Zomebazam
Identifiers
  • 1,3,8-trimethyl-4-phenylpyrazolo[3,4-b][1,4]diazepine-5,7-dione
CAS Number
PubChem CID
ChemSpider
UNII
Chemical and physical data
FormulaC15H16N4O2
Molar mass284.319 g·mol−1
3D model (JSmol)
  • O=C1N(c2c(N(C(=O)C1)C)n(nc2C)C)c3ccccc3
  • InChI=1S/C15H16N4O2/c1-10-14-15(18(3)16-10)17(2)12(20)9-13(21)19(14)11-7-5-4-6-8-11/h4-8H,9H2,1-3H3 ☒N
  • Key:BFWACMHTIVUWJS-UHFFFAOYSA-N ☒N
 ☒NcheckY (what is this?)  (verify)

Zomebazam[1] produced by Hoechst is a pyrazolodiazepinone derivative drug with anxiolytic properties. It is structurally related to razobazam and zometapine.[2]

Synthesis

Synthesis:[3] Patent:[4]

The catalytic hydrogenation of N,2,5-trimethyl-4-phenyldiazenylpyrazol-3-amine CID:136203602 (1) over Raney Nickel gives 4-amino-1,3-dimethyl-5-methylaminopyrazole, CID:10219477 (2). Treatment with methyl malonyl chloride [37517-81-0] (3) gives 4-a-ethoxycarbonylacetylamino-1,3-dimethyl-5-methylaminopyrazole, CID:20561101 (4). Base catalyzed lactamization gives (5). The Goldberg reaction completes the synthesis Zomebazam (6).

See also

References

  1. ↑ US 3558605, "4-Aryl-5,6,7,8-tetrahydropyrazolo(3,4-B)-(1,5)diazepine-1H,4H-5,7-diones and medicaments containing same"
  2. ↑ "Zomebazam". psychotropics.dk. 2003. Retrieved 7 December 2009.
  3. ↑ Renger B (1985). "Direkte N-Arylierung von Amiden: Eine Verbesserung der Goldberg-Reaktion". Synthesis. 1985 (9): 856–560. doi:10.1055/s-1985-31364.
  4. ↑ US 4302468, Rackur G, Hoffmann I, issued 1981, assigned to Hoechst Aktiengesellschaft
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