Method for the preparation of 1-benzotriazolyl carbonate esters of poly(ethylene glycol)
View Patent ↗The invention provides a method for preparing a 1-benzotriazolylcarbonate ester of a water-soluble and non-peptidic polymer by reacting a terminal hydroxyl group of a water-soluble and non-peptidic polymer with di(1-benzotriazolyl)carbonate in the presence of an amine base and an organic solvent. The polymer backbone can be poly(ethylene glycol). The 1-benzotriazolylcarbonate ester can then be reacted directly with a biologically active agent to form a biologically active polymer conjugate or reacted with an amino acid, such as lysine, to form an amino acid derivative.
1. A method for making a polymer conjugate, said method comprising:
(i) providing a water-soluble and non-peptidic polymer having at least one terminal hydroxyl group;
(ii) reacting the terminal hydroxyl group of the water-soluble and non-peptidic polymer with di(1-benzotriazolyl)carbonate (di-BTC) to form a 1-benzotriazolylcarbonate ester of the water-soluble and non-peptidic polymer (polymer BTC ester), and
(iii) reacting the 1-benzotriazolylcarbonate ester of the water-soluble and non-peptidic polymer with a biologically active agent under conditions effective to form a polymer conjugate.
2. The method of claim 1 , wherein the biologically active agent comprises a nucleophilic functional group capable of reacting with said polymer BTC ester; and said BTC ester is reacted with said biologically active agent.
3. The method of claim 2 , wherein said nucleophilic functional group is an amine.
4. The method of claim 1 , wherein said biologically active agent is selected from the group consisting of peptides, proteins, enzymes, small molecule drugs, dyes, lipids, nucleosides, oligonucleotides, cells, viruses, liposomes, microparticles and micelles.
5. The method of claim 1 , wherein the water-soluble and non-peptidic polymer is selected from the group consisting of poly(alkylene glycol), poly(oxyethylated polyol), poly(olefinic alcohol), poly(vinylpyrrolidone), poly(hydroxypropylmethacrylamide), poly(α-hydroxy acid), poly(vinyl alcohol), polyphosphazene, polyoxazoline, poly(N-acryloylmorpholine), and copolymers, terpolymers, and mixtures thereof.
6. The method of claim 5 , wherein the water-soluble and non-peptidic polymer is a poly(ethylene glycol).
7. The method of claim 6 , wherein the poly(ethylene glycol) is selected from the group consisting of alkoxy poly(ethylene glycol), difunctional poly(ethylene glycol), multi-armed poly(ethylene glycol), forked poly(ethylene glycol), branched poly(ethylene glycol), and pendent poly(ethylene glycol).
8. The method of claim 6 , wherein the poly(ethylene glycol) comprises a degradable linkage.
9. The method of claim 6 , wherein the poly(ethylene glycol) has an average molecular weight from about 200 Da to about 100,000 Da.
10. The method of claim 6 , wherein the poly(ethylene glycol) comprises the formula: —CH 2 CH 2 O—(CH 2 CH 2 O) n —CH 2 CH 2 —, where n is from about 3 to about 4000.
11. The method of claim 10 , wherein the poly(ethylene glycol) comprises the formula: —CH 2 CH 2 O—(CH 2 CH 2 O) n —CH 2 CH 2 —, where n is from about 3 to about 2000.
12. The method of claim 7 , wherein the poly(ethylene glycol) is branched.
13. The method of claim 12 , wherein the poly(ethylene glycol) has a central branch core and a plurality of linear poly(ethylene glycol) chains linked to the central branch core.
14. The method of claim 13 , wherein said central branch core is derived from a polyol selected from glycerol, pentaerythritol, and sorbitol.
15. The method of claim 1 , wherein the water-soluble and non-peptidic polymer in step (i) has the structure R′-POLY-OH and the 1-benzotriazolylcarbonate ester of the water-soluble and non-peptidic polymer has the structure:
wherein POLY is a water-soluble and non-peptidic polymer backbone and R′ is a capping group.
16. The method of claim 15 , wherein R′ is methoxy.
17. The method of claim 15 , wherein R′ is a functional group selected from the group consisting of hydroxyl, protected hydroxyl, active ester, active carbonate, acetal, aldehyde, aldehyde hydrates, alkenyl, acrylate, methacrylate, acrylamide, active sulfone, protected amine, protected hydrazide, thiol, protected thiol, carboxylic acid, protected carboxylic acid, isocyanate, isothiocyanate, maleimide, vinylsulfone, dithiopyridine, vinylpyridine, iodoacetamide, epoxide, glyoxal, dione, mesylate, tosylate, and tresylate.
18. The method of claim 1 , wherein said reacting step (ii) is conducted in an organic solvent.
19. The method of claim 18 , wherein the organic solvent is selected from the group consisting of methylene chloride, chloroform, acetonitrile, tetrahydrofuran, dimethylformamide, dimethyl sulfoxide, and mixtures thereof.
20. The method of claim 1 , wherein said reacting step (ii) is conducted in the presence of a base.
21. The method of claim 20 , wherein the base is selected from the group consisting of pyridine, dimethylaminopyridine, quinoline, trialkylamines, and mixtures thereof.
22. The method of claim 1 , wherein the molar ratio of di(1-benzotriazolyl) carbonate to the water-soluble and non-peptidic polymer is about 30:1 or less.
23. The method of claim 6 , wherein said biologically active agent is a peptide or protein, and said polymer conjugate comprises a carbamate linkage between said protein or peptide and said polymer.
24. The method of claim 4 , wherein said biologically active agent is a small molecule drug.
25. The method of claim 23 , wherein step (iii) results in formation of a mixture of polymer conjugates selected from the group consisting of mono-PEGylated peptide or protein, di-PEGylated peptide or protein, tri-PEGylated peptide or protein, and tetra-PEGylated peptide or protein.