Metal-free para-selective C-H amination and azidation of N-arylhydroxylamines

Abstract

Due to the universality of arylamine and arylazide building blocks in pharmaceuticals, natural products and functional materials, the formation of aryl C-N bonds from readily available materials appears to be highly appealing, especially for the exclusive regioselective C-H amination. Despite substantial advancements in the synthesis of aryl C-N bonds, achieving a general, efficient, and para-selective C-H amination under mild conditions remains a significant challenge. Here we showcase a fluorosulfuryl imidazolium triflate-mediated para-selective C-H amination of N-arylhydroxylamines employing primary and secondary amines, diphenylmethanimine and azides as nitrogen source, affording structurally diverse 1,4-diaminoarenes or para-azidoanilides in the absence of oxidants and transition-metal catalysts. This effective protocol exhibits exclusive para-selectivity and good functional group tolerance for both N-arylhydroxylamines and N-nucleophiles (>90 examples). DFT calculations have been performed to elucidate the high chemoselectivity observed amidst multiple nucleophilic and electrophilic species.

Achieving general, efficient, and para-selective C-H amination under mild conditions remains a significant challenge. Here the authors report a fluorosulfuryl imidazolium triflate-mediated para-selective C-H amination of N-arylhydroxylamines for the synthesis of 1,4-diaminoarenes or para-azidoanilides.

Introduction

The aryl amine moiety represents privileged structural motif due to its widespread applications and presence in pharmaceuticals, natural products, dye industry, and material science^{1, 2, 3, 4, 5–6}. Examples include Binimetinib⁷, Murrastifoline B⁸, Erdafitinib⁹ and P2Y₁₂ receptor antagonist¹⁰ (Fig. 1). Additionally, aryl amines serve as highly versatile intermediates or synthons in organic synthesis, readily convertible into a wide range of structurally diverse functional groups¹¹. Therefore, the construction of C-N bonds towards the synthesis of aryl amines has emerged as a significant research area in organic chemistry. Conventional methods for the synthesis of aryl amines majorly rely on the nitration of arenes followed by metal-catalyzed nitro reduction, and transition-metal-catalyzed cross-coupling reactions of amines with prefunctionalized aryl substrates (e.g., Ullman-Goldberg¹², Buchwald-Hartwig^{13, 14–15}, Chan-Lam^16,17 C-N bond formation reactions) (Fig. 2a). In addition, the employment of NaN₃ or hydroxylamine as amination reagents to achieve C (sp²) amination through C-C bond cleavage^18,19 or direct C(sp²)-H-amination^{20, 21, 22, 23, 24–25} are also representative strategies. Over the past two decades, remarkable advances have been made in the transition-metal-catalyzed C-H amination of arenes, in particular, the directed ortho-C-H amination has been relatively well studied for the construction of aryl C-N bond in the presence of a variety of metal-catalysts, such as Pd^{26, 27, 28, 29–30}, Rh^{31, 32, 33, 34, 35, 36–37}, Ir^{38, 39, 40–41}, Ru^{42, 43, 44, 45, 46, 47, 48, 49–50}, Cu^51,52, Co^{53, 54, 55–56}, Fe^23,57 et al. (Fig. 2b). Despite the remarkable success of these strategies, challenges remain, including the employment of transition metals or harsh reagents, the need for specific directing groups, and limitations in substrate scope.

Fig. 1 Biologically active aryl amine scaffold. [Images not available. See PDF.]

Representative pharmaceuticals and natural products with aryl amine structural motif.

Fig. 2 Synthetic approaches to aryl amines. [Images not available. See PDF.]

a Conventional methods. b Directed ortho-C-H amination. c Directed para-C-H amination. d This work: Metal-, oxidant-, directing-group-free para-C-H amination.

