Synthesis of Organometallic Oligonucleotides through Oximation with Metalated Benzaldehydes.

A phthaloyl-protected aminooxymethyl-C-2'-deoxyriboside building block has been prepared and incorporated in the middle of an oligodeoxyribonucleotide. Removal of the phthaloyl protection followed by on-support oximation with either mercurated or palladated benzaldehydes yielded oligonucleotides bearing the respective benzaldoxime metallacycles.

Introduction

Oligonucleotides functionalized with transition metal ions are studied intensively for potential applications in DNA nanotechnology[1−4] as well as diagnostics and chemotherapy.[5−8] Such structures are typically obtained through coordination of the desired metal ion to a high-affinity ligand within the oligonucleotide. We, on the other hand, have recently become interested in an alternative approach in which the metal ion is held in place by an organometallic bond formed by postsynthetic metalation of an oligonucleotide, incorporating an appropriate “hot spot” in a solution.[9] The main advantage of this strategy is that the organometallic complex resists dissociation even at extreme dilution, widening the scope of metal ions usable in intracellular applications from the kinetically inert Pt(II) and Ru(II) to more labile ones, such as Pd(II) and Hg(II). For example, the high thermodynamic stability of kinetically labile metal-mediated base pairs[2,3] could be harnessed to promote hybridization of therapeutic oligonucleotides with their target sequences.[10] A notable disadvantage is that the formation of carbon–metal bonds often requires conditions hardly compatible with the solubility or chemical stability of oligonucleotides. Even when the metalation is achieved under sufficiently mild conditions, the removal of excess free transition metal ions from the product mixture can present a problem.

Herein, we describe the synthesis of a modified oligonucleotide containing an aminooxymethyl-functionalized residue for the introduction of diverse organometallic complexes through oxime coupling on a solid support. A deoxyribose scaffold bearing the aminooxymethyl function on its β face was chosen so that the resulting benzaldoxime metallacycles would resemble natural nucleosides, allowing high-affinity metal-mediated base pairing with a complementary oligonucleotide. For the same reason, the sequences flanking the metallacyclic residue were the same as in our previous studies on metal-mediated base pairing.[11,12] The method described effectively removes the limitations on the reaction conditions used in the preparation of the organometallic complex. Furthermore, the use of oximation for the introduction of conjugate groups to oligonucleotides is well established[13] and should proceed predictably, exhibiting little dependence on the structure of the organometallic complex. Finally, any excess reagent is conveniently removed by washing the solid support with appropriate solvents. The utility of the method has been demonstrated with one arylmercury(II) compound and one arylpalladium(II) compound.

Results and Discussion

Synthesis of the phthaloyl-protected aminooxy sugar 1 and the corresponding phosphoramidite building block 2 is described in Scheme . First, lactone 3 was transformed to the corresponding lactol 4 by treatment with DIBAL-H, as described previously.[14] The reaction with vinyl magnesium bromide then provided compound 5 as a mixture of two diastereomers ((5R)-5 and (5S)-5). Chromatographic separation of the desired diastereomer (5S)-5 followed by mesyl chloride-promoted ring closure afforded the β-vinyl C-glycoside 6. Synthesis of an analogous compound with tert-butyldiphenylsilyl, rather than tert-butyldimethylsilyl, protections by the same pathway has been described in the literature.[15] The desired β-stereochemistry was confirmed by a 1D NOESY experiment, where irradiation of the anomeric proton (H1) at 4.58 ppm lead to a single positive NOE enhancement at 4.35 ppm, corresponding to H4 (Figure S1, spectra presented in the Supporting Information).

