9-Bromo-6H-[1,2,4]triazolo[1,5-c]quinazolin-5-one
- Product Name
- 9-Bromo-6H-[1,2,4]triazolo[1,5-c]quinazolin-5-one
- CAS No.
- 882517-92-2
- Chemical Name
- 9-Bromo-6H-[1,2,4]triazolo[1,5-c]quinazolin-5-one
- Synonyms
- Bromo-6H-[1,2,4]triazolo[1,5-c]quinazolin-5-one;9-Bromo-6H-[1,2,4]triazolo[1,5-c]quinazolin-5-one;9-Bromo-[1,2,4]triazolo[1,5-c]quinazolin-5(6H)-one;9-bromo-[1,2,4]triazolo[4,3-c]quinazolin-5(6H)-one;[1,2,4]Triazolo[1,5-c]quinazolin-5(6H)-one,9-bromo-
- CBNumber
- CB22487548
- Molecular Formula
- C9H5BrN4O
- Formula Weight
- 265.07
- MOL File
- 882517-92-2.mol
9-Bromo-6H-[1,2,4]triazolo[1,5-c]quinazolin-5-one Property
- Density
- 2.09
- storage temp.
- Sealed in dry,Room Temperature
- pka
- 7.00±0.20(Predicted)
Safety
- HS Code
- 2933599590
N-Bromosuccinimide Price
- Product number
- 4072AC
- Product name
- 9-Bromo-[1,2,4]triazolo[1,5-c]quinazolin-5(6H)-one
- Packaging
- 250mg
- Price
- $358
- Updated
- 2021/12/16
- Product number
- HCH0368537
- Product name
- 9-BROMO-[1,2,4]TRIAZOLO[1,5-C]QUINAZOLIN-5(6H)-ONE
- Purity
- 95.00%
- Packaging
- 5MG
- Price
- $504.69
- Updated
- 2021/12/16
- Product number
- A120522
- Product name
- 9-Bromo-[1,2,4]triazolo[1,5-c]quinazolin-5(6H)-one
- Purity
- 95%
- Packaging
- 100mg
- Price
- $110
- Updated
- 2021/12/16
- Product number
- A120522
- Product name
- 9-Bromo-[1,2,4]triazolo[1,5-c]quinazolin-5(6H)-one
- Purity
- 95%
- Packaging
- 250mg
- Price
- $176
- Updated
- 2021/12/16
- Product number
- CD11035305
- Product name
- 9-Bromo-[1,2,4]triazolo[1,5-c]quinazolin-5(6H)-one
- Purity
- 95+%
- Packaging
- 250mg
- Price
- $226
- Updated
- 2021/12/16
9-Bromo-6H-[1,2,4]triazolo[1,5-c]quinazolin-5-one Chemical Properties,Usage,Production
Synthesis
220269-80-7
624-84-0
882517-92-2
General procedure for the synthesis of 9-bromo-[1,2,4]triazolo[1,5-c]quinazolin-5(6H)-one from (4-bromo-2-cyanophenyl)carbamic acid ethyl ester and formylhydrazine: to a solution of (4-bromo-2-cyanophenyl)carbamic acid ethyl ester (40.4 g, 150 mmol) in N-methyl pyrrolidone (NMP, 170 mL), was added formylhydrazine ( 10.0 g, 150 mmol). The reaction mixture was stirred at 160°C for 1.5 hours in a mild nitrogen atmosphere. Upon completion of the reaction, the mixture was cooled to below 100°C and water (340 mL) was slowly added. The resulting slurry was further cooled to 25°C and stirred continuously for 15 minutes. The precipitated solid was collected by filtration and washed sequentially with water and 2-propanol. Finally, the product was dried under vacuum to afford 9-bromo-[1,2,4]triazolo[1,5-c]quinazolin-5(6H)-one (32.4 g, 81% yield) as a light yellow solid. Mass spectrometry (MS) analysis result: m/e = 264.9/267.0 (M + H+).
References
[1] Patent: US2006/84642, 2006, A1. Location in patent: Page/Page column 9
[2] Patent: US2006/84801, 2006, A1. Location in patent: Page/Page column 12
[3] Patent: US2006/79507, 2006, A1. Location in patent: Page/Page column 18
[4] Bioorganic and Medicinal Chemistry Letters, 2009, vol. 19, # 20, p. 5940 - 5944
9-Bromo-6H-[1,2,4]triazolo[1,5-c]quinazolin-5-one Preparation Products And Raw materials
Raw materials
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