Cyclising peptides

Abstract

A method for preparing a cyclic peptide, derivative or analogue thereof is described. The method comprises contacting a peptide, derivative or analogue thereof with a fluoro-heteroaromatic compound to cyclise the peptide, derivative or analogue thereof.

Claims

1. A method for preparing a bridged peptide, derivative or analogue thereof, the method comprising contacting a reactant comprising a peptide, derivative or analogue thereof with a fluoro-heteroaromatic compound to form a bridged structure with the peptide, derivative or analogue thereof, wherein the fluoro-heteroaromatic compound comprises at least two halogen atoms, wherein all of the at least two halogen atoms are fluorine atoms or the at least two halogen atoms comprise at least one fluorine atom and at least one chlorine atom, the reactant comprises at least two nucleophilic side chains at least one of which comprises a thiol group, and the method is carried out with the reactant in solution using a solvent and the solvent is 2,2,2-trifluoroethanol (TFE), and the reactant is: a) a peptide; b) a peptide where one or more of the amino acids residues of the peptide are replaced by residues with similar side chains or peptide backbone properties; c) a peptide where terminal groups thereof are protected by N- and C- terminal protecting groups with similar properties to acetyl or amide groups; d) a peptoid; e) a retropeptoid; f) a peptide-peptoid hybrid; or g) a peptide where at least one of the amino acids residues of the peptide is a D-amino acid.

2. The method according to claim 1, wherein the bridged peptide comprises at least two, three, four or five amino acid residues.

3. The method according to claim 1, wherein the fluoro-heteroaromatic compound contains one, two or three nitrogen atoms in the aromatic ring.

4. The method according to claim 1, wherein the fluoro-heteroaromatic compound comprises at least one hydrogen atom.

5. The method according to claim 1, wherein a first nucleophilic side chain reacts in an S.sub.NAr type reaction with the fluoro-heteroaromatic compound to displace a fluorine atom and create a covalent bond between the first nucleophilic side chain and the fluoro-heteroaromatic compound, and subsequently a second nucleophilic side chain reacts in an S.sub.NAr type reaction with the fluoro-heteroaromatic compound, which is covalently bonded to the first nucleophilic side chain, to displace a further fluorine atom and create a covalent bond between the second nucleophilic side chain and the fluoro-heteroaromatic compound, thereby creating a linker between the first and second nucleophilic side chains, and thereby forming the bridged peptide, derivative or analogue thereof.

6. The method according to claim 1, wherein at least one of the nucleophilic side chains comprises an amine group, and/or an alcohol group.

7. The method according to claim 6, wherein the or each thiol is provided on a cysteine residue or modified cysteine residue in the reactant, or the or each amine group is provided on a lysine residue in the reactant, and/or the or each alcohol group is provided on a tyrosine, serine or threonine residue within the reactant.

8. The method according to claim 1, wherein the bridged peptide, derivative or analogue thereof that is prepared comprises one bridging structure.

9. The method according to claim 1, wherein the bridged peptide, derivative or analogue thereof that is prepared comprises multiple bridging structures.

10. The method according to claim 1, wherein the at least two nucleophilic side chains comprise at least one thiol group and at least one phenol group and the fluoro-heteroaromatic compound reacts selectively with the at least one thiol group.

11. The method according to claim 1, wherein the at least two nucleophilic side chains comprise at least one amine group and at least one phenol group and the fluoro-heteroaromatic compound reacts selectively with the at least one amine group.

12. The method according to claim 1, wherein the at least two nucleophilic side chains comprise at least one thiol group and at least one amine group and the fluoro-heteroaromatic compound reacts selectively with the at least one thiol group.

13. The method according to claim 1, wherein the method comprises dissolving a peptide, derivative or analogue thereof in a solvent, and adding a base thereto before the fluoro-heteroaromatic compound is added to the dissolved peptide to create a reaction solution.

14. The method according to claim 13, wherein the method further comprises subjecting the solution to a vacuum to remove a volatile liquid, and/or wherein the step of mixing the solution is undertaken at at least 30 C.

15. The method according to claim 1, wherein the molar ratio of the peptide, derivative or analogue thereof to the fluoro-heteroaromatic compound is between 1:1 and 1:100.

16. A method for producing a bridged peptide, derivative or analogue thereof in a step-wise fashion, the method comprising at least two steps sequentially, wherein the first step comprises contacting a reactant comprising a peptide, derivative or analogue thereof with a fluoro-heteroaromatic compound to create a chemically modified peptide, derivative or analogue thereof, and the second step comprises contacting the chemically modified peptide, derivative or analogue thereof with a fluoro-heteroaromatic compound to cyclise the chemically modified peptide, derivative or analogue thereof, wherein the fluoro-heteroaromatic compound comprises at least two halogen atoms, wherein all of the at least two halogen atoms are fluorine atoms or the at least two halogen atoms comprise at least one fluorine atom and at least one chlorine atom, the reactant comprises at least two nucleophilic side chains at least one of which comprises a thiol group, the solvent for the first step is 2,2,2-trifluoroethanol (TFE) and the solvent for the second step is dimethylformamide (DMF), and the reactant is: a) a peptide; b) a peptide where one or more of the amino acids residues of the peptide are replaced by residues with similar side chains or peptide backbone properties; c) a peptide where terminal groups thereof are protected by N- and C- terminal protecting groups with similar properties to acetyl or amide groups; d) a peptoid; e) a retropeptoid; f) a peptide-peptoid hybrid; or g) a peptide where at least one of the amino acids residues of the peptide is a D-amino acid.

17. The method according to claim 16, wherein the second step comprises contacting the chemically modified peptide, derivative or analogue thereof with a fluoro-heteroaromatic compound which is added to the reaction during the second step, or further contacting the chemically modified peptide, derivative or analogue thereof with a fluoro-heteroaromatic compound which is already attached to the chemically modified peptide, derivative or analogue thereof by at least one chemical bond.

18. The method according to claim 1, wherein the fluoro-heteroaromatic compound comprises a perfluoroheteroaromatic compound.

Description

(1) For a better understanding of the invention, and to show how embodiments of the same may be carried into effect, reference will now be made, by way of example, to the accompanying Figures, in which:

(2) FIG. 1 shows two chemical reactions, the first resulting in the formation of a mono-cyclic peptide, and the second resulting in the formation of a multi-cyclic peptide;

(3) FIG. 2 is a schematic diagram showing the different types of cyclisation reactions for peptides;

(4) FIG. 3 shows the reagents used in the prior art by Pepscan Therapeutics NV;

(5) FIG. 4 shows the reagents used in the prior art by the Pentelute group at MIT;

(6) FIG. 5 shows a chemical reaction from the prior art resulting in the formation of a cyclic peptide-peptoid hybrid;

(7) FIG. 6 shows a chemical reaction between a peptide and a perfluoro-heteroaromatic reagent;

(8) FIG. 7 shows a chemical reaction for peptide cyclisation using perfluoro-heteroaromatic reagents according to an embodiment of the invention;

(9) FIG. 8 is an LCMS spectrum and chromatogram at 280 nm for peptide 1, which has the structure AcNHYC-G-G-G-C-A-L-CONH.sub.2;

(10) FIG. 9 is an LCMS spectrum and chromatogram at 280 nm for peptide 2, which has the structure AcNHYS-G-G-G-S-A-L-CONH.sub.2;

(11) FIG. 10 is an LCMS spectrum and chromatogram at 280 nm for peptide 3, which has the structure AcNHYK-G-G-G-K-A-L-CONH.sub.2;

(12) FIG. 11 shows the possible positions of nitrogen atoms in the fluoro-hereroaromatics which may be used in accordance with the present invention;

(13) FIG. 12 shows the structure, chemical formula and molecular weight of a product formed by reacting peptide 1 with pentafluoropyridine according to procedure A or B;

(14) FIG. 13 is an LCMS spectrum and chromatogram at 280 nm for the products formed by reacting peptide 1 with pentafluoropyridine according to procedure A;

(15) FIG. 14 is a .sup.19F NMR spectrum for the products formed by reacting peptide 1 according to procedure A, with the solvent used for the NMR being H.sub.2O/MeCN/D.sub.2O in a ratio of 1:1:0.2;

(16) FIG. 15 shows the expansions of the peaks of the spectrum of FIG. 14;

(17) FIG. 16 is an LCMS chromatogram at 280 nm of the products formed by reacting peptide 1 according to procedure B;

(18) FIG. 17 shows the structure for the product formed by reacting peptide 1 with fluoro-heteroaromatic (I) according to procedure A;

(19) FIG. 18 shows the structure for the product formed by reacting peptide 1 with fluoro-hereroaromatic (III) according to procedure A;

(20) FIG. 19 shows the structure for the product formed by reacting peptide 1 with fluoro-heteroaromatic (IV) according to procedure A;

(21) FIG. 20 shows the structure for the products formed by reacting peptide 1 with fluoro-heteroaromatic (V) according to procedure A;

(22) FIG. 21 shows the structure for the products formed by reacting peptide 1 with fluoro-heteroaromatic (VI) according to procedure A;

(23) FIG. 22 shows the structure for the products formed by reacting peptide 1 with fluoro-heteroaromatic (VII) according to procedure A;

(24) FIG. 23 shows the structure for the products formed by reacting peptide 1 with fluoro-aromatic (VIII) according to procedure A;

(25) FIG. 24 is a crude .sup.19F NMR spectrum for the products formed by reacting peptide 5 according to procedure F;

(26) FIG. 25 shows the structure, chemical formula and molecular weight of a product formed by reacting peptide 2 according to procedure A or C;

(27) FIG. 26 is a .sup.19F NMR spectrum for the products formed by reacting peptide 2 according to procedure A, with the solvent used for the NMR being H.sub.2O/MeCN/D.sub.2O in a ratio of 1:1:0.2;

(28) FIG. 27 shows the expansions of the peaks of the spectrum of FIG. 26;

(29) FIG. 28 shows the structure for the products formed by reacting peptide 2 with fluoro-heteroaromatic (I) according to procedure A;

(30) FIG. 29 shows the structure for the products formed by reacting peptide 2 with fluoro-heteroaromatic (III) according to procedure A;

(31) FIG. 30 shows the structure for the products formed by reacting peptide 2 with fluoro-heteroaromatic (VI) according to procedure A;

(32) FIG. 31 shows the structure for the products formed by reacting peptide 2 with fluoro-hereroaromatic (VII) according to procedure A;

(33) FIG. 32 shows the structure, chemical formula and molecular weight of a product formed by reacting peptide 3 according to procedure A;

(34) FIG. 33 shows the structure of a product formed by reacting peptide 3 according to procedure C;

(35) FIG. 34 shows the structure for the products formed by reacting peptide 3 with fluoro-heteroaromatic (I) according to procedure A;

(36) FIG. 35 shows the structure for the products formed by reacting peptide 3 with fluoro-heteroaromatic (III) according to procedure A;

(37) FIG. 36 shows the structure for the products formed by reacting peptide 3 with fluoro-heteroaromatic (IV) according to procedure A;

(38) FIG. 37 shows the structure for the products formed by reacting peptide 3 with fluoro-heteroaromatic (V) according to procedure A;

(39) FIG. 38 shows the structure for the products formed by reacting peptide 3 with fluoro-heteroaromatic (VI) according to procedure A;

(40) FIG. 39 shows the structure for the products formed by reacting peptide 3 with fluoro-heteroaromatic (VII) according to procedure A;

(41) FIG. 40 shows the structure of a product formed by reacting peptide 1 according to procedure D;

(42) FIG. 41 shows the chemical structure for product P7a;

(43) FIG. 42 shows the chemical structure for product P14;

(44) FIG. 43 is an LCMS chromatogram for the crude products formed by reacting peptide 4 according to procedure E, where the solvent for the reaction was DMF;

(45) FIG. 44 is an LCMS chromatogram for the crude products formed by reacting peptide 4 according to procedure F, where the solvent for the reaction was DMF;

(46) FIG. 45 is an LCMS chromatogram for the crude products formed by reacting peptide 4 according to procedure E, where the solvent for the reaction was TFE;

(47) FIG. 46 is an LCMS chromatogram for the crude products formed by reacting peptide 4 according to procedure F, where the solvent for the reaction was TFE;

(48) FIG. 47 shows the structure for peptoid 1;

(49) FIG. 48 shows the structure for peptoid 2;

(50) FIG. 49 is the LCMS spectrum and chromatogram at 220 nm and 280 nm for the products formed by reacting peptoid 1 with pentafluoropyridine according to procedure I;

(51) FIG. 50 shows the structure, of a product formed by reacting peptoid 1 with pentafluoropyridine according to procedure I;

(52) FIG. 51 is the MALDI-Tof spectra for the products formed by reacting peptoid 1 with fluoro-heteroaromatic (I) according to procedure I;

(53) FIG. 52 shows the structure of a product formed by reacting peptoid 1 with fluoro-heteroaromatic (I) according to procedure I;

(54) FIG. 53 shows the structure of a product formed by reacting peptoid 1 with fluoro-heteroaromatic (I) according to procedure I;

(55) FIG. 54 shows the structure of a product formed by reacting peptoid 1 with fluoro-heteroaromatic (I) according to procedure I;

(56) FIG. 55 is the LCMS spectrum and chromatogram at 220 nm and 280 nm for the products formed by reacting peptoid 2 with pentafluoropyridine according to procedure I;

(57) FIG. 56 shows the structure of a product formed by reacting peptoid 2 with pentafluoropyridine according to procedure I;

(58) FIG. 57 is the MALDI-Tof spectra for the products formed by reacting peptoid 1 with fluoro-heteroaromatic (I) according to procedure I;

(59) FIG. 58 shows the structure of a product formed by reacting peptoid 2 with fluoro-heteroaromatic (I) according to procedure I;

(60) FIG. 59 shows the structure of a product formed by reacting peptoid 2 with fluoro-heteroaromatic (I) according to procedure I;

(61) FIG. 60 shows the structure of a product formed by reacting peptoid 2 with fluoro-heteroaromatic (I) according to procedure I;

(62) FIG. 61 shows the structure of a product formed by reacting peptoid 2 with fluoro-heteroaromatic (I) according to procedure I and

(63) FIG. 62 shows the chemical structure for product P5;

(64) FIG. 63 shows the chemical structure for products P6a and P6b;

(65) FIG. 64 shows the chemical structure for products P7a and P7b;

(66) FIG. 65 shows the chemical structure for products P8a and P8b;

(67) FIG. 66 shows the chemical structure for products P9a and P9b;

(68) FIG. 67 shows the chemical structure for product P10;

(69) FIG. 68 shows the chemical structure for product P11; and

(70) FIG. 69 shows the chemical structure for product P12.

EXAMPLES

(71) As mentioned previously, it is desirable to be able to react peptides, derivatives or analogues thereof to form mono-cyclic or multi-cyclic products. These reactions can be at least one of: head-to-tail cyclisation; side chain-to-tail cyclisation; head-to-side chain cyclisation and/or side chain-to-side chain cyclisation, as shown in FIG. 2.

(72) The reagents and methods used in the prior art have a number of drawbacks as discussed above. FIG. 3 shows reagents used by Pepscan. These reagents all contain bromine which does not allow for easy monitoring of the reactions. The reagents used by the Pentelute group are shown in FIG. 4. These reagents are fairly unreactive so, as with the Pepscan, they can only be used with peptides which contain cysteine. Finally, the reaction scheme developed by the Lim group is shown in FIG. 5. However, to avoid unwanted by-products this reaction must be carried out on resin. Additionally, as with the Pepscan reagents, the cyanuric chloride used by the Lim group does not allow for easy monitoring of the reactions.

(73) The inventors' work has lead to the discovery of using fluoro-heteroaromatic compounds as a reagent in the cyclisation reactions of peptides, peptoids and peptide-peptoid hybrids. This can either be done as a one step reaction, as illustrated in FIGS. 1 and 7, or as a two step process, where the peptide, peptoid or peptide-peptoid hybrid is first tagged, as illustrated in FIG. 6, and then further reacted to cyclise.

