Enantioselective synthesis of Iboga alkaloids and vinblastine via rearrangements of quaternary ammoniums

We present an efficient and unified strategy for the enantioselective syntheses of various iboga alkaloids and vinblastine, involving gold-catalyzed oxidation and Stevens rearrangement. New vinblastine analogs were prepared by our 10-step synthesis.


Introduction
The total synthesis of complex natural product small molecules invites the examination of various methodologies in a complicated system, which at times reveals current limitations and inspires new advances. 1 Importantly, total synthesis could also provide valuable analogs to explore the structure-activity relationships of targeted chemotypes. 2 We have been interested in using rearrangement reactions that lead to dramatic changes in molecular skeletons to develop novel and efficient synthetic routes towards various biologically active natural products. 3 Herein, we describe a concise and collective synthesis 4 of iboga alkaloids and vinblastine which further substantiates these concepts.
The iboga alkaloid family of natural products comprises over 60 members of monoterpene indoles that share a common pentacyclic skeleton of ibogamine ( Fig. 1). 5 Among the various neurological activities of ibogamine (1) and ibogaine (2), the most exciting one is their capability to attenuate the addiction to a number of drugs, although the molecular mechanism of action remains largely elusive. 6 Ibogaine, as the most abundant alkaloid in the root bark of the shrub Tabernanthe iboga, has even been studied in a clinical setting. 6 Interestingly, both enantiomers of ibogamine are not only active in reducing the self-administration of cocaine and morphine in rats but are also devoid of tremorigenic activity-a side effect exhibited by ibogaine, which hence deserves further investigation. 7 Catharanthine (3) and its derivative dihydrocatharanthine (4) have recently been identied as among the most potent TRPM8 antagonists and modulate cold-induced pain signals as well as mammalian thermoregulation. 8 More importantly, the conversion of catharanthine to the potent anti-cancer drug vinblastine (5) via a one-pot procedure has boosted the value of this iboga alkaloid, and its derivatives have led to vinblastine analogs revealing insightful structure-activity relationships. 9 Despite the variety of synthetic approaches towards different iboga alkaloids that have been reported, the enantioselective total syntheses remain relatively sparse. 10-13 Since Trost's group published the elegant synthesis of enantioenriched ibogamine in 1978, 11 the preparation of chiral isoquinuclidine fragments followed by the construction of a C2-C16 bond in the late stages (catharanthine numbering, throughout) has become the focus of asymmetric synthesis studies. 12 The only two exceptions are the efficient syntheses of (À)-ibogamine and (À)-catharanthine by White's group and Oguri's group respectively, both employing the asymmetric Diels-Alder reaction. 13 An alternative approach to prepare such a privileged skeleton, especially in an enantioselective manner, would be a valuable addition to current synthetic endeavours and more importantly, would enable exible structural changes of this chemotype.

