Synthesis of cocoa flavanol metabolites
Although the health benefits of cocoa flavanols have been well-established,2-10 the precise biological mechanisms that give rise to these effects are poorly understood. The major challenge associated with these studies results from the complex mixture of metabolites believed to be responsible for the biological activities. (-)-Epicatechin, the major constituent in cocoa is rapidly metabolized in vivo to give a wide variety of methylated, sulfated and glucuronidated products. Since each of these unique compounds, within a given class, have the same molecular weight, it is very difficult to determine which specific isomers are formed and how they exert their biological effects. As a critical first step towards solving this complex problem, analytical standards for each metabolite were needed.
A general synthetic strategy was envisioned where a series of late-stage orthogonally protected intermediates could be used to prepare all target compounds. As illustrated in Scheme 1, selectively protected acetophenone and benzaldehyde moieties would be coupled using an Aldol condensation. Reduction of the ketone followed by Sharpless dihydroxylation and cyclization would give the (-)-epicatechin core structure. Selective deprotection of this late-stage intermediate would allow introduction of the desired sulfate or glucuronide, then deprotection would give the desired product. By varying the specific protecting groups in the initial starting materials, the sulfate or glucuronide could be introduced at the desired position.
Scheme 1: general synthetic strategy for (-)-epicatechin metabolites
Successful implementation of this strategy resulted in the synthesis of all possible mono-glucuronides and mono-sulfates (10 each) of (-)-epicatechin, 3’-OMe and 4’-OMe-(-)-epicatechin. An example of the final method is illustrated in Scheme 2 with synthesis of (-)-epicatechin-5-sulfate ammonium salt. Here the trihydroxy acetophenone is selective protected with benzyl and methoxymethyl groups at the 4’ and 6’-positions respectively (4). Aldol condensation, followed by protection of the free hydroxyl, Luche reduction of the ketone and Sharpless dihydroxylation gives diol 9 with > 99% ee. Cyclization with triethylorthofomate and PPTS gives protected intermediate 10. Hydrolysis, followed by inversion of the hydroxyl group stereochemistry via Dess-Martin oxidation and reduction with Al(Oi-Pr)3 gives hydroxy intermediate 11. Treatment with BnBr and base and selective deprotection of the methoxymethyl ether gives key intermediate 12. Here either the sulfate or glucuronide can be conveniently introduced. Once complete, deprotection of the remaining benzyl groups give the desired product 14.
Scheme 2: Synthesis of (-)-Epicatechin-5-sulfate ammonium salt
Using this general strategy, the hydroxyl groups of 2,4,6-trihydroxy acetophenone and 3,4,-dihydroxybenzaldehyde are selectively protected as benzyl ethers or a methoxymethyl ether, then combined in an Aldol reaction. The Aldol product is converted to a late-stage intermediate over several steps (e.g. 12), where either a trichloroethylsulfonyl chloride or 2,3,4-tri-O-acetyl-1-O-(trichloroacetimidoyl)-α-D-glucuronate is coupled to the single free hydroxy group. Then a two-step deprotection give the target compounds.
With all twenty target compounds complete, analytical HPLC methods were developed to separate each of the sulfate and glucuronide products. Results from this work are being used to decipher the specific metabolic profile of (-)-epicatechin and understand the biological activities of each specific phase II metabolite.
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