].Furthermore, regioselective C-O-bond-forming reactions are interesting in organic synthesis due to the presence of these bonds in numerous natural products, biological compounds, pharmaceuticals, fragrances, cosmetics and polymers [11][12][13][14][15][16][17].Among others Buchwald, Hartwing and co-workers followed by many other groups during the past decade reported the metalcatalyzed formation of carbon-heteroatom bonds [18][19][20][21][22][23][24][25][26][27][28][29][30].Most of the literature reports are limited to aryl halides and indoles only.Clearly, each of these protocols has its own virtues; however, limitations still exist with respect to substrate scope, reagents and solvents, etc.Thus, palladium-catalyzed intra-and intermolecular cross-coupling reactions of azaindoles with amides, amines, amino acid esters or phenols offer an interesting complementary method for the synthesis of C-N and C-O bonds under comparably mild conditions.It is important to note that, in contrast to well-established palladium-catalyzed coupling reactions of indole with amines, alcohols and phenols [5,7,[31][32][33][34][35][36], very few studies on the formation of C-N and C-O bond formation over 7-azaindole have been performed [37][38][39].On the other hand, the chemistry of 4-bromo-7-azaindole has not been explored in depth until today.Amino and phenyl-substituted 7-azaindole scaffolds appear in various pharmaceutically important molecules (Figure 1), which are very challenging and lengthy to prepare by the traditional methods [40,41].In general, nucleophilic aromatic substitution (S N Ar) reaction of a halo-precursor of 7-azaindole with a large excess of amine counterpart under high reaction temperatures, preferably under heating to more than 180 °C or through the use of microwave irradiation, results in the amino-7-azaindole in moderate to low yield [5,7].Primary alkylamines or anilines under similar reaction conditions provided the displacement rearrangement products 4-amino-5-azaindole as the sole product [7].Very recently Buchwald et al. [39] reported a palladium-catalyzed amination of unprotected halo-7-azaindoles using biarylphosphine ligands (DavePhos), palladium precatalyst (RuPhos)-based reagents, and LiHDMS as a base.However, inconsistency of the results was observed when the reactions were carried out on a large scale.As part of continuing efforts in our laboratory [42][43][44][45][46] toward the development of new and improved methods in organic synthesis, we became interested in the possibility of developing an efficient palladium-mediated coupling of amides, amines, amino acid esters and phenols with N-protected 7-azaindole derivatives for one of our medicinally important drug-development programs.
We herein report on Pd-catalyzed coupling reactions of N-protected 4-bromo-7-azaindoles with amides, amines, amino acid esters and phenols (Scheme 1), to yield new important intermediates for one of our medicinal chemistry programs.To the best of our knowledge this is the first report on intermolecular coupling of 4-bromo-7-azaindole with amides, amino acid esters and phenols.
With optimized conditions in hand, we embarked on an investigation of the reaction scope by subjecting various N-protected 7-azaindoles 1 to a wide range of amides 2. The experimental results are summarized in Table 2.The reaction did not proceed at all without N-protection (1a, Table 2, entry 1).When the reaction was carried out with N-sulfonyl-protected 4-bromo-7azaindole 1b only the desulfonated product (Table 2, entry 2) was obtained.It is worth mentioning that the N-sulfonyl protected 7-azaindole 1b was efficiently deprotected under basic conditions in dioxane [57].The optimized reaction conditions worked well with benzamide (2a) (   2, entry 8).We found that amide is more reactive than amine under the reaction conditions studied.The use of Cs 2 CO 3 as the base is advantageous because the common functional groups such as fluoro, methoxy, etc., are well tolerated.We found that the N-protection of 4-bromo-7-azaindoles 1 has a marginal effect on the reaction yield and time.The coupling of amides with N-protected 4-bromo-7-azaindoles 1 was demonstrated in multi-gram synthesis in our hands.Next we diverted our attention towards coupling of N-protected 4-bromo-7-azaindoles 1 with amines 4.
Synthesis of 4-amino-7-azaindoles was generally achieved from the corresponding halide by S N Ar displacement reactions, which typically require very high temperatures, extended reaction times, and a large excess of the amine counterpart [5].