(74) Materials and Methods

(75) The following examples were carried out on ten different peptides, referred to as peptides 1 to 10, and two different peptoids, referred to as peptoids 1 and 2, where:

(76) Peptide 1 has the structure AcNHYC-G-G-G-C-A-L-CONH.sub.2;

(77) Peptide 2 has the structure AcNHYS-G-G-G-S-A-L-CONH.sub.2;

(78) Peptide 3 has the structure AcNHYK-G-G-G-K-A-L-CONH.sub.2;

(79) Peptide 4 has the structure AcNHFK-A-C-G-K-G-C-A-CONH.sub.2;

(80) Peptide 5 is glutathione;

(81) Peptide 6 has the structure AcNHFC(Acm)-G-G-C-G-G-C(Acm)-A-L-CONH.sub.2;

(82) Peptide 7 has the structure AcNH-A-CW-G-SI-L-A-R-T-CONH.sub.2;

(83) Peptide 8 has the structure AcNH-A-CY-G-SI-L-A-R-T-CONH.sub.2;

(84) Peptide 9 has the structure AcNHFC-G-G-G-C-A-L-CONH.sub.2; and

(85) Peptide 10 has the structure AcNHFS-G-G-G-S-A-L-CONH.sub.2;

(86) Peptoid 1 is [(Nae-Nspe-Nspe)(NCys-Nspe-Nspe)].sub.2; and

(87) Peptoid 2 is [Nae-NCys-Nspe)].sub.4.

(88) Peptides 1 to 4 and 6 to 10 were prepared using automated Fmoc-SPPS methods on a Liberty 1 peptide synthesiser (CEM) with microwave-assisted couplings (single coupling per amino acid; 10 min, 75 C. (50 C. for Fmoc-cys(trt)-OH coupling). Solid phase synthesis was conducted using Rink amide resin (0.7 mol/g loading) on a 0.1 mol scale, employing PyBOP and DIPEA as activator and base, respectively. Following on-resin synthesis of the appropriate sequence, N-terminal capping was achieved using Ac.sub.2O/DMF (20%, 215 min) with shaking at room temperature. Finally, peptides were cleaved from the resin as the C-terminal amide by treatment of beads with a cleavage cocktail containing 90% TFA, 5% TIPS and 5% water with shaking at room temperature for 4 h. After removal of volatiles in vacuo, the product was triturated and washed using Et.sub.2O.

(89) Peptide 5, glutathione, can be bought commercially.

(90) Peptoids 1 and 2 were prepared via automated peptoid synthesis using an Aapptec Apex 396 synthesiser. Solid phase synthesis was conducted using Rink Amide resin (0.1 mmol, loading 0.54 mmol g-1) by cycles of haloacetylation (either bromo- or chloroacetic acid, 1 ml, 0.6M in DMF) using DIC as activator (0.18 ml, 50% v/v in DMF, 20 min at RT) followed by halide displacement by the desired amine (1 ml, 1.5M in DMF, 60 min at RT) until the desired sequence was achieved. Finally peptoids were cleaved off the resin using 95:5:5 TFA:TIPS:H2O (4 ml, 30 min, RT). The cleavage cocktail containing the target peptoids was then filtered from the resin and evaporated in vacuuo and the resulting residue precipitated in Et2O (20 ml). The crude peptoid was obtained via centrifugation to yield the crude product as a white/yellow powder.

(91) Mass spectroscopy data was collected for peptides 1 to 3 and is shown in FIGS. 8 to 10. FIG. 8, for peptide 1, shows an [M+H].sup.+ peak at 783.747 m/z, FIG. 9, for peptide 2, shows an [M+H].sup.+ peak at 751.946 m/z and FIG. 10, for peptide 3, shows an [M+H].sup.+ peak at 834.290 m/z and an [M+H].sup.2+ peak at 418.366 m/z.

(92) The peptides or peptoids were reacted according to procedures A, B, D, E, F, G, H or I as described below:

(93) Procedure A

(94) Solid peptide (approx. 2 mg, 2.5 mol) was dissolved in DMF (0.5 mL) in a 1.5 mL plastic Eppendorf tube, to which DIPEA (50 mM in DMF, 0.5 mL) was added. The required fluoroheteroaromatic or fluoro-aromatic was added in 25 equivalents and the tube was shaken at room temperature for 4.5 h. After removal of volatiles under vacuum, each reaction mixture was redissolved in a 1:1 mixture of H.sub.2O and MeCN (1 mL) and analysed by LCMS (ESI+) and .sup.19F NMR (100 L D.sub.2O added).

(95) Procedure B

(96) Solid peptide (approx. 2 mg, 2.5 mol) was dissolved in DMF (0.5 mL) in a 1.5 mL plastic Eppendorf tube, to which DIPEA (50 mM in DMF, 0.5 mL) was added. The required fluoro-heteroaromatic or fluoro-aromatic was added in 5 equivalents and the tube was shaken at room temperature for 4.5 h. After removal of volatiles under vacuum, each reaction mixture was redissolved in a 1:1 mixture of H.sub.2O and MeCN (1 mL) and analysed by LCMS (ESI+) and .sup.19F NMR (100 L D.sub.2O added).

(97) Procedure C

(98) Solid peptide (approx. 2 mg, 2.5 mol) was dissolved in DMF (0.5 mL) in a 1.5 mL plastic Eppendorf tube, to which DIPEA (50 mM in DMF, 0.5 mL) was added. The required fluoro-heteroaromatic or fluoro-aromatic was added in 25 equivalents and the tube was shaken at 50 C. for 4.5 h. After removal of volatiles under vacuum, the solid was washed with DCM (21 mL) and the residual solid was redissolved in a 1:1 mixture of H.sub.2O and MeCN (1 mL) and analysed by LCMS (ESI+) and .sup.19F NMR (100 L D.sub.2O added).

(99) Procedure D

(100) Solid peptide (approx. 2 mg, 2.5 mol) was dissolved in TFE (0.5 mL) in a 1.5 mL plastic Eppendorf tube, to which DIPEA (so mM in TFE, 0.5 mL) was added. The required fluoro-heteroaromatic (or fluoro-aromatic) was added in 25 equivalents and the tube was shaken at room temperature for 4.5 h. After removal of volatiles under vacuum, each reaction mixture was redissolved in a 1:1 mixture of H.sub.2O and MeCN (1 mL) and analysed by LCMS (ESI+) and .sup.19F NMR (100 L D.sub.2O added).

(101) Procedure E

(102) A stock solution of peptide was prepared by dissolving in the appropriate solvent (approx. 2 mg/mL). In a 2.0 mL glass vial peptide stock solution was added (1.0 mL), to which DIPEA (20 L) was added. An aliquot of stock pentafluoropyridine solution (200 L, 9.0 mM in the respective solvent) was added and the volume adjusted to a final volume of 2.0 mL by addition of appropriate solvent. The resulting mixture was shaken at room temperature for 4.5 h. After removal of volatiles under vacuum, each reaction mixture was redissolved in DMF/D.sub.2O (9:1, 1 mL) and analysed by LCMS (ESI+) and .sup.19F NMR.

(103) Procedure F

(104) A stock solution of peptide was prepared by dissolving in the appropriate solvent (approx. 2 mg/mL). In a 2.0 mL glass vial peptide stock solution was added (1.0 mL), to which DIPEA (20 L) was added. An aliquot of stock pentafluoropyridine solution (70 L, 9.0 mM in the respective solvent) was added and the volume adjusted to a final volume of 2.0 mL by addition of appropriate solvent. The resulting mixture was shaken at room temperature for 4.5 h. After removal of volatiles under vacuum, each reaction mixture was redissolved in DMF/D.sub.2O (9:1, 1 mL) and analysed by LCMS (ESI+) and .sup.19F NMR.

(105) Procedure G

(106) Solid peptide (approx. 2 mg, 2.5 mol) was dissolved in DMF (4.5 mL) in a sealed glass vial, to which DIPEA (50 mM in DMF, 0.5 mL) was added. The required perfluoroheteroaromatic was added in 25 equivalents and the tube was shaken at room temperature for 4.5 h. After removal of volatiles under vacuum, each reaction mixture was redissolved in a 1:1 mixture of H.sub.2O and MeCN (1 mL) and analysed by LCMS (ESI+) and .sup.19F NMR (100 L D.sub.2O added).