Scheme 1

Synthesis of Aminooxy Sugar 1 and the Corresponding Phosphoramidite Building Block 2

Reagents and conditions: (a) DIBAL-H, THF, −78 °C, 1 h; (b) C2H3MgBr, THF, 0 °C, 4 h; (c) MsCl, pyridine, CH2Cl2, −25 °C, 12 h; (d) (i) RuCl3, NaIO4, CeCl3, MeCN, EtOAc, H2O, 25 °C, 10 min; (ii) NaIO4, THF, H2O, Et2O, 25 °C, 90 min; (e) NaBH4, EtOH, Et2O, 25 °C, 3 h; (f) MsCl, pyridine, CH2Cl2, 25 °C, 3 h; (g) Et3N·3HF, THF, 25 °C, 16 h; (h) HONPhth, DIPEA, DMF, 70 °C, 30 h; (i) DMTrCl, pyridine, 25 °C, 12 h; and (j) 2-cyanoethyl-N,N-diisopropylchlorophosphoramidite, Et3N, CH2Cl2, N2 atmosphere, 25 °C, 2 h.

RuO4 (generated in situ from RuCl3)-catalyzed dihydroxylation of the vinyl group to a vicinal diol[16] followed by oxidative cleavage with NaIO4 gave the formyl C-glycoside 7 in excellent yield. Based on 1H and 13C NMR spectra, the product was identical to the authentic compound reported previously,[17] further confirming the stereochemical assignment of the two diastereomers of compound 5. Aldehyde 7 was then reduced to the corresponding alcohol 8 by treatment with NaBH4, and the newly created hydroxy function was mesylated to give compound 9. The hydroxy functions at positions 4 and 6, in turn, were desilylated by treatment with Et3N·3HF to yield intermediate 10, which was further converted to the phthaloyl-protected aminooxy sugar 1 by nucleophilic displacement of the mesylate leaving group with an N-hydroxyphthalimide anion. It is worth pointing out that attempts to introduce the phthaloyl-protected aminooxy group to intermediate 8 by the Mitsunobu reaction failed, even though various reagent combinations were used. Similarly, the reaction between the protected mesylate 9 and N-hydroxyphthalimide afforded only traces of the desired product, the main product being a monodesilylated mesylate. Finally, the primary hydroxy group was protected as a 4,4′-dimethoxytrityl ether to give compound 11, and the secondary one was phosphitylated with 2-cyanoethyl-N,N-diisopropylchlorophosphoramidite to give the protected phosphoramidite building block 2.

To demonstrate functionalization with organometallic complexes, an oligonucleotide incorporating a single phthaloyl-protected aminooxy sugar in the middle of the chain was first assembled on an automated DNA synthesizer by the standard phosphoramidite protocol using an extended coupling time (600 s) for incorporation of the phosphoramidite building block 2. Normal (>99%) coupling yields were obtained throughout the synthesis. Selective removal of the phthaloyl protection was achieved by treatment with a mixture of hydrazine hydrate, pyridine, and acetic acid, as described previously (Scheme ).[18] Immediately after liberation of the aminooxy function, the support-bound oligonucleotide was immersed in a solution of either acetato(2-formyl-6-hydroxyphenyl)mercury (12) in DMSO or bromo(2-formylphenyl)bis(triphenylphosphine)palladium (13) in CH2Cl2. These organometallic complexes were prepared as described previously.[19,20] The mixtures were shaken for 12 h at 25 °C, after which the solid supports were washed with appropriate solvents, and the oligonucleotide products were deprotected and released by treatment with a mixture of aqueous MeNH2 and NH3 at 65 °C. A short treatment of only 10 min was used to avoid demetalation of the organomercury or organopalladium residue. Finally, the modified oligonucleotides ON1-Hg and ON1-Pd thus obtained were purified by RP-HPLC and characterized by ESI-TOF-MS.

Scheme 2

Synthesis of the Organomercury and Organopalladium Oligonucleotides ON1-Hg and ON1-Pd

Reagents and conditions: (a) H2NNH2, AcOH, pyridine, 25 °C, 45 min; (b) 12, DMSO, 25 °C, 12 h; (c) 13, CH2Cl2, 25 °C, 12 h; and (d) MeNH2, NH3, H2O, 65 °C, 10 min.

