Oxazolidinone

Oxazolidinone Structure
CAS No.
51667-26-6
Chemical Name:
Oxazolidinone
Synonyms
Oxazolidinone;(R)-(-)-4-ISOPROPYL-3-PROPIMYL-2-OXAZOLIDINOE
CBNumber:
CB01028254
Molecular Formula:
C3H5NO2
Molecular Weight:
87.0773
MOL File:
Mol file
Modify Date:
2023/5/9 9:30:18

Oxazolidinone Chemical Properties,Uses,Production

Preparation

The amino alcohol 761 (1 equiv.) was dissolved in dichloromethane (10 mL/mmol) and triphosgene (0.3 equiv.) and triethylamine (1 equiv.) were added. After 1 h, the reaction mixture was hydrolyzed with H2O. The organic layer was separated, washed successively with saturated aq. NaHCO3 solution and saturated brine, dried over Mg2SO4, and concentrated in vacuo. The residue was chromatographed on silica gel (n-hexane/ethyl acetate, 1:1); threo isomer 762: 54.6 mg (67%) from 85 mg (0.35 mmol) of threo-761 as a pale oil; erythro isomer 762: 124 mg (91%) from 100 mg (0.26 mmol) of erythro-761.
The preparation of Oxazolidinone

Pharmaceutical Applications

The oxazolidinones are a novel class of synthetic antimicrobial agents unrelated to any other antibacterial drug class. They were originally developed as monoamine oxidase inhibitors for treatment of depression, with subsequent recognition of their antimicrobial properties. The first members of the group to emerge exhibited potent activity against Gram-positive organisms, but were not developed for human use owing to toxicity in animal models. In the 1990s two less toxic oxazolidinones were developed: eperezolid, a piperazine derivative, and linezolid, a morpholine derivative. Linezolid exhibited the more favorable pharmacokinetic profile and was subsequently licensed for human use.
Numerous chemical analogs have been screened in a search for compounds with enhanced potency, a broader spectrum of activity or a more favorable side effect profile. Several promising candidates have been described, but linezolid remains the only oxazolidinone currently available.
These drugs are characterized by activity against Gram-positive organisms including methicillin-resistant Staphylococcus aureus, penicillin-resistant pneumococci and vancomycin-resistant enterococci. They are inactive against most Gram-negative species, although some investigational compounds are active against fastidious Gramnegative bacteria including Haemophilus influenzae. They have potentially useful activity against mycobacteria, including multiresistant isolates of Mycobacterium tuberculosis. Resistance among Grampositive organisms remains very uncommon (<0.5%) among clinical isolates.

Oxazolidinone Preparation Products And Raw materials

Raw materials

Preparation Products

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Oxazolidinone (R)-(-)-4-ISOPROPYL-3-PROPIMYL-2-OXAZOLIDINOE 51667-26-6 Oxazolidinone