The effect of the change of synthetic route on the product 73590-85-9

Compounds in my other articles are similar to this one(5-Methoxy-2-[[(4-methoxy-3,5-dimethyl-2-pyridyl)methyl]thio]benzimidazole)Formula: C17H19N3O2S, you can compare them to see their pros and cons in some ways,such as convenient, effective and so on.

Most of the natural products isolated at present are heterocyclic compounds, so heterocyclic compounds occupy an important position in the research of organic chemistry. A compound: 73590-85-9, is researched, SMILESS is CC1=CN=C(CSC2=NC3=CC(OC)=CC=C3N2)C(C)=C1OC, Molecular C17H19N3O2SJournal, Tetrahedron: Asymmetry called Asymmetric synthesis of esomeprazole, Author is Cotton, H.; Elebring, T.; Larsson, M.; Li, L.; Sorensen, H.; von Unge, S., the main research direction is esomeprazole asym synthesis.Formula: C17H19N3O2S.

A highly efficient synthesis of esomeprazole – the (S)-enantiomer of omeprazole – via asym. oxidation of prochiral sulfide I is described. The asym. oxidation was achieved by titanium-mediated oxidation with cumene hydroperoxide (CHP) in the presence of (S,S)-diethyl tartrate [(S,S)-DET]. The enantioselectivity was provided by preparing the titanium complex in the presence of I at an elevated temperature and/or during a prolonged preparation time and by performing the oxidation of I in the presence of an amine. An enantioselectivity of >94% ee was obtained using this method.

Compounds in my other articles are similar to this one(5-Methoxy-2-[[(4-methoxy-3,5-dimethyl-2-pyridyl)methyl]thio]benzimidazole)Formula: C17H19N3O2S, you can compare them to see their pros and cons in some ways,such as convenient, effective and so on.

Reference:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem