Bi ( OTf ) 3-catalyzed three-component synthesis of α-amino acid derivatives †

α-Arylglycines are interesting and important non-proteinogenic amino acids. The α-arylglycine motif is found in many significant drugs and natural products including glycopeptide antibiotics (e.g. vancomycin and teicoplanins) and the widely used β-lactam antibiotics (e.g. norcardicins, amoxicillins and cephalecins) (Fig. 1). Arylglycines have been shown to selectively modulate the activity of metabotropic glutamate receptors, a promising new approach for the treatment of neurodegenerative disorders such as Parkinson’s disease. Due to this impressive range of biological activities, various methods for the synthesis of arylglycine derivatives have been developed during the last few decades. Reactions based on the addition of a carbon nucleophile to a reactive imineor iminium-species, such as the Strecker reaction, the Mannich reaction or the Petasis reaction, are widely used in industry and academia. Recently, we have developed an efficient iron-catalyzed three-component synthesis of arylglycines from simple starting materials (Scheme 1). Although this method provides an atom-economic and cost-effective route to arylglycines, it has some limitations. Sulfonamides or unhindered secondary amides do not react in the presence of an iron-catalyst and only reactions with at least moderately electron-rich aromatic components, such as m-xylene, provide the desired products in reasonable yields. The observed modest catalytic activity of the employed iron(III) salts can be rationalized by their moderate Lewis acidity. We anticipated that substitution of the iron-catalyst with a stronger Lewis acid should lead to a more general three-component reaction. In previous studies, we had already identified Bi(OTf)3 as a very effective catalyst for three-component amidoalkylation reactions. Since Bi(OTf)3 is commercially available for a reasonable price, nontoxic, airand moisture-stable, it is a very attractive catalyst. Indeed, Bi(OTf)3 could catalyze the reaction between benzamide, ethyl glyoxalate and m-xylene very efficiently even at low catalyst loadings (Table 1, entries 1–4). Other Bi salts or HOTf, a possible byproduct from the hydrolysis of Bi(OTf)3, displayed reduced catalytic activity. To exclude a possible Fig. 1 Arylglycine moieties in biologically active molecules. Scheme 1 Three-component synthesis of arylglycines.

