Total synthesis of sulfolipid-1 †

Sulfolipid-1, a tetra-acylated sulfotrehalose from Mycobacterium tuber-culosi s, was isolated over 40 years ago. Being a main component of the mycomembrane of M. tuberculosis , its biosynthesis and function have been studied in depth

Sulfolipid-1, a tetra-acylated sulfotrehalose from Mycobacterium tuberculosis, was isolated over 40 years ago.Being a main component of the mycomembrane of M. tuberculosis, its biosynthesis and function have been studied in depth, but the chemical synthesis of sulfolipid-1 has not been reported.The synthesis presented here is based on iterative catalytic asymmetric conjugate additions of methylmagnesium bromide for the preparation of the phthioceranic and hydroxyphthioceranic acid side chains, a double regioselective reductive ring-opening and a fivefold deprotection in the final step.
Mycobacterium tuberculosis (M.tuberculosis), isolated by Koch 130 years ago, is at present still the cause of the most widespread bacterial infectious disease. 1 Much of the molecular research on M. tuberculosis, considerably stimulated by the sequencing of the bacterial genome, has focused on the composition and biosynthesis of its unusual waxy cell envelope. 2The outer membrane of the cell envelope, the mycomembrane, is composed of long-tailed (glyco) lipids and, as a consequence, this hydrophobic layer functions as a very efficient barrier for antibiotics. 3 number of these mycomembrane glycolipids are known to modulate the immune response of the host, and several specific glycolipids act as ligands for the CD1 immune system. 4One of the most prominent and most complex glycolipids present is sulfolipid-1 (1), a 2,3,6,6 0 -tetraacyl-a,a-trehalose 2 0 -sulfate, decorated with phthioceranic, hydroxyphthioceranic, and palmitic acid residues (Fig. 1).Remarkably, 1 is only present in pathogenic mycobacteria but its function remains largely unknown.Sulfolipid-1 was isolated, and its structure elucidated using scrupulous degradation studies, by Goren more than 40 years ago. 5Recently, Gilleron et al. showed, using mass spectrometry and 2D-NMR spectroscopy, that the composition, abundance, and position of the fatty acids on the trehalose core of 1 varies per strain. 6The role of 1 in the pathogenicity of M. tuberculosis has not been demonstrated and in addition could be species specific, a phenomenon not uncommon in mycobacterial infections. 7Studies with knockout mutants, unable to produce the negatively charged 1, indicate that 1 has a role in host-pathogen interactions by mediating between a cationic human antimicrobial peptide and the bacterium. 8n a series of studies, the group of Bertozzi has unraveled the biosynthesis of 1, that starts with the sulfation of trehalose. 9n addition, its membrane transport is a topic of interest. 9 comprehensive view on the biosynthesis and role of trehalosecontaining lipids in mycobacteria is expected to originate from a bioorthogonal chemistry approach. 10As far as synthetic precursors and model compounds have been involved in these studies, the multimethyl-branched phthioceranic acid residues were replaced by mono-or disubstituted analogues for synthetic reasons. 11lso the hydroxy group in hydroxyphthioceranic acid was omitted; in addition its stereochemistry was unknown.Stratingh Institute for Chemistry, University of Groningen, Nijenborgh 7, NL-9747 AG Groningen, The Netherlands.E-mail: a.j.minnaard@rug.nl† Electronic supplementary information (ESI) available: Experimental procedures, spectral data, and a HRMS-spectrum of synthetic Recently, we reported the first total synthesis of Ac 2 SulfoGlycoLipid (Ac 2 SGL, 2), a biosynthetic precursor of 1. 12,13 Ac 2 SGL is a potent antigen in M. tuberculosis-infected humans, specifically recognized by antigen presenting cells expressing CD1b.This points to the potential use of (analogues of) Ac 2 SGL in a TB vaccine. 14In these studies the stereochemistry of the hydroxy group in hydroxyphthioceranic acid was also established.Although still challenging, with the experience gained in the synthesis of Ac 2 SGL, a total synthesis of 1 has come within reach.This would potentially assist in the research on M. tuberculosis and in addition serve as an illustration of the power of asymmetric catalysis in the synthesis of complex deoxypropionates. 15ey to the successful synthesis of 1 is the regioselective esterification and sulfation of trehalose, with minimal loss of the precious phthioceranic acids 3 and 4 (Fig. 2).Commencing with intermediate 6, 16 prepared from trehalose in three steps, esterification with 3 (Scheme 1), followed by regioselective reductive ring-opening of the benzylidene acetals, should produce 8 with the 6-and 6 0 -OH liberated.Subsequent esterification of both 6-positions with 5 should provide 9, which upon desilylation, regioselective sulfation and overall deprotection would afford 1.
