Methods of synthesizing and using derivatives of [2-(2-aminoethoxy)ethoxy] acetic acid

Abstract

A synthetic reaction to produce [2-(2-aminoethoxy)ethoxy] acetic acid (AEEA) derivatives. This synthetic reaction does not require isolation and purification of intermediates. The AEEA derivatives can be used to synthesize high load polystyrene-polyethylene glycol-like resins having excellent swelling characteristics.

Description

CROSS REFERENCE TO RELATED APPLICATION [0001] This Patent Application is a Continuation-in-part Patent Application of PCTUS01 / 44382, filed 26 Nov. 2001, and claims the benefit of U.S. Provisional Application No. 60 / 253,242, filed 27 Nov. 2000. CROSS REFERENCE TO RELATED APPLICATION [0002] This application claims the benefit of U.S. Provisional Application No. 60 / 253,242, filed 27 Nov. 2000.STATEMENT REGARDING FEDERALLY SPONSORED RESEARCH [0003] This invention was made with the support of the U.S. Government under Grant No. NIDA DA-10035 awarded by the National Institutes of Health. The U.S. Government has certain rights in this invention.BACKGROUND OF THE INVENTION [0004] 1. Field of the Invention [0005] The present invention is directed to a facile synthesis of polyethylene glycol (PEG)-like compounds of defined lengths (i.e., fixed monomer units). Specifically, a method is enumerated for the facile and cost-efficient synthesis of a suitably protected PEG-like spacer, for use under...

AI Technical Summary

Benefits of technology

[0037] The AEEA derivatives can be used to synthesize high load polystyrene-polyethylene glycol-like (PPL) resins having excellent swelling characteristics. More particularly, the AEEA derivatives can be used to synthesize “designer resins” in which the properties of the resin can be easily optimized. This type of synthesis also permits the variation of the PEG-like content in order to optimize the physicochemical characteristics versus the loading capacity. The resins can be readily synthesized using fluorenylmethoxy carbonyl-(aminoethoxy)ethyl acetic acid (Fmoc-AEEA) and an aminomethylated polystyrene (AMS) resin by standard solid-phase conditions.

Problems solved by technology

Although PEGylated molecules have numerous advantages as exemplified above, there are also disadvantages associated with these polymeric compounds.

The main problem associated with PEG chains has been the lack of well-defined fixed molecular weight of the PEG chains.

The variable chain lengths of high molecular weight PEGs (MW=1000 to 20,000 Da) not only impedes purification by size exclusion chromatography and characterization by mass spectrometry, but the problem multiplies if more than one PEG chain is attached per molecule.

Thus, advances in analytical chemistry have made the use of polymeric PEG chains impractical in many instances.

Although there has been a recent spurt in interest in these short chain PEG-like molecules, a low-cost commercial source of these compounds is still lacking.

This spacer unit can be attached to peptides under solid-phase reaction conditions using a commercial reagent, but the high cost of the reagent (U.S.$466 / g,.

Oxidation of this compound with Jones reagent leads to the formation of carboxylic acid.

The two main drawbacks of the above two schemes are the low overall yields (23% and 32%, respectively) and the necessity for purification (by flash column chromatography, ion-exchange chromatography, etc.) of the intermediates at almost every step.

These resins were therefore ideal candidates to be developed for SPOS, however the low initial loading of the reacting functional group (the free amine in the case of an amino resin) on these resins (typically 0.1-0.4 mmol / g) results in small quantities (typically ˜50-100 mg / g of resin) of the molecules being synthesized.

However, the acid lability of its benzylic ether linkage can be problematic.

Reactions will go to completion only if they are carried out in solvents that adequately swell the resins, and many poor synthetic results are probably due to poor swelling of the resin.

However, introduction of large PEG-based chains decreases resin loading so that loadings are typically much lower for PS-PEG resins (0.8-2.0 mmol / g).

Also, the polymeric nature of the PEG chains can result in variable PEG content of the resin, which in turn affects loading.

Although the PEG-PS based resins have been ideal for the synthesis of peptides, the low substitution level (0.1-0.7 mmol / g) is a problem.

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