(107) Procedure H

(108) Solid peptide (approx. 2 mg, 2.5 mol) was dissolved in the appropriate solvent (0.5 mL) in a 1.5 mL plastic Eppendorf tube, to which Cs.sub.2CO.sub.3 or DIPEA stock solutions (50 mM DMF, 0.5 mL) was added. The fluoro-aromatic or fluoro-heteroaromatic was then added (25 equivalents with respect to the peptide) and the tube was shaken at room temperature for 4.5 h. After removal of volatiles under vacuum, each reaction mixture was redissolved in a 8:1:1 mixture of DMF/H.sub.2O/ACN-d3 (1 mL) and analysed by LCMS (ESI+) and 19F NMR. Large scale reactions for product isolation and purification were run under the same parameters in Ar flushed syringes, in order to avoid air bubbles where volatile aromatic compounds may concentrate.

(109) Procedure I

(110) Solid peptoid (approx. 2 mg, 2.5 mol) was dissolved in DMF (0.5 mL) in a 1.5 mL plastic Eppendorf tube, to which DIPEA (50 mM in DMF, 0.5 mL) was added. The required fluoro-aromatic or fluoro-heteroaromatic was then added (25 equivalents with respect to the peptoid) and the tube was shaken at room temperature for 4.5 h. After removal of volatiles under vacuum, each reaction mixture was redissolved in a 1:1 mixture of H.sub.2O and MeCN (1 mL) and analysed by LC-MS (ESI+) and .sup.19F NMR. Due to the observation of N-terminal (Nae) mass loose in ESI+ mode, samples were also analysed by Maldi-ToF in order to confirm that fragmentation was induced by ionization and not by peptoid degradation. When LC-MS (ESI+) analysis was not possible due to poor solubility of the reaction products in H.sub.2O/MeCN mixtures and/or molar mass of the expected products was beyond LC-MS (ESI+) range, analitycal HPLC with detection at 220 nm was used in order to obtain the reaction profile of products in DMF (95% H.sub.2O to 95% MeCN in 40 min, 1 mL/min) and Maldi-ToF analysis was employed to verify the mass of the final products present in the sample.

(111) LC-MS Conditions:

(112) Peptides and peptoids were characterised by LC-MS, ESI-LC MeCN (TQD mass spectrometer and an Acquity UPLC from Waters) using an Acquity UPLC BEH C8 1.7 M (2.1 mm50 mm) column and (C18 as of Jun. 2, 2015 3 pm) with a flow rate of 0.6 ml min.sup.1, a linear gradient of 5-95% of solvent B over 3.8 min (A=0.1% formic acid in H.sub.2O, B=0.1% formic acid in MeCN) and injection volume of 1 l.

(113) QToF (mass spectrometer and an Acquity UPLC from Waters) using an Acquity UPLC BEH C8 1.7 m (2.1 mm50 mm) column with a flow rate of 0.6 ml min.sup.1, a linear gradient of 0-99% of solvent B over 5 min (A=0.1% formic acid in H.sub.2O, B=0.1% formic acid in MeCN) and injection volume of 3 l.

(114) Peptides and peptoids identities were also confirmed by MALDI-TOF mass spectra analysis (Autoflex II ToF/ToF mass spectrometer Bruker Daltonik GmBH) operating in positive ion mode using an -cyano-4-hydroxycinnamic acid (CHCA or CHHA) matrix. Data processing was done with MestReNova Version 10.0.

(115) TQD

(116) ESI-LC MeCN (TQD): Acquity UPLC BEH C8 1.7 m (2.1 mm50 mm) (C18 as of Jun. 2, 2915 3 pm)

(117) Mobile phase: water containing formic acid (0.1% v/v): Acetonitrile

(118) Flow rate: 0.6 ml min.sup.1

(119) Injection volume: 1 l

(120) Gradient:

(121) TABLE-US-00001 Time (min) % A % B 0 95 5 0.2 95 5 4 5 95 4.5 5 95 5 95 5

(122) Data processing: MestReNova 10.0

(123) QToF

(124) Accurate mass: Acquity UPLC BEH C18 1.7 m (2.1 mm100 mm)

(125) Mobile phase: water containing formic acid (0.1% v/v): Acetonitrile

(126) Flow rate: 0.6 ml min.sup.1

(127) Injection volume: 3 l

(128) Gradient:

(129) TABLE-US-00002 Time (min) % A % B 0 100 0 5 1 99 6 1 99 6.1 100 0 7 100 0

(130) Data processing: MestReNova 10.0

(131) MALDI

(132) Autoflex II ToF/ToF mass spectrometer Bruker Daltonik GmBH 337 nm nitrogen laser

(133) Sample preparation 1 mg/ml, 1 l spotted on matrix

(134) Operating in positive ion mode using an -cyano-4-hydroxycinnamic acid (CHCA or HCCA) matrix

(135) Data acquisition: reflecton mode of analysis

(136) Data processing: MestReNova 10.0

(137) The fluoro-heteroaromatic used in the reactions had to contain at least one nitrogen atom in the aromatic ring. However, it could contain two or three nitrogens in the aromatic ring. FIG. 11 shows five different heterocyclic ring systems which illustrate the possible positions of nitrogen atoms in the fluoro-heteroaromatic reagents. The fluorine atoms are not shown. However, it will be readily understood that for use in cyclisation reactions each ring must contain at least two halogen atoms, and at least one of the halogen atoms must be a fluorine atom.

(138) Ring system A could therefore contain 2, 3, 4 or 5 halogen atoms, and 1, 2, 3, 4 or 5 fluorine atoms. Accordingly, it could be bifluoropyridine, trifluoropyridine, tetrafluoropyridine or pentafluoropyridine.

(139) Similarly, ring systems B, C and D could contain 2, 3 or 4 halogen atoms, and 1, 2, 3, or 4 fluorine atoms, and ring system E could contain 2 or 3 halogen atoms, and 1, 2 or 3 flouorine atoms.

Example 1

Tagging of Cysteine-Containing Peptides with Fluoro-Heteroaromatics

(140) Peptide 1, was reacted according to procedures A and B. The reaction is shown below and the products for each reaction are shown in table 1.

(141) ##STR00001##

(142) TABLE-US-00003 TABLE 1 Reaction of peptide 1 with pentafluoropyridine using procedures A and B Procedure ArF Products formed A B

(143) In the prior art hexafluorobenzene has been shown to react with peptide 1 to generate a cyclic peptide..sup.vi,vii The introduction of nitrogen atom into the aromatic ring increases the reactivity of the perfluoroaromatic systems considerably as pentafluorpyridine and its derivatives are significantly more reactive than hexafluorobenzene. Therefore, pentafluorpyridine reacted with peptide 1 to give a multiply tagged peptide rather than a cyclic product, as explained below. Interestingly reports of sulphur nucleophiles reacting with pentafluoropyridine are not well documented in the literature.

(144) The crude reaction products were analysed used LCMS. The LCMS spectrum and chromatogram of the reaction of peptide 1 according to procedure A is shown in FIG. 13. This shows one major peak in the LCMS chromatogram with a retention time of 3.234 minutes. The spectrum for this peak shows an [M+H].sup.+ peak at 1231.929 m/z, which indicates a tri-substituted product was formed. The structure of this product is shown in FIG. 12.

(145) The LCMS chromatogram of the reaction of peptide 1 according to procedure B is shown in FIG. 16. This shows three major peaks in the LCMS chromatogram with retention times of 1.946, 2.706, 3.074 and 3.175 minutes. Analysis of these peaks was carried out and the results are summarised in table 2.

(146) TABLE-US-00004 TABLE 2 Products of the reaction of peptide 1 according to procedure B identified using LCMS spectroscopy Peak Retention time m/z Identity 1 1.946 820 Starting peptide MeCN adduct 2 2.706 1082 Double ArF addition 3 3.074 1138 ? 4 3.175 1231 Triple ArF addition

(147) This shows that both bi-substituted and tri-substituted products were formed.

(148) Owing to the presence of fluorine atoms in the reagents, it was possible to monitor in situ the outcome of these reactions rapidly using .sup.19F NMR spectra. Moreover, fluorine is very sensitive to changes in local environment, which made it possible to gain structural details which include the substitution pattern around the ring and number of fluoro-heteroaryl groups that have been added.

