Combinatorial synthesis of PEG oligomer libraries
View Patent ↗A simple chain-extending approach was established for the scale-up of the monoprotected monodisperse PEG diol materials. Reactions of THP-(OCH 2 CH 2 ) n —OMs (n=4, 8, 12) with a large excess of commercially available H—(OCH 2 CH 2 ) n —OH (n=1-4) under basic conditions led to THP-(OCH 2 CH 2 ) n —OH (n=5-15). Similarly, Me-(OCH 2 CH 2 ) n —OH (n=4-11, 13) were prepared from Me-(OCH 2 CH 2 ) n —OMs (n=3, 7, 11). For the chain elongation steps, 40-80% yields were achieved through extraction purification. PEG oligomer libraries I and II were generated in 50-95% overall yields by alkylation or acylation of THP-(OCH 2 CH 2 ) n —OH (n=1-15) followed by deprotection. Alkylation of Me-(OCH 2 CH 2 ) n —OH (n=1-11, 13) with X—(CH 2 ) m —CO 2 R (X=Br or OMs) and subsequent hydrolysis led to PEG oligomer library III in 30-60% overall yields. Combinatorial purification techniques were adapted to the larger-scale library synthesis. A total of 498 compounds, each with a weight of 2-5 g and a minimum purity of 90%, were synthesized.
1. A PEG oligomer combinatorial library consisting of three different groups of compounds having structurally diverse amphiphilic block co-polymer oligomers with permutations of number of poly(ethylene glycol) (PEG) monomers and alkyl chains and a conjugation site for binding with a testing drug candidate, the groups consisting of:
(a) a first group of oligomers consisting of two or more oligomers having the formula CH 3 (CH 2 ) m —(OCH 2 CH 2 ) n —OH wherein m is 3-17 and n is 1-15, wherein hydrophilic and lipophilic components are connected via a nonhydrolyzable ether bond and a hydroxyl group for subsequent conjugation to the testing drug candidate;
(b) a second group of oligomers consisting of two or more oligomers having the formula CH 3 (CH 2 ) m′ —C(O)O—(CH 2 CH 2 O) n′ ,—H wherein m′ is 2-8, 10, 12, 14, and 16 and n′ is 1- 15, wherein hydrophilic and lipophilic components are joined together by a hydrolyzable ester bond and a hydroxyl group for subsequent conjugation to the testing drug candidate; and
(c) a third group of oligomers consisting of two or more oligomers having the formula CH 3 (OCH 2 CH 2 ) n″ —O—(CH 2 ) m″ CO 2 H wherein m″ is 4-7, 9-11, 14, and 15 and n″ is 1-11, and 13 wherein hydrophilic and lipophilic components are connected via a nonhydrolyzable ether bond and the hydrophilic and lipophilic components are inverted relative to the first group and a carboxylic acid group for subsequent conjugation to the testing drug candidate;
and wherein each compound has a weight of from 2-5 grams and a minimum purity of 90% to provide three different groups for the combinational library for drug discovery.
2. The oligomer library of claim 1 wherein the first group consists of 225 compounds.
3. The oligomer library of claim 1 , wherein the second group consists of 165 compounds.
4. The oligomer library of claim 1 , wherein the third group consists of 108 compounds.