The mass spectra of ON1-Hg and ON1-Pd corresponded to the expected structures, showing incorporation of exactly one Hg(II) ion and one Pd(II) ion, respectively. On the other hand, no exchangeable ligands of the metal centers could be detected. In ON1-Pd, the oxime nitrogen probably occupies one coordination site. While oxime coupling can yield both E and Z isomers of the C=N bond, ortho-palladated benzaldoximes have invariably been reported as palladacycles with the oxygen and the phenyl carbon trans to each other and the nitrogen coordinated to palladium.[21−23] Hg(II) tends to form linear complexes, but weak N–Hg bonds in organomercury complexes similar to the one in ON1-Hg have nonetheless been proposed based on X-ray crystallographic evidence.[24] Possible candidates for the remaining ligands (one in ON1-Hg and two in ON1-Pd) include methylamine and ammonia used for deprotection of the oligonucleotides as well as the HPLC buffer components triethylamine and acetate ion. With ON1-Pd, the presence of a triphenylphosphine ligand was ruled out by 31P NMR (spectrum presented in the Supporting Information).

Conclusions

In summary, we have developed a method for the preparation of covalently metalated oligonucleotides through oxime coupling between aminooxy-functionalized oligonucleotides and organometallic benzaldehyde derivatives. The scope of the method has been demonstrated with Hg(II) and Pd(II) but, in all likelihood, can be expanded to other metals. The most important improvement compared to previously reported methods is that the metalation conditions are not limited by the solubility or chemical stability of oligonucleotides. The metal as well as the organic ligand can be easily varied without the need to synthesize new phosphoramidite building blocks. We therefore believe that our method will enable rapid synthesis of previously unattainable metalated oligonucleotides.

Experimental Section

General Information

All experiments involving air- and/or moisture-sensitive compounds were performed using oven-dried glassware under an argon atmosphere. For the preparation of HPLC elution buffers, freshly distilled triethylamine was used. Other commercially available chemicals were used without further purification, unless otherwise stated. The solvents for organic synthesis were of reagent grade and were dried over 4 Å molecular sieves. All reactions were monitored by thin-layer chromatography (TLC), performed on Merck 60 (silica gel F254) plates. Chromatographic purification of products was accomplished using flash column chromatography on a silica gel (230–400 mesh). 1H, 13C, and 31P NMR spectra were recorded in deuterated solvents on Bruker Biospin 500 and 600 MHz NMR spectrometers. Chemical shifts (δ, ppm) are quoted relative to the residual solvent peak as an internal standard. Mass spectra were recorded on a Bruker micrOTOF-Q ESI mass spectrometer.

Oligonucleotide Synthesis

The modified oligonucleotide scaffold was assembled on an Applied Biosystems Incorporated 3400 automated DNA/RNA synthesizer by a conventional phosphoramidite strategy. The exocyclic amino functions of adenine, cytosine, and guanine bases were protected by the standard acyl-protecting groups (benzoyl, acetyl, and isobutyryl, respectively). For the phthaloyl-protected aminooxy-C-deoxyriboside phosphoramidite building block 2, the coupling time was extended to 600 s. The support-bound oligonucleotide was then treated with a mixture of H2NNH2·H2O, pyridine, and AcOH (1:32:8, v/v) for 45 min. The support was washed subsequently with pyridine, methanol, and acetonitrile and dried under vacuum. The support-bound oligonucleotide was placed in two microcentrifuge tubes (approximately 0.25 μmol each), and a solution of either acetato(2-formyl-6-hydroxyphenyl)mercury[19] (12, 10 μmol) in dry DMSO (100 μL) or bromo(2-formylphenyl)bis(triphenylphosphine)palladium[20] (13, 10 μmol) in dry CH2Cl2 (200 μL) was added. Note that the organomercury compound 12 is potentially highly toxic and should be handled appropriately. The resulting mixtures were shaken for 12 h at 25 °C. The solutions were discarded, and the solid supports were washed with either DMSO or CH2Cl2 and then treated with a mixture of methylamine and 25% aqueous ammonia (1:1, v/v) for 10 min at 65 °C. The solutions were recovered and evaporated to dryness, and the crude products thus obtained were purified by RP-HPLC on a Hypersil ODS C18 column (250 × 4.6 mm, 5 μm), eluting with a linear gradient (10 to 30% over 30 min for ON1-Hg and 5 to 30% over 30 min for ON1-Pd; flow rate = 1.0 mL min–1) of MeCN in 50 mM aq triethylammonium acetate. Detection was performed by UV absorbance at λ = 260 nm. Finally, the purified oligonucleotides were characterized by ESI-TOF-MS and quantified spectrophotometrically using an implementation of the nearest neighbors method. Isolated yields of oligonucleotides ON1-Hg and ON1-Pd were approximately 1 and 11%, respectively. The low yields stem from general difficulties in the chromatographic purification of covalently metalated oligonucleotides and is not an inherent property of the method reported in the present study. In particular with covalently mercurated oligonucleotides, ligand exchange of Hg(II) causes severe broadening of the peaks, making isolation of the oligonucleotide in a high yield challenging. Efforts to improve the purification methods for covalently metalated oligonucleotides are underway in our laboratory.