(149) FIG. 14 shows the .sup.19F NMR spectrum of the products of reaction of peptide 1 according to procedure A and FIG. 15 shows expansions of the peaks. The spectrum shows six different peaks which is consistent with the six different fluorine environments you would expect for a tri-substituted product.

(150) Peptide 1, was reacted according to procedure A with either a fluoro-heteroaromatic (I-VII) or a fluoro-aromatic (VIII). The chemical structures for each of the various fluoro-heteroaromatics (I-VII) or fluoro-aromatic (VIII) are shown in table 3. The crude reaction products for the reactions were analysed using LCMS, and the results are also shown in table 3.

(151) TABLE-US-00005 TABLE 3 Reaction of peptide 1 with various fluoro-heteroaromatics (I-VII) or fluoro- aromatic (VIII) reagents using procedure A LCMS spectrum and Entry ArF chromatogram Products 1 One major peak in the LCMS chromatogram with a retention time of 2.472 minutes, the spectrum for this peak shows an [M + H].sup.+ peak at 1027.676 m/z. Cyclic product, see FIG. 17. 2 One major peak in the LCMS chromatogram with a retention time of 1.942 minutes, the spectrum for this peak shows an [M + H].sup.+ peak which corresponds to starting peptide 1. No detectable new products. 3 One major peak in the LCMS chromatogram with a retention time of 3.104 minutes, the spectrum for this peak shows an [M + H].sup.+ peak at 1255.52 m/z. Di-substituted product, see FIG. 18. 4 One major peak in the LCMS chromatogram with a retention time of 2.665 minutes, the spectrum for this peak shows an [M + H].sup.+ peak at 1045.674 m/z. Di-substituted product, see FIG. 19. 5 0 A major peak in the LCMS chromatogram with a retention time of 3.071 minutes, the spectrum for this peak shows an [M + H].sup.+ peak at 1231.929 m/z. Cyclic mono-substituted product, see FIG. 20. 6 Two major peaks in the LCMS chromatogram with retention times of 2.950 minutes and 3.394 minutes. The spectrum for these peaks show an [M + H].sup.+ peak at 1203.590 m/z and [M + H].sup.+ peak at 1328.009 m/z respectively. Di-substituted and the tri-substituted products were formed, see FIG. 21. 7 A major peak in the LCMS chromatogram with a retention times 3.180 minutes, the spectrum for this peaks shows an [M + H].sup.+ peak at 1280.062 m/z. Tri-substituted product, see FIG. 22. 8 One major peak in the LCMS chromatogram with a retention time of 2.265 minutes, the spectrum for this peak shows an [M + H].sup.+ peak at 929.874 m/z. Cyclic product see FIG. 23.

(152) As mentioned previously, in the prior art hexafluorobenzene was found to readily react with peptides containing two cysteine residues to generate a cyclic peptide. Accordingly, the result obtained for entry 8 of table 3 is consistent with the teachings of the prior aft.

Example 2

Reaction of Glutathione with Pentafluoropyridine

(153) Peptide 5, was reacted according to procedure E. The reaction is shown below. This shows a single mono-substituted product was formed.

(154) ##STR00014##

(155) Analysis of the crude reaction products was carried out using .sup.19F NMR spectroscopy, and the spectrum is shown in FIG. 24. Residual pentafluoropyridine is seen at 93.36, 137.42 and 164.43 ppm. However, the peaks at 102.76 and 171.46 ppm relate to the tagged peptide and are consistent with a single, mono-substituted product.

Example 3

Tagging of Tyrosine-Containing Peptides with Fluoro-Heteroaromatics

(156) Peptide 2, was reacted according to procedures A and C. The reaction is shown below and the products for each reaction are shown in table 4.

(157) ##STR00015##

(158) TABLE-US-00006 TABLE 4 Reaction of peptide 2 with perfluoro-heteroaromtics using procedures A and C Procedure ArF Products formed A C

(159) At room temperature pentafluoropyridine was found to only react with the phenolic OH on the tyrosine (Y) residue.

(160) The crude reaction products were analysed used LCMS. The LCMS spectrum and chromatogram of the reaction of peptide 2 according to procedure A shows one major peak in the LCMS chromatogram with a retention time of 2.455 minutes. The spectrum for this peak shows an [M+H].sup.+ peak at 900.688 m/z, which indicates a mono-substituted product was formed. The structure of this product is shown in FIG. 25.

(161) Similarly, the LCMS spectrum and chromatogram of the reaction of peptide 2 according to procedure C shows one major peak in the LCMS chromatogram with a retention time of 2.261 minutes. The spectrum for this peak shows an [M+H].sup.+ peak at 900.358 m/z, which also indicates a mono-substituted product was formed.

(162) Again .sup.19F NMR spectroscopy was used to analysis the results. FIG. 26 shows the .sup.19F NMR spectrum of the products of reaction of peptide 2 according to procedure A and FIG. 27 shows expansions of the peaks. The spectrum shows two different peaks which is consistent with the two different fluorine environments you would expect for a mono-substituted product.

Example 4

Tagging of Serine-Containing Peptides with Fluoro-Heteroaromatics

(163) Peptide 2, was reacted according to procedure A with either a fluoro-heteroaromatic (I-VII) or a fluoro-aromatic (VIII). The chemical structures for each of the various fluoro-heteroaromatics (I-VII) or fluoro-aromatic (VIII) are shown in table 5. The crude reaction products for the reactions were analysed using LCMS, and the results are also shown in table 3.

(164) TABLE-US-00007 TABLE 5 Reaction of peptide 2 with various fluoro-heteroaromatics (I-VII) or fluoro- aromatic (VIII) reagents using procedure A. LCMS spectrum and Entry ArF chromatogram Products 1 0 Four major peak in the LCMS chromatogram with retention times of 2.625 minutes. 2.763 minutes, 2.818 minutes and 2.946 minutes. The spectrum for the peak at 2.625 minutes shows an [M + H].sup.+ peak at 883.918 Mono-substituted, di- substituted, tri- substituted and cyclic products, see FIG. 28. m/z. The spectrum for the peak at 2.763 minutes shows an [M + H]+ peak at 995.921 m/z. The spectrum for the peak at 2.818 minutes shows an [M + H].sup.+ peak at 1015.805 m/z. The spectrum for the peak at 2.946 minutes shows an [M + H].sup.+ peak at 1148.058 m/z. 2 One major peak in the LCMS chromatogram with a retention time of 1.828 minutes, the spectrum for this peak shows an [M + H]+ peak at 753.132 m/z. Unreacted peptide 2 detected. 3 One major peak in the LCMS chromatogram with a retention time of 3.007 minutes, the spectrum for this peak shows an [M + H].sup.+ peak at 1221.554 m/z. Di-substituted product, see FIG. 29. 4 One major peak in the LCMS chromatogram with a retention time of 1.842 minutes, the spectrum for this peak shows an [M + H].sup.+ peak at 752.061 m/z. Unreacted peptide 2 detected. 5 One major peak in the LCMS chromatogram with a retention time of 3.1 minutes. Structure of this product could not be assigned. 6 Two major peaks in the LCMS chromatogram with retention times of 2.490 minutes and 2.931 minutes. The spectrum for these peaks show an [M + H].sup.+ peak at 932.907 m/z, and an [M + H].sup.+ peak 1115.768 m/z. Mono-substituted and the di-substituted products were formed, see FIG. 30. 7 Two major peaks in the LCMS chromatogram with a retention times of 2.426 minutes and 2.758 minutes. The spectrum for these peaks show an [M + H].sup.+ peak at 916.777 m/z, and an [M + H].sup.+ peak at 1081.649 m/z. Mono-substituted and the di-substituted products were formed, see FIG. 31. 8 One major peak in the LCMS chromatogram with a retention time of 1.810 minutes, the spectrum for this peak shows an [M + H].sup.+ peak at 752.026 m/z. Unreacted peptide 2 detected.

(165) While hexafluorobenzene (VIII) was found to readily react with peptides containing two cysteine residues to generate a cyclic peptide, it was found to be completely unreactive towards nucleophilic attack by serine or tyrosine.

Example 5

Tagging of Lysine-Containing Peptides with Fluoro-Heteroaromatics

(166) Peptide 3, was reacted according to procedures A and C. The reaction is shown below and the products for each reaction are shown in table 6.

