Enantioselective synthesis of anti-3-alkenyl-2-amido-3-hydroxy esters: application to the total synthesis of (+)-alexine

Abstract

A straightforward synthesis of anti-3-alkenyl-2-amido-3-hydroxy esters from the corresponding racemic α-amino-β-keto esters by using a ATH/DKR protocol has been developed. This method gives moderate to excellent yields with high chemo-, diastereo- and enantioselectivities for a broad range of substrates. In order to highlight the versatility of the methodology it was applied in an efficient asymmetric synthesis of the polyhydroxylated pyrrolizidine alkaloid (+)-alexine.

A straightforward synthesis of anti-3-alkenyl-2-amido-3-hydroxy esters from the corresponding racemic α-amino-β-keto esters by using a ATH/DKR protocol has been developed.

β-Hydroxy-α-amino esters and their derivatives are important structural motif in a number of biologically relevant compounds.¹ As a consequence, several elegant methods have been developed for the stereoselective² and asymmetric³ synthesis of such compounds. We speculated that the versatility of this scaffold could be expanded by the incorporation of a vinyl moiety in 3-position (e.g.2, Scheme 1), thus allowing for additional stereoselective manipulation. For example, stereoselective epoxidation⁴ or dihydroxylation⁵ of the carbon–carbon double bond in compound 2, or cross metathesis, could furnish advanced such intermediates for the synthesis of polyhydroxylated alkaloids (Scheme 1), compounds with diverse biological activities.⁶ Compound 2, in turn, was excepted to be derived through a chemoselective asymmetric transfer hydrogenation (ATH) of α-amido-β-keto ester 1. Herein we detail our efforts towards realizing this methodology and its application to the synthesis of (+)-alexine (3).

Scheme 1. Proposed route from α-amido- β-keto ester 1 to polyhydroxylated pyrrolizidine and indolizidine alkaloids.

ATH coupled with a dynamic kinetic resolution (DKR) of configurationally labile α-amido-β-keto ester has been proven to be a powerful method for the synthesis of syn- or anti β-hydroxy-α-amino esters.⁷ In such transformation two contiguous stereocenters can be constructed in high er and dr in a single operation from a racemic starting material. We have previously developed a ATH process coupled with DKR for preparation aryl, alkyl or heterocyclic anti-β-hydroxy-α-amido ester in organic solvents, emulsions or water system.⁸ For the present investigation it was of interest to expand the substrate scope to encompass substrates having an vinylic group in 3-position, e.g. compound 1, and to investigate the possibility of developing a chemoselective 1,2-reduction of the carbonyl group in preference of a 1,4-reduction of the enone moiety.

The investigation was initiated by examining the ATH of ester 1a using our previously optimized conditions ([RuCl₂(benzene)]₂/(S,S)-BnDPAE), yielding a mixture of the desired anti-amino alcohol 2a, having low dr and er, and the over-reduced compound 4 in poor selectivity (Table 1, entry 1). Subjecting 2a to the reactions conditions did not afford 4 and it is believed that the latter compound is formed by an initial 1,4-reduction of the enone moiety in 1a followed by a 1,2-reduction of the resultant carbonyl group. Screening of different ligands gave 2a with increased diastereoselectivity, but in all cases the chemoselectivity remained low (entries 2–4). It was noted, however, that the use of (S,S)-DPAE resulted in the formation of 2a in high enantiomeric excess (er 95 : 5, entry 4). It was then decided to explore different ruthenium dimer catalysts together with the (S,S)-DPAE ligand (entries 5–7). The use of ruthenium(ii) dichloride dimer catalyst incorporating a substituted arene moiety resulted in an improved chemoselectivity with only traces of the over reduced compound 4 being observed, the best result being obtained with [RuCl₂(mesitylene)]₂ (entry 6). Encouraged by this result, other reaction parameters (solvent and catalyst loading) were screened in order to improve the reaction outcome. Performing the reaction in MeOH or CH₃CN did not improve the outcome (entries 8–9), while the use of dioxane or CHCl₃ afforded similar results in terms of yields and stereoselectivities as CH₂Cl₂ (entries 8–11). Since the reaction run in dioxane gave the best result this solvent was selected for the final screening of catalyst loading (entries 12–14). It was observed that similar yields but with improved diastereoselectivity could be achieved when lowering the amount of catalyst from 20 mol% to 5 mol%. The best result, 72% yield of 2a with 95 : 5 dr and 96.5 : 3.5 er, was obtained when using 2.5 mol% of [RuCl₂(mesitylene)]₂ and 5 mol% (S,S)-DPAE (entry 14).

Optimization of the ATH Reaction of 1a^a.

Entry	Ru dimer	Ligand	Solvent	1a/2a/4 (%)b	dr (anti : syn)c	er (anti)d
1	Benzene	L1	CH2Cl2	5/50/20	55 : 45	88.5 : 11.5
2	Benzene	L2	CH2Cl2	21/41/16	89 : 11	7 : 93
3	Benzene	L3	CH2Cl2	35/15/5	87 : 13	12.5 : 87.5
4	Benzene	L4	CH2Cl2	<5/52/20	80 : 20	95 : 5
5	p-Cymene	L4	CH2Cl2	33/47/<5	85 : 15	90.5 : 9.5
6	Mesitylene	L4	CH2Cl2	20/65/<5	91.5 : 8.5	93 : 7
7	Hexamethylbenzene	L4	CH2Cl2	34/28/<5	83 : 17	58 : 42
8	Mesitylene	L4	MeOH	49/24/<5	86 : 14	89.5 : 10.5
9	Mesitylene	L4	CH3CN	26/37/<5	85 : 15	85 : 15
10	Mesitylene	L4	Dioxane	8/68/<5	93 : 7	95.5 : 4.5
11	Mesitylene	L4	CHCl3	13/57/<5	94.5 : 5.5	96 : 4
12e	Mesitylene	L4	Dioxane	11/68/<5	93 : 7	96 : 4
13f	Mesitylene	L4	Dioxane	15/60/<5	94 : 6	96 : 4
14g	Mesitylene	L4	Dioxane	12/72/<5	95 : 5	96.5 : 3.5

^aReactions preformed with [RuCl₂(arene)]₂ (0.1 eq.) and ligand (0.2 eq.) heated in 2-propanol (0.3 mL) at 80 °C for 1 h. After cooling to room temperature, the catalyst was then added to a solution of 1a (0.2 mmol, 1 eq.) and HCO₂H/Et₃N (1.5 : 3, 1.5 eq.) in solvent (1 mL).

^bIsolated yields.

^cDetermined by NMR analysis of the crude reaction mixture.

^dDetermined by chiral HPLC.

^eReaction run with 0.075 eq. of [RuCl₂(mesitylene)]₂ and 0.15 eq. of (S,S)-DPAE.

^fReaction run with 0.05 eq. of [RuCl₂(mesitylene)]₂ and 0.1 eq. of (S,S)-DPAE.

^gReaction run with 0.025 eq. of [RuCl₂(mesitylene)]₂ and 0.05 eq. of (S,S)-DPAE.

Next the scope of the ATH reaction was investigated by screening a variety of γ-alkenyl-β-keto-α-amido esters 1 and the results are summarized in Table 2. The influence of the ester moiety in the substrate was negligible as compounds 1a–d all gave the corresponding aminoalcohols 2a–d, respectively, in good yields and high selectivities. However, the choice of N-protecting group influenced the reaction outcome, with N-acetyl and N-benzoate protected substrates 1f and 1g furnishing the corresponding products in lower yields and selectivities compared to 1a, while N-Boc protected 1e performed equally well as 1a. The ATH reaction proved to be sensitive to the substitution at the olefin moiety with substrate 1h, having a disubstituted alkene, giving mostly over-reduced products derived from both 1,4- and 1,2-reductions and only minor amounts of 2h. Substrate 1i and 1j, having a trisubstituted and 1,1-disubstituted olefin moiety, respectively, performed well in the ATH reaction and deliver the corresponding products in good yields, dr and er. Similarly, substrates 1k–m, having a conjugated olefin moiety, all performed well in the reduction, while alkynyl 1n was unreactive under these conditions and 1o gave a complicated mixture of products.

Exploration of substrates scope^a,b,c,d.

^aReaction preformed with [RuCl₂(mesitylene)]₂ (0.025 eq.) and (S,S)-DPAE (0.05 eq.) heated in 2-propanol (0.3 mL) at 80 °C for 1 h. After cooling to room temperature, the catalyst was then added to the β-keto ester 1 (0.2 mmol, 1 eq.) and HCO₂H/EtN₃ (1.5 : 3, 1.5 eq.) in dioxane (1 mL).

^bIsolated yields.

^cdr determined by ¹H NMR analysis of the crude reaction mixture.

^der determined by chiral HPLC.

^eIsolated yields based on recovered start material.

^fNo reaction.

^gThe reaction gave a complicated mixture of product.

To demonstrate the applicability of the developed methodology it was decided to apply it to the total synthesis of the polyhydroxylated pyrrolizidine alkaloid (+)-alexine.⁹ Previous syntheses of this natural product has relied on carbohydrate derived strategies and relatively high steps strategies, while the present approach relies on an efficient and non-carbohydrate entry into this class of compounds. Our retrosynthetic analysis is summarized in Scheme 2 and relies on the known cyclization of amino epoxides 10 into (+)-alexine.¹⁰ Compound 10, in turn is derived from alkene 8, which can be derived from 2b using standard transformations (Scheme 2).

Scheme 2. Retrosynthetic analysis of (+)-alexine.

Subjecting ester 1b (4 g) to the ATH reaction, using the optimized conditions, furnished anti-α-amido-β-hydroxy ester 2b (87% brsm) in high diastereo- and enantioselectivity (anti/syn 96 : 4, er 97 : 3), which also indicate that the ATH/DKR protocol is scalable. Reduction of 2b with NaBH₄, followed by protection of the resulting 1,3-diol as the bis-BOM ether provided 5 (78%, two steps). Ozonolysis of this material followed by a chelation controlled addition of vinylmagnesium bromide afforded compound 7 (58%, dr 75 : 25).¹¹ Attempts to improve the dr of this step involved screening different solvents, Lewis acids, temperatures and hydroxyl protecting groups, but did not improve the situation.¹² The cross metathesis reaction of mixture 7 with 4-butenol p-tolyl-sulfonate in the presence of Grubbs' 2nd generation catalyst provided the trans olefin (64% brsm). After the deprotection of benzyloxymethyl group, an undesired diastereomer of compound 8 could be separated by column chromatography, and compound 8 was obtained (67%, dr > 95 : 5) as a pure form. Next the stage was set for the neighbouring group directed epoxidation of 8, which was accomplished using Ti(OiPr)₄ and β-hydroperoxy alcohol 9, yielding anti epoxide 10 (78%) as the only detectable isomer.¹³ Deprotection of 10 (Pd/C, H₂, MeOH) followed by purification on silica gel afforded (+)-alexine (3) in 76% yield as a white solid. The ¹H-NMR, ¹³C-NMR data, melting point and the optical rotation (mp 160–162 °C, [α]²⁰_D = +42.1 (c 0.3H₂O)) were in good agreement with the published data for (+)-alexine⁹ (mp 162–163 °C, [α]²⁰_D = +40 (c 0.25 in H₂O)) (Scheme 3).

Scheme 3. Total synthesis of (+)-alexine.

In summary, we have developed an operationally straightforward synthesis of anti-3-alkenyl-2-amido-3-hydroxy esters from the corresponding racemic α-amino-β-keto esters by using a ATH/DKR protocol. This method gives moderate to excellent yields, diastereoselective and enantioselectivities for a broad range of substrates. In order to highlight the versatility of the methodology it was applied in an asymmetric synthesis of the polyhydroxylated pyrrolizidine alkaloid (+)-alexine (3, 8 steps and 11.5% overall yield from 2b).

Conflicts of interest

There are no conflicts to declare.