Compared to the well-established directed ortho-C-H amination methods, the meta^{58, 59, 60–61} and para-selective C-H amination of arenes are considerably less explored and only limited examples have been reported across this field in recent years. In 2011, Zhang and co-workers⁶² disclosed a palladium-catalyzed, highly selective para-C-H amination of arenes by using N-fluorobenzenesulfonimide (NFSI) as nitrogen source and an alkoxyl group at the ortho position of the amide as a directing group [Fig. 2c, panel (1)]. Subsequently, several groups reported similar para-amination strategies for sp² C-H bonds, utilizing hypervalent iodine reagent or metal catalyst employing a variety of nitrogen source, such as NFSI⁶³, dibenzenesulfonimide⁶⁴, azodicarboxylates^65,66 and azoles⁶⁷ [Fig. 2c, panel (2)]. In 2015, Nicewicz and co-workers reported an elegant site-selective C-H amination protocol of electron-rich arenes promoted by an organic photoredox-based catalytic system using azoles or ammonium salts as nitrogen source albeit with moderate to good regioselectivity (para Vs ortho) [Fig. 2c, panel (3)]⁶⁸. Very recently, Zhang, Lei and Cai developed a facile, metal-free, dehydrogenative para-selective amination of nitroarenes through an aminyl radical coupling mechanism employing cyclic and acyclic secondary amine as nitrogen source and environmentally friendly O₂ as an oxidant [Fig. 2c, panel (4)]⁶⁹. However, the involvement of aminyl radicals excluded the employment of primary amines and non-nitroarenes. While these transformations have established the feasibility of the para-selective C-H amination of arenes with a variety of directing groups, the development of an effective regio-selective cross coupling of arenes with a number of N-nucleophiles under mild conditions is still in high demand. Herein, we report a practical, oxidant- and metal-free umpolung para-selective C-H amination and azidation of N-arylhydroxylamines with a wide range of N-nucleophiles. This transformation is efficiently promoted by FluoroSulfuryl Imidazolium Triflate (FSIT) under mild conditions (Fig. 2d).

Over the past decade, Sulfur(VI) Fluoride Exchange (SuFEx) chemistry, pioneered by Sharpless, Dong and co-workers^{70, 71–72},has been extensively applied to the synthesis of numerous target molecules or functional materials employing SO₂F₂ or its surrogates (such as FSIT and AISF < ([4-(Acetylamino)phenyl]-ImidodiSulfuryl diFluoride>)) as effective and powerful hub. Moreover, in our recent studies, FSIT has been found to be an unique activator to achieve the umpolung cascade cross-coupling of N-arylhydroxylamines with various O- and S-nucleophiles for the efficient construction of para-functionalized anilides under simple conditions⁷³. Inspired by the aforementioned protocols, we began to evaluate the possibility of realizing the metal- and directing-group-free para-C-H amination of N-arylhydroxylamines with diverse N-nucleophiles.

Results

Condition screening

We started our investigation by choosing N-phenylhydroxylamine 1a and aniline 2a as model substrates (Table 1). Screening of a series of bases, such as Et₃N, DBU, DMAP, K₂CO₃, NaHCO₃ and Na₂CO₃, was firstly conducted using MeCN as solvent at 0 ^oC under air atmosphere, indicating Na₂CO₃ was relatively promising with the generation of the desired product 3 in 33% yield (Table 1, entries 1-6). Notably, only trace amount of phenylsulfamoyl fluoride 1a′′, which was formed by the reaction of aniline 2a with FSIT⁷², could be observed. The subsequent solvent screening revealed that the participation of 1,4-dioxane was helpful, affording to the para-aminated anilide 3 in 49% yield using the mixed solvent of acetonitrile and 1,4-dioxane in 3:1 ratio (Table 1, entries 7-11). To our delight, the yield of product 3 could be further increased to 66% when the reaction was carried out at -20 ^oC, although the generation of N-phenylbenzamide 1a′ from the decomposition of N-phenylhydroxylamine 1a could not be fully suppressed (Table 1, entries 12-13). The employment of N₂ atmosphere did not affect the yield of the target product 3 (Table 1, entry 14). Decreasing the loading equivalents of FSIT resulted in lower yield of para-aminated anilide 3 (Table 1, entry 15). Thus, the combination of 1.0 equivalent of N-arylhydroxylamine, 2.0 equivalents of aniline, 1.5 equivalents of FSIT, 2.0 equivalents of Na₂CO₃ as base, the 3:1 mixture of acetonitrile and 1,4-dioxane as solvent at -20 °C under air for 3 h, was selected as the optimal conditions for this cascade transformation. (Table 1, entry 12).

