3-(Trifluoromethyl)-1,2,4-triazolo[4,3-a]pyrazine
3-(Trifluoromethyl)-1,2,4-triazolo[4,3-a]pyrazine Basic information
- Product Name:
- 3-(Trifluoromethyl)-1,2,4-triazolo[4,3-a]pyrazine
- Synonyms:
-
- 3-(TRIFLUOROMETHYL)-1,2,4-TRIAZOLO[4,3-A]-PYRAZINE
- 3-(TRIFLUOROMETHYL)-[1,2,4]TRIAZOLO[4,3-A]PYRAZINE,95% MIN(HPLC)
- 1,2,4-Triazolo[4,3-a]pyrazine, 3-(trifluoromethyl)-
- CAS:
- 486460-20-2
- MF:
- C6H3F3N4
- MW:
- 188.11
- Mol File:
- 486460-20-2.mol
3-(Trifluoromethyl)-1,2,4-triazolo[4,3-a]pyrazine Chemical Properties
- Density
- 1.69±0.1 g/cm3(Predicted)
- storage temp.
- 2-8°C
- pka
- -2.40±0.30(Predicted)
3-(Trifluoromethyl)-1,2,4-triazolo[4,3-a]pyrazine Usage And Synthesis
Uses
3-(Trifluoromethyl)-[1,2,4]triazolo[4,3-a]pyrazine can be used as reactant/reagent in synthetic preparation of 3-amino-4-phenylbutanoic acid derivatives as dipeptidyl peptidase inhibitors for treatment or prevention of diabetes.
Synthesis
1447800-65-8
486460-20-2
General method: 10 mmol of compound 3 (CAS:1447800-65-8) was dissolved in 50 mL of toluene and 20 mmol of triethylamine was slowly added to the reaction system at room temperature with continuous stirring for 1 hour. The reaction process was monitored by thin layer chromatography (TLC). After the reaction was complete, the reaction mixture was slowly poured into 25 g of ice-water mixture, stirred thoroughly and left to stratify. The organic phase was separated and washed with 2 x 10 mL of cold water, followed by drying the organic phase with anhydrous sodium sulfate. Finally, the organic phase was concentrated under reduced pressure to give compound 4 in good yield.
References
[1] Letters in Organic Chemistry, 2013, vol. 10, # 5, p. 348 - 352
3-(Trifluoromethyl)-1,2,4-triazolo[4,3-a]pyrazine Preparation Products And Raw materials
Raw materials
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