A Novel One-pot Three-step Synthesis of 2-( 1-Benzofuran-2-yl ) quinoline-3-carboxylic Acid Derivatives

A facile and efficient one-pot three-step procedure for the preparation of 2-(1-benzofuran2-yl)quinoline-3-carboxylic acid derivatives is described, featuring three different synthetic transformations, namely Williamson ether synthesis, hydrolysis of an ester group at the quinoline ring C-3 position, and intramolecular electrophilic cyclization reaction between the aldehyde group of salicylaldehyde and the methylene at the quinoline ring C-2 position.

2][23][24] For example, chimanine alkaloids, simple 2-substituted quinolines, isolated from the bark of Galipea longiflora trees of the Rutaceae family, are effective against the parasites Leishmania sp., which are the reagents of leishmaniasis, a protozoan disease of the tropical areas in South America.9][30][31][32][33] Recently, there is much current interest in Vol.5][36][37][38] For example, 2-(furan-2-yl) quinoline-4-carboxylic acid as well as analogues (Figure 1) was reported to have the inhibition of C. albicans prolyl-tRNA synthetase and showed potent in vitro antifungal activities against dermatophytes. 39,40 light of the above reports and because of the potent biological activities of quinoline ring system and 2-substituted benzo[b]furan derivatives, we felt that there is a real need for the synthesis of new prototypes by combining both quinoline ring system and benzo [b]  furan moiety in the same molecule at 2-position, which might be important for pharmacological studies or creating new medicinal properties.Therefore, we would like to report herein a facile and inexpensive one-pot three-step procedure for the preparation of novel hybrid molecules 2-(1-benzofuran-2-yl)quinoline-3-carboxylic acid derivatives under mild conditions.

Results and Discussion
In Scheme 1 is outlined the synthetic route developed in our laboratory.The starting material ethyl 2-(bromomethyl) quinoline-3-carboxylate (1) was prepared according to the method of literature. 41The one-pot three-step reaction reported here represents a new synthetic method for the preparation of novel 2-(1-benzofuran-2-yl)quinoline-3-carboxylic acid derivatives (3a-i), involving the in situ formation of ether by Williamson reaction between compound 1 and various substituted salicylaldehydes 2a-i followed by the hydrolysis and intramolecular cyclization reactions.This novel procedure provides quick and easy access to the incorporation of benzo[b]furan core to the quinoline nucleus at 2-position, with good yields and simple workup.
Recently, we have reported the one-pot two-step reaction of bromomethylquinolines with substituted phenols or naphthols to give the corresponding quinoline carboxylic acid ethers as key precursors of heterocycle-fused quinoline compounds. 42,43In order to continue our interest in the development of bioactive quinoline alkaloids, our initial intention was to extend the method to the reaction of monobromide 1 with salicylaldehydes, in which the presence of aldehyde functionality may provide opportunity for further manipulation.Thus, monobromide 1 was first subjected to the Williamson reaction with salicylaldehyde (2a) to give the corresponding ethyl 2-[(2-formylphenoxy)methyl] quinoline-3-carboxylate (4), which structure has already been characterized by spectroscopic method.Because the resulting 4 does not interfere with further hydrolysis reaction, purification at this stage is unnecessary.Thus, we simply added 10% ethanolic potassium hydroxide solution 10 mL to this reaction mixture under reflux.After the reaction was complete, it was found that the major product was identified as 2-(1-benzofuran-2-yl)quinoline-3-carboxylic acid (3a).In its 1 H NMR spectrum the presence of a distinct singlet, integrating for one proton resonating at d 7.56 ppm, assignable to be the proton attached on the furan moiety and the absence of both the exocyclic methylene protons and the aldehyde proton resonances in product 3a indicated the possibility of cyclization through intramolecular condensation along with the elimination of H 2 O.Moreover, the proposed structure of 3a was also confirmed by its 13 C NMR spectrum, which revealed besides the signals due to aromatic carbons the presence of carboxyl carbon at 168.16 ppm and the absence of the exocyclic methylene carbon as well as the aldehyde carbon.The IR spectrum also showed the absence of aldehyde group and exocyclic methylene absorption bands.Further, the structure assigned for this reaction product was fully supported by its mass spectrum, which showed molecular ion (M + ) peak at 289 m/z and matched the expected molecular weight of 3a.Moreover, the obtained elemental analysis values are also in agreement with theoretical data.
The formation of 3a may be interpreted by the following proposed mechanism as shown in Scheme 2. The in situ base-mediated ester hydrolysis of the initially formed 4 resulted in the abstraction of acidic proton of the active methylene within the molecule 6 and subsequent attack of the carbanion at aldehydic carbon to form a five-membered cyclic system 8.After this cyclization, dehydration led to the formation of a benzofuran ring 3a.The proposed mechanism was similar to that of the formation of naphthofurans via intramolecular condensation under the action of triethyl amine reported by Srivastava et al. 44 It is noteworthy that the use of 10% ethanolic potassium hydroxide solution is sufficient to promote the reaction and there were no improvements in the reaction rates and yields by increasing the amount of KOH or using other bases.
Encouraged by the experimental result, we attempted the reaction of monobromide 1 with a series of other salicylaldehydes (2b-i) with differing electronic properties under the similar conditions, furnishing the respective 2-benzofuranyl-quinoline-3-carboxylic acids (3b-i) in good yields as shown in Table 1.
In Table 1, a series of salicylaldehydes 2a-i (entries 1-9) reacted with 1 to give the corresponding 2-benzofuranylquinoline-3-carboxylic acids (3a-i) in 55-75% yields.It seems that the electronic nature of the substituents has no significant effect on the reactions; all the salicylaldehydes with electron-donating (entries 2 and 3), electronwithdrawing (entries 4-6), or the halo-and t-butyldisubstituted groups (entries 7-9) worked well and gave the corresponding 2-benzofuranyl-quinoline-3-carboxylic acids in good yields, showing little distinction.The ease of isolation of all the products was notable; after acidification workup with 1 mol L -1 HCl, the products were isolated as the main products.
Additionally, since the naphthofuran backbone is a part of some natural compounds such as maturin, maturin acetate and 14-methoxydehydrocacalohastine, and novel strategies for the synthesis of naphthofuran backbone continue to receive considerable attention in the field of synthetic organic chemistry, [45][46][47] we also attempted the reaction of 1 with

Conclusions
In summary, the present method offered a facile synthetic route to a variety of 2-benzofuranyl-quinoline-3carboxylic acids (3a-i) as well as 2-naphtho[2,1-b]furan-2yl-quinoline-3-carboxylic acid (3j), which would provide new leads in the search for future drug candidates.Readily availability of starting material, mild reaction conditions, short reaction times, experimental simplicity and satisfactory yields contribute to the usefulness of this method.Possible biological activity of the described compounds possessing the benzofuran and quinoline skeletons remains to be studied.In addition, the products represent potentially useful synthetic building blocks in medicinal chemistry.

Chemical analysis
Melting points (uncorrected) were determined by using WRS-1B melting points apparatus and are uncorrected. 1H NMR and 13 C NMR spectra were recorded on a Varian Inova 400 MHz or Brucker AVANCE 600 MHz NMR spectrometer using CDCl 3 or DMSO-d 6 as the solvent.The reported chemical shifts (d values) are given in parts per million downfield from tetramethylsilane (TMS) as the internal standard.EI-MS (70 eV): Finningan-MAT-8430 mass spectrometer.The elemental analyses was performed for C, H, and N using an Elementar Vario EL-III element analyzer and found within ±0.4%.The progress of reactions was monitored by thin-layer chromatography (TLC) on silica gel GF254 using ethyl acetate as eluent.
The mass spectra and elemental analysis data were in agreement with the proposed structures.

General procedure for the preparation of 2-(1-benzofuran-2-yl)quinoline-3-carboxylic acids 3a-i
A mixture of ethyl 2-(bromomethyl)quinoline-3carboxylate (1 mmol, 0.294 g), each salicylaldehyde (1 mmol) and K 2 CO 3 (4 mmol, 0.552 g) was stirred in refluxing CH 3 CN (12 mL).The conversion was monitored by TLC.After completion, 10% ethanolic potassium hydroxide solution 10 mL was added to the reaction mixture continued to reflux for 2 h, cooled, and acidified with 1 mol L -1 HCl solution.The resulting crude product was recrystallized from ethanol to afford the corresponding products 3a-i in 55-75% yields.The melting pints and yields of all the compounds are summarized in Table 1 and the spectral and analytical data are given below.