Uldazepam

In today's world, Uldazepam is a topic that has gained relevance in different areas of society. For years, Uldazepam has been the subject of debate and analysis due to its impact on people's daily lives. Whether in the scientific, social, political or cultural field, Uldazepam has proven to be a constant point of interest for researchers, experts and the general public. In this article, we will explore how Uldazepam has influenced various areas of society and what its implications are for the present and future. Through deep analysis, we seek to better understand the importance and scope of Uldazepam today.

Uldazepam
Clinical data
Other names7-chloro-5-(2-chlorophenyl)-N-prop-2-enoxy-3H-1,4-benzodiazepin-2-amine
ATC code
  • none
Identifiers
  • (2Z)-7-Chloro-5-(2-chlorophenyl)-1,3-dihydro-2H-1,4-benzodiazepin-2-one O-allyloxime
CAS Number
PubChem CID
ChemSpider
UNII
KEGG
CompTox Dashboard (EPA)
Chemical and physical data
FormulaC18H15Cl2N3O
Molar mass360.24 g·mol−1
3D model (JSmol)
  • Clc3ccccc3C/2=N/CC(=N/c1c\2cc(Cl)cc1)\NOC\C=C
  • InChI=1S/C18H15Cl2N3O/c1-2-9-24-23-17-11-21-18(13-5-3-4-6-15(13)20)14-10-12(19)7-8-16(14)22-17/h2-8,10H,1,9,11H2,(H,22,23) checkY
  • Key:DTMPGSXFUXZBDK-UHFFFAOYSA-N checkY
 ☒NcheckY (what is this?)  (verify)

Uldazepam is a drug which is a benzodiazepine derivative. It has sedative and anxiolytic effects similar to those of other benzodiazepines.

Synthesis

Thio thionamide is even more prone to amidine formation than the lactam itself.

Uldazepam synthesis: J. B. Hester, Jr., (1970); Chem. Abstr., 73: 99,001t (1970).

Reaction of thionamide (2) with O-allyl-hydroxylamine gave the oximino (3) uldazepam.

See also

References

  1. ^ "Uldazepam U 31920". Psychotropics. Retrieved 12 June 2013.
  2. ^ Oelschläger H, Ellaithy MM, Volke J (February 1988). "". Archiv der Pharmazie (in German). 321 (2): 69–72. doi:10.1002/ardp.19883210205. PMID 3369929. S2CID 96356746.
  3. ^ Itil TM, Akpinar S, Ozkut H, Balki N, Herrmann WM (June 1974). "Clinical and computerized EEG effects of U-31,920, a new anxiolytic". Current Therapeutic Research, Clinical and Experimental. 16 (6): 642–54. PMID 4211146.
  4. ^ DE 2005176, Hester Jr., Jackson Boling, "3H-1,4-benzodiazepine und Verfahren zu deren Herstellung ", published 1970-09-10, assigned to The Upjohn Co. 
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