Method for preparing water-soluble polymer derivatives bearing a terminal carboxylic acid
View Patent ↗A method is provided for preparing water-soluble polymer derivatives bearing a terminal carboxylic acid or ester thereof. The method involves the hydrolyzing an ortho ester of a water-soluble polymer so as provide the corresponding acid. In addition, the invention provides water-soluble polymers bearing a terminal carboxylic acid or ester thereof, intermediates and reagents useful in carrying out the method, as well as gels, pharmaceutical formulations, conjugates related to the described water-soluble polymer derivatives.
1. A polymer having the following structure:
wherein:
POLY is a water-soluble polymer segment having a nominal average molecular weight of from about 2,000 daltons to about 25,000 daltons;
(a) is either zero or one;
X, when present, is a spacer moiety;
(z) is an integer from 1 to 24;
R 1 , in each occurrence, is in dependently H or an organic radical selected from the group consisting of alkyl, substituted alkyl, alkenyl, substituted alkenyl, alkynyl, substituted alkynyl, aryl, and substituted aryl;
R 2 , in each occurrence, is independently H or an organic radical selected from the group consisting of alkyl, substituted alkyl, alkenyl, substituted alkenyl, alkynyl, substituted alkynyl, aryl, and substituted aryl; and
each R 4 is a either (i) an organic radical independently selected from the group consisting of alkyl, substituted alkyl, alkenyl, substituted alkenyl, alkynyl, substituted alkynyl, aryl, and substituted aryl, or (ii) one or more atoms that combine with another R 4 or the remaining R 4 moieties to form a cyclic ortho ester structure.
2. The polymer of claim 1 , wherein (z) equals three and the polymer has the following structure:
3. The polymer of claim 2 , wherein each occurrence of R 1 and R 2 is H.
4. The polymer of claim 2 , wherein the R 1 attached to the carbon α to the carbon in the ortho ester moiety is alkyl, all other R 1 variables are H, and all R 2 variables are H.
5. The polymer of claim 1 , wherein POLY is selected from the group consisting of a poly(alkylene oxide), poly(vinyl pyrrolidone), poly(vinyl alcohol), polyoxazoline, poly(acryloylmorpholine), and poly(oxyethylated polyol).
6. The polymer of claim 5 , wherein POLY is a poly(alkylene oxide).
7. The polymer of claim 6 , wherein the poly(alkylene oxide) is a poly(ethylene glycol).
8. The polymer of claim 7 , wherein the poly(ethylene glycol) is terminally capped with an end-capping moiety.
9. The polymer of claim 8 , wherein the end-capping moiety is independently selected from the group consisting alkoxy, substituted alkoxy, alkenyloxy, substituted alkenyloxy, alkynyloxy, substituted alkynyloxy, aryloxy, substituted aryloxy, and hydroxy.
10. The polymer of claim 9 , wherein the end-capping moiety is alkoxy.
11. The polymer of claim 10 , wherein the alkoxy is methoxy.
12. The polymer of claim 9 , wherein the end-capping moiety is hydroxy.
13. The polymer of claim 7 , wherein the poly(ethylene glycol) has a nominal average molecular weight of from about 5,000 daltons to about 20,000 daltons.
