Synthesis and NMR studies of malonyl-linked glycoconjugates of N-(2-aminoethyl)glycine. Building blocks for the construction of combinatorial glycopeptide libraries

  1. ,
  2. and
Institute of Organic Chemistry, University of Tuebingen, Auf der Morgenstelle 18, 72076 Tuebingen, Germany
  1. Corresponding author email
Associate Editor: N. Sewald
Beilstein J. Org. Chem. 2016, 12, 1939–1948. https://doi.org/10.3762/bjoc.12.183
Received 10 Jun 2016, Accepted 16 Aug 2016, Published 30 Aug 2016
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Abstract

Four glycoconjugate building blocks for the construction of combinatorial PNA like glycopeptide libraries were prepared in 75–79% yield by condensing tert-butyl N-[2-(N-9-fluorenylmethoxycarbonylamino)ethyl]glycinate (AEG) 5 with 3-oxo-3-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosylamino)- (6a), 3-oxo-3-(β-D-galactopyranosylamino)- (6b), 3-oxo-3-(2-acetamido-2-deoxy-3,4,6-tetra-O-acetyl-β-D-glucopyranosylamino)- (6c) and 3-oxo-3-(2-acetamido-2-deoxy-3,4,6-tetra-O-acetyl-β-D-galactopyranosylamino)propanoic acid (6d), respectively. The resulting AEG glycoconjugates 1a–d were converted into the corresponding free acids 2a–d in 97–98% yield by treatment with aqueous formic acid. The Fmoc group of compound 1c was removed and the intermediate amine 9 was condensed with 2a to afford the corresponding glycosylated AEG dipeptide 4 in 58% yield. All glycoconjugate building blocks showed the presence of cis and trans rotamers. Compounds 1a, 1b and 4 were subjected to temperature dependent 1H NMR spectroscopy in order to determine the coalescence temperature which resulted in calculated rotation barriers of 17.9–18.3 kcal/mol for the rotamers.

Introduction

The glycocalyx is a fringy or fuzzy polysaccharide layer coating most animal and many bacterial cells. It is covalently bound to the surface of the cell membrane through glycoproteins and plays a major role in numerous biologically important recognition mechanisms like cell–cell recognition, signal transduction and immunological processes [1-4]. Therefore, investigating the delicate carbohydrate–protein interactions on a molecular level is an inalienable prerequisite for a deep understanding of the fundamental cellular recognition processes involving the complex saccharides of the glycocalyx [5-8]. Unfortunately, isolation of pure carbohydrate material or specific glycoconjugates from natural sources remains a difficult, sometimes even an unrealizable task, for naturally occurring saccharides exhibit micro-heterogenity which makes it nearly impossible to obtain pure material from such sources. Chemical or chemoenzymatic syntheses of complex oligosaccharides, on the other hand, may provide sufficient amounts of pure material for such studies. Despite the great achievements in oligosaccharide synthesis during the past decades, the preparation of complex oligosaccharides can be tedious, lengthy or circuitous, and the often intrinsic intricacy of a chemical saccharide synthesis makes it sometimes impossible to prepare a certain saccharide or glycoconjugate [9]. Therefore, gaining access to new glycoconjugates which are easily accessible by chemical synthesis and which are able to mimic the interaction between a specific protein and its natural oligosaccharide ligand are highly desirable [10-13]. In our previous work we introduced various trifunctional glycopeptide building blocks derived from aspartic acid, 3-aminomethyl-5-aminobenzoic acid [14] and from the PNA-like N-(2-aminoethyl)glycine (AEG) backbone to which sugar moieties were linked through either simple alkyl chains [15,16], amino alcohols [17,18] or 1,2,3-triazoles [19-21]. These building blocks were used for automated SPOT synthesis on a cellulose surface in order to construct complex glycoconjugates which are able to specifically bind to lectins [15,18,20].

In continuation of these studies, we now describe the preparation of PNA-based glycoconjugate building blocks 1–3 as well as a dimeric glycoconjugate 4 in which the sugar moieties are attached through a malonyl linker (Figures 1–3). For these compounds we studied the cis/trans-rotameric structures via temperature-dependent 1H NMR spectroscopy. Unfortunately, the amidic protons of the rotamers of the unprotected glycoconjugates could not be observed in the 1H NMR spectra in D2O due to the fast H/D exchange with the solvent (Figure 2). Nevertheless, we could identify two rotameric forms exhibiting a cis/trans ratio of 2:1 which was in accordance with similar rotamers described in literature [22]. Hereupon, we report on our investigations concerning the structures of the fully protected conjugates 1 and 4 for the rotamers of which around the C–N bond we calculated the respective ΔGr-values.