(2R,3S,5S)-1,3-Bis((tert-butyldimethylsilyl)oxy)hept-6-ene-2,5-diol ((5S)-5) and (2R,3S,5R)-1,3-Bis((tert-butyldimethylsilyl)oxy)hept-6-ene-2,5-diol ((5R)-5)

To a stirred solution of lactol 4 (3.62 g, 9.99 mmol) in dry THF (30 mL) at 0 °C was slowly added vinylmagnesium bromide (1.0 M THF, 30.0 mL, 30.0 mmol). The resulting mixture was stirred for 4 h at 0 °C, after which the reaction was then quenched by addition of 30 mL of saturated aqueous ammonium chloride and extracted with diethyl ether (2 × 50 mL). The organic phase was dried over anhydrous sodium sulfate and evaporated to dryness. The residue was purified by flash chromatography eluting with a mixture of MeOH and CH2Cl2 (1:99, v/v), yielding 1.70 g (43%) of (5S)-5 and 1.10 g (28%) of (5R)-5 as colorless oils. 1H NMR (500 MHz, CDCl3, (5S)-5): δ = 5.91 (ddd, J = 17.0, 10.5, 5.5 Hz, 1H), 5.30 (m, 1H), 5.10 (m, 1H), 4.43 (t, J = 7.0 Hz, 1H), 3.94 (dd, J = 11.0, 5.5 Hz, 1H), 3.79 (dd, J = 10.0, 4.0 Hz, 1H), 3.74 (m, 1H), 3.60 (dd, J = 10.0, 7.0 Hz, 1H), 3.16 (s, 1H), 2.66 (s, 1H), 1.90 (m, 1H), 1.72 (ddd, J = 15.0, 10.0, 4.5 Hz, 1H), 0.93 (s, 9H), 0.92 (s, 9H), 0.15 (s, 3H), 0.12 (s, 3H), 0.10 (s, 6H). 13C NMR (125 MHz, CDCl3, (5S)-5): δ = 141.4, 113.8, 73.9, 71.5, 69.8, 64.1, 40.3, 25.9, 25.8, 18.3, 18.0, −4.4, −4.7, −5.3, −5.4. 1H NMR (500 MHz, CDCl3, (5R)-5): δ = 5.89 (ddd, J = 17.0, 10.5, 5.5 Hz, 1H), 5.27 (dt, J = 17.0, 1.5 Hz, 1H), 5.10 (dt, J = 10.5, 1.5 Hz, 1H), 4.43 (brs, 1H), 3.93 (q, J = 5.5 Hz, 1H), 3.76–3.72 (m, 2H), 3.62 (m, 1H), 3.33 (s, 1H), 2.92 (s, 1H), 1.89 (m, 1H), 1.77 (m, 1H), 0.92–0.91 (m, 18H), 0.10 (s, 3H), 0.09 (s, 3H), 0.08 (s, 6H). 13C NMR (125 MHz, CDCl3, (5R)-5): δ = 141.2, 114.0, 74.5, 70.8, 69.0, 64.0, 40.5, 25.9, 25.8, 18.3, 18.0, −4.4, −4.6, −5.36, −5.41. HRMS (ESI+): m/z calcd for C19H42O4Si2Na [M + Na]+, 413.2514; found, 413.2513.