Results and discussion
While seeking a unied strategy to access iboga alkaloids with and without the methoxycarbonyl group at C16, we envisioned two late-stage intermediates 6a and 6b (Fig. 2). The C20 carbonyl group of 6 could be a versatile handle for the preparation of bioactive natural products and small-molecule probes. Inspired by the transannular cyclization accomplished by Kutney and co-workers, 10b as well as recent advances in the fragmentation of the C16-C21 bond, 14 we decided to explore the [1,2]-Stevens rearrangement of ammonium ylide 7 to construct the C16-C21 bond and give the structurally compact product 6. 15 Given that zwitterion 7 could be generated from the quaternary ammonium cation 8 upon treatment with base due to the enhanced acidity at C21, 6 would therefore be accessible from 8 in one step. This key precursor 8 could be prepared by intramolecular alkylation of the tertiary amine 9, for which we hypothesized that the recently developed gold-catalyzed conversion of terminal alkynes to a-chloromethyl ketones could nd application. 16 Thus, the tertiary amine 10 became the precursor for 9, which could be traced back to the known amide 11 via propargylation and reduction. 17,18 We commenced our studies with the chiral amide 11a, which was prepared from tryptamine in 3 steps via the organocatalytic Pictet-Spengler reaction reported by Jacobsen's group (Scheme 1). 17 The introduction of the propargyl group was achieved with the protection of the nitrogen atom, and the following deprotection afforded a pair of readily separable diastereomers, where the desired stereoisomer 13a was isolated as the major product in 52% yield over 3 steps. The subsequent reduction of 13a by LiAlH 4 produced the tertiary amine 10a smoothly in 85% yield. We ultimately developed a one-pot procedure that converted 10a to the quaternary ammonium compound 8a in good yield (see the ESI † for the determination of the counteranion).
The extensive optimization of this gold-catalyzed reaction followed by intramolecular alkylation was carried out using racemic 10a (Table 1 and S1 †). The basicity of the tertiary amine 10a is detrimental to the cationic gold catalysis and needs to be neutralized with the addition of another equivalent of acid. 16b,19 Using a 10 mol% (Ph 3 P)AuNTf 2 catalyst and 2 equiv. of MsOH additive, we examined a variety of oxidants and identied 2-bromopyridine N-oxide 14 as the optimal one (Table S1 †  solution of sodium bicarbonate. The end product 8a was obtained in 47% yield with the recovery of 39% starting material 10a (Table 1, entry 1). Inspired by the screening of the acid additives to improve the conversion in similar transformations, 20 we discovered that complete consumption of 10a was achieved in 20 h at room temperature with 1.3 equiv. MsOH and 1.1 equiv. TFA as the acid additives to afford 8a in 63% isolated yield (entry 2). The addition of 3 mol% AgOTf signicantly accelerated the reaction, 21 which gave 8a in 69% yield on an even larger scale (200 mg scale, entry 3). We intentionally lowered the gold catalyst loading to 5 mol% for the gram scale reaction and found that the rst step went to completion in 8 h at room temperature but 8a was isolated in only 51% yield aer workup (entry 4). The conditions for the gram scale reaction were further improved by discovering that the addition of 1 equiv. AgOTf effectively promoted the cyclization step, which eventually afforded 8a in 74% isolated yield (entry 5).
With abundant 8a in hand, we proceeded to test the Stevens rearrangement. Initial efforts in base, solvent and temperature screening proved unfruitful, leading to either starting material recovery or decomposition (Table S2 †). Inspired by the development of organocatalytic sigmatropic reactions, 22 we shied our focus to exploiting a novel Stevens rearrangement through the intermediacy of an enamine. 23 By examining a variety of amines (Table S3 †), we identied that 5 equiv. of piperidine 16 could promote the desired transformation in methanol even if the isolated yield of 6a was only 11% aer heating at 170 C for 8 h in a sealed tube (Table 2, entry 1). 24 We therefore turned to microwave technology and found that it was more effective than conventional thermal conditions (entry 2). 25 Through a series of optimization procedures including the amount of 16 (entry 3), solvent (entry 4), concentration and heating sequence (entry 5), the iboga alkaloid framework 6a was eventually obtained from 8a in 50-60% isolated yield (over 90% yield based on starting material recovery). Furthermore, when N-methylmorpholine was employed in place of piperidine 16 under the optimized reaction conditions, we did not observe the formation of 6a and the starting material 8a was recovered in 88% yield, thus suggesting that the formal Stevens rearrangement was not base mediated. To the best of our knowledge, this transformation represents the rst example of Stevens rearrangement through secondary amine catalysis.
The stage was set for the late-stage functional group manipulations of 6a (Scheme 2). First, the addition of an organocerium reagent, prepared from ethylmagnesium bromide, to the ketone afforded 17 as a single diastereomer, effectively completing the formal synthesis of (+)-catharanthine (3). 10d,12c The Wittig reaction was then employed to convert 6a to olen 18, where the Z conguration of the trisubstituted olen was assigned by a NOESY experiment (see ESI † for details). Hydrogenation of alkene 18 using activated Pd/C as the catalyst afforded epiibogamine 19 in 97% yield. 26 The high stereoselectivity could be attributed to the preferential addition of H 2 to the less hindered side of the molecule. Therefore we turned to the radical-based hydrogenation of electron-neutral alkenes initiated by hydrogen atom transfer. 27 While manganese and cobalt-based catalyst precursors also produced 19 as the predominant product (Table S4 †), we were delighted to nd that Fe(acac) 3 , the precatalyst reported by Baran and co-workers for reductive alkene coupling, 28 afforded separable 19 and (+)-ibogamine 1 in 34% and 26% yields, respectively. The key intermediate 6a could be expediently decorated to other interesting derivatives with an iboga alkaloid skeleton. For instance, the reductive cyanation of ketone 6a with tosylmethylisocyanide produced a pair of separable diastereomers 20 and 21 in 25% and 54% yields, respectively. 29 The structures of racemic 19 and 20 were determined unambiguously by X-ray crystallography, 30 AgOTf was added as an additive. e 1 g scale reaction, 5% PPh 3 AuNTf 2 , 2% AgOTf as an additive. f 3 g scale reaction, 5% PPh 3 AuNTf 2 , 2% AgOTf as an additive, 1 equiv. AgOTf was added with NaHCO 3 (s, aq.) to facilitate the cyclization. while the analytical data of 1 and 17 corresponded well with that in the literature. 12a,c Encouraged by the completion of (+)-ibogamine (1), we moved towards the synthetic study of the iboga alkaloids with the methoxycarbonyl group at C16 (Scheme 3). The amide 13b was prepared from the known compound 11b with excellent enantiopurity 18 following the same procedures depicted in Scheme 1, while the undesired diastereomeric amide could also be converted to 13b readily (see ESI † for details). The selective reduction of the amide carbonyl group in 13b subsequently afforded the tertiary amine 10b. 31 We fortunately isolated a trace amount of the rearranged product 6b aer the work-up of the gold-catalyzed oxidation reaction of 10b, indicating that the [1,2]-shi was quite facile in the presence of the C16 methoxycarbonyl group. Therefore, the gold-catalyzed oxidation was followed by the addition of a saturated aqueous solution of sodium bicarbonate and excess triethylamine to promote the cyclization and rearrangement. Gratifyingly, this one-pot procedure afforded ketone 6b in 51% yield from 10b under mild reaction conditions. The Wittig reaction of 6b gave rise to 22a catharanthine isomer with an exocyclic versus endocyclic double bond. Hydrogenation of 22 afforded dihydrocatharanthine (4) in 79% yield. Interestingly, 22 differs from a known compound derived from catharanthine in the olen geometry. 32 Eventually, employing the conditions reported by Boger and coworkers, 32a we successfully made vinblastine (5) in 50% yield by coupling 22 with commercially available vindoline 23.

Conclusions
In summary, we have accomplished a unique and general route for the enantioselective synthesis of iboga alkaloids by developing a Stevens rearrangement through secondary amine catalysis and an oxidation/cyclization/rearrangement tandem sequence. The precise mechanism of the rearrangement remains to be investigated to identify whether a radical or an ionic intermediate is involved. Nonetheless, both reactions have the potential to be applied in the synthesis of a myriad of complex alkaloids. This study nicely exemplies the total synthesis of complex natural products serving as not only a driving force for advancing the synthetic methodology but also as an important source for providing analogs. Furthermore, this practical approach to modify iboga alkaloids and vinblastine paves the way for studies into their pronounced pharmacological properties using state-of-the-art chemical biology technologies, which are underway in our group and will be reported in due course.