[1860-5397-12-183-1]

Figure 1: cis- and trans rotamer of protected PNA building blocks 1a–d and 2a–d.

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Figure 2: cis- and trans rotamer of unprotected PNA-building block 3.

[1860-5397-12-183-3]

Figure 3: Rotameric structures of dimeric PNA glycoconjugate 4.

Results and Discussion

Synthesis of building blocks

The preparation of building blocks 1a–d and 2a–d started from tert-butyl N-[2-(N-9-fluorenylmethoxycarbonyl)aminoethyl)]glycinate hydrochloride (5) which was synthesized in 39% yield from tert-butyl bromoacetate according to the procedure published by Thomson et al. [23]. Acetyl protected glycosylaminomalonic acids 6a–d were prepared from the corresponding tert-butyl esters as previously described [14]. Coupling of 5 with acids 6a–d was achieved with either N,N,N′,N′-tetramethyl-O-(1H-benzotriazol-1-yl)uronium hexafluorophosphate (HBTU) or 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide (EDCI) (Scheme 1, Table 1). In general, HBTU gave higher yields of malonamides 1a–d than EDCI. Previously, we used EDCI for coupling acids 6a–d to aniline derivatives because HBTU resulted in byproducts which were difficult to be removed [14]. Such byproducts were not observed here though.

[1860-5397-12-183-i1]

Scheme 1: Synthesis of building blocks 1a–d and 2a–d (a stands for D-glucose, b stands for D-galactose, c stands for N-acetylglucosamine, d stands for N-acetylgalactosamine).

Table 1: Synthesis of building blocks 1a–d.

Entry Starting material Coupling method Product Yield (%)
1 [Graphic 1]
6a
A) HBTU
B) EDCI
[Graphic 2]
1a
A) 79%
B) 40%
2 [Graphic 3]
6b
A) HBTU
B) EDCI
[Graphic 4]
1b
A) 79%
B) 47%
3 [Graphic 5]
6c
A) HBTU
B) EDCI
[Graphic 6]
1c
A) 75%
B) 57%
4 [Graphic 7]
6d
A) HBTU
B) EDCI
[Graphic 8]
1d
A) 77%
B) 42%

Next, the tert-butyl ester groups of building blocks 1a–d were removed under acid conditions with a 2:1 mixture of formic acid and dichloromethane at room temperature to give the corresponding free acids 2a–d in 97–98% yield (Scheme 1, Table 2).

Table 2: Synthesis of building blocks 2a–d.

Entry Starting material Product Yield (%)
1 [Graphic 9]
1a
[Graphic 10]
2a
98%
2 [Graphic 11]
1b
[Graphic 12]
2b
97%
3 [Graphic 13]
1c
[Graphic 14]
2c
97%
4 [Graphic 15]
1d
[Graphic 16]
2d
97%

Partially deprotected building block 3 was prepared from 1a as follows. First, removal of the Fmoc group in 1a under basic conditions with triethylamine in DMF gave the crude amino derivate which was acetylated with Ac2O to give building block 7 in 60% yield. Removal of the acetyl groups of the sugar moiety in 7 to afford compound 3 could be achieved in a virtually quantitative yield by subjection 7 to a saturated solution of NH3 in MeOH (7 N) (Scheme 2).

[1860-5397-12-183-i2]

Scheme 2: Synthesis of building block 3.

In addition to the monomeric glycoconjugates 1a–d and 2a–d we also prepared dimer 4 from the glucose containing conjugate 2a and the N-acetylglucosamine containing conjugate 1c. Treatment of 1c with 20% piperidine in DMF at room temperature for 3.5 h gave partially protected compound 8 which was used for the next step without further purification. Coupling of 2a with crude 8 using HBTU, 1-hydroxytriazole (HOBt) and diisopropylethylamine (DIPEA) in DMF gave dipeptide 4 in 58% yield (Scheme 3).

[1860-5397-12-183-i3]

Scheme 3: Synthesis of the dimeric glycoconjugate 4.

1D-NMR investigation

Glycoconjugates 1a,b and 4 were submitted to temperature-dependent 1H NMR spectroscopy in order to reveal, verify and determine their cis- and trans-rotameric structures (see also Figures 1–3). The 1H NMR spectra of 1a and 1b in CDCl3 at room temperature revealed two separate doublets at 8.19 and 7.99 ppm for 1a and 8.26 and 7.99 ppm for 1b, respectively for the anomeric amide proton indicating the presence of two rotamers (Figure 4 and Figure 5). The signals at lower field were assigned to the respective trans rotamers whereas the signals at higher field were assigned to the corresponding cis rotamers of 1a and 1b (see 2D NMR investigations below).

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Figure 4: 1H NMR (400 MHz) of building block 1a in CDCl3. The amide signals of the rotamers are marked.

[1860-5397-12-183-5]

Figure 5: 1H NMR (400 MHz) of building block 1b in CDCl3. The amide signals of the rotamers are marked.

The 1H NMR spectrum of the dimeric PNA glycoconjugate 4 in CDCl3 showed the presence of four different rotameric structures (see also Figure 3). This was evident from eight distinct doublet signals for the anomeric amide protons (Figure 6). Here, no unambiguous assignment of the observed doublets to respective cis/trans rotameric forms could be achieved by 2D NMR spectroscopy.

[1860-5397-12-183-6]

Figure 6: 1H NMR (400 MHz) of PNA glycoconjugate 4 in CDCl3. The amide signals of the rotamers of 4 (2 doublets for each rotamer) are marked 1/2, 3/4, 5/6 and 7/8.

Since deuterochloroform is not suitable for temperature-dependent 1H NMR experiments at higher temperatures which, in turn, are necessary for determining the coalescence temperature of both rotamers we measured the 1H NMR of 1a in DMSO-d6, DMF-d7, and chlorobenzene-d5 as well (Figure 7). In DMSO-d6 and DMF-d7 which both are common solvents for temperature-dependent NMR spectroscopy [24] the anomeric amide protons of the two rotamers of 1a were not sufficiently separated. Furthermore, Fmoc groups are known to be unstable in DMSO and DMF at higher temperatures [24,25]. Indeed, when 1a was heated in DMSO-d6 above 60 °C a signal of dibenzofulvene at 6.21 ppm appeared, indicating the cleavage of the Fmoc group in 1a (Figure 8). In chlorobenzene-d5 (bp 131 °C), however, sufficient separation of the two anomeric amide protons of the rotamers of 1a were observed and no cleavage of the Fmoc group occurred. Höck et al. [24] could also show that chlorobenze-d5 does not cause cleavage of Fmoc groups in peptides up to 120 °C.

[1860-5397-12-183-7]

Figure 7: Building block 1a in CDCl3, DMSO-d6, DMF-d7 and chlorobenzene-d5.

[1860-5397-12-183-8]

Figure 8: Temperature-dependent 1H NMR (600 MHz) spectra of building block 1a in DMSO-d6.

Figure 9 shows the temperature-dependent 1H NMR spectra (7.65–8.30 ppm area only) of 1a in the temperature range between 25 and 100 °C. Heating the sample caused a downfield shift of the anomeric amide protons with coalescence (Tc) at 90–95 °C (363–368 K). Unfortunately, the amide signals partially overlapped with the proton signals of the Fmoc group at the coalescence temperature so that no exact coalescence temperature could be determined.

[1860-5397-12-183-9]

Figure 9: Temperature-dependent 1H NMR (600 MHz) spectra of building block 1a in chlorobenzene-d5, broadened signals near the coalescence temperature are marked.

Figure 10 shows the temperature-dependent 1H NMR spectra (7.65–8.50 ppm area only) of 1b in the range between 25 and 100 °C. In this case the corresponding coalescence temperature (Tc) could be determined at 90–95 °C (363–368 K).

[1860-5397-12-183-10]

Figure 10: Temperature-dependent 1H NMR (600 MHz) spectra of building block 1b in chlorobenzene-d5, broadened signals near the coalescence temperature are marked.

Figure 11 finally shows the temperature-dependent 1H NMR spectra (9.10–7.80 ppm are only) of 4 in the range between 25 and 100 °C. In this case, the corresponding coalescence temperature (Tc) could also be determined at 90–95 °C (363–368 K).