3,5-Di-O-(tert-butyldimethylsilyl)-C-ethenyl-2-deoxy-β-d-ribofuranose (6)

To a solution of (5S)-5 (1.10 g, 2.82 mmol) in CH2Cl2 (15 mL) was added 3.4 mL of dry pyridine. The solution was cooled to −25 °C, and a solution of MsCl (502 μL, 6.49 mmol) in CH2Cl2 (3.0 mL) was added gradually over 30 min with stirring. After standing overnight at −25 °C, the reaction mixture was quenched by addition of 5.0 mL of saturated aqueous NH4Cl. The aqueous phase was extracted with diethyl ether (2 × 20 mL), and the combined organic extracts were dried over anhydrous Na2SO4 and evaporated to dryness. The residue was purified by silica gel flash column chromatography eluting with a mixture of hexane and EtOAc (24:1, v/v), yielding 343 mg (69%) of 6 as a colorless oil. 1H NMR (500 MHz, CDCl3): δ = 5.84 (ddd, J = 17.0, 10.0, 7.0 Hz, 1H), 5.30 (d, J = 17.0 Hz, 1H), 5.12 (d, J = 10.5 Hz, 1H), 4.58 (m, 1H), 4.35 (d, J = 5.0 Hz, 1H), 3.87 (m, 1H), 3.68 (dd, J = 10.5, 4.0 Hz, 1H), 3.47 (dd, J = 10.5, 6.5 Hz, 1H), 1.92 (m, 1H), 1.74 (m, 1H), 0.92 (s, 18H), 0.10 (s, 6H), 0.08 (s, 6H). 13C NMR (125 MHz, CDCl3): δ = 138.8, 116.0, 87.8, 79.6, 74.3, 63.9, 41.6, 26.0, 25.8, 18.4, 18.0, −4.67, −4.69, −5.3, −5.4. HRMS (ESI+): m/z calcd for C19H40O3Si2K [M + K]+, 411.2148; found, 411.2146.

3,5-Di-O-(tert-butyldimethylsilyl)-C-formyl-2-deoxy-β-d-ribofuranose (7)

NaIO4 (379 mg, 1.77 mmol) and CeCl3·7H2O (88.0 mg, 0.236 mmol) were taken in a 10 mL round-bottom flask. H2O (0.54 mL) was added, and the resulting mixture was gently heated until a bright yellow suspension was formed. After cooling to 0 °C, EtOAc (1.48 mL) and MeCN (1.78 mL) were added, and the mixture was stirred for 2 min. A 0.1 M aqueous solution of RuCl3 (60 μL, 5.95 μmol) was added, and the mixture was stirred for another 2 min. A solution of compound 6 (440.0 mg, 1.181 mmol) in EtOAc (0.3 mL) was then added in one portion, and the resulting slurry was stirred for 10 min. The mixture was poured into a mixture of saturated aqueous NaHCO3 (10 mL) and saturated aqueous Na2S2O3 (10 mL). Phases were separated, and the aqueous phase was extracted with EtOAc (3 × 50 mL). The combined organic extracts were dried over anhydrous Na2SO4 and evaporated to dryness. The residue was dissolved in a mixture of THF, H2O, and Et2O (1:1:1, v/v, 5.0 mL), and the resulting solution was cooled to 0 °C. NaIO4 (470 mg, 2.2 mmol) was added, and the solution was stirred for 90 min at 25 °C. Brine (10.0 mL) was added, and the resulting mixture was extracted with EtOAc (3 × 20 mL). The combined organic extracts were dried over anhydrous Na2SO4 and evaporated to dryness. The residue was purified by silica gel flash column chromatography eluting with a mixture of hexane and EtOAc (17:3, v/v), yielding 351 mg (74% over two steps) of 7 as a colorless syrup. 1H NMR (500 MHz, CDCl3): δ = 9.69 (d, J = 2.0 Hz, 1H), 4.48 (m, 1H), 4.37 (m, 1H), 3.99 (m, 1H), 3.71 (dd, J = 11.0, 3.5 Hz, 1H), 3.60 (dd, J = 11.0, 5.5 Hz, 1H), 2.09–2.02 (m, 2H), 0.92–0.91 (m, 18H), 0.10–0.08 (m, 12H). 13C NMR (125 MHz, CDCl3): δ = 202.8, 88.6, 82.6, 73.3, 63.4, 37.0, 25.9, 25.7, 18.3, 17.9, −4.7, −4.8, −5.4, −5.5. HRMS (ESI+): m/z calcd for C18H38O4Si2Na [M + Na]+, 397.2201; found, 397.2202.

