Design and synthesis of a cyclitol-derived scaffold with axial pyridyl appendages and its encapsulation of the silver(I) cation

Conversion of a myo-inositol derivative into a scyllo-inositol-derived scaffold with C3v symmetry bearing three axial pyridyl appendages is presented. This pre-organized hexadentate ligand allows complexation of silver(I). The crystal structure of the complex was established.


Introduction
Despite its recognized potential for nuclear medicine applications [1], the β − emitter 111 Ag (t 1/2 = 7.47 d), which can be produced carrier-free and with high specific activity [2,3], has not yet found widespread uses [4,5].This is due in part to the lack of suitable Ag complexing agents and in this work the synthesis of an cyclitol-derived scaffold designed to sequester Ag is presented.Interaction of myo-inositol-derived podands [6] and crown ethers [7] with Ag salts has been shown to depend on the relative spatial orientation of the binding sites moreover, in mono-orthoesters of scyllo-inositol the three axial hydroxy groups can be used to link substituents in a pre-organized manner [8][9][10].Thus the introduction of pyridine groups (known to bind Ag(I) efficiently [11][12][13][14]) on a scyllo-inositol orthoester was considered, which led to the design of scaffold 1 (Figure 1).Indeed, upon complexation with participation of three oxygen atoms in the binding, no substantial rearrangement of this semi-rigid structure is to be expected.In addition, reductive cleavage of one of the ortho-ester C-H benzylic bonds, which is known to yield a free hydroxy group [15,16], would allow ligation of this scaffold.
Compounds 5 and 7 were also acetylated (to 8 and 9, respectively) and the chemical shift of the acetyl methyl group of 9 (δ = 1.7 ppm) displayed an upfield shift compared to that of 8 (δ = 2.1 ppm) due to ring-current effects from through-space interactions with the pyridyl groups.That a scyllo-inositol derivative had been obtained was confirmed after the introduction of the third pyridyl group (NaH, 2-picolyl chloride).In the resulting tri-picolyl derivative 1 (71%) a C 3v axis of symmetry is now present, which leads to simplification of NMR spectra.The structure of 1 was subsequently confirmed (see below) by X-ray diffraction of a single crystal of its Ag-complex.

Complexation
Incremental addition of silver(I) trifluoromethanesulfonate to a solution of 1 in 1:1 CD 3 OD/CDCl 3 was monitored by NMR.A single set of resonances was observed at all concentrations.That the pyridine rings and the "oxygenated cavity" were involved in silver binding was shown by the relevant shifts in both the 1 Hand 13 C-NMR spectra (see Supporting Information File 1).However, in the absence of characteristic signals for Ag(I)complex (even at low temperature: −50 °C) NMR methods cannot be used for the determination of the complex stability constant.The electrospray mass spectrum (from the solution contained in the NMR tube) revealed a 1:1 complex, with the expected 107 Ag/ 109 Ag isotopic ratio.The stability constant of the complex could be determined by spectrophotometric titration, which was carried out in 1:1 aqueous methanol (the complex is not water soluble) and its value (log K 1•Ag = 3.8 ± 0.2) is in agreement with that of a previously described Ag(I) complex in a N 3 O 3 environment [13].
Study of the molecular structure of the complex was made possible as a single crystal could be grown by slow evaporation of a methanol/ethanol solution of stoichiometric amounts of 1 and silver trifluoromethanesulfonate. The complex crystallises in the triclinic system, with a pseudo-ternary axis of symmetry.Its coordination sphere involves all 3 nitrogen atoms as well as the 3 oxygen atoms which are implied in the linkage of the pyridines (Figure 3).Bond distances and angles (see Supporting Information File 1) are in accord with those of known silver complexes which are hexa-coordinated with pyridyl groups and oxygen atoms [13,14].

Conclusion
A rigid scaffold with C 3v symmetry bearing three appendages in a pre-organized manner, 1, could be synthesized in 6 steps from myo-inositol orthobenzoate and in 25% overall yield.Noteworthy is that the synthetic scheme may allow variation of heterocyclic substituents, which need not be the same since they are introduced at different stages of the synthesis.The complex formed with silver cation (log K 1•Ag = 3.8 ± 0.2) was shown to involve N 3 O 3 coordination with the Ag(I) ion lying within the cage.However, the complex is not water soluble (which precludes its use for biomedical applications) although the grafting of hydrophilic appendages to aromatic residues could increase its hydrophilicity.

Figure 3 :
Figure 3: ORTEP drawing for the 1•Ag(I) cation complex (ellipsoids are drawn at the 50% probability level and H atoms are omitted for clarity).