[1860-5397-12-183-11]

Figure 11: Temperature-dependent 1H NMR (600 MHz) spectra of dimeric glycoconjugate 4 in chlorobenzene-d5, broadened signals near the coalescence temperature are marked.

2D-NMR investigation

In order to unambiguously assign the anomeric amide signals (doublets) from the proton NMR spectra above to the corresponding cis/trans rotamers of 1a we measured the NOESY spectrum of conjugate 1a in CDCl3 (see Supporting Information File 2). The spectrum indicates that the direct assignment of the amidic doublets to the respective cis- or trans rotamers is not possible due to missing crosspeaks between the amidic signals and the methylene or 2-aminoethyl protons of the PNA backbone (Figure 12).

[1860-5397-12-183-12]

Figure 12: A) Missing correlation between the amidic proton and the methylene or 2-aminoethyl protons of the PNA backbone; B) Observed NOE-correlations of PNA building block 1a.

Nevertheless, crosspeaks between the amidic protons and the malonyl protons could be observed, and were used for an indirect assignment of the amidic doublets. Stronger NOE crosspeaks between the methylene protons of the side chain (3.20 ppm) and the methylene protons of the PNA backbone (3.93 ppm) indicated that the distance between these protons should be shorter in comparison to the distance of the protons with a chemical shift at 3.36 and 3.93 ppm. Therefore, the signal of the protons at 3.20 ppm and the doublet at 8.18 ppm belong to the trans rotamer whereas the doublet at 8.01 ppm should belong to the cis rotameric structure.

Calculation of ΔGr-values

In order to evaluate the rotation barrier around the tertiary peptide bond (C–N bond) we calculated the corresponding ΔGr values for building blocks 1a,b from the measured coalescence temperatures (Tc) by using the Eyring model [26]. The ΔGc values of the dimeric glycoconjugate 4 could not be determined though because no unambiguous assignment of the rotameric structures to the corresponding specific proton signals could be made. Nevertheless, the rotation barriers of glycoconjugate 4 should be rather similar to the barriers of building blocks 1a,b due to the almost identical coalescence temperatures (Tc).

[Graphic 17]

[Graphic 18]

[Graphic 19]

The respective Δ[Graphic 20] values (NHtrans – NHcis) were extracted from the corresponding 1H NMR spectra of the specific building blocks 1a,b in chlorobenzene-d5 at 25 °C (298 K). Table 3 summarizes the calculated ΔGc values and illustrates that there is only a small difference between the calculated ΔGr values of building blocks 1a and 1b in chlorbenzene-d5. It is obvious that the different saccharide moieties do not significantly influence the rotation barrier around the tertiary peptide bond. Furthermore, the calculated ΔGr values are in good accordance with those of other PNA derivates (17.9–19 kcal/mol) [27,28].

Table 3: ΔGc values of building blocks 1a,b.

Entry building block Tc in °C (K) Δ[Graphic 21] in ppm kr in Hz ΔGr in kcal/mol
1 1a 90–95
(363–368)
0.07 93.2 18.1–18.3
2 1b 90–95
(363–368)
0.09 119.9 17.9–18.1

Conclusion

We have described the efficient chemical synthesis of a series of novel PNA-based glycopeptoids. We also studied the cis/trans rotamers of these glycopeptoids via temperature-dependent 1H NMR spectroscopy by determining the corresponding coalescence temperatures (Tc = 90–95 °C) and by calculating the specific rotation barrier (ΔGr) using the Eyring model. The found ΔGr values (17.9–18.3 kcal/mol) were in good accordance with those of other known PNA-derivates (17.9–19 kcal/mol). The PNA-based glycoprotein building blocks described here will be used in combination with previously described benzoic acid-based glycopeptoids to generate glycopeptide libraries of more complex nature by automated SPOT synthesis.

Supporting Information

Supporting Information File 1: Experimental data.
Format: PDF Size: 536.5 KB Download
Supporting Information File 2: NMR spectra of building blocks 1a–d, 2a–d, 3, 4 and 7; 2D NMR spectra of building block 1a.
Format: PDF Size: 1.5 MB Download

Acknowledgements

We thank Dr. Dorothee Wistuba for the measurement of the high resolution mass spectra, Dr. Markus Kramer and the members of the NMR-division of the Institute of Organic Chemistry for recording the NMR spectra and Petra Krüger for performing the elemental analyses. We also thank Dr. Gregor Lemanski for numerous discussions on the topic.

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