(167) ##STR00028##

(168) TABLE-US-00008 TABLE 6 Reaction of peptide 3 with perfluoro-heteroaromatics using procedures A and C Procedure ArF Products formed A 0 C

(169) The crude reaction products were analysed used LCMS. The LCMS spectrum and chromatogram of the reaction of peptide 3 according to procedure A shows one major peak in the LCMS chromatogram with a retention time of 3.209 minutes. The spectrum for this peak shows an [M+H].sup.+ peak at 1281.571 m/z, which indicates a tri-substituted product was formed. The structure of this product is shown in FIG. 32.

(170) However, the LCMS spectrum and chromatogram of the reaction of peptide 3 according to procedure C is shows one major peak in the LCMS chromatogram with a retention time of 3.086 minutes. The spectrum for this peak shows an [M+H].sup.+ peak at 1131.913 m/z, which indicates a bi-substituted product was formed. The structure of this product is shown in FIG. 33.

(171) Peptide 3, was reacted according to procedure A with either a fluoro-heteroaromatic (I-VII) or a fluoro-aromatic (VIII). The chemical structures for each of the various fluoro-heteroaromatics (I-VII) or fluoro-aromatic (VIII) are shown in table 7.

(172) TABLE-US-00009 TABLE 7 Reaction of peptide 3 with various fluoro-heteroaromatics (I-VII) or fluoro- aromatic (VIII) reagents using procedure A. LCMS spectrum and Entry ArF chromatogram Products 1 One major peak in the LCMS chromatogram with a retention time of 2.608 minutes, the spectrum for this peak shows an [M + H].sup.+ peak at 1229.630 m/z. Tri-substituted product, see FIG. 34. 2 Three major peaks in the LCMS chromatogram. Structure of these products could not be assigned. 3 One major peak in the LCMS chromatogram with a retention time of 3.115 minutes, the spectrum for this peak shows an [M + H].sup.+ peak at 1303.728 m/z. Di-substituted product, see FIG. 35. 4 One major peak in the LCMS chromatogram with a retention time of 2.659 minutes, the spectrum for this peak shows an [M + H].sup.+ peak at 1086.348 m/z. Di-substituted product, see FIG. 36. 5 This shows one major peak in the LCMS chromatogram with a retention time of 3.261 minutes, the spectrum for this peak shows an [M + H].sup.+ peak at 1263.562 m/z. Di-substituted product, see FIG. 37. 6 Two major peaks in the LCMS chromatogram with retention times of 2.874 minutes and 3.343 minutes. The spectrum for these peak shows an [M + H].sup.+ peak at 1197.389 m/z and an [M + H].sup.+ peak at 1378.105 m/z. Di-substituted and tri- substituted products, see FIG. 38. 7 This shows two major peaks in the LCMS chromatogram with retention times of 2.807 minutes and 3.245 minutes. The spectrum for these peak shows an [M + H].sup.+ peak at 1165.693 m/z, and an [M + H].sup.+ Di-substituted and tri- substituted products, see FIG. 39. peak at 11328.587 m/z. 8 0 One major peak in the LCMS chromatogram with a retention time of 1.680 minutes. This peak corresponds to unreacted peptide 3. Unreacted peptide 3 detected.

(173) While, hexafluorobenzene (VIII) will readily react with peptides containing two cysteine residues it was found to be completely unreactive towards nucleophilic attack by lysine.

Example 6

Effective on Cysteine, Lysine and Serine Tagging Using Fluoro-Heteroaromatics or Fluoro-Aromatics in the Presence of Organic or Inorganic Bases

(174) Peptides 1-3, were reacted according to procedure H, where the solvent used was DMF and the base used was caesium carbonate. A reaction scheme is shown below, although the products obtained varied, as shown in table 8.

(175) ##STR00041##

(176) TABLE-US-00010 TABLE 8 Summary of the reactions of peptides 1-3 carried according to reaction procedure H where the base used was caesium carbonate. [m/z].sub.obs Entry ArF Peptide Products Position (Da) Product R1.4 1, X = Cys Tri-substituted (main) Di-substituted (minor) Mono- substituted 2Cys and Tyr Cys and Tyr Cys/Tyr mixture 1231.28 1138.35 1048.3 P5, see FIG. 62 P6a and P6b, see FIG. 63 P7a and P7b, see (minor) FIG. 64 R1.5 2, X = Ser Mono- substituted Di-substituted Tri-substituted Tyr/Ser mixture Tyr and Ser 2 Ser and Tyr 901.34 1050.34 1199.33 P8a and P8b, see FIG. 65 P9a and P9b, see FIG. 66 P10, see FIG. 67 R1.6 3, X = Lys Tri-substituted 2Lys and Tyr 1281.45 P11, see FIG. 68

(177) Peptides 1-3, were reacted according to procedure H, where the solvent used was DMF and the base used was N,N-diisopropylethylamine (DIPEA). A reaction scheme is shown below, although the products obtained varied, as shown in table 9.

(178) ##STR00045##

(179) TABLE-US-00011 TABLE 9 Summary of tagging reactions of peptides 1-3 carried out according to reaction procedure H where the base used was DIPEA. Pep- Pro- Posi- [m/z].sub.obs Entry ArF tide ducts tion (Da) Product R2.4 1, X = Cys Tri- sub- stituted 2Cys and Tyr 1233.7 P5, see FIG. 62 R2.5 2, X = Ser Mono- sub- stituted Tyr 901.35 P12, see FIG. 69 R2.6 3, X = Lys Tri- sub- stituted 2Lys and Tyr 1281.45 P11, see FIG. 68

(180) It will be noted that there are clear differences in the products obtained depending on the base used.

(181) For example; DIPEA provides less of a mixture of products. This is evident when comparing entries R1.4 (table 8) and R2.4 (table 9). Here it can be seen that when the reaction of peptide 1 and pentafluoropyridine is carried out using DIPEA as the base (R2.4, table 9) only one main product is formed. When the analogous reaction is carried out with caesium carbonate as the base (R1.4, table 8) three products were observed and isolated.

Example 7

Selective Cysteine Tagging Using Fluoroheteroaromatics in the Presence of Tyrosine Employing 2,2,2-trifluoroethanol (TFE) as Solvent

(182) Peptide 1, was reacted according to procedure D. The reaction is shown below and the product for the reaction is shown in table 10.

(183) ##STR00049##

(184) TABLE-US-00012 TABLE 10 Reaction of peptide 1 with fluoro-heteroaromatics using Procedure D Stapling Procedure reagent Comments/Products formed D 0

(185) The crude reaction products were analysed used LCMS. The LCMS spectrum and chromatogram of the reaction of peptide 1 according to procedure D shows one major peak in the LCMS chromatogram with a retention time of 2.617 minutes. The spectrum for this peak shows an [M+H].sup.+ peak at 1081.629 m/z, which indicates a bi-substituted product was formed. The structure of this product is shown in FIG. 40.

(186) Peptides 1-3 were reacted with both hexafluorobenzene and pentafluoropyridine according to procedure D. A reaction scheme is shown below, although the products obtained varied, as shown in table 11.

(187) ##STR00052##

(188) TABLE-US-00013 TABLE 11 Reaction of peptides 1-3 with hexafluorobenzene and pentafluoropyridine according to procedure D. [m/z].sub.obs Entry ArF Peptide Products Position (Da) Product 1 1, X = Cys No reaction 2 2, X = Ser No reaction 3 3, X = Lys No reaction 4 1, X = Cys Mono- substituted Di-substituted Cys 2Cys 989.36 1038.29 P7a P14 5 2, X = Ser No reaction 6 3, X = Lys No reaction

(189) The crude reaction products were analysed used LCMS.

(190) The reaction of peptides 1-3 with hexafluorobenezne according to procedure D did not yield any products (table 11, entries 1-3). Similarly, the reaction of peptides 2 and 3 with pentafluoropyridine according to procedure D also did not yield any products (table 11, entries 5 and 6).

