Extracurricular laboratory: Synthetic route of 3724-19-4

Here is just a brief introduction to this compound(3724-19-4)Electric Literature of C8H9NO2, more information about the compound(3-Pyridinepropionic acid) is in the article, you can click the link below.

The preparation of ester heterocycles mostly uses heteroatoms as nucleophilic sites, which are achieved by intramolecular substitution or addition reactions. Compound: 3-Pyridinepropionic acid( cas:3724-19-4 ) is researched.Electric Literature of C8H9NO2.Lu, Shui-Yu; Chin, Frederick T.; McCarron, Julie A.; Pike, Victor W. published the article 《Efficient O- and N-(β-fluoroethylation)s with NCA [18F]β-fluoroethyl tosylate under microwave-enhanced conditions》 about this compound( cas:3724-19-4 ) in Journal of Labelled Compounds & Radiopharmaceuticals. Keywords: fluorine 18 beta microwave fluoroethylation amine phenol carboxylic acid; pipecolinic acid chemoselective fluorine 18 beta microwave fluoroethylation. Let’s learn more about this compound (cas:3724-19-4).

Reactions of no-carrier-added (NCA) [18F]β-fluoroethyl tosylate with amine, phenol or carboxylic acid in the presence of base (e.g. Cs2CO3) to form the corresponding [18F]N-(β-fluoroethyl)amine, [18F]β-fluoroethyl ether or [18F]β-fluoroethyl ester, are rapid (2-10 min) and efficient (51-89% conversion) under microwave-enhanced conditions. These conditions allow reactants to be heated rapidly to 150° in a low b.p. solvent, such as MeCN, and avoid the need to use high b.p. solvents, such as DMSO and DMF, to promote reaction. The microwave-enhanced reactions gave ∼20% greater radiochem. yields than thermal reactions performed at similar temperatures and over similar reaction times. With a bi-functional mol., such as DL-pipecolinic acid, [18F]β-fluoroethyl tosylate reacts exclusively with the amino group.

Here is just a brief introduction to this compound(3724-19-4)Electric Literature of C8H9NO2, more information about the compound(3-Pyridinepropionic acid) is in the article, you can click the link below.

Reference:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem