“On Water” Palladium Catalyzed Direct Arylation of 1H-Indazole and 1H-7-Azaindazole

The C3 direct arylation of 1H-indazole and 1H-7-azaindazole has been a significant challenge due to the lack of the reactivity at this position. In this paper, we describe a mild and an efficient synthesis of new series of C3-aryled 1H-indazoles and C3-aryled 1H-7-azaindazoles via a C3 direct arylation using water as solvent. On water, PPh3 was effective as a ligand along with a lower charge of the catalyst Pd(OAc)2 (5 mol%) at 100 °C, leading to C3-aryled 1H-indazoles or C3-aryled 1H-7-azaindazoles in moderate to good yields.


Introduction
In recent years, the C-H activation has risen as an increasingly powerful tool for molecular sciences with notable applications in organic synthesis [1][2][3][4][5]. This method has gained considerable recent momentum as a significantly environmentally and economically attractive alternative to classical cross-coupling such as Suzuki-Miyaura, Negishi, and Stille reactions [6][7][8][9][10]. With fewer steps and accessible reagents, complex organic molecules are nowadays easily accessible with C-H activation [11][12][13][14][15][16][17][18][19][20]. Nevertheless, this reaction usually requires high temperatures and organic solvents to achieve new C(sp 2 )-C(sp 2 ) bonds [21]. For economic and environmental concerns, we are aiming at developing a new C-H direct arylation of 1H-indazole and 1H-7-azaindazole by using water as a green solvent. Water is nature's primordial solvent to carry out synthesis [22]. It is known that water can increase the rate and affect the selectivity of a wide variety of organic reactions [23][24][25][26]. It was also found that on watery conditions, the heterogeneous mixture of substrates and catalyst can be very effective for direct arylation under mild conditions [27].
1H-indazoles and 2H-indazoles have widespread utility as highly bioactive molecules [28]. For such reasons, various researchers were inspired to develop and optimize new methods for their synthesis and functionalization [29][30][31][32]. Recently, different research groups have investigated the C3 direct arylation of indazole, including our own. In 2012, our group [33] in parallel with the Itami group [34] developed, for the first time, conditions to realize the direct arylation of 1H-indazole series. The key of this success was the use of bidentate ligand (1,10-phenanthroline) with a high catalyst Scheme 1. Reported methods on C3 arylation of 1H-indazoles and 1H-azaindazoles versus our new procedure.
Herein, we reported a new path for the direct and selective C3 arylation of 1H-indazoles on water. We showed, for the first time, that a phosphine ligand (PPh 3 ), contrary to the bidentate (Phen) ligand used in the case of organic solvent, is crucial to achieve the arylation reaction (Scheme 1). We are striving also to report the first examples of "on water" C3 arylation of 1H-7-azaindazoles. We showed as well that a low charge of the catalyst (5 mol%) and ligand (10 mol%) leads to desired products in acceptable to good yields.
It is noticed that Knochel et al. used 3-zincated indazoles which undergo palladium-catalyzed Negishi cross-couplings to give the C3 substituted indazole derivatives [40], while, Burton et al. described a regioselective iridium-catalyzed C3 borylation of 1H-indazoles, followed by subsequent Suzuki-Miyaura coupling with aryl chlorides [41]. Compared to the methodology described in our manuscript, the two methodologies cited above are more difficult to implement and also less economical.
Then, in the presence of palladium(II)acetate and 1,10-phenanthroline as a bidentate ligand, again no reaction was observed, and only starting material 1 was recovered (Table 1, entry 2). Changing the type of the ligand to triphenylphosphine, a monodentate ligand, which may form a stronger coordination with Pd(II) centers, led to the desired arylated product 1a in 40% yield (Table 1, entry 3). Encouraged by this result, we decided to improve the reaction's conversion by screening different conditions. At first, we tried to increase the temperature and to change the heating system with our efforts leading to no avail (Table 1, entries [4][5][6]. Water/ethanol solution was also used to increase the solubility, but only a decrease of the reaction yield (17%) was observed (Table 1, entry 7). Using (2 equiv.) of iodotoluene slightly improved the reaction yield (entry 8). Luckily, increasing the amount of iodotoluene to (3 equiv.) furnished 1a to 86% isolated yield and with a total conversion (Table 1, entry 9). Furthermore, we succeeded in reducing the loading of both palladium and PPh 3 ligand to 5 and 10% respectively (Table 1, entry 11). When the reaction was run for 24 h instead of 48 h, the yield dramatically decreased (Table 1, entry 12). Notably, the reaction temperature can be reduced to 100 • C without affecting the reaction yield (Table 1, entry 13). Using Phen instead of Ph 3 P as a ligand, under the optimized reaction conditions, led to a total loss of the reactivity (Table 1, entry 14). The reaction under reflux of water in an open flask was not total and 10% of starting material 1 was recovered (Table 1, entry 15). In addition, when 4-iodotoluene was replaced by 4-bromotoluene, the arylation did not occur, and only starting material 1 was recovered (Table 1, entry 16).
The scope and limitation of the C3 arylation reaction of various substituted indazoles 1 and 2 were examined (their preparation is described in the Supporting Information). We used various iodoaryl derivatives carrying electron-donating or electron-withdrawing groups (such as methoxy, chlorine, ester, nitro, trifluoromethyl, or methyl groups) under the most optimal reaction conditions [5 mol% Pd(OAc) 2 as the catalyst, 10% PPh 3 as the ligand, and Ag 2 CO 3 as the base in water at 100 • C (Scheme 2)]. The results showed that the expected C3-arylated products 1a-g were regioselectivity obtained. First, using indazole 1 with 4-iodotoluene gave 1a in 80% yield (Scheme 2). Afterwards, the coupling of 1 with various aryl iodides was studied. Thus, the reactions with iodobenzene, 4-iodoanisole, 4-iodobenzotrifluoride, 1-chloro-4-iodobenzene, ethyl 4-iodobenzoate, and 1-iodo-4-nitrobenzene afforded 1b-g in 54-87% yields (Scheme 2). A moderate yield was observed when 3-iodoanisole was used. In this case, the desired product 1h was isolated in 45% yield. No reaction was observed when indazole 1 was treated by 2-iodoanisole presumably as a result of its steric hindrance (methoxy group at the 2-position of the aromatic ring) and 4-iodopyridine (Scheme 2). It is noticeable that iodoaryl, containing electron-donating groups, was crucial for the achievement of C3 arylation reactions in good reaction yields (63-87%). In our second attempt, we used indazole 2 in order to see if the nitro group on position C7 affects the arylation regioselectivity. The treatment of indazole 2 with various substituted aryl iodides as coupling partners showed that the nature of the substituents (electron-donating or electron-withdrawing groups) did not affect the reaction yields or regioselectivity (compounds 2a-f). Thus, the desired products 2a-f were obtained in yields ranging between 41 and 68%. As described in the previous results, we also observed no arylation when indazole 2 was treated by 2-iodoanisole and hetero-aryl iodide as coupling partners (compounds 2g-h) (Scheme 2). chlorine, ester, nitro, trifluoromethyl, or methyl groups) under the most optimal reaction conditions [5 mol% Pd(OAc)2 as the catalyst, 10% PPh3 as the ligand, and Ag2CO3 as the base in water at 100 °C (Scheme 2)]. The results showed that the expected C3-arylated products 1a-g were regioselectivity obtained. First, using indazole 1 with 4-iodotoluene gave 1a in 80% yield (Scheme 2). Afterwards, the coupling of 1 with various aryl iodides was studied. Thus, the reactions with iodobenzene, 4iodoanisole, 4-iodobenzotrifluoride, 1-chloro-4-iodobenzene, ethyl 4-iodobenzoate, and 1-iodo-4nitrobenzene afforded 1b-g in 54-87% yields (Scheme 2). A moderate yield was observed when 3iodoanisole was used. In this case, the desired product 1h was isolated in 45% yield. No reaction was observed when indazole 1 was treated by 2-iodoanisole presumably as a result of its steric hindrance (methoxy group at the 2-position of the aromatic ring) and 4-iodopyridine (Scheme 2). It is noticeable that iodoaryl, containing electron-donating groups, was crucial for the achievement of C3 arylation reactions in good reaction yields (63-87%). In our second attempt, we used indazole 2 in order to see if the nitro group on position C7 affects the arylation regioselectivity. The treatment of indazole 2 with various substituted aryl iodides as coupling partners showed that the nature of the substituents (electron-donating or electron-withdrawing groups) did not affect the reaction yields or regioselectivity (compounds 2a-f). Thus, the desired products 2a-f were obtained in yields ranging between 41 and 68%. As described in the previous results, we also observed no arylation when indazole 2 was treated by 2-iodoanisole and hetero-aryl iodide as coupling partners (compounds 2gh) (Scheme 2).
Finally, we decided to run the reaction under our reaction conditions using the starting material 3 previously used without success by Greaney and his group [32]. As expected, we succeeded in achieving the desired arylated products 3a and 3b in 58 and 51% yield, respectively (Scheme 3).
Finally, we decided to run the reaction under our reaction conditions using the starting material 3 previously used without success by Greaney and his group [32]. As expected, we succeeded in achieving the desired arylated products 3a and 3b in 58 and 51% yield, respectively (Scheme 3). Finally, we decided to run the reaction under our reaction conditions using the starting material 3 previously used without success by Greaney and his group [32]. As expected, we succeeded in achieving the desired arylated products 3a and 3b in 58 and 51% yield, respectively (Scheme 3).
After succeeding in developing a "greener" pathway to synthesize C3-arylated 1H-indazole, we extended the methodology to prepare C3-arylated pyrazolo [3,4-b]pyridine, also known as azaindazole, which is an 1H-indazole isostere and is often used as a key pharmacophore in drug design [42][43][44][45][46][47][48][49][50][51][52][53][54][55][56][57]. Despite the enormous biological interest of C3-arylated pyrazolo [3,4-b]pyridines, only one work has been reported by Lavard and Popowycz [38], addressing the functionalization of this motif via direct arylation. Although this reported method is efficient, it is relatively energywasting, using heating at 160 °C for a long period of 3 days and organic solvent. For this reason, we decided to test our conditions developed to prepare C3-arylated pyrazolo [3,4-b]pyridine using the starting material 4 containing a benzyl group (the preparation of starting material 4 is described in the Supporting Information) with various aryl iodides as arylating partners. As expected, this procedure also showed a very high tolerance to various substituents on the aryl rings and the arylated products 4b-d were isolated with yields ranging between 56 and 67% (Scheme 4).