(191) However, the reaction of peptide 1 with pentafluoropyridine according to procedure D produced two products that were isolated, purified and characterised. The first of the products was P7a, the chemical structure of which is shown in FIG. 41. The second product, was characterised to be the di-cysteine substituted product P14. The chemical structure for P14 are shown in FIG. 42. Both P7a and P14 have no substitution on the tyrosine residue of peptide 1. This shows that by using TFE as the solvent, it is possible to selectively introduce fluoro-heteroaromatic groups at the sulphur (cysteine) positions of peptide 1 over the oxygen-containing tyrosine position.

(192) Perfluorinated solvents have been shown to accelerate organic chemistry reactions,.sup.viii including S.sub.NAr reactions of fluoropurines..sup.ix 2,2,2-Trifluoroethanol (TFE) has also been the subject of several studies involving peptides and proteins and has been shown to stabilise -helical secondary structures..sup.x,xi,xii,xiii Using the procedures developed previously.sup.viii we have demonstrated that, rather than enhancing reactivity, employing 2,2,2-trifluoroethanol (TFE) as the solvent in our system broadly attenuated the reactivity of the electrophiles under investigation. Under these conditions hexafluorobenzene did not react with any peptide side chain (see table 11 entries 1-3). Previously, regiocontrol using pentafluoropyridine was challenging and multiple substitution products were observed, including substitution on the competing tyrosine. Replacement of DMF with TFE afforded a mild method for controlled introduction of fluoro-heteroaromatics at cysteine.

(193) Also as table 11, entries 5 and 6 show in the presence of the solvent TFE peptide 2 (di-serine peptide) and peptide 3 (di-lysine peptide) do not react with pentafluoropyridine.

(194) Accordingly, TFE can be used to allow selective tagging of cysteine (or sulphur nucleophiles) in the presence of serine and lysine residues.

Example 8

Selective Cysteine Tagging Using with Fluoro-Heteroaromatics in the Presence of Lysine Employing TFE as Solvent

(195) Based on the results from Example 7, the inventors subsequently wanted to apply the application of TFE induced selectivity to peptide systems containing mixed cysteine and lysine side chain functionalities, such as peptide 4, to provide further evidence that they could obtain selective functionalization between sulphur (cysteine) and nitrogen (lysine).

(196) Peptide 4, was reacted according to procedures E and F. The general reaction is shown below. The differences between the various reactions and the relative ratio of the products obtained is outlined below and is summarised in table 14.

(197) ##STR00059##

(198) As can be seen above, two products were obtained. The main peak in the mass spectrum for product P15 was at 1265.84 m/z, which corresponds to product P15 with an MeCN adduct. Similarly, the main peak in the mass spectrum for product P16 is at 1565.99 m/z, which corresponds to product P16 with an MeCN adduct.

(199) The LCMS chromatogram of the reaction of peptide 4 according to procedure E, using DMF as the solvent for the reaction is shown in FIG. 43. This shows two major peaks in the LCMS chromatogram, with retention times of 5.77 minutes and 6.98 minutes, and a smaller peak with a retention time of 6.44 minutes. It was found that the peak at 5.77 minutes corresponded to unreacted peptide 4, the peak at 6.44 minutes corresponded to product P15 and the peak at 6.98 minutes corresponded to product P16.

(200) The LCMS chromatogram of the reaction of peptide 4 according to procedure F, using DMF as the solvent for the reaction is shown in FIG. 44. As before, this shows two major peaks in the LCMS chromatogram, with retention times of 5.77 minutes (corresponding to unreacted peptide) and 7.04 minutes (corresponding to product P16), and a smaller peak with a retention time of 6.49 minutes (corresponding to product P15).

(201) Both these show that while product P15 was present, the predominant product formed when the solvent was DMF was product P16.

(202) The LCMS chromatogram of the reaction of peptide 4 according to procedure E, using TFE as the solvent for the reaction is shown in FIG. 45. This shows a major peak in the LCMS chromatogram, with a retention time of 6.33 minutes (corresponding to product P15), and a smaller peak with a retention time of 7.01 minutes (corresponding to product P16). There was no peak present corresponding to unreacted peptide.

(203) The LCMS chromatogram of the reaction of peptide 4 according to procedure F, using TFE as the solvent for the reaction is shown in FIG. 46. This shows a major peak in the LCMS chromatogram, with a retention time of 6.31 minutes (corresponding to product P15), and a smaller peak with a retention time of 6.87 minutes (corresponding to product P16). There was no peak present corresponding to unreacted peptide.

(204) Both these show that while product P16 was present, the predominant product formed when the solvent was TFE was product P15. Thus, when TFE was used as the solvent the cystenine was tagged selectively in the presence of lysine.

(205) The relative ratios of products P15 and P16 for the various reactions are set out in table 12 below.

(206) TABLE-US-00014 TABLE 12 Differences between the reaction procedures used and the ratio of the products obtained when peptide was reacted according to procedures E and F Relative Molar equivalents ratio Procedure of of products Solvent used pentafluoropyridine P15 P16 DMF E 3 1 10.7 DMF F 1 1 9.6 TFE E 3 13.3 1 TFE F 1 2.8 1

(207) As explained above, treatment of the mixed functionality peptide with pentafluopyridine in DMF led to almost complete reaction at both cysteine and both lysine side chains, whereas, the reaction carried out in TFE afforded reaction almost exclusively at both cysteine, leaving the lysines free.

Example 9

Preparing Cyclic Peptides Using Perfluoroheteroaromatics

(208) Peptide 1, was reacted according to procedure G. The reaction is shown below and the product for the reaction is shown in table 12.

(209) ##STR00060##

(210) TABLE-US-00015 TABLE 13 Reaction of peptide 1 with perfluoroheteroaromatics using procedure G Procedure ArF Products formed G

(211) The crude reaction products were analysed used LCMS. The LCMS chromatogram had a peak with a retention time of 2.90 minutes, which was analysed and showed an [M+H].sup.+ peak at 1063.544 m/z, which indicated a cyclic product was formed, as shown above.

(212) This shows that when the concentration of the reagents is lower the reaction favours the formation of a cyclic peptide in a one step synthesis as opposed to a multiply substituted product, as described in many of the previous examples.

Example 10

Preparation of Multi-Cyclic Peptides Using Fluoro-Heteroaromatics

(213) It is also possible to prepare multi cyclic peptide constructs from linear peptide and peptide mimetic sequences containing 3 or more nucleophilic side chains using the methods outlined previously.

(214) These multicyclic peptides (or peptide mimetics may be prepared in a one-pot fashion by nucleophilic aromatic substitution reaction of an appropriate perfluoro heteroaromatic with a peptide (or peptide mimic) containing 3 or more nucleophilic side chains according to the general reaction set out below. Examples of mutli-cyclic peptoid constructs prepared using this approach are detailed in Example 11.

(215) ##STR00063##

(216) It is also conceivable that multicyclic peptides (or peptide mimetics) can be accessed in a regioselective step-wise fashion by sequential reaction of judiciously positioned thiol (e.g. cysteine) residues with a chosen perfluoroheteroaromatic using TFE as the solvent to selectively form a first macrocycle, followed by reaction in DMF with a second perfluoro heteroaromatic to furnish a second attached macrocycle through reaction at amine (e.g. lysine) side chains as shown below.

(217) ##STR00064##

(218) Alternatively, a peptide (or peptide mimetics) can initially form a monocyclic peptide as in Method 2, however, rather than reacting with a second perfluoro heteroaromatic, the available amine (e.g. lysine) functionality can react further at available positions on the attached perfluoro heteroaromatic to form a multicyclic system as shown below.

(219) ##STR00065##

(220) Alternatively, a peptide (or peptide mimetic) can initially be prepared where only one reactive site is revealed and the remaining nucleophilic side chains are protected. An example of this peptide is peptide 6. Peptide 6 can then be reacted selectively with a fluoro-heteroaromatic as shown in the two examples below.

(221) The LCMS chromatogram (280 nm) for purified P17 has a peak with a retention time of 2.622 minutes and the mass spectrum for that peak has an [M+H].sup.+ peak at 1235.84 m/z. The LCMS chromatogram (280 nm) for purified P18 has a peak with a retention time of 2.571 minutes and the mass spectrum for that peak has an [M+H].sup.+ peak at 1219.037 m/z.

