ChemicalBook > CAS DataBase List > ethyl [1,2,4]triazolo[1,5-a]pyridine-2-carboxylate

ethyl [1,2,4]triazolo[1,5-a]pyridine-2-carboxylate

Product Name
ethyl [1,2,4]triazolo[1,5-a]pyridine-2-carboxylate
CAS No.
62135-58-4
Chemical Name
ethyl [1,2,4]triazolo[1,5-a]pyridine-2-carboxylate
Synonyms
ethyl [1,2,4]triazolo[1,5-a]pyridine-2-carboxylate;[1,2,4]Triazolo[1,5-a]pyridine-2-carboxylic acid, ethyl ester
CBNumber
CB02506128
Molecular Formula
C9H9N3O2
Formula Weight
191.19
MOL File
62135-58-4.mol
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ethyl [1,2,4]triazolo[1,5-a]pyridine-2-carboxylate Property

Melting point:
136-138 °C(Solv: ethanol (64-17-5))
Density 
1.33±0.1 g/cm3(Predicted)
storage temp. 
Inert atmosphere,Room Temperature
pka
0.03±0.30(Predicted)
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

TRC
Product number
B441295
Product name
ethyl[1,2,4]triazolo[1,5-a]pyridine-2-carboxylate
Packaging
10mg
Price
$45
Updated
2021/12/16
American Custom Chemicals Corporation
Product number
CHM0392187
Product name
ETHYL-[1,2,4]TRIAZOLO[1,5-A]PYRIDINE-2-CARBOXYLATE
Purity
95.00%
Packaging
5MG
Price
$496.2
Updated
2021/12/16
Crysdot
Product number
CD11088168
Product name
Ethyl[1,2,4]triazolo[1,5-a]pyridine-2-carboxylate
Purity
95+%
Packaging
1g
Price
$594
Updated
2021/12/16
Alichem
Product number
62135584
Product name
Ethyl[1,2,4]triazolo[1,5-a]pyridine-2-carboxylate
Packaging
1g
Price
$842.4
Updated
2021/12/16
Crysdot
Product number
CD11088168
Product name
Ethyl[1,2,4]triazolo[1,5-a]pyridine-2-carboxylate
Purity
95+%
Packaging
5g
Price
$1782
Updated
2021/12/16
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ethyl [1,2,4]triazolo[1,5-a]pyridine-2-carboxylate Chemical Properties,Usage,Production

Synthesis

56000-35-2

4755-77-5

62135-58-4

The general procedure for the synthesis of ethyl [1,2,4]triazolo[1,5-a]pyridine-2-carboxylate from ethyl [1,2,4]triazolo[1,5-a]pyridine-2-carboxylate using 2,4-trimethylbenzenesulfonate 1,2-diaminopyridinium (10.9 g, 35.2 mmol) and ethyl monooxynitrate of oxalyl chloride (9.62 g, 7.84 mL, 70.5 mmol) was as follows: at room temperature, ethyl monooxynitrate of oxalyl chloride was added slowly to a light red solution of 2,4-trimethyl benzenesulfonic acid 1,2-diaminopyridinium pyridine (50 mL) in a light red solution, noting that the reaction is exothermic. The color of the solution changed from light red to dark red. Subsequently, the reaction mixture was heated to 100 °C with continuous stirring overnight. After completion of the reaction, the solvent was removed by evaporation and the black residue obtained was ground with saturated aqueous sodium carbonate solution (300 mL) for 30 minutes. The reaction mixture was extracted with dichloromethane (4 x 250 mL), the organic layers were combined and dried with anhydrous magnesium sulfate. After drying, the organic phase was concentrated in vacuum to give 6.64 g of crude product. The crude product was suspended in ether (30 mL), filtered and washed with ether. The resulting precipitate was dried under vacuum to give the light brown solid product ethyl [1,2,4]triazolo[1,5-a]pyridine-2-carboxylate (6.1 g, 31.9 mmol, 90.6% yield). Mass spectral analysis showed M = 192.2 (M + H)+.

References

[1] Patent: US2013/59833, 2013, A1. Location in patent: Paragraph 0515-0516
[2] Patent: WO2013/34506, 2013, A1. Location in patent: Page/Page column 88

ethyl [1,2,4]triazolo[1,5-a]pyridine-2-carboxylate Preparation Products And Raw materials

Raw materials

Preparation Products

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ethyl [1,2,4]triazolo[1,5-a]pyridine-2-carboxylate Suppliers

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62135-58-4, ethyl [1,2,4]triazolo[1,5-a]pyridine-2-carboxylateRelated Search:


  • ethyl [1,2,4]triazolo[1,5-a]pyridine-2-carboxylate
  • [1,2,4]Triazolo[1,5-a]pyridine-2-carboxylic acid, ethyl ester
  • 62135-58-4