Bromazolam

 化学構造式
71368-80-4
CAS番号.
71368-80-4
化学名:
别名:
英語名:
Bromazolam
英語别名:
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;Bromazolam;Bromazolon;New Bromazolam;Dechlorothiazole;Bromazolam 71368-80-four;8-Bromo-1-methyl-6-phenyl-4H-
CBNumber:
CB12657919
化学式:
C17H13BrN4
分子量:
353.22
MOL File:
71368-80-4.mol

Bromazolam 物理性質

融点 :
272.0-275℃
沸点 :
519.8±60.0 °C(Predicted)
比重(密度) :
1.54±0.1 g/cm3 (20 ºC 760 Torr)
溶解性:
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
外見 :
A crystalline solid
酸解離定数(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

安全性情報

Bromazolam 価格

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Bromazolam 化学特性,用途語,生産方法

使用

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.

主な応用

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.

合成

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.
説明図

Bromazolam 上流と下流の製品情報

原材料

準備製品


Bromazolam 生産企業

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