α-Arylglycines are interesting and important non-proteinogenic amino acids.The α-arylglycine motif is found in many significant drugs and natural products including glycopeptide antibiotics (e.g.vancomycin and teicoplanins) and the widely used β-lactam antibiotics (e.g.norcardicins, amoxicillins and cephalecins) (Fig. 1). 1 Arylglycines have been shown to selectively modulate the activity of metabotropic glutamate receptors, a promising new approach for the treatment of neurodegenerative disorders such as Parkinson's disease. 2 Due to this impressive range of biological activities, various methods for the synthesis of arylglycine derivatives have been developed during the last few decades. 3,4Reactions based on the addition of a carbon nucleophile to a reactive imine-or iminium-species, 5,6 such as the Strecker reaction, 7 the Mannich reaction 8 or the Petasis reaction, 9 are widely used in industry and academia.Recently, we have developed an efficient iron-catalyzed three-component synthesis of arylglycines from simple starting materials (Scheme 1). 10 Although this method provides an atom-economic and cost-effective route to arylglycines, it has some limitations.Sulfonamides or unhindered secondary amides do not react in the presence of an iron-catalyst and only reactions with at least moderately electron-rich aromatic components, such as m-xylene, provide the desired products in reasonable yields.The observed modest catalytic activity of the employed iron(III) salts can be rationalized by their moderate Lewis acidity. 11We anticipated that substitution of the iron-catalyst with a stronger Lewis acid should lead to a more general three-component reaction.In previous studies, we had already identified Bi(OTf ) 3 as a very effective catalyst for three-component amidoalkylation reactions. 12][16][17] Indeed, Bi(OTf ) 3 could catalyze the reaction between benzamide, ethyl glyoxalate and m-xylene very efficiently even at low catalyst loadings (Table 1, entries 1-4).Other Bi 3+ salts or HOTf, a possible byproduct from the hydrolysis of Bi(OTf ) 3 , displayed reduced catalytic activity.To exclude a possible "hidden" catalysis 18 by in situ generated Brønsted acids, we performed the reaction in the presence of 2,6-di-tert-butylpyridine (dbpy), a selective proton scavenger. 19Since no decrease in catalytic activity was observed, we assume that a Bi 3+ -species is the active catalyst.In general, best yields were obtained in nitromethane as a solvent (entries 1-4 and 9).
With the optimized conditions established, the scope of the method was explored.As shown in Scheme 2, reactions with electron rich arenes such as mesitylene (3b), 4-bromophenol (3n) 20 or anisole (3c) and its derivatives (3d-j) furnished the desired products in good to excellent yields (4b-i, 4n).The high catalytic activity of Bi(OTf ) 3 allows reactions with less nucleophilic arenes, such as toluene or N-protected aniline derivatives ( products 4k-m). 21In most cases the regioselectivity of the reaction is good to excellent.Only in a few cases, for example with anisole (3c) or toluene (3k), a mixture of regioisomers was obtained.
The reaction of various primary aryl or alkyl amides with ethyl glyoxalate and mesitylene provided the desired products in good to excellent yields (see Scheme 3, 5a-f ).Even acid sensitive functionalities such as an acrylamide ( product 5c) were well tolerated.Using carbamates as the amide component, the corresponding N-protected arylglycines, useful building blocks for further transformations, were obtained in 86% and 65% yield (5g and 5h).Also, in the case of the amide component, the high catalytic activity of Bi(OTf ) 3 leads to a broader substrate scope and facilitates reactions with unhindered cyclic secondary amides or carbamates ( products 5i-j).Sterically more demanding acyclic secondary amides, such as 1j, or tert-butyl carbamate (1i) did not react under the standard conditions.‡ To our delight, also sulfonamides are suitable amide components (Scheme 4).Reactions with alkyl-as well as arylsulfonamides furnished the desired products in good to excellent yields (7a-e).
With heteroarenes as nucleophilic compounds, lower reaction temperatures were necessary to avoid direct addition of the heteroarene to the aldehyde (Scheme 5).In general, better results were obtained with urethane as the amide component and DCE as a solvent.Under these modified conditions, several heterocycles such as thiophenes (8a-c), N-tosylpyrrole (8d), N-tosylindole (8e) and benzofuran (8f ) could be utilized as the nucleophilic component.
This method is not limited to ethyl glyoxalate as the aldehyde component.Reaction with different glyoxalates, such as isopropyl or benzyl glyoxalate, furnished the desired amino  acid derivatives in 50-69% yield (Scheme 6, products 10b-c).This reaction is quite insensitive to air or moisture and therefore very simple to perform.Even an aqueous solution of glyoxylic acid could be used as an aldehyde source.In this case the free acid 10a could be obtained in 71% yield.
In order to expand the utility of this method, we investigated possible diastereoselective reactions with chiral amide components.To our surprise, reaction with the chiral oxazolidione 11 yielded the cyclic amino acid 12 as a single product, even if an excess of the nucleophilic arene component 3b was used (Scheme 7).This reactivity can be rationalized by an intramolecular addition of the phenyl group to the formed acyliminium species.Unfortunately, other chiral oxazolidiones, derived from valine or norephedrine, did not react under the standard conditions.
Therefore we examined reactions with chiral primary amides derived from amino acids.The three-component reaction with N-phthalyl-protected valinamide 13 afforded the desired dipeptide 14 in high yield and moderate diastereoselectivity (Scheme 8). 22Since both diastereomers can be separated by simple chromatography, this reaction could be used for an unusual synthesis of dipeptides.

Conclusions
In summary, we have developed an efficient Bi(OTf ) 3 -catalyzed three-component synthesis of α-amino acid derivatives from readily available starting materials.This practical and operationally simple approach has a very broad scope and water is generated as the only by-product.In addition, we have demonstrated that reactions with chiral amide components proceed with moderate diastereoselectivity.The scope of these diastereoselective reactions and further asymmetric transformation are currently being investigated in our laboratory and will be reported in due course.(Ludwigshafen) and Evonik Industries (Darmstadt) for the generous gift of chemicals.
Notes and references ‡ General procedure for reactions with ethyl glyoxalate: A 10 mL screw-cap vial was charged with Bi(OTf ) 3 (1-5 mol%), amide (1.0 equiv.), and nitromethane (2 mL mmol −1 amide).Ethyl glyoxalate (1.2 equiv.) in nitromethane (2 mL mmol −1 amide) and the aromatic compound (3.0-4.0 equiv.)were added under vigorous stirring.The mixture was heated to 60-100 °C and stirred at this temperature for 16 h.After cooling to room temperature, the reaction mixture was diluted with EtOAc and filtered through a short plug of Celite.The plug was rinsed with additional EtOAc.The combined filtrates were concentrated under reduced pressure.Purification of the crude residue by column chromatography (hexane-EtOAc) afforded the analytically pure product.

aScheme 2 Scheme 3
Scheme 2 Variation of arenes a .a Isolated yield of analytically pure product.b Reaction with 1 mol% Bi(OTf ) 3 .c Reaction with 2 mol% Bi(OTf ) 3 .d Reaction with 5 mol% Bi(OTf ) 3.e Obtained as a mixture of regioisomers; the ratio of regioisomers is given in parentheses.

Scheme 5 Scheme 6 Scheme 8 Scheme 7
Scheme 5 Variation of heteroarenes a .a Isolated yields of analytically pure products.b Reaction in nitromethane.cObtained as a mixture of regioisomers; the ratio of regioisomers is given in parentheses.

Table 1
Survey of catalysts a