Other alternative methods employ the amino-substituted azaindole as the key intermediate, which are challenging to prepare [6].Initially, coupling of 4-bromo-1-ethyl-1H-pyrrolo[2,3b]pyridine (1d) with phenylmethanamine (4a) was selected as a model reaction to optimize the reaction condition of C-N-bond formation of amines.The experimental results are summarized in Table 3.After the screening of various ligands (Scheme 1), palladium catalysts, and bases (Table 1), the catalyst combination of Pd 2 (dba) 3 , Xantphos and Cs 2 CO 3 in dioxane was found     to be crucial.The cross-coupling reaction of 4-bromo-1-ethyl-1H-pyrrolo[2,3-b]pyridine (1d) with phenylmethanamine (4a) proceeded rapidly by using the combination of Pd 2 (dba) 3 , Xantphos and Cs 2 CO 3 in dioxane at 100 °C for 1 h (Table 3, entry 1).When K 2 CO 3 was used as base along with Pd 2 (dba) 3 as catalyst and XantPhos (L 1 ) as ligand, slightly lower yield (~85%) was obtained (Table 3, entry 2) in 3 h.Other ligands SPhos (L 2 ) and XPhos (L 3 ) with Pd 2 (dba) 3 as catalyst provided average yields of 60 and 62%, respectively, in 6 h (Table 3, entries 3 and 4).However, the tertiary phosphine ligand PCy 3 (L 4 ) was ineffective in generating any product (Table 3, entries 5 and 12).Interestingly, Pd(OAc) 2 results in poor yields of the product (Table 3, entries [6][7][8][9][10][11][12].Given this surprising result, we hypothesized that the amination product 5 may interfere with catalyst turnover by promoting the formation of an inactive Pd-chelate complex. With a viable coupling procedure in hand, attention was turned to the generality of the process and couplings of structurally diverse nucleophilic amines.As seen from Table 4, the crosscoupling reaction of N-protected 4-bromo-7-azaindoles 1a-1d with various amines 4a-4f proved to be general under the optimized conditions to get the coupled products 5a-5f in very good yield (88-94%) within a reasonable time of 2.5 to 3 h.The C-N-bond-forming reaction of primary aromatic amines (Table 4, entries 3, 4 and 6) proceeded smoothly under the optimized conditions to provide excellent yields of the corresponding coupling products 5a, 5b and 5d, respectively.The reaction was also effective for cyclic amine morpholine (Table 4, entry 5) and Boc-protected piperazine (Table 4, entry 8).The reaction works equally well for aliphatic primary amine too (Table 4, entry 7) resulting in 90% isolated yield.There was a feeble change in yield by varying the substitution on the 7-azaindole nitrogen (N1) from a methyl to an ethyl group (Table 4, entries 6-8).There was no reaction without the N-protection (Table 4, entry 1).Heating of the reaction mixture of 4-bromo-1-(phenylsulfonyl)-1H-pyrrolo[2,3-b]pyridine (1b) with phenylmethanamine (4a) in the presence of base and palladium catalyst resulted in the desulfonated 4-bromo-7-azaindole as the sole product (Table 4, entry 2).
Our continuous efforts to develop synthetic methods for the formation of C-N bonds by coupling of N-protected 7-azaindoles 1 with amino acids or esters result in the development of interesting intermediates in our own medicinal chemistry program based on 7-azaindole.Large molecular architectures designed by cross-coupling strategies with the introduction of an amino acid functionality on 7-azaindole, result in new scaffolding.N-aryl-amino acids are reported as important synthetic intermediates and structural motifs for various drug-development programs by various medicinal and process-research chemists.Therefore, transition metal-catalyzed coupling of amino acids and its derivatives finds popularity in various coupling protocols [58].A copper(I) iodide catalyzed coupling reaction of haloindoles with α-amino acids was reported by Ishikawa et al. [59].
Indole and azaindole moieties functionalized with amino acid ester scaffold are believed to be important synthetic intermediates and structural components of various medicinal and pharmaceutical candidates.The coupling of N-methyl-4-bromo-7azaindole (1c) with D-alanine methyl ester 6b was chosen as the model reaction to test the feasibility of the palladium-assisted coupling reaction of 7-azaindole and amino acids.The experimental results are summarized in Table 5.In our initial endeavor the coupling of N-methyl-4-bromo-7-azaindole (1c) with D-alanine (6a) resulted in only a trace amount of product 7a with Xantphos (L 1 ) as a ligand (Table 5, entry 1) .Other bidentate aryl phosphine ligands L 2 and L 3 did not result in any product formation (Table 5, entries 2 and 3).The tertiary phosphine ligand PCy 3 (L 4 ) was ineffective in the arylation of N-methyl-4-bromo-7-azaindole (1c) with D-alanine (6a) (Table 5, entry 4).It is believed that the coordination of the central metal of the oxidative addition complex with the carboxyl functionality of the amino acid scaffold retained the Pd-N bond, making the 7-azaindole-Pd-N complexes too stable for reductive elimination [58].As can be seen from Table 5, the reaction of N-methyl-4-bromo-7-azaindole (1c) with D-alanine methyl ester (6b) occurred rapidly with Pd 2 (dba) 3 as a catalyst, Xantphos (L 1 ) as ligand, and Cs 2 CO 3 as base in dioxane at 100 °C in a short reaction time of 1 h (Table 5, entry 5).When K 2 CO 3 was used as a base with Pd 2 (dba) 3 as a catalyst, and Xantphos (L 1 ) as a ligand, 85% of the product conversion was observed in 3 h (Table 5, entry 6).
With a viable coupling procedure in hand, attention was turned to the generality of the process and couplings of structurally  diverse amino acid building blocks.Results summarized in Table 6 show that the optimized conditions described proved to be general for the coupling with a wide variety of amino acid building blocks.As can be seen from Table 6, the catalytic system works well with diversified amino acid building blocks.
Coupling of N-methyl-4-bromo-7-azaindole (1c) with D-alanine methyl ester (6b) resulted in good yield of the product 7b in a short reaction time (Table 6, entry 2).The chiral purity of the product was determined by chiral HPLC using Chiral Pak AD-H column.Amino acids without extra coordinating groups gave good coupling yields (Table 6, entries 3, 6 and 7).
