Late-stage ortho-C-H alkenylation of 2-arylindazoles in aqueous medium by Manganese(i)-catalysis.

Earth-abundant and water-tolerant manganese(i) catalyzed alkenylation of 2-arylindazole with alkyl and aryl alkynes through C-H bond activation is described with a unique level of E-selectivity. The reaction proceeds through the control of C3 nucleophilicity of 2-aryl indazoles. This method is applied to the late-stage functionalization of complex molecules including ethinylestradiol, norethisterone, and N-protected amino acid derivatives. The kinetic isotope studies suggest that the C-H bond activation step may not be the rate-determining step. This journal is © The Royal Society of Chemistry.

Introduction

Direct functionalization of inert C–H bonds is still one of the most attractive strategies due to the formation of the versatile fundamental linkage in organic compounds.[1] In this context, noble metals such as iridium,[2] ruthenium,[2] rhodium,[2] and palladium[2] have been extensively employed for C–C and C–hetero atom bond formation reactions in the past two decades because of their high catalytic performance. However, these noble metal catalysts usually suffer from toxicity, low natural abundance, and high cost. In recent years, remarkable progress in 3d-transition metals such as Mn,[3] Fe,[3] Co,[3] Ni,[3] and Cu[3] based C–H activations have been observed due to the metals' low price, high earth abundance, low toxicity, and potential to develop unique reactivity. In this topic, Mn-complexes typically exhibit low toxicity, thus the utilization in C–H functionalization is highly desirable.[4] The Wang group first reported the alkenyation of hetero-arene with alkynes via C–H bond activation using Mn(CO)5Br as a catalyst.[5] Afterward, various research groups such as Ackermann,[6] Glorius,[6] Kuninobu[6] and others[6] independently developed Mn-catalyzed C–H functionalization. Even though C–H bond activation in an aqueous medium is sought after, only a few examples of such reactions are known that occur in water.[7]

Indazole, a nitrogen-containing heterocycle is widely used in pharmaceutical and material science. In particular, antitumor, antiplatelet, anticancer, anti-inflammatory, HIV-protease inhibition, etc., are shown by indazole.[8] Various marketed drugs contain indazole moiety, such as pazopanib, gamendazole, anticancer agent (MK-4827), bendazac (tyrosine kinase inhibitor, votrient), etc.[9] Therefore, various methodologies have been developed for the synthesis and functionalization of indazoles because of their extensive biological applications.[10]

Recently few methodologies of ortho C–H activation in 2-arylindazole moiety have been developed.[11] However, C–H activation of 2-aryl indazoles using water-tolerant metal-catalyst has not been explored yet. We concentrated our focus on Mn-catalyzed selective ortho-C–H functionalization of 2-aryl indazoles through the control of C3 nucleophilicity.[12] Herein, we have described manganese-catalyzed ortho-C–H alkenylation of 2-arylindazole with alkyl and aryl alkynes in water (Scheme 1).

Scheme 1

Indazole-Directed C–H Alkenylation.

Results and discussion

The study was initiated by investigating the reaction of 2-phenyl-2H-indazole (1a) and prop-2-yn-1-yl 4-methylbenzoate (2a) in the presence of Mn-catalyst. The reaction was performed using 10 mol% MnBr(CO)5 as a catalyst and 20 mol% NaOAc as an additive in 1,4-dioxane at 100 °C under N2 atmosphere. Gratifyingly, the coupling product (E)-3-(2-(2H-indazol-2-yl)phenyl)allyl 4-methylbenzoate (3aa) was obtained in 85% yield after 8 h (Table 1, entry 1). Next, we screened the effect of various Mn-catalyst like Mn2(CO)10, MnCl2, and Mn(OAc)2. But in all the cases, unsatisfactory results were observed (Table 1, entries 2–4). Further optimization was carried out using various solvents such as 1,2-DCE, THF, Toluene, DMF, CH3CN, and H2O (Table 1, entries 5–10). It was found that polar protic solvent H2O afforded the desired product in 91% yield (Table 1, entry 10). No significant improvement of the yield was observed on further screening of additives like KOAc, K2CO3, K3PO4, and Et3N (Table 1, entries 11–14). However, no product was formed in the absence of catalyst (Table 1, entry 15). Next, we checked the reaction without additives (Table 1, entry 16). In addition, varying the reaction temperature did not improve the yield of the product (Table 1, entry 17). The reaction yield did not enhance under air atmosphere, and no difunctionalized product was obtained in the presence of 2.0 equiv. of 2a (Table 1, entry 18). From these results, the optimum reaction conditions was determined to be those in entry 10.

Optimization of the reaction conditionsa

Entry	Catalyst (10 mol%)	Additives (20 mol%)	Solvent (2.0 mL)	Yield (%)
1	MnBr(CO)5	NaOAc	1,4-Dioxane	85
2	Mn2(CO)10	NaOAc	1,4-Dioxane	65
3	MnCl2	NaOAc	1,4-Dioxane	nr
4	Mn(OAc)2	NaOAc	1,4-Dioxane	nr
5	MnBr(CO)5	NaOAc	1,2-DCE	61
6	MnBr(CO)5	NaOAc	THF	46
7	MnBr(CO)5	NaOAc	Toluene	52
8	MnBr(CO)5	NaOAc	DMF	21
9	MnBr(CO)5	NaOAc	CH3CN	10
10	MnBr(CO) 5	NaOAc	H 2 O	91
11	MnBr(CO)5	KOAc	H2O	78
12	MnBr(CO)5	K2CO3	H2O	62
13	MnBr(CO)5	K3PO4	H2O	57
14	MnBr(CO)5	Et3N	H2O	45
15	—	NaOAc	H2O	nr
16	MnBr(CO)5	—	H2O	36
17	MnBr(CO)5	NaOAc	H2O	67b, 62c
18	MnBr(CO)5	NaOAc	H2O	69d, 72e

Reaction conditions: All reactions were carried out with 0.25 mmol of 1a, 0.3 mmol of 2a, 10 mol% of MnBr(CO)5, 20 mol% NaOAc in 2.0 mL solvent for 8 h at 100 °C under N2.

Stirred at 120 °C.

Stirred at 80 °C.

Under air.

2.0 equiv. of 2a was used. nr = no reaction.

After getting the optimized reaction conditions for the manganese-catalyzed C–H alkenylation in hand, we next investigated its versatility (Table 2). The electron-donating (–Me), halogen (–Cl), and electron-withdrawing (–CN) substituted benzoic acid derived alkynes smoothly underwent with indazole (1a) through C–H activation, effectively providing the expected products (3aa–3ac) with excellent yields even on a gram scale of 3aa. Nicotinic acid derived alkyne was examined, furnishing the corresponding alkenylated product 3ad in 78% yield. It is noteworthy that aliphatic acids like pivalic acid, cyclohexanecarboxylic acid, and adamantane-1-carboxylic acid derived alkynes were successfully employed, leading to the desired products 3ae–3ag in good to excellent yields of 89–96%. Pent-4-yn-1-yl benzoate (2h) was treated with 2-phenyl-2H-indazole (1a), and the expected alkenylation reaction occurred with moderate yield. Remarkably, phenol, aniline, and thiophenol derivatives alkynes were efficiently converted to the desired products 3ai–3ak with complete E-selectivity. Specifically, N-Boc-protected amino acid derivatives 2l and 2m were well tolerated, which will be precious for further post-synthetic application. Furthermore, N-Boc-protected indoline-2-carboxylic acid derived alkyne (2n) was converted to the desired product in 72% yield. Inspired by the incredible versatility of Mn(i)-catalyzed alkenyation, we became interested in performing this alkenylation reaction with more challenging steroid structures. In this regard, ethinylestradiol and norethisterone took part effectively in the reaction to deliver 3ao and 3ap in 68% and 60% yields, respectively. Again, 1-octyne was smoothly reacted, giving the desired product 3aq in 57% yield with excellent E-selectivity. Moreover, 3-hexyne was reacted with 2-phenyl-2H-indazole (1a) under the standard reaction conditions, but unfortunately obtained an inseparable mixture.

Substrate Scope of Alkynesa

Reaction conditions: 0.25 mmol of 1, 0.3 mmol of 2 in presence of 10 mol% of MnBr(CO)5, 20 mol% NaOAc in 2.0 mL of H2O at 100 °C for 8 h under N2.

