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Sulazepam

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
Sulazepam
Clinical data
ATC code
  • none
Legal status
Legal status
Identifiers
  • 7-Chloro-1-methyl-5-phenyl-1,3-dihydro- 2H-1,4-benzodiazepine-2-thione
CAS Number
PubChemCID
ChemSpider
UNII
KEGG
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC16H13ClN2S
Molar mass300.80 g·mol−1
3D model (JSmol)
  • ClC1=CC=C(N(C)C(CN=C2C3=CC=CC=C3)=S)C2=C1
  • InChI=1S/C16H13ClN2S/c1-19-14-8-7-12(17)9-13(14)16(18-10-15(19)20)11-5-3-2-4-6-11/h2-9H,10H2,1H3 checkY
  • Key:MWGWTOPCKLQYEU-UHFFFAOYSA-N checkY
  (verify)

Sulazepam is abenzodiazepine derivative. It is thethioamide derivative ofdiazepam. It is metabolised intodiazepam,desmethyldiazepam andoxydiazepam[citation needed]. It hassedative,muscle relaxant,hypnotic,anticonvulsant andanxiolytic properties like those of other benzodiazepines.[1][2] It was never marketed.

Synthesis

[edit]
Sulazepam synthesis:[3]U.S. patent 3,141,890

Treatment of diazepam withphosphorus pentasulfide produces the correspondingthionamide, sulazepam.

See also

[edit]

References

[edit]
  1. ^"sulazepam". psychotropics.dk. 2003. Retrieved29 December 2008.
  2. ^Golovenko NI, Zin'kovskii VG (September 1976). "[Analysis of the structure of the components of the convulsive action of corazole following administration of sulazepam and its metabolites to mice]" [Analysis of the structure of the components of the convulsive action of corazole following administration of sulazepam and its metabolites to mice].Biulleten' Eksperimental'noi Biologii I Meditsiny (in Russian).82 (9):1078–81.PMID 11012.
  3. ^Archer GA, Sternbach LH (1964). "Quinazolines and 1,4-Benzodiazepines. XVI. Synthesis and Transformations of 5-Phenyl-1,4-benzodiazepine-2-thiones".The Journal of Organic Chemistry.29: 231.doi:10.1021/jo01024a511.
1,4-Benzodiazepines
1,5-Benzodiazepines
2,3-Benzodiazepines*
Triazolobenzodiazepines
Imidazobenzodiazepines
Oxazolobenzodiazepines
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Pyridodiazepines
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Pyrazolodiazepines
Pyrrolodiazepines
Tetrahydroisoquinobenzodiazepines
Pyrrolobenzodiazepines*
Benzodiazepine prodrugs
* atypical activity profile (notGABAA receptor ligands)
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Nonbenzodiazepines
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