Coupling of L-serine(O-t-Bu)-OMe (6d) with 1c resulted in moderate yield of the product in 3 h (Table 6, entry 4).The catalytic system developed by us for the coupling of amino acid esters with N-protected 7-azaindoles was ineffective for L-proline (6f), L-serine (6g), and L-glutamic acid (6h) (Table 6, entries 8-10).This may be ascribed to the fact that these amino acids contain more heteroatoms that bind to the central palla- dium atom and enhance the stability of the 7-azaindole-Pd-N complexes, making them too stable for reductive elimination.
After successful demonstration of the C-N-bond-formation reaction of 4-bromo-7-azaindole derivatives with amides, amines and amino acid esters, we wanted to expand the scope of the reaction towards C-O-bond formation.Until today no general method has been described for the C-O-bond-formation reaction of 4-halo-azaindole with phenols or alcohols.Most of the literature reports described on C-O-bond-formation reactions are limited to aryl halides and phenols or alcohols only [36,[60][61][62][63]. Functionalization of 4-substituted-7-azaindole scaffolds with 4-amino-2-fluorophenol was reported to be ineffective upon heating in the presence of a strong base such as KOt-Bu [35].In addition, the N-oxide derivative of 4-substituted 7-azaindole fails to provide the desired product under similar conditions [48].Further, on utilizing palladium or copper-mediated cross-coupling reactions of N-protected amino-2-fluorophenol with 4-chloro-or 4-bromo-1Hpyrrolo[2,3-b]pyridine, the desired diaryl ether could not be isolated in acceptable yield [5,35].To select the best reaction conditions for C-O-bond formation, we envisaged the synthesis of an activated 7-azaindole building block that could be coupled with phenols.To select the best coupling conditions for C-O bond formation, the coupling of 4-bromo-1-methy-1Hpyrrolo[2,3-b]pyridine (1c) with m-cresol (8a) was selected as a model reaction to find the suitable ligands (Scheme 1), palladium catalysts, bases and organic solvents.The experimental findings are summarized in Table 7.The coupling of 1c with 8a by using a combination of Pd(OAc) 2 , Xantphos (L 1 ) and K 2 CO 3 in dioxane at 100 °C in 10 h of time provided 70% of the desired diaryl ether 9a (Table 7, entry 3).The reaction rate is slow, i.e., when run for 3 h at 100 °C, only 30% product was obtained (Table 7, entry 2).But upon continuous heating for 7 h we observed 70% (Table 7, entry 3) of the expected product.Interestingly, usage of Pd 2 (dba) 3 resulted in poor yields of the product (Table 7, entries 5 and 6).In most of the cases we observed decomposition of the Pd 2 (dba) 3 reagent.In comparison to the conditions described for the amines and amides, a much longer reaction time was required for the C-O-bond formation when treated with phenols.K 2 CO 3 was found to be a suitable base for the C-O-bond formation under the experimental conditions we studied.When Cs 2 CO 3 was used as base, settling of the base was observed even under heating and stir-ring of the reaction mixture at 100 °C.The probable reason may be that Cs 2 CO 3 is much heavier than K 2 CO 3 and tends to settle in the bottom of the reaction vessel or reactor when run on a larger scale, causing improper mixing of the heterogeneous mixture.
With a viable coupling procedure in hand, attention was turned to the generality of the process and couplings of structurally diverse phenols.Results are summarized in Table 8.The C-Obond formation was established with good yields with phenol derivatives and 1-naphthol (Table 8, entries 1-3).Moreover, the outcome of the reaction strongly depended on the electronic character of the appropriate phenol (Table 8).The more-electron-rich nucleophiles 8a, 8b furnished the desired ethers 9a and 9b in good yields.Further studies are in progress in our laboratory to investigate different substrate scope and mechanistic aspects of the C-O-bond-forming reaction.

Conclusion
In conclusion, we have developed the best coupling conditions for C-N-bond formation of N-substituted 4-bromo-7-azaindoles with amides, amines, and amino acid esters and demonstrated well for the synthesis of various N-substituted 7-azaindole compounds, which are very difficult to synthesize otherwise.The combination of Xantphos, Cs 2 CO 3 and dioxane was found to be crucial for all the C-N cross-coupling reactions.However, different Pd-catalyst precursors were used for different amines/amides and amino acid esters.We have enhanced the methodology towards the C-O-bond formation with various phenols, which is very difficult to achieve.K 2 CO 3 was found to be better for C-O cross-coupling reactions.This protocol provides a nice alternative for the synthesis of N-substituted 7-azaindole derivatives, which exist extensively in natural products and pharmaceuticals.This is the first report on coupling of amides, amino acid esters and phenols with N-substituted 4-bromo-7-azaindole.Hence, we feel that our methodology will serve as an excellent tool in medicinal chemistry, organic synthesis and process research worldwide.

Table 1 :
Reaction optimization for coupling of 1e with benzamide (2a) under various conditions a .
dNo reaction occurred at room temperature.