Table 1. Optimization of reaction conditions

Entry[a]	conditions					Yield (%)[b]
	Solvent	Base	T (oC)		3	1a′	1a′′
1	MeCN	Et3N	0		21	18	<5
2	MeCN	DBU	0		9	18	<5
3	MeCN	DMAP	0		24	15	<5
4	MeCN	K2CO3	0		29	23	<5
5	MeCN	NaHCO3	0		17	5	<5
6	MeCN	Na2CO3	0		33	18	<5
7	DCM	Na2CO3	0		17	13	<5
8	THF	Na2CO3	0		23	23	<5
9	MeCN/THF(1/1)	Na2CO3	0		36	18	<5
10	MeCN/1,4-Dioxane (1/1)	Na2CO3	0		45	13	0
11	MeCN/1,4-Dioxane (3/1)	Na2CO3	0		49	18	0
12	MeCN/1,4-Dioxane (3/1)	Na2CO3	−20		66	13	0
13	MeCN/1,4-Dioxane (3/1)	Na2CO3	-40		55	13	0
14[c]	MeCN/1,4-Dioxane (3/1)	Na2CO3	−20		66	18	0
15[d]	MeCN/1,4-Dioxane (3/1)	Na2CO3	-20		54	15	0

^aReaction conditions: 1a (0.2 mmol, 1.0 equiv.), 2a (0.4 mmol, 2.0 equiv.), FSIT (0.3 mmol, 1.5 equiv.), base (0.4 mmol, 2.0 equiv.) in solvent at a specific temperature for 3 h. ^bIsolated yield. ^cAtmosphere of N₂ was used. ^d1.2 equivalents of FSIT were used. FSIT fluorosulfuryl imidazolium triflate, DBU 1,8-Diazabicyclo[5.4.0]undec-7-ene, DMAP 4-Dimethylaminopyridine.

Mechanistic studies

To better understand the good chemoselectivity observed in this tandem transformation, particularly in the presence of multiple nucleophilic species and its reaction mechanism, we conducted a DFT study using the B3LYP-D3 functional (see pages S52-53 of the Supplementary Information and source data for computational details.). First, experimental data show that N-phenylhydroxylamine (1a) reacts more readily with FSIT than aniline (2a). The initial step involves the reaction of either nucleophile, 1a or 2a, with Na₂CO₃ to form an anionic nucleophile (as a Na-salt). Accordingly, we calculated the free energy changes for these reactions. As shown in Fig. 3a, the reaction between 1a and the base is exergonic by 5.9 kcal/mol, leading to the formation of the 1a-O nucleophile. In contrast, the reaction between 2a and the base is endergonic by 15.6 kcal/mol, forming the 2a-N nucleophile, indicating this reaction is thermodynamically less favorable than that of 1a. Therefore, thermodynamic calculations suggest that the N-phenylhydroxylamine anion forms more easily under basic conditions, supporting the experimental observation that the primary reaction occurs between 1a and FSIT.

Fig. 3 DFT studies. [Images not available. See PDF.]

a Reactions of 1a and 2a with the Na₂CO₃ base. b Reactions of IN1 with 2a and NaOSO₂F. c Free energy profile for the reaction starting from imine cation IN1 (bond distances are given in Å).

Following the reaction of 1a with FSIT, the N-O bond undergoes cleavage, generating an imine cation. This cation can react with either aniline (2a) or the NaOSO₂F nucleophile in solution. We calculated the free energy for both reactions, and the results show that the reaction between 2a and the imine cation is exergonic by 25.9 kcal/mol, whereas the reaction between NaOSO₂F and the imine cation is only exergonic by 3.2 kcal/mol (Fig. 3b). These calculations demonstrate that, at this stage, it is more favorable for the imine cation to react with aniline (2a) rather than with other nucleophiles, which is consistent with experimental observations. Notably, we also considered the anionic forms of both nucleophiles (i.e., PhNH⁻ and FSO₃⁻) in the free energy calculations, and found that the reaction of the imine cation with deprotonated aniline (PhNH⁻) is still much more favorable than with FSO₃⁻ (see pages S52-53 of the Supplementary Information and source data for details). Thus, these calculations clearly explain why 1a, but not 2a, reacts with FSIT, and why the imine cation intermediate preferentially reacts with aniline over fluorosulfonate-based nucleophiles.

