5285-41-6Relevant articles and documents
A method for synthesizing anti-mildew agent O
-
Paragraph 0010; 0024; 0026; 0027, (2017/04/06)
The invention discloses a synthesis method of mildew preventive O. The synthesis method comprises the following steps: carrying out condensation reaction on 5-chloro-2-hydroxyaniline and urea under existence of hydrochloric acid to prepare 5-chlorobenzene oxazolone intermediate; carrying out substitution reaction on 5-chlorobenzene oxazolone, the hydrochloric acid and aqueous hydrogen peroxide solution under existence of polar solvent acetic acid, wherein the mass ratio of the 5-chlorobenzene oxazolone to the acetic acid to the hydrochloric acid to the aqueous hydrogen peroxide solution is 1 to 2.5 to 1.25 to 0.9; the reaction temperature is controlled at 50-75 DEG C; the reaction time is 3 hours; carrying out post-treatment such as cooling, washing and the like on the prepared product, so as to obtain a mildew preventive O crude product; recrystallizing by 95% of ethanol, so as to obtain a pure mildew preventive O product. The mildew preventive O is similar to white in appearance; the content is 96%; the melting point range is 185.0 DEG C to 187.0 DEG C; the product yield is over 80%.
BENZOXAZOLONE DERIVATIVES AS ACID CERAMIDASE INHIBITORS, AND THEIR USE AS MEDICAMENTS
-
Page/Page column 40; 44, (2015/12/11)
The present invention relates to benzoxazolone derivatives as acid ceramidase inhibitors, pharmaceutical compositions containing these inhibitors and methods of inhibiting acid ceramidase for the treatment of disorders in which modulation of the levels of ceramide is clinically relevant. The invention also provides benzoxazolone derivatives for use as a medicament in the treatment of cancer, inflammation, pain, inflammatory pain or pulmonary diseases.