3,5-Di-O-(tert-butyldimethylsilyl)-C-hydroxymethyl-2-deoxy-β-d-ribofuranose (8)

Aldehyde 7 (351 mg, 0.939 mmol) was dissolved in a mixture of EtOH and H2O (2/1, v/v, 25.0 mL), and the resulting solution was cooled to 0 °C. NaBH4 (142.1 mg, 3.760 mmol) was added, and the resulting mixture was stirred for 3 h at 25 °C. The reaction mixture was then poured into brine (20 mL) and extracted with EtOAc (2 × 20 mL). The combined organic extracts were dried over anhydrous Na2SO4 and evaporated to dryness. The residue was purified by silica gel flash column chromatography eluting with a mixture of hexane and EtOAc (17:3, v/v), yielding 311 mg (88%) of 8 as a white solid. 1H NMR (500 MHz, CDCl3): δ = 4.43 (dt, J = 6.0, 4.0 Hz, 1H), 4.33 (ddd, J = 10.0, 7.0, 3.0 Hz, 1H), 3.85–3.81 (m, 2H), 3.73–3.67 (m, 2H), 3.46 (ddd, J = 12.0, 8.5, 3.0 Hz, 1H), 2.47 (dd, J = 8.5, 3.0 Hz, 1H), 2.11 (m, 1H), 1.87 (m, 1H), 0.93 (s, 9H), 0.91 (s, 9H), 0.10–0.09 (m, 12H). 13C NMR (125 MHz, CDCl3): δ = 87.0, 78.8, 73.1, 64.9, 63.3, 36.9, 25.9, 25.8, 18.4, 18.0, −4.6, −4.8, −5.48, −5.51. HRMS (ESI+): m/z calcd for C18H40O4Si2Na [M + Na]+, 399.2357; found, 399.2359.

3,5-Di-O-(tert-butyldimethylsilyl)-C-methanesulfonyloxymethyl-2-deoxy-β-d-ribofuranose (9)

To a solution of 8 (218.0 mg, 0.579 mmol) in CH2Cl2 (5 mL) was added 0.58 mL of dry pyridine, and the resulting solution was cooled to 0 °C. MsCl (85.0 μL, 0.869 mmol) was then added slowly, and the mixture was stirred for 3 h at 25 °C, after which it was poured into a saturated aqueous solution of NaHCO3. The phases were separated, and the aqueous phase was extracted with CH2Cl2 (2 × 20 mL). The combined organic extracts were dried over anhydrous Na2SO4 and evaporated to dryness. The residue was purified by silica gel flash column chromatography eluting with a mixture of hexane and EtOAc (4:1, v/v), yielding 246 mg (94%) of 9 as a colorless oil. 1H NMR (500 MHz, CDCl3): δ = 4.46 (m, 1H), 4.36–4.33 (m, 2H), 4.20 (m, 1H), 3.89 (ddd, J = 6.0, 4.0, 2.0 Hz, 1H), 3.64 (dd, J = 11.0, 4.0 Hz, 1H), 3.49 (dd, J = 11.0, 5.5 Hz, 1H), 3.07 (s, 3H), 1.89–1.81 (m, 2H), 0.92 (s, 9H), 0.91 (s, 9H), 0.09 (s, 6H), 0.08 (s, 6H). 13C NMR (125 MHz, CDCl3): δ = 88.3, 76.0, 73.6, 71.4, 63.6, 37.7, 37.0, 25.9, 25.8, 18.3, 18.0, −4.69, −4.75, −5.38, −5.46. HRMS (ESI+): m/z calcd for C19H42O6SSi2Na [M + Na]+, 477.2133; found, 477.2132.

