Synthetic Route of C11H19NO4S. The protonation of heteroatoms in aromatic heterocycles can be divided into two categories: lone pairs of electrons are in the aromatic ring conjugated system; and lone pairs of electrons do not participate. Compound: (R)-3-(tert-Butoxycarbonyl)-5,5-dimethylthiazolidine-4-carboxylic acid, is researched, Molecular C11H19NO4S, CAS is 117918-23-7, about Attachment of basic amino group to plasmepsin inhibitors exhibiting potent antimalarial activity. Author is Kashimoto, Keisuke; Hidaka, Koushi; Uemura, Tsuyoshi; Miura, Takuya; Freire, Ernesto; Kimura, Tooru; Kiso, Yoshiaki.
Plasmepsin (Plm) is a target for new antimalarial drugs, but most reported Plm inhibitors have relatively low antimalarial activities. So, we attached substituents on a structure of the highly potent Plm inhibitor KNI-10006. Among the derivatives, amino-substituted compound such as KNI-10538 exhibited enhanced antimalarial activity maintaining potent Plm II inhibitory activity. These results suggest that auxiliary substituents of specific basic group contribute to deliver the inhibitors to the target Plm. We further synthesized the alkylamino derivatives
After consulting a lot of data, we found that this compound(117918-23-7)Synthetic Route of C11H19NO4S can be used in many types of reactions. And in most cases, this compound has more advantages.
Reference:
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts