ETHYL 1,5-DIMETHYL-1H-PYRAZOLE-3-CARBOXYLATE Chemical Properties

Melting point:

39-41°C

Boiling point:

154°C 10mm

Density 

1.12±0.1 g/cm3 (20 ºC 760 Torr)

Flash point:

110.3±21.8℃

storage temp. 

under inert gas (nitrogen or Argon) at 2–8 °C

form 

powder to crystal

pka

0.54±0.10(Predicted)

color 

Light orange to Yellow to Green

InChI

InChI=1S/C8H12N2O2/c1-4-12-8(11)7-5-6(2)10(3)9-7/h5H,4H2,1-3H3

InChIKey

OJPXVXXMBWKEAT-UHFFFAOYSA-N

SMILES

N1(C)C(C)=CC(C(OCC)=O)=N1

CAS DataBase Reference

5744-51-4(CAS DataBase Reference)

Safety Information

Hazard Codes 

Xi,Xn

Risk Statements 

36/37/38-22

Safety Statements 

26-36/37/39

WGK Germany 

3

HazardClass 

IRRITANT

HS Code 

29331990

ETHYL 1,5-DIMETHYL-1H-PYRAZOLE-3-CARBOXYLATE Usage And Synthesis

Chemical Properties

White to light yellow solid

Uses

Ethyl 1,5-dimethyl-1H-pyrazole-3-carboxylate is a biochemical reagent that can be used as a biological material or organic compound for life science related research.

Synthesis

1. Dissolve ethyl 3-methylpyrazole-5-carboxylate (30.8 g, 200 mmol) in 200 mL of anhydrous tetrahydrofuran. Under cooling in an ice bath, sodium hydride (4.8 g, 200 mmol) was added slowly, making sure that the sodium hydride was completely incorporated. The reaction mixture was warmed to 50 °C, stirred for 1 h and cooled to room temperature. 2. Dissolve iodomethane (28.2 g, 200 mmol) in 100 mL of tetrahydrofuran and slowly add dropwise to the above reaction mixture. After the dropwise addition was completed, the reaction was continued to be heated at 50°C for 2 hours. 3. After completion of the reaction, cool to room temperature and remove the tetrahydrofuran by distillation under reduced pressure. 100 mL of water was added and extracted with ethyl acetate (100 mL x 3), the organic layers were combined, dried and the solvent was removed under reduced pressure to give ethyl 1,5-dimethyl-1H-pyrazole-3-carboxylate (26.6 g, 85% yield). 4. To a dry three-necked flask was added lithium aluminum hydride (3.8 g, 100 mmol) and 200 mL of anhydrous tetrahydrofuran. Ethyl 1,5-dimethyl-1H-pyrazole-3-carboxylate (16.8 g, 100 mmol) was dissolved in 100 mL of dry tetrahydrofuran and slowly added dropwise to the three-necked flask. After the dropwise addition, stirring was continued for 4 hours. 5. Upon completion of the reduction reaction, anhydrous ethanol was added dropwise to quench the remaining lithium aluminum hydride and the tetrahydrofuran was removed under reduced pressure. Add 500 mL of methanol, adjust the pH to neutral, heat and reflux for 6 hours and then filter. The filtrate was concentrated, dissolved in 100 mL of dichloromethane, washed twice with 50 mL of saturated aqueous sodium chloride, the organic layer was dried and concentrated to give 5-methyl-1-methylpyrazole methanol (8.8 g, 70% yield). 6. 5-methyl-1-methylpyrazolemethanol (6.3 g, 50 mmol) was dissolved in 20 mL of dichloromethane and thionyl chloride (6 g, 50 mmol) was added dropwise slowly. After dropwise addition, stirring was continued for 2 hours. 7. After completion of the reaction, slowly add saturated sodium bicarbonate aqueous solution to adjust the pH to neutral, extracted with 200 mL of dichloromethane. The organic layers were combined, dried and concentrated to give 3-chloromethyl-1,5-dimethylpyrazole (6.5 g, 90% yield). 8. To a 50 mL round bottom flask was added 3-chloromethyl-1,5-dimethylpyrazole (1.44 g, 10 mmol), N-(2,4,6-trimethylphenyl)imidazole (1.86 g, 10 mmol), and 20 mL of acetonitrile, and heated to reflux for 6 hours. After cooling to room temperature, the solvent was removed by distillation under reduced pressure. The resulting solid was dissolved in water, filtered, and the filtrate was saturated with aqueous ammonium hexafluorophosphate to precipitate the solid, which was dried to give the imidazolium salt ligand (HL1PF6, 3.8 g, 88% yield).

References

[1] Patent: CN106478734, 2017, A. Location in patent: Paragraph 0027; 0028; 0029
[2] Journal of Medicinal Chemistry, 2015, vol. 58, # 5, p. 2180 - 2194
[3] Medicinal Chemistry Research, 2012, vol. 21, # 10, p. 2772 - 2778,7

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