C-Methanesulfonyloxymethyl-2-deoxy-β-d-ribofuranose (10)

To a stirred solution of compound 9 (246 mg, 0.542 mmol) in dry THF (4 mL) under argon at 0 °C was added Et3N·3HF (265 μL, 1.63 mmol). The resulting mixture was stirred for 16 h at 25 °C, after which it was passed through a short silica gel plug eluting with EtOAc. The EtOAc filtrate was evaporated, and the residue was purified by silica gel flash column chromatography eluting with a mixture of MeOH and CH2Cl2 (1:9, v/v), yielding 114 mg (93%) of 10 as a white foam. 1H NMR (500 MHz, MeOD): δ = 4.42 (m, 1H), 4.36 (dd, J = 11.0, 3.0 Hz, 1H), 4.26–4.21 (m, 2H), 3.87 (m, 1H), 3.60–3.54 (m, 2H), 3.13 (s, 3H), 1.95 (dd, J = 8.0, 4.5 Hz, 2H). 13C NMR (125 MHz, MeOD): δ = 87.7, 76.0, 72.2, 71.5, 62.4, 36.1, 36.0. HRMS (ESI+): m/z calcd for C7H14O6SNa [M + Na]+, 249.0403; found, 249.0401.

C-Phthalimidooxymethyl-2-deoxy-β-d-ribofuranose (1)

To a solution of compound 10 (114 mg, 0.504 mmol) and N-hydroxyphthalimide (165 mg, 1.01 mmol) in DMF (1.5 mL) was added diisopropylethylamine (351 μL, 2.02 mmol). The resulting red solution was stirred at 70 °C for 30 h, after which it was evaporated to dryness. The residue was purified by silica gel flash column chromatography eluting with a mixture of MeOH and CH2Cl2 (1:19, v/v), yielding 69.2 mg (47%) of 1 as a syrup. 1H NMR (500 MHz, MeOD): δ = 7.87–7.83 (m, 4H), 4.51 (m, 1H), 4.30–4.25 (m, 3H), 3.82 (dd, J = 8.0, 5.0 Hz, 1H), 3.60–3.51 (m, 2H), 2.09–1.98 (m, 2H). 13C NMR (125 MHz, MeOD): δ = 163.5, 134.4, 128.9, 122.9, 87.7, 79.5, 76.1, 72.1, 62.4, 36.6. HRMS (ESI+): m/z calcd for C14H15O6NNa [M + Na]+, 316.0792; found, 316.0792.

5-O-(4,4′-Dimethoxytrityl)-C-phthalimidooxymethyl-2-deoxy-β-d-ribofuranose (11)