5 mmol scale.

A number of electron-neutral and -donating (–Me, –OMe) and electron-deficient (–F) phenylacetylenes (2) were taken part in the reaction with 2-arylindazole (1a) to afford the desired products (3ar–3au) up to 87% yields. 2-Ethynyl-6-methoxynaphthalene (2v) was also amenable to this method. Moreover, internal alkyne (2w and 2x) also provided ortho-alkenyated product 3aw–3bx in moderated yields (55–82%). Interestingly, heteroaryl substituted alkyne such as 3-ethynyl thiophene (2y) was successfully converted into the corresponding alkenylated product 3ay in decent yields. The regioselectivity of unsymmetrical alkynes (direction of alkynes) have been determined from the 1H-NMR data and coupling constant (J) values.

Motivated by the versatility of the Mn(i)-catalysis, a variety of indazoles were examined. Electron-donating group (–Me) at the phenyl ring of 2-arylindazole gave the corresponding alkenylated product 3br in excellent yields. Halogen (–F, –Cl, and –Br) containing substrates produced the desired products (3cr–3er) in moderate to good yields. An electron-withdrawing (–COOEt) group containing 2H-indazole was well tolerated in this method and gave the expected products in moderate yields (3fr). meta-Substituted 2-arylindazoles (1g and 1h) were also reacted under the optimal reaction conditions (3gr and 3hr) with good yields. 2H-indazoles, bearing halogens (–F and –Cl) on the C-5 position of arene, successfully reacted to produce the desired products (3ir and 3kr). Furthermore, disubstituted indazoles (1j, 1l, and 1m) were explored and gave the corresponding products without any difficulties (3jr, 3lr, and 3mr). On the other side, due to the difficulty in the formation of a five-membered mangancyclic intermediate, indazole substituted at the ortho-position did not produce the desired product. Interestingly, similar N-containing heterocycles such as 2-phenylpyridine (1n) and 1-phenyl-1H-pyrazole (1o) also reacted with N-Boc-protected amino acid derivative alkyne (2l) and provided their corresponding products 3nl and 3ol in 86% and 88% yields, respectively (Table 3).

Substrate Scope of Hetrocyclesa

Reaction conditions: 0.25 mmol of 1, 0.3 mmol of 2 in presence of 10 mol% of MnBr(CO)5, 20 mol% NaOAc in 2.0 mL of H2O at 100 °C for 8 h under N2.

The deuterium labeling experiment, kinetic isotope effect (KIE), and parallel experiments were performed to realize the mechanistic pathway of this reaction (Scheme 2). Initially, a H/D exchange experiment was executed under the optimized reaction conditions using D2O as a co-solvent which led to the incorporation of deuterium at ortho-position of the phenyl ring (Scheme 2a). This result indicated that the reversible cleavage of C–H bonds might be involved in the reaction. In addition, the intermolecular competition reaction (Scheme 2b) and parallel reaction (Scheme 2c) gave low KIE values of 1.0 and 1.1, respectively. This data suggested that the C–H bond cleavage step was unlikely to be the rate-determining step.

Scheme 2

Control experiments.

Based on the above results and previous reports,[4,5] a plausible reaction mechanism is shown in Scheme 3. At first, NaOAc-assisted cyclomanganation of 2H-indazole (1b) forms a five-membered manganacycle A. Coordination of alkyne (2) with A gives intermediate B. Subsequently, migratory insertion of alkyne generates intermediate C. Finally, protonation of C furnishes the desired product, and regenerate the active Mn(i) complex to complete the catalytic cycle.

Scheme 3

Plausible mechanistic pathway.

Conclusions

In summary, we have successfully developed a highly stereo- and regioselective Mn(i)-catalyzed ortho-alkenylation of indazole with various alkynes. The salient features of this methodology includes (1) robust C–H activation in H2O, (2) Mn(i)-catalyzed C–H functionalization, (3) broad substrate scope and good to excellent yields, (4) excellent E-stereoselectivity, (5) the late-stage functionalization of complex molecules, (6) scalable. We believe this method will gain much attraction in organic synthesis, pharmaceutical chemistry, and as well as in material sciences.

Conflicts of interest

There are no conflicts to declare.