Simplified one-pot synthesis of [
View Patent ↗A non-aqueous single pot synthesis of [ 18 F]SFB is set forth. The [ 18 F]SFB produced with this method is then used, for example, to label a peptide or an engineered antibody fragment (diabody) targeting human epidermal growth factor receptor 2 (HER2) as representative examples of labeled compounds for use as an injectable composition to locate abnormal tissue, specifically tumors within an animal or human using a PET scan.
1. An anhydrous process for preparing 18 F labeled compounds comprising
a labeling step comprising, in the presence of carbonate ions, reacting an alkyl or aryl 4-trimethylammoniumbenzoate triflate with a dried potassium-Kryptofix-2.2.2 complex salt of [ 18 F]fluoride in dimethylsulfoxide (DMSO), or cesium carbonate as a source of the activating counter ion for [ 18 F]fluoride, to provide a reaction vial containing a corresponding alkyl or aryl 4-[ 18 F]fluorobenzoate solution, and removing any water in the solution containing the alkyl or aryl 4-[ 18 F]fluorobenzoate,
a deprotecting step comprising dissolving the alkyl or aryl 4-[ 18 F]fluorobenzoate in a basic anhydrous and aprotic solvent to provide a reaction mixture containing 4[ 18 F] fluorobenzoid salt, and
a coupling step comprising adding a solution of an activating agent to the reaction mixture contained 4-[ 18 F]fluorobenzoate to provide an activated ester.
2. The process of claim 1 wherein a N-succinimidyl 4-[ 18 F]fluorobenzoate ([ 18 F]SFB) is dissolved in a solvent and is purified by using a solid phase extraction system, the [ 18 F]SFB then being eluted from the solid phase extraction system.
3. The process of claim 2 wherein the solvent is a weak acidic aqueous solution.
4. The process of claim 3 wherein the weak acidic aqueous solution is an acetic acid solution.
5. The process of claim 2 wherein the [ 18 F]SFB is eluted using an organic solvent.
6. The process of claim 5 wherein the organic solvent is ethyl ether.
7. The process of claim 1 wherein the labeling step is conducted at 90-100° C. for 5-15 minutes, the deprotection step is conducted at from about 90° C. to about 100° C. for about 5-10 minutes and the coupling step is conducted at 85° C.-90° C. for about 9-10 minutes, the heat being provide by a heat source external to the reaction vial.
8. The process of claim 1 wherein a microwave source provides energy to the reaction vial and the labeling step is conducted with the microwave source operating at 20 W-60 W for 1-3 min, the deprotection step is conducted with the microwave source operating at from about 40 W-50 W for about 1 minute and the coupling step is performed with the microwave source operating at about 30-40 W for about 2 minutes.
9. The process of claim 1 further including reacting a N-succinimidyl 4-[ 18 F]fluorobenzoate ([ 18 F]SFB) with a primary amine containing compound to provide a radiation emitting compound.
10. The process of claim 9 wherein the primary amine containing compound is a virus, cell, peptide, protein, lipid, sugar, polymer, nanoparticle, nanowire, nanorod, small molecule or drug.
11. The process of claim 9 wherein the primary amine containing compound is a protein selected from the group consisting of an anti-HER/anti-EGFR antibody, antiHER2/anti-HER 3 diabody, Annexin V and anti-CEA diabody and anti-0066 antibody, a peptide selected from the group consisting of a proinsulin connecting peptide, C-peptide, endothelin-1, αmelanocyte stimulating hormone and its analogs, neurotensin, bombesin and its analogs, vasoactive intestinal peptide and its analogs, arginine-glycine-aspartic acid peptide, BBN-RGD heterodimer and its analogs, (δ-opoid receptor antagonist and urortensin-II; and small molecules selected from the group consisting of prostate specific membrane antigen and (PSMA) inhibitor.
12. The process of claim 1 wherein the alkyl groups are methyl, ethyl, i-propyl or benzyl and the aryl groups are phenyl or substituted phenyls.
13. The process of claim 1 wherein the alkyl or aryl 4-trimethylammoniumbenzoate triflate is ethyl 4-trimethylammoniumbenzoate triflate.
14. The process of claim 1 wherein the basic anhydrous and aprotic solvent is selected from the group consisting of potassium tert-butoxide (t-BuOK) in anhydrous DMSO, LiCl in DMF or pyridine, NaCN in DMSO, KO 2 , 18-crown-6 in benzene, Lil in EtOAc, TMSCl or NaI in MeCN, MgI 2 in toluene or (Bu 3 Sn) 2 O in benzene.
15. The process of claim 1 wherein the activating agent is O—(N-succinimidyl)-N,N,N′,N′-tetrame.