Lastly, we computed the reaction mechanism starting from the imine cation species. As shown in the free energy profile (Fig. 3c), the reaction between the imine cation (IN1) and aniline (2a) is exergonic by 25.9 kcal/mol, yielding the amine cation (IN2). Subsequent deprotonation of IN2 by Na₂CO₃ leads to IN3, which is exergonic by 23.1 kcal/mol. The carbonate base then interacts with the para-C-H bond of IN3 via hydrogen bonding to form intermediate IN4. This is followed by the deprotonation transition state (TS1), resulting in the formation of IN5. This step is facile (∆G^≠ = 1.2 kcal/mol) and highly exergonic (∆G = 39.2 kcal/mol) relative to IN3, likely driven by aromatization. Finally, proton transfer from the carbonate back to the anionic nitrogen, along with the release of Na₂CO₃, yields the final product, IN6, with a slight exergonicity of 0.6 kcal/mol. Overall, the imine cation intermediate undergoes nucleophilic attack, deprotonation, rearomatization, and proton transfer to give the final amine product. It is important to note that the carbonate base plays a key role in this proton-shuttling process: deprotonating the para-C-H bond and returning the proton to the anionic nitrogen.

Substrate scope

With the optimal reaction conditions in hand, we began investigating the substrate scope of this cascade protocol by verifying the different amine nucleophiles (Fig. 4). Pleasingly, a wide array of primary anilines bearing halogen atom, cyanide, aldehyde, ketone, ester, sulfone, nitro, hydroxyl, alkyl and alkoxyl groups at the para, ortho or meta positions readily reacted with N-phenylhydroxylamine 1a under standard conditions, delivering the desired para-aminated anilides products 4-23 in moderate to good yields. In addition, 2,4-, 3,4-di- and 2,4,6-trisubstituted anilines and naphthylamines were well tolerated to give the corresponding products 24-30 in 41−73% yields. Notably, the excellent chemoselectivity of this cascade protocol could be proven by the aniline substrates with OH group, which could exclusively generate the N-attack products 19 and 25 rather than the O-attack products. We were pleased to find that herteroaryl amines, such as quinolinyl-, isoquinolinyl-, pyridinylamines with diverse substituents, were amenable to our current reaction conditions to afford the expected aminated products 31-41 in moderate to good yields, showing the potential applications of this methodology in preparing the pharmaceutical-relevant compounds. For the secondary amine substrates, such as N-methyl, N-phenyl amines, 1,2,3,4-tetrahydroquinoline, 2,3,4,5-tetrahydro-1H-benzo[b]azepine and pyrazole, this FSIT-promoted umpolung para-amination process still occurred to give the corresponding products 42-47 albeit with relatively lower yields. In addition to the above-mentioned nitrogen nucleophiles, we also explored other representative amination reagents, especially aliphatic amines. Unfortunately, they are not well applicable to the reaction to obtain the corresponding products (For details, see page S47 of the Supplementary Information.).

Fig. 4 Substrate scope for the para-C-H amination. [Images not available. See PDF.]

Method. A: 1a (0.20 mmol, 1.0 equiv.), 2 (0.40 mmol, 2.0 equiv.), Na₂CO₃ (0.40 mmol, 2.0 equiv.), FSIT (0.30 mmol, 1.5 equiv.) in 4 ml of MeCN/1,4-Dioxane (3/1) at −20 ^oC for 3 h. For 45: 2.0 equivalents of K₂CO₃ rather than Na₂CO₃ was employed as base. Yields were determined by the isolated products. FSIT fluorosulfuryl imidazolium triflate.

Given the good results with diverse arylamine nucleophiles, we decided to explore the substrate scope of N-arylhydroxylamine for this metal-free amination reaction, as shown in Fig. 5. N-Phenylhydroxylamines with several frequently-used N-protective groups (such as Ac, Cbz and Fmoc) smoothly reacted with 4-chloroaniline 2c under the standard conditions, affording to the corresponding para-aminated products 48-50 in high yields (70-78%). A broad range of N-phenylhydroxylamine with ortho- and meta-substituents, including electron-withdrawing and electron-donating functionalities, were well compatible to form the desired para-aminated products 51-62 in moderate to good yields. The 2,3-, 2,5-, and 3,5-disubstituted N-phenylhydroxylamines with various substituents were demonstrated as the suitable candidates for this cascade transformation to generate the desired products 63-71 in 53–75% yields. More importantly, N-phenylhydroxyl-amines connected with complex rings or natural product-relevant structures, such as cycloheptanol, adamantanol, furan-2-ylmethanol, menthol and perillyl alcohol, could also be compatible with this amination reaction to furnish the corresponding products 72-76 in good yields (58-80%) under the optimal conditions.

Fig. 5 Scope of the N-arylhydroxylamines. [Images not available. See PDF.]

Method. A: 1 (0.20 mmol, 1.0 equiv.), 2c (0.40 mmol, 2.0 equiv.), FSIT (0.30 mmol, 1.5 equiv.), Na₂CO₃ (0.40 mmol, 2.0 equiv.) in 4 ml of MeCN/1,4-Dioxane (3/1) at -20 ^oC for 3 h. Yields were determined by the isolated products. FSIT fluorosulfuryl imidazolium triflate.

Encouraged by the successful assembling of secondary and tertiary amine at the para-position of the anilides, we were interested in the direct primary amination of our N-arylhydroxylamine substrates. Due to the strong coordinating property and nucleophilicity of ammonia and its analogs, the direct primary amination was much more challenging than the secondary and tertiary aminations in both metal-catalyzed and metal-free amination reactions. As far as we know, there are very rare examples for the efficient para-primary amination of arenes except for limited reports on metal-catalyzed cross-coupling amination reactions. After systematic screening of various aminating reagents and reaction conditions, we delightedly found that readily available diphenylmethanimine 77 can be employed as effective nitrogen source to accomplish the C-N bond formation in our protocol, followed by the practical removal of benzophenone under acidic conditions to obtain the para-primary aminated product 90 (For detailed optimization study, see page S9 of the Supplementary Information.). Gratifyingly, this facile successive protocol has a wide range of substrate scope (Fig. 6). N-Arylhydroxylamines bearing variety of substituents were compatible with this cascade reaction system, providing the corresponding products in both steps in good to excellent yields. Notably, the yields of p-aminobenzenamines 90-101 on the right side of Fig. 6 refer to the yields after hydrolysis of compounds 78-89 on the left side.

Fig. 6 Scope of para-amination of N-arylhydroxylamines. [Images not available. See PDF.]

Method B: Step 1: 1 (0.20 mmol, 1.0 equiv.), 77 (2.0 mmol, 10.0 equiv.), FSIT (0.30 mmol, 1.5 equiv.), Na₂CO₃ (0.40 mmol, 2.0 equiv.) in 4 ml of MeCN/1,4-Dioxane (3/1) at -20 ^oC for 3 h. Step 2: Compounds 78-89 in 5 ml of THF/HCl (2.5/2.5) at 25 ^oC for 4 h, followed by treatment of 1 mol/l of KOH solution after removal of solvent. All yields were determined by the isolated products. FSIT fluorosulfuryl imidazolium triflate.

Having developed an efficient metal-free protocol for the synthesis of structurally diverse para-aminated anilides, we assumed that this method might provide a good opportunity to realize the goal of expanding the chemical space to other nitrogen-containing molecules, such as aryl azides. Due to their versatile reactivities and unique biological properties, organic azides have become widely applied in organic synthesis as highly valuable building blocks for the preparation of various nitrogen-containing heterocycles^{74, 75–76}, peptide molecules, functional materials and had extensive applications in polymer chemistry, drug discovery, biology and interface chemistry^{77, 78, 79, 80–81}. Although great effort has been devoted into the installation of the azide group onto the aromatic rings^82,83, such as nucleophilic aromatic substitution^84,85, diazotization pretreatment of aromatic amines followed by diazo transfer^86,87, sonication-mediated Friedel-Crafts C-H azidation⁸⁸ and copper-catalyzed cross-coupling of preactivated arenes^89,90 or direct C-H bond azidation of anilines⁹¹, these methods still suffer from the harsh reaction conditions or the limited functional group tolerance.

To our delight, our current FSIT-promoted umpolung para-C-H functionalization strategy can be successfully extended to the direct para-C-H azidation of N-arylhydroxylamines using TMSN₃ as azide source under the similar conditons (For detailed optimization study on para-azidation, see page S10 of the Supplementary Information.). A broad array of N-arylhydroxylamines bearing electron-withdrawing and electron-donating groups on the phenyl ring were well tolerated in this cascade transformation, affording the corresponding para-azidized anilide products 103-114 in moderate to good yields under standard conditions (Fig. 7).

Fig. 7 Substrate scope of para-azidation of N-arylhydroxylamines. [Images not available. See PDF.]

Method C: 1 (0.20 mmol, 1.0 equiv.), FSIT (0.4 mmol, 2.0 equiv.), TMSN₃ (0.60 mmol, 3.0 equiv.), K₂CO₃ (0.40 mmol, 2.0 equiv.) in 4 ml of MeCN/1,4-Dioxane (3/1) at −20 ^oC for 3 h. Yields were determined by the isolated products. FSIT fluorosulfuryl imidazolium triflate.

Gram-scale reactions and synthetic applications

With these para-aminated anilide products in hand, a preliminary survey of their optical properties was carried out by choosing compound 33 as a representative. Similar to the general D-π-A system, the absorption of compound 33 does not change significantly in different polar solvents, while the emission shows a significant solvation effect. The maximum emission wavelength of compound 33 has been redshifted by ~70 nm from the non-polar solvent cyclohexane to the highly polar tetrahydrofuran (Fig. 8). To demonstrate the synthetic practicability of this protocol, a gram-scale synthesis of 5 was carried out under standard conditions. It was found that the gram-scale reaction proceeded smoothly to afford 1.08 grams of 5 in 67% yield (Fig. 9, panel 1). To illustrate the synthetic potential of the newly formed 1,4-diaminoaryl compounds, various reactions were performed under different conditions by choosing compound 6 as a representative (Fig. 9, paths a-e). For instance, the classical palladium-catalyzed Suzuki coupling of compound 6 with phenylboronic acid was accomplished to produce the corresponding biaryl product 115 in 70% yield (Fig. 9, path a)⁹²; both nitrogen atoms of 6 could be efficiently methylated in the presence of iodomethane and sodium tert-butoxide to furnish 116 in 73% yield (Fig. 9, path b)⁹³; compound 6 could be efficiently oxidized into N-((1E,4E)-4-((4-bromophenyl)imino)-cyclohexa-2,5-dien-1-ylidene)benzamide 117 in 82% yield employing iodobenzene diacetate as oxidant (Fig. 9, path c)⁹⁴; the benzoyl group of 6 could be readily removed by hydrazine hydrate to afford N-(4-bromophenyl)benzene-1,4-diamine 118⁹⁵, which could be further converted into 1-(3,5-bis(trifluorom-ethyl)phenyl)-3-(4-((4-bromophenyl)-amino)phenyl)thiourea 119 in 90% yield by the treatment with isothiocyanate (Fig. 9, path d and e)⁹⁶.

Fig. 8 Optical properties. [Images not available. See PDF.]

Absorption spectrum in DCM and emission spectra in various solvents for compound 33 (λ_ex = 350 nm).

Fig. 9 Grams-scale reaction and synthetic applications of the para-aminated products. [Images not available. See PDF.]

Reaction conditions: a Phenylboronic acid, Pd(OAc)₂, Xphos, K₃PO₄, THF, N₂, 55 ^oC, 12 h. b ^tBuONa, CH₃I, DMF, 4 h. c PhI(OAc)₂, MeOH, 0 ^oC, 5 min. d Hydrazine hydrate, 150 ^oC, 12 h. e Isothiocyanate, THF, 30 ^oC, 12 h. FSIT fluorosulfuryl imidazolium triflate.

In summary, we have developed a one-pot, metal-free, direct aromatic para-C-H amination and azidation of N-arylhydroxylamines, promoted by fluorosulfuryl imidazolium triflate (FSIT) under mild conditions. This cascade protocol exhibits excellent functional group tolerance, accommodating N-arylhydroxylamines with diverse functionalities and motifs relevant to natural products. A wide range of readily available nitrogen nucleophiles such as primary anilines, secondary amines, diphenylmethanimine and TMSN₃, could be successfully introduced at the para-position of the anilides with moderate to good yields and excellent chemo- and regioselectivity. DFT studies were also carried out to explain the excellent chemoselectivity in the presence of multiple nucleophilic and electrophilic species. Ongoing research in our laboratory aims to extend this method to other nucleophiles and explore its synthetic applications in the preparation of more complex bioactive molecules.

