Some scientific research about 152305-23-2

We¡¯ll also look at important developments in the pharmaceutical industry because understanding organic chemistry is important in understanding health, medicine, the role of 152305-23-2, and how the biochemistry of the body works.Electric Literature of 152305-23-2

Electric Literature of 152305-23-2, The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.152305-23-2, Name is (S)-4-(4-Aminobenzyl)oxazolidin-2-one, molecular formula is C10H12N2O2. In a Patent£¬once mentioned of 152305-23-2

ONE POT SYNTHESIS OF 2-OXAZOLIDINONE DERIVATIVES

The present invention provides an improved process for preparing (S)-4-{[3-[2-(dimethylamino)ethyl]-1H-indol-5-yl]methyl}-2-oxazolidinone which comprises: a) forming a carbamate of formula (III), from methyl 4-nitro-(L)-phenylalaninate hydrochloride; b) reducing the compound of formula (III) to give the compound of formula (IV); c) reducing the methyl ester grouping in the compound of formula (IV) to give the compound of formula (V); d) ring closure of the compound of formula (V) to give the compound of formula (VI); e) diazonium salt formation from the compound of formula (VI) followed by reduction to give the compound of formula (VII); f) Fischer reaction of the compound of formula (VII) to give (S)-4-{[3-[2-(dimethylamino)ethyl]-1H-indol-5-yl]methyl}-2-oxazolidinone

We¡¯ll also look at important developments in the pharmaceutical industry because understanding organic chemistry is important in understanding health, medicine, the role of 152305-23-2, and how the biochemistry of the body works.Electric Literature of 152305-23-2

Reference£º
Oxazolidine – Wikipedia,
Oxazolidine | C3H2217NO – PubChem