Instrumenttion
The reactions were monitored by thin-layer chromatography (TLC) analysis using silica gel (60 F254) plates. Compounds were visualized by UV irradiation. Flash column chromatography was performed on silica gel 60 (230-400.13 mesh, 0.040, 0.063 mm). Melting points (mp [°C]) were taken on samples in open capillary tubes and are uncorrected. The infrared spectra of compounds were recorded at room temperature on a Thermo Scientific Nicolet IS50 FT-IR. 1 H and 13 C NMR spectra were recorded on a Bruker Avance II 400 MHz ( 13 C, 100 MHz) or on a Bruker Avance DPX 250 MHz ( 13 C, 62.9 MHz). Chemical shifts are given in parts per million from tetramethylsilane (TMS) as internal standard. The multiplicities of the spectra are reported as follows: singlet (s), doublet (d), triplet (t), quartet (q), and multiplet (m). Coupling constants (J) are reported in hertz (Hz). Highresolution mass spectra (HRMS) were performed on a Maxis Bruker 4G.
N-Arylation of indazole [42]: iodobenzene (204 mg, 1 mmol) and dimethyl sulfoxide 1 mL was added to the mixture of 1H-indazole (141.7 mg, 1.2 mmol), KOH (67.3 mg, 1.2 mmol), and copper iodide (I) (19.1 mg, 0.1 mmol), and the reaction was for 12 h at 120 °C. After the completion of the reaction, cooled to room temperature, 2 mL of water and ethyl acetate 2 mL was added, and liquid separation was done. 1-phenyl indazole was obtained as a main component of the organic layer (80% yield).

Instrumenttion
The reactions were monitored by thin-layer chromatography (TLC) analysis using silica gel (60 F254) plates. Compounds were visualized by UV irradiation. Flash column chromatography was performed on silica gel 60 (230-400.13 mesh, 0.040, 0.063 mm). Melting points (m p [ • C]) were taken on samples in open capillary tubes and are uncorrected. The infrared spectra of compounds were recorded at room temperature on a Thermo Scientific Nicolet IS50 FT-IR. 1 H and 13 C NMR spectra were recorded on a Bruker Avance II 400 MHz ( 13 C, 100 MHz) or on a Bruker Avance DPX 250 MHz ( 13 C, 62.9 MHz). Chemical shifts are given in parts per million from tetramethylsilane (TMS) as internal standard. The multiplicities of the spectra are reported as follows: singlet (s), doublet (d), triplet (t), quartet (q), and multiplet (m). Coupling constants (J) are reported in hertz (Hz). High-resolution mass spectra (HRMS) were performed on a Maxis Bruker 4G.

Preparation of Starting Compounds 1-4
N-Methylation of indazole [33]: the indazole (1 g, 1 equivalent) was dissolved in acetone (10 mL) at 0 • C in a 50 mL flask. KOH (3 equivalent) was added, and then CH 3 I (1.5 equivalent) was added dropwise. The reaction mixture was filtered and separated by flash chromatography on silica gel (75% yield).

General Experimental
Procedure for the Synthesis of Products 1a-h, 2a-f, 3a-b and 4a-d A 5 mL sealed tube was charged with 1-methyl-7-nitro-1H-indazole 1, 1-methyl-1H-indazole 2, 1-phenyl-1H-indazole 3, or 1-benzyl-1H-pyrazolo[3,4-b]pyridine 4 (1.0 equivalent), iodoaryl (3.0 equivalent), Pd(OAc) 2 (0.05 equivalent), PPh 3 (0.1 equivalent) and Ag 2 CO 3 (1.5 equivalent). The mixture of solids was stirred for a few seconds to ensure all solids were well mixed. Then, 3 mL of distilled water was added, the mixture was degassed for few minutes, and the vial was covered with a serum cap. Then, the vial and its contents were heated and stirred at 100 • C for 24 h. After it was cooled to room temperature, the mixture was filtered through celite, and the organic phase was extracted three times with ethyl acetate, dried over magnesium sulfate, and then concentrated under reduced pressure. The residue was purified by flash chromatography to provide the desired products. N-Arylation of indazole [42]: iodobenzene (204 mg, 1 mmol) and dimethyl sulfoxide 1 mL was added to the mixture of 1H-indazole (141.7 mg, 1.2 mmol), KOH (67.3 mg, 1.2 mmol), and copper iodide (I) (19.1 mg, 0.1 mmol), and the reaction was for 12 h at 120 °C. After the completion of the reaction, cooled to room temperature, 2 mL of water and ethyl acetate 2 mL was added, and liquid separation was done. 1-phenyl indazole was obtained as a main component of the organic layer (80% yield).

General Experimental Procedure for the Synthesis of Products
, Pd(OAc)2 (0.05 equivalent), PPh3 (0.1 equivalent) and Ag2CO3 (1.5 equivalent). The mixture of solids was stirred for a few seconds to ensure all solids were well mixed. Then, 3 mL of distilled water was added, the mixture was degassed for few minutes, and the vial was covered with a serum cap. Then, the vial and its contents were heated and stirred at 100 °C for 24 h. After it was cooled to room temperature, the mixture was filtered through celite, and the organic phase was extracted three times with ethyl acetate, dried over magnesium sulfate, and then concentrated under reduced pressure. The residue was purified by flash chromatography to provide the desired products.  1-Methyl-7-nitro-3-phenyl-1H-indazole 1b: Data for compound 1b were previously reported [11]. N-Arylation of indazole [42]: iodobenzene (204 mg, 1 mmol) and dimethyl sulfoxide 1 mL was added to the mixture of 1H-indazole (141.7 mg, 1.2 mmol), KOH (67.3 mg, 1.2 mmol), and copper iodide (I) (19.1 mg, 0.1 mmol), and the reaction was for 12 h at 120 °C. After the completion of the reaction, cooled to room temperature, 2 mL of water and ethyl acetate 2 mL was added, and liquid separation was done. 1-phenyl indazole was obtained as a main component of the organic layer (80% yield).

General Experimental Procedure for the Synthesis of Products
, Pd(OAc)2 (0.05 equivalent), PPh3 (0.1 equivalent) and Ag2CO3 (1.5 equivalent). The mixture of solids was stirred for a few seconds to ensure all solids were well mixed. Then, 3 mL of distilled water was added, the mixture was degassed for few minutes, and the vial was covered with a serum cap. Then, the vial and its contents were heated and stirred at 100 °C for 24 h. After it was cooled to room temperature, the mixture was filtered through celite, and the organic phase was extracted three times with ethyl acetate, dried over magnesium sulfate, and then concentrated under reduced pressure. The residue was purified by flash chromatography to provide the desired products.  5 equivalent). The lids was stirred for a few seconds to ensure all solids were well mixed. Then, 3 mL of r was added, the mixture was degassed for few minutes, and the vial was covered with Then, the vial and its contents were heated and stirred at 100 °C for 24 h. After it was m temperature, the mixture was filtered through celite, and the organic phase was ee times with ethyl acetate, dried over magnesium sulfate, and then concentrated under ssure. The residue was purified by flash chromatography to provide the desired  N-Arylation of indazole [42]: iodobenzene (204 mg, 1 mmol) and dimethyl sulfoxide 1 mL was added to the mixture of 1H-indazole (141.7 mg, 1.2 mmol), KOH (67.3 mg, 1.2 mmol), and copper iodide (I) (19.1 mg, 0.1 mmol), and the reaction was for 12 h at 120 °C. After the completion of the reaction, cooled to room temperature, 2 mL of water and ethyl acetate 2 mL was added, and liquid separation was done. 1-phenyl indazole was obtained as a main component of the organic layer (80% yield). [33]: 1H-pyrazolo[3,4-b]pyridine (1 g, 8.39 mmol, 1.00 equivalent) was dissolved in acetone (10 mL) at 0 °C in a 50 mL flask, along with KOH (1.41 g, 25.19 mmol, 3.00 equivalent). After few minutes of stirring, benzyl chloride (1.59 g, 12.59 mmol, 1.50 equivalent) was added dropwise. The reaction mixture was filtered, and the two isomers N1 and N2 were separated by flash chromatography on silica gel (N1: 50%/N2: 45%).

General Experimental Procedure for the Synthesis of Products 1a-h, 2a-f, 3a-b and 4a-d
A 5 mL sealed tube was charged with 1-methyl-7-nitro-1H-indazole 1, 1-methyl-1H-indazole 2, 1-phenyl-1H-indazole 3, or 1-benzyl-1H-pyrazolo[3,4-b]pyridine 4 (1.0 equivalent), iodoaryl (3.0 equivalent), Pd(OAc)2 (0.05 equivalent), PPh3 (0.1 equivalent) and Ag2CO3 (1.5 equivalent). The mixture of solids was stirred for a few seconds to ensure all solids were well mixed. Then, 3 mL of distilled water was added, the mixture was degassed for few minutes, and the vial was covered with a serum cap. Then, the vial and its contents were heated and stirred at 100 °C for 24 h. After it was cooled to room temperature, the mixture was filtered through celite, and the organic phase was extracted three times with ethyl acetate, dried over magnesium sulfate, and then concentrated under reduced pressure. The residue was purified by flash chromatography to provide the desired products.  1-phenyl-1H-indazole 3, or 1-benzyl-1H-pyrazolo [3,4-b]pyridine 4 (1.0 equivalent), iodoaryl (3.0 equivalent), Pd(OAc)2 (0.05 equivalent), PPh3 (0.1 equivalent) and Ag2CO3 (1.5 equivalent). The mixture of solids was stirred for a few seconds to ensure all solids were well mixed. Then, 3 mL of distilled water was added, the mixture was degassed for few minutes, and the vial was covered with a serum cap. Then, the vial and its contents were heated and stirred at 100 °C for 24 h. After it was cooled to room temperature, the mixture was filtered through celite, and the organic phase was extracted three times with ethyl acetate, dried over magnesium sulfate, and then concentrated under reduced pressure. The residue was purified by flash chromatography to provide the desired products.  160.2, 145.3, 133.3, 132.7, 130.2, 128.7,128.2, 126.8, 124.7, 120.5, 120.1, 114.7, 113.4 25.19 mmol, 3.00 equivalent). After few minutes of stirring, benzyl chloride (1.59 g, 12.59 mmol, 1.50 equivalent) was added dropwise. The reaction mixture was filtered, and the two isomers N1 and N2 were separated by flash chromatography on silica gel (N1: 50%/N2: 45%).