In the synthesis of Ac 2 SGL, the preparation of 3 and 5 had already been combined, thereby minimizing the total number of reactions and purification steps. 12To study the reductive ring-opening of the benzylidene acetals in 7, a less precious substrate carrying (S)-methylbutyric acid was prepared. 17Whereas a combination of borane and CoCl 2 , contrary to literature reports, gave no conversion, 18 its combination with Cu(OTf) 2 19 and TMSOTf 20 afforded 10, albeit in low yield.The main side product in these reactions was the fully deprotected 4,6-4 0 ,6 0 -tetraol. 21Increasing the amount of BH 3 ÁTHF to 12 eq. in combination with TMSOTf gave the product in a satisfactory 59% yield.Also the regioselectivity affording the free 6-and 6 0 -OH was excellent using this approach.A successive double esterification of 10 with (S)-methylbutyric acid under Yamaguchi conditions, however, gave mainly a disappointing mixture of 6-and 6 0 -monoacylated products.The desired diacylated 11 could, on the other hand, be obtained in very good yield using an EDC-promoted esterification (Scheme 2).Straightforward removal of the bis(diisopropylsilyl) ether with buffered TBAF, followed by regioselective introduction of a 2,2,2-trichloroethyl-protected sulfate at the 2-OH, 22 and removal of all protecting groups under hydrogenolysis conditions, led to the corresponding analogue of 1 (see ESI, † compounds 15-17).
In order to synthesize 1, 6 was efficiently acylated with 3 at the 3-position, by Yamaguchi esterification, to afford 7 (Scheme 3).Applying the optimized conditions for regioselective reductive ring-opening with TMSOTf and BH 3 ÁTHF, 8 was obtained in 59% yield, similar to the model substrate.EDC-promoted double esterification of 8 using the previously prepared benzyl ether-protected 5 initially proved rather sluggish.Addition of an excess of EDC (8 eq.) and DMAP (8 eq.) was required to obtain complete conversion of the starting material.This diminished reactivity of long-chain fatty acids has been reported before. 23Despite the formation of 10% of the tri-acyl product, tetraacyl 9 was obtained in 71% yield.Deprotection of the bis(diisopropylsilyl) ether under buffered conditions proved to be facile affording the 2 0 ,3 0 -diol 12 in 84% yield.Subsequent introduction of the 2,2,2-trichloroethyl protected sulfate at the 2 0 -OH using 13 turned out to be not completely regioselective. 22In the synthesis of Ac 2 SGL, only introduction of the TCE-sulfate at the 2 0 -OH and minor amounts of difunctionalization was observed.In the current case, also trace amounts of, assumed, 3 0 -OH sulfated products were obtained.This can be subscribed to the diminished rigidity of the substrate as a consequence of the previously effected benzylidene ring-opening.Nevertheless, pure 14 was isolated in 58% yield.To circumvent the purification of highly polar and charged intermediates, we envisioned, as our final step, the complete removal of all protecting groups using hydrogenolysis.Previously, the fivefold deprotection of our model system had shown to be straightforward.With a combination of ammonium formate, Pd(OH) 2 /C and hydrogen at atmospheric pressure, the benzyl groups on both the 4-and 4 0 -OH, the benzyl group in the side chain and the TCE group were removed. 12In 14, however, the benzyl groups on the 4-and 4 0 -OH were not removed under these conditions.While 15 bar of hydrogen pressure did not lead to full deprotection, prolonged hydrogenolysis at 30 bar hydrogen finally led to 1 in a low, but delivering 15% yield.The low yield is a result of the multiple attempts to remove all protecting groups causing desulfation of the variety of intermediates and the product.Indeed, also a small amount of the desulfated product was isolated. 16An explanation given earlier, 23b to account for the reluctant hydrogenolysis, is most likely the steric hindrance caused by the long-tailed lipids that prevents the approach of the heterogeneous Pd-catalyst.Although natural 1 is isolated as a mixture of homologues, the 1 H-NMR spectrum of synthetic 1 is similar to the one reported for natural 1 (Fig. S1, ESI †).Sulfolipid-1 turned out unstable in CDCl 3 solution (most probably desulfation takes place), 5a accounting for the minor differences.High resolution mass analysis (ESI) confirmed the formation of the desired product.
In summary, forty years after its first isolation as a main component of the mycomembrane of Mycobacterium tuberculosis, sulfolipid-1 has been synthesized and its structure confirmed.The availability of synthetic 1 and its precursors will accommodate research on its biosynthesis and function.Key steps in the synthesis are the preparation of hydroxyphthioceranic acid, the regioselective reductive ringopening of the benzylidene acetals and a final fivefold deprotection.