(222) ##STR00066##

(223) Removal of the Acm protecting group and subsequent cyclisation onto the fluoro-heteroaromatic rings would give rise to multi-cyclic peptide systems. An overview of this stepwise approach to prepare multi-cyclic peptide constructs is shown below.

(224) ##STR00067##

Example 11

Reaction of Cysteine-Containing Peptoids with Fluoro-Heteroaromatics

(225) The chemical structures for peptoid 1 and 2 is given in FIGS. 47 and 48 respectively.

(226) Peptoids 1 and 2 were reacted according to procedure I, and the results are shown in table 14.

(227) TABLE-US-00016 TABLE 14 Reaction of peptoids 1 and 2 with pentafluoropyridine and fluoro- heteroaromatic (I) using procedure I. Entry Peptoid ArF Analysis Products 1 1 LCMS shown in FIG. 49. A mixture of products were obtained. The main product observed was a tetra- substituted, see FIG. 50 2 1 MALDI- Tof analysis shown in FIG. 51. A bi-cyclic product, see FIG. 52, a mono-cyclic, di- substituted product, see FIG. 53, and a tetra-substituted product, see FIG. 54, were obtained. 3 2 0 LCMS shown in FIG. 55. A mixture of products were obtained. The main product observed was an octa-substituted, see FIG. 56. 4 2 MALDI- Tof analysis shown in FIG. 57. A mono-cyclic, di-substituted product, see FIG. 58, a tetra- substituted product, see FIG. 59, a di-cyclic, tetra- substituted product, see FIG. 60, and a mono-cyclic, hexa-substituted product, see FIG. 61, were obtained.

(228) The reaction of peptoids 1 and 2 with pentafluoropyridine according to procedure I results predominately in the formation of linear multiply substituted products (FIGS. 50 and 56).

(229) However, the reaction peptoids 1 and 2 with fluoro-heteroaromatic (I) according to procedure I results predominately in the formation of cyclic (FIGS. 53, 58, 61) and multi-cyclic (FIGS. 52 and 60) products.

Example 12

Cyclisation with Further Heteroaromatics

(230) To show that further fluoro-heteroaromatic compounds could be used to cyclise peptides further reactions were carried out on peptides 7 to 10 using procedure D, and the results are shown below in table 15.

(231) TABLE-US-00017 TABLE 15 Reaction of peptides 7 to 10 according to procedure D LCMS Fluoro- spectrum and Peptide heteroaromatic chromatogram Product 7 Peak in LCMS chromatogram with retention time of 3.183 minutes/ The spectrum for this peak shows an [M + H].sup.+ peak at 1254.47 m/z. 8 Two major peaks in the LCMS chromatogram with retention times of 2.750 minutes and 3.833 minutes. The spectrum for these peaks show an [M + 2 MeCN + H].sup.+ peak at 1288 m/z and an [M + H].sup.+ peak at 1686 m/z. 9 One major peak in the LCMS chromatogram with a retention time of 2.292 minutes, the spectrum for this peak shows an [M + H].sup.+ peak at 880 m/z. 9 Two peaks in the LCMS chromatogram with retention times of 3.650 minutes and 3.125 minutes. The spectrum for these peaks show an [M + H].sup.+ peak at 1238 m/z and an [M + H].sup.+ peak at 982 m/z. 0 9 Two major peaks in the LCMS chromatogram with retention times of 3.558 minutes and 2.583 minutes. The spectrum for these peaks showed an [M + H].sup.+ peak at 1132 m/z, and [M + H].sup.+ peak at and 929 m/z 9 Two major peaks in the LCMS chromatogram with retention times of 3.208 minutes and 2.417 minutes. The spectrum for these peaks show an [M + H].sup.+ peak at 1064 m/z, and [M + H].sup.+ peaks at 896 m/z and 879 m/z. 10 Two peaks in the LCMS chromatogram with retention times of 2.125 minutes and 2.197 minutes. The spectrum for these peaks show [M + H].sup.+ peaks at 868 m/z, , 1000 m/z and 848 m/z. 0 10 Two peaks in the LCMS chromatogram with retention times of 3.650 minutes and 2.708 minutes. The spectrum for these peaks show [M + H].sup.+ peaks at 1206 m/z and 951 m/z.

(232) Accordingly, it will be apparent that a range of fluoro-heteroaromatic compounds can be used to produce cyclic peptide scaffolds. It should also be noted that peptide cyclisation is also possible via two serine residues which is not possible using current published work.

(233) Summary

(234) Advantages of the invention include the possibility of stapling a range of amino acid residues not only on cysteine as with other published methodologies. Use of fluorinated reagents allows monitoring and analysis to be carried out using .sup.19F NMR, which is not available in other heteroaromatic tag methods and selectivity for specific amino acids can be tuned by varying the solvent e.g. using TFE no tagging is observed at tyrosine or lysine.

REFERENCES

(235) .sup.iBlackwell, H. E. and Grubbs, R. H. Highly Efficient Synthesis of Covalently Cross-Linked Peptide Helices by Ring-Closing Metathesis. Angew. Chem. Int. Ed. 1998, 37, 3281-3284.

(236) .sup.iiSchafmeister, C. E. et al. An All-Hydrocarbon Cross-Linking System for Enhancing the Helicity and Metabolic Stability of Peptides. J. Am. Chem. Soc. 2000, 122, 5891-5892. .sup.iiiVerdine, G. L. and Hilinski, G. J. Stapled Peptides for Intracellular Drug Targets. Methods in Enzymology, Elsevier Inc, 2012, Vol. 503. .sup.ivCraik, D. J. et al. The Future of Peptide-based Drugs. Chem. Biol. Drug. Des. 2013, 81,136-147.

(237) .sup.vChristopher J. White and Andrei K. Yudin. Contemporary strategies for peptide macrocyclization. Nature Chemistry, 2011, 3, 509-524

(238) .sup.viHudson, A. S. et al. Synthesis of a novel tetrafluoropyridine-containing amino acid and tripeptide. Tet. Lett, 2013, 54, 4865-4867.

(239) .sup.viiAlexandra M. Webster et al. A Mild Method for the Synthesis of a Dehydrobutyrine Containing Amino Acid. Tetrahedron, 2014, article accepted

(240) .sup.viiiCoxon, C. R. et al. Investigating the potential application of pentafluoropyridine based reagents in the preparation of novel peptide systems. Org. Biomol. Chem.

(241) Manuscript in Preparation

(242) .sup.ixAlexander M. Spokoyny et al. A Perfluoroaryl-Cysteine S.sub.NAr Chemistry Approach to Unprotected Peptide Stapling. J. Am. Chem. Soc. 2013, 135, 5946-5949.

(243) .sup.xYekui Zou et al. Convergent diversity-oriented side-chain macrocyclization scan for unprotected peptides. Org. Biomol. Chem. 2014, 135, 5946-5949

(244) .sup.xi A. Berkessel et al. Dramatic Acceleration of Olefin Epoxidation in Fluorinated Alcohols: Activation of Hydrogen Peroxide by Multiple H-Bond Networks. J. Am. Chem. Soc., 2006, 128, 8421-8426.

(245) .sup.xiiTrifluoroacetic Acid in 2,2,2-Trifluoroethanol Facilitates S.sub.NAr Reactions of Heterocycles with Arylamines. Benoit Carbain et al. Chem. Eur. J. 2014, 20, 2311-2317

(246) .sup.xiiiKentaro Shiraki et al. Trifluoroethanol-induced Stabilization of the -Helical Structure of -Lactoglobulin: Implication for Non-hierarchical Protein Folding. J. Mol. Biol. 1995, 245, 180-194.

(247) .sup.xivF. D. Sonnichsen et al. Effect of trifluoroethanol on protein secondary structure: an NMR and CD study using a synthetic actin peptide. Biochemistry, 1992, 31, 8790-8798.

(248) .sup.xvPeizhi Luo and Robert L. Baldwin. Mechanism of Helix Induction by Trifluoroethanol: A Framework for Extrapolating the Helix-Forming Properties of Peptides from Trifluoroethanol/Water Mixtures Back to Water. Biochemistry, 1997, 36, 8413.

(249) .sup.xviK. Gast et al. Trifluoroethanol-induced conformational transitions of proteins: insights gained from the differences between alpha-lactalbumin and ribonuclease A. Protein Sci. 1999, 8, 625-634.