General Experimental
Procedure for the Synthesis of Products 1a-h, 2a-f, 3a-b and 4a-d A 5 mL sealed tube was charged with 1-methyl-7-nitro-1H-indazole 1, 1-methyl-1H-indazole 2, 1-phenyl-1H-indazole 3, or 1-benzyl-1H-pyrazolo [3,4-b]pyridine 4 (1.0 equivalent), iodoaryl (3.0 equivalent), Pd(OAc)2 (0.05 equivalent), PPh3 (0.1 equivalent) and Ag2CO3 (1.5 equivalent). The mixture of solids was stirred for a few seconds to ensure all solids were well mixed. Then, 3 mL of distilled water was added, the mixture was degassed for few minutes, and the vial was covered with a serum cap. Then, the vial and its contents were heated and stirred at 100 °C for 24 h. After it was cooled to room temperature, the mixture was filtered through celite, and the organic phase was extracted three times with ethyl acetate, dried over magnesium sulfate, and then concentrated under reduced pressure. The residue was purified by flash chromatography to provide the desired products. 1-Methyl-3-(p-tolyl)-1H-indazole 2a: Data for compound 2a were previously reported [35].

General Experimental
Procedure for the Synthesis of Products 1a-h, 2a-f, 3a-b and 4a-d A 5 mL sealed tube was charged with 1-methyl-7-nitro-1H-indazole 1, 1-methyl-1H-indazole 2, 1-phenyl-1H-indazole 3, or 1-benzyl-1H-pyrazolo[3,4-b]pyridine 4 (1.0 equivalent), iodoaryl (3.0 equivalent), Pd(OAc)2 (0.05 equivalent), PPh3 (0.1 equivalent) and Ag2CO3 (1.5 equivalent). The mixture of solids was stirred for a few seconds to ensure all solids were well mixed. Then, 3 mL of distilled water was added, the mixture was degassed for few minutes, and the vial was covered with a serum cap. Then, the vial and its contents were heated and stirred at 100 °C for 24 h. After it was cooled to room temperature, the mixture was filtered through celite, and the organic phase was extracted three times with ethyl acetate, dried over magnesium sulfate, and then concentrated under reduced pressure. The residue was purified by flash chromatography to provide the desired products.  1,3-Diphenyl-1H-indazole 3a: Data for compound 3a were previously reported [34].

General Experimental
Procedure for the Synthesis of Products 1a-h, 2a-f, 3a-b and 4a-d A 5 mL sealed tube was charged with 1-methyl-7-nitro-1H-indazole 1, 1-methyl-1H-indazole 2, 1-phenyl-1H-indazole 3, or 1-benzyl-1H-pyrazolo[3,4-b]pyridine 4 (1.0 equivalent), iodoaryl (3.0 equivalent), Pd(OAc)2 (0.05 equivalent), PPh3 (0.1 equivalent) and Ag2CO3 (1.5 equivalent). The mixture of solids was stirred for a few seconds to ensure all solids were well mixed. Then, 3 mL of distilled water was added, the mixture was degassed for few minutes, and the vial was covered with a serum cap. Then, the vial and its contents were heated and stirred at 100 °C for 24 h. After it was cooled to room temperature, the mixture was filtered through celite, and the organic phase was extracted three times with ethyl acetate, dried over magnesium sulfate, and then concentrated under reduced pressure. The residue was purified by flash chromatography to provide the desired products.
3.3. General Experimental Procedure for the Synthesis of Products 1a-h, 2a-f, 3a-b and 4a-d A 5 mL sealed tube was charged with 1-methyl-7-nitro-1H-indazole 1, 1-methyl-1H-indazole 2, 1-phenyl-1H-indazole 3, or 1-benzyl-1H-pyrazolo[3,4-b]pyridine 4 (1.0 equivalent), iodoaryl (3.0 equivalent), Pd(OAc)2 (0.05 equivalent), PPh3 (0.1 equivalent) and Ag2CO3 (1.5 equivalent). The mixture of solids was stirred for a few seconds to ensure all solids were well mixed. Then, 3 mL of distilled water was added, the mixture was degassed for few minutes, and the vial was covered with a serum cap. Then, the vial and its contents were heated and stirred at 100 °C for 24 h. After it was cooled to room temperature, the mixture was filtered through celite, and the organic phase was extracted three times with ethyl acetate, dried over magnesium sulfate, and then concentrated under reduced pressure. The residue was purified by flash chromatography to provide the desired products.

Conclusions
In summary, we have developed a new palladium catalyzed direct C3 arylation of 1H-indazole using a low charge of 5 mol% of Pd(OAc) 2 along with 10 mol % of PPh 3 on water as solvent at 100 • C. This new procedure afforded a board of arylated indazoles differently substituted at the C3 position in moderate to good yields. The application of this protocol on 1H 7-azaindazole was fruitful, and four examples of C3-arylated pyrazolo [3,4-b]pyridine were successfully reported.