Methods

Method A

The system of a mixture of 1 (0.2 mmol, 1.0 equiv.), 2 (0.4 mmol, 2.0 equiv.), Na₂CO₃ (0.4 mmol, 2.0 equiv.) in 1,4-dioxane (1 ml) and MeCN (3 ml), FSIT (0.3 mmol, 1.5 equiv.) was added in one portion. The reaction mixture was stirred at -20 ^oC for 3 h until the complete consumption of 1, which was monitored by TLC analysis. The reaction mixture was evaporated under reduced pressure and purified by column chromatography to give the desired product 3-76.

Method B

The system of a mixture of 1 (0.2 mmol, 1.0 equiv.), 77 (2 mmol, 10.0 equiv.) and Na₂CO₃ (0.4 mmol, 2.0 equiv.) in 1,4-dioxane (1 ml) and MeCN (3 ml), FSIT (0.3 mmol, 1.5 equiv.) was added in one portion. The reaction mixture was stirred at -20 ^oC for 3 h until the complete consumption of 1, which was monitored by TLC analysis. Afterwards, the reaction mixture was concentrated in vacuo and the residue was purified by flash column chromatography to afford the target compound 78-89.

The ketimine 78-89 (0.2 mmol, 1.0 equiv.) was suspended in 1/1 (v/v) ratio of 1 N HCl:THF (5 ml) solution and stirred at 25 ^oC for 4 h. Upon consumption of the ketimine as determined by TLC, THF was removed and the aqueous residue was basified using 1 N KOH to a pH of 10–14. The aqueous layer was then extracted three times with ethyl acetate (30 ml). The organic layer was dried with anhydrous Na₂SO₄, filtered and concentrated in vacuo to give the crude amine. Upon purification via column chromatography, the pure product 90-101 was obtained after solvent removal.

Method C

To a solution of 1 (0.2 mmol, 1.0 equiv.), TMSN₃102 (0.6 mmol, 3.0 equiv.) and K₂CO₃ (0.4 mmol, 2.0 equiv.) in 1,4-dioxane (1 ml) and MeCN (3 ml), FSIT (0.2 mmol, 1.0 equiv.) was added every half an hour in one portion until FSIT was completely added. The reaction mixture was stirred violently at -20 ^oC under air atmosphere for 3 h until the complete consumption of 1, which was monitored by TLC analysis. Afterwards, the reaction mixture was concentrated in vacuo and the residue was purified by flash column chromatography to afford the title compound 103-114.

Acknowledgements

H.G. thanks the financial supports from the National Natural Science Foundation of China (22271176, 22471144), the Taishan Scholar Project of Shandong Province (tsqn202306015), Shandong University and Ningxia University. L.X. thanks the financial supports from the Taishan Scholar Project of Shandong Province (tsqn202312066), Shandong Provincial Natural Science Foundation Outstanding Youth Fund (ZR2024YQ016), Youth Innovation Team Program in Colleges and Universities of Shandong Province (2022KJ228) and Qilu Young Scholar Program of Shandong University.

Author contributions

H.G. conceived and directed the project. Y.B. designed and performed experiments. H.J. performed the density functional theory calculations and mechanistic analysis. W.X. helped with the collection of some new compounds and data analysis. H.G. and L.X. wrote the manuscript with input from all other authors. All authors discussed the results and commented on the manuscript.

Peer review

Peer review information

Nature Communications thanks Zhen Zhang and the other anonymous reviewer(s) for their contribution to the peer review of this work. A peer review file is available.

Data availability

The X-ray crystallographic coordinates for the products reported in this Article have been deposited at the Cambridge Crystallographic Data Centre (CCDC), under deposition nos. CCDC 2376503 (58) and CCDC 2392892 (81). Copies of the data can be obtained free of charge via https://www.ccdc.cam.ac.uk/structures/. Experimental procedures and characterization of new compounds are available in the Supplementary Information. Source data are provided with this paper. All data are available from the corresponding author upon request.  are provided with this paper.

Competing interests

The authors declare no competing interests.

Supplementary information

The online version contains supplementary material available at https://doi.org/10.1038/s41467-025-63534-8.

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