14. The polymer of claim 1 , wherein (a) equals zero.
15. The polymer of claim 1 , wherein (a) equals one.
16. The polymer of claim 15 , wherein X is independently selected from the group consisting of —O—, —S—, —C(O)—, —C(O)—NH—, —NH—C(O)—NH—, —O—C(O)—NH—, —C(S)—, —CH 2 —, —CH 2 —CH 2 —, —CH 2 —CH 2 —CH 2 —, —CH 2 —CH 2 —CH 2 —CH 2 —, —O—CH 2 —, —CH 2 —O—, —O—CH 2 —CH 2 —, —CH 2 —O—CH 2 —, —CH 2 —CH 2 —O—, —O—CH 2 —CH 2 —CH 2 —, —CH 2 —O—CH 2 —CH 2 —, —CH 2 —CH 2 —O—CH 2 —, —CH 2 —CH 2 —CH 2 —O—, —O—CH 2 —CH 2 —CH 2 —CH 2 —, —CH 2 —O—CH 2 —CH 2 —CH 2 —, —CH 2 —CH 2 —O—CH 2 —CH 2 —, —CH 2 —CH 2 —CH 2 —O—CH 2 —, —CH 2 —CH 2 —CH 2 —CH 2 —O—, —C(O)—NH—CH 2 —, —C(O)—NH—CH 2 —CH 2 —, —CH 2 —C(O)—NH—CH 2 —, —CH 2 —CH 2 —C(O)—NH—, —C(O)—NH—CH 2 —CH 2 —CH 2 —, —CH 2 —C(O)—NH—CH 2 —CH 2 —, —CH 2 —CH 2 —C(O)—NH—CH 2 —, —CH 2 —CH 2 —CH 2 —C(O)—NH—, —C(O)—NH—CH 2 —CH 2 —CH 2 —CH 2 —, —CH 2 —C(O)—NH—CH 2 —CH 2 —CH 2 —, —CH 2 —CH 2 —C(O)—NH—CH 2 —CH 2 —, —CH 2 —CH 2 —CH 2 —C(O)—NH—CH 2 —, —CH 2 —CH 2 —CH 2 —C(O)—NH—CH 2 —CH 2 —, —CH 2 —CH 2 —CH 2 —CH 2 —C(O)—NH—, —C(O)—O—CH 2 —, —CH 2 —C(O)—O—CH 2 —, —CH 2 —CH 2 —C(O)—O—CH 2 —, —C(O)—O—CH 2 —CH 2 —, —NH—C(O)—CH 2 —, —CH 2 —NH—C(O)—CH 2 —, —CH 2 —CH 2 —NH—C(O)—CH 2 —, —NH—C(O)—CH 2 —CH 2 —, —CH 2 —NH—C(O)—CH 2 —CH 2 —, —CH 2 —CH 2 —NH—C(O)—CH 2 —CH 2 —, —C(O)—NH—CH 2 —, —C(O)—NH—CH 2 —CH 2 —, —O—C(O)—NH—CH 2 —, —O—C(O)—NH—CH 2 —CH 2 —, —NH—CH 2 —, —NH—CH 2 —CH 2 —, —CH 2 —NH—CH 2 —, —CH 2 —CH 2 —NH—CH 2 —, —C(O)—CH 2 —, —C(O)—CH 2 —CH 2 —, —CH 2 —C(O)—CH 2 —, —CH 2 —CH 2 —C(O)—CH 2 —, —CH 2 —CH 2 —C(O)—CH 2 —CH 2 —, —CH 2 —CH 2 —C(O)—, —CH 2 —CH 2 —CH 2 —C(O)—NH—CH 2 —CH 2 —NH—, —CH 2 —CH 2 —CH 2 —C(O)—NH—CH 2 —CH 2 —NH—C(O)—, —CH 2 —CH 2 —CH 2 —C(O)—NH—CH 2 —CH 2 —NH—C(O)—CH 2 —, —CH 2 —CH 2 —CH 2 —C(O)—NH—CH 2 —CH 2 —NH—C(O)—CH 2 —CH 2 —, —O—C(O)—NH—[CH 2 ] h —(OCH2CH2) j —, —C(O)—NH—(CH 2 ) 1-6 —NH—C(O)—, —NH—C(O)—NH—(CH 2 ) 1-6 —NH—C(O)—, and —O—C(O)—NH—(CH 2 ) 1-6 —NH—C(O)-,bivalent cycloalkyl group, an amino acid, —N(R 6 )—, and combinations of two or more of any of the foregoing, wherein R 6 is H or an organic radical selected from the group consisting of alkyl, substituted alkyl, alkenyl, substituted alkenyl, alkynyl, substituted alkynyl, aryl and substituted aryl, (h) is zero to six, and (j) is zero to 20.
17. The polymer of claim 1 , wherein each R 4 combines with another R 4 or the remaining R 4 moieties to form an ortho ester cyclic structure.
18. The polymer of claim 17 , wherein each R 4 combines with another R 4 or the remaining R 4 moieties to form an ortho ester cyclic structure selected from the group
consisting of
19. The polymer of claim 1 , selected from the group consisting of
wherein H 3 CO—(CH 2 CH 2 O) m — is the Poly and wherein said Poly is a polyethylene glycol terminally capped with methoxy.