Bromazolam

Bromazolam Struktur
71368-80-4
CAS-Nr.
71368-80-4
Englisch Name:
Bromazolam
Synonyma:
Bromazola;8-Bromo-1-methyl-6-phenyl-4H-s-triazolo[4,3-a][1,4]benzodiazepine;8-BROMO-1-METHYL-6-PHENYL-4H-BENZO[F][1,2,4]TRIAZOLO[4,3-A][1,4]DIAZEPINE;Benzos;Brozolam;Bromazolam;Bromazolon;New Bromazolam;Dechlorothiazole;Bromazolam 71368-80-four
CBNumber:
CB12657919
Summenformel:
C17H13BrN4
Molgewicht:
353.22
MOL-Datei:
71368-80-4.mol

Bromazolam Eigenschaften

Schmelzpunkt:
272.0-275℃
Siedepunkt:
519.8±60.0 °C(Predicted)
Dichte
1.54±0.1 g/cm3 (20 ºC 760 Torr)
Löslichkeit
DMF: 30 mg/ml; DMF:PBS(pH 7.2)(1:1): 0.5 mg/ml; DMSO: 20 mg/ml; Ethanol: 10 mg/ml; Methanol: 1 mg/ml
Aggregatzustand
A crystalline solid
pka
2.37±0.40(Predicted)
InChI
InChI=1S/C17H13BrN4/c1-11-20-21-16-10-19-17(12-5-3-2-4-6-12)14-9-13(18)7-8-15(14)22(11)16/h2-9H,10H2,1H3
InChIKey
KCEIOBKDDQAYCM-UHFFFAOYSA-N
SMILES
N12C(C)=NN=C1CN=C(C1=CC=CC=C1)C1=CC(Br)=CC=C12

Sicherheit

Bromazolam Chemische Eigenschaften,Einsatz,Produktion Methoden

Verwenden

8-Bromo-1-methyl-6-phenyl-4H-s-triazolo[4,3-a][1,4]benzodiazepine is used to study the antianxiety activity, antidepressant and psychotropics for central nervous system.

Application

Bromazolam(8bromo) is a synthetic cannabinoid that has been used as an alternative to marijuana. It has been shown to induce psychosis in animals and humans and is associated with high rates of depression. 8bromo was found to be effective against cancer cells in vitro and in vivo, but not against bacteria or fungi. In humans, 8bromo increased the levels of liver enzymes. This agent has also been shown to have antiinflammatory properties that are mediated by prostaglandin synthesis inhibition.

Synthese

The synthesis of Bromazolam is as follows:
A solution of 1 (1 g, 3.07 mmol of 7-bromo-5-phenyl-1,4-benzodiazepine-2-one) in dry THF (20 mL) was cooled in an ice-water bath and a 60% dispersion of sodium hydride (152.2 mg) was added in one portion. After 20 minutes, di-4-morpholinylphosphinic chloride (943.9 mg, 4.76 mmol) was added at 0° C. and this was stirred for 30 minutes and allowed to warm to room temperature (Ning, R Y., et al., (1976) J Org Chem 41: 2724-2727). The mixture was stirred for 1.5 hours. To this mixture was then added a solution of acetylhydrazide (521.9 mg, 7.14 mmol) in dry butanol (5 mL) and stirring was continued at room temperature for 10 min. The solvents were evaporated and the residue was dissolved in butanol (10 mL) and heated to reflux for 5 hours. Butanol was removed under reduced pressure and the residue was partitioned between CH2Cl2 (50 mL) and water (50 mL). The water layer was extracted by CH2Cl2 (3×30 mL). The combined organic layer was washed by brine (30 mL). The organic layer was dried (Na2SO4) and the solvent was removed under vacuum. The residue was purified by flash chromatography (silica gel) to provide pure 8 [539.5 mg (40% yield)] as a white solid.
synthesis of Bromazolam.png

Bromazolam Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


  • 8-Bromo-1-methyl-6-phenyl-4H-[1,2,4]triazolo[4,3-a][1,4]benzodiazepine
  • 4H-[1,2,4]Triazolo[4,3-a][1,4]benzodiazepine, 8-bromo-1-methyl-6-phenyl-
  • Bromazolam 71368-80-four
  • 8-Bromo-1-methyl-6-phenyl-4H-S-triazolo[...
  • Bromazolon
  • Bromazolam
  • 8-BROMO-1-METHYL-6-PHENYL-4H-BENZO[F][1,2,4]TRIAZOLO[4,3-A][1,4]DIAZEPINE
  • 8-Bromo-1-methyl-6-phenyl-4H-s-triazolo[4,3-a][1,4]benzodiazepine
  • Bromazola
  • 8-Bromo-1-methyl-6-phenyl-4H-
  • Bromazolam, 2'-Desfluoroflubromazolam, 8-Bromodeschloroalprazolam
  • Bromazolam/8-Bromo-1-methyl-6-phenyl-4H-
  • Bromazolam Two appearances: pale pink powder and white powder
  • New Bromazolam
  • Dechlorothiazole
  • Benzos
  • RC or synthetic chemicals rc benzos
  • Brozolam
  • 71368-80-4
  • 71368-80-4
  • 1
  • Pharm
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