Compound 1 (69.0 mg, 0.235 mmol) was coevaporated from dry pyridine (2 × 10 mL), and the residue was dissolved in dry pyridine (5 mL). DMTrCl (88.0 mg, 0.260 mmol) was added, and the resulting mixture was stirred at room temperature for 12 h, after which it was concentrated under reduced pressure. The residue was diluted with CH2Cl2 (20 mL), washed with saturated aqueous NaHCO3 (20 mL), dried over anhydrous Na2SO4, and filtered. The filtrate was evaporated to dryness, and the residue was purified by silica gel flash chromatography eluting with a mixture of hexane, EtOAc, and Et3N (38:57:5, v/v) to yield 84.2 mg (60%) of 11 as a white foam. 1H NMR (500 MHz, CDCl3): δ = 7.83–7.80 (m, 2H), 7.75–7.72 (m, 2H), 7.42–7.40 (m, 2H), 7.32–7.28 (m, 6H), 7.21 (m, 1H), 6.88–6.84 (m, 4H), 4.61 (m, 1H), 4.35 (m, 1H), 4.33–4.28 (m, 2H), 3.95 (m, 1H), 3.81 (s, 6H), 3.21 (dd, J = 9.5, 4.5 Hz, 1H), 3.13 (dd, J = 10.0, 5.5 Hz, 1H), 2.11–2.07 (m, 2H). 13C NMR (125 MHz, CDCl3): δ = 163.3, 158.5, 144.8, 136.0, 134.4, 130.1, 130.0, 129.0, 128.1, 127.8, 126.8, 123.5, 113.1, 86.2, 79.9, 76.0, 74.1, 64.5, 55.2, 37.4. HRMS (ESI+): m/z calcd for C35H33O8NNa [M + Na]+, 618.2098; found, 618.2096.

3-O-[(2-Cyanoethoxy)(N,N-diisopropylamino)phosphinyl]-5-O-(4,4′-dimethoxytrityl)-C-phthalimidooxymethyl-2-deoxy-β-d-ribofuranose (2)

To a stirred solution of compound 11 (108.0 mg, 0.181 mmol) in dry CH2Cl2 (1.5 mL) were added Et3N (152 μL, 1.09 mmol) and 2-cyanoethyl-N,N-diisopropylchlorophosphoramidite (49 μL, 0.22 mmol). The reaction mixture was stirred at 25 °C under a N2 atmosphere for 2 h, after which it was diluted with CH2Cl2 (20 mL) and washed with saturated aqueous NaHCO3 (20 mL). The organic phase was dried over anhydrous Na2SO4 and evaporated to dryness. The residue was purified by silica gel flash column chromatography eluting with a mixture of hexane, EtOAc, and Et3N (57:38:5, v/v) to yield 108.4 mg (75% as a mixture of RP and SP diastereomers) of 2 as a white foam. 1H NMR (500 MHz, CDCl3, a mixture of RP and SP diastereomers): δ = 7.84–7.81 (m, 2H), 7.74–7.71 (m, 2H), 7.43–7.41 (m, 2H), 7.33–7.27 (m, 6H), 7.22–7.18 (m, 1H), 6.85–6.82 (m, 4H), 4.62 (m, 1H), 4.44 (m, 1H), 4.37–4.35 (m, 2H), 4.13 (m, 1H), 3.81–3.80 (m, 6H), 3.69 (m, 1H), 3.63–3.54 (m, 2H), 3.19 (m, 1H), 3.10 (m, 1H), 2.64 (t, J = 6.5 Hz, 1H), 2.45 (t, J = 6.5 Hz, 1H), 2.14–2.03 (m, 2H), 1.20–1.16 (m, 10H), 1.08–1.07 (m, 3H). 13C NMR (125 MHz, CDCl3, a mixture of RP and SP diastereomers): δ = 163.31, 163.29, 158.4, 144.9, 136.1, 136.07, 136.04, 136.03, 134.4, 130.13, 130.13, 130.10, 129.0, 128.3, 128.2, 127.77, 127.76, 126.69, 126.66, 123.5, 117.6, 117.5, 113.09, 113.08, 86.19, 86.16, 86.0, 79.96, 79.86, 76.4, 76.3, 75.4, 75.2, 75.0, 74.9, 64.1, 64.0, 58.41, 58.39, 58.3, 58.2, 55.22, 55.20, 43.3, 43.22, 43.19, 43.1, 37.09, 37.06, 36.93, 36.89, 24.65, 24.63, 24.59, 24.57, 24.50, 24.46, 24.45, 24.41, 20.4, 20.3, 20.2, 20.1. 31P (162 MHz, CDCl3, a mixture of RP and SP diastereomers): δ = 148.1, 147.8. HRMS (ESI+): m/z calcd for C44H50O9N3PNa [M + Na]+, 818.3177; found, 818.3175.