Basic information Safety Supplier Related

ETHYL IMIDAZO[2,1-B][1,3]THIAZOLE-6-CARBOXYLATE

Basic information Safety Supplier Related

ETHYL IMIDAZO[2,1-B][1,3]THIAZOLE-6-CARBOXYLATE Basic information

Product Name:
ETHYL IMIDAZO[2,1-B][1,3]THIAZOLE-6-CARBOXYLATE
Synonyms:
  • Ethyl imidazo[2,1-b][1,3]thiazole-6-carboxylate 97%
  • Ethyl imidazo[2,1-b]thiazole-6-carboxylate
  • IMIDAZO[2,1-B]THIAZOLE-6-CARBOXYLIC ACID ETHYL ESTER
  • ETHYL IMIDAZO[1,2-A]THIAZOLE-6-CARBOXYLATE
  • ETHYL IMIDAZO[2,1-B][1,3]THIAZOLE-6-CARBOXYLATE
  • 6-(Ethoxycarbonyl)imidazo[2,1-b][1,3]thiazole
  • Ethylimidazo[2,1-b][1,3]thiazole-6-carboxylate97%
  • SKL392
CAS:
64951-04-8
MF:
C8H8N2O2S
MW:
196.23
Mol File:
64951-04-8.mol
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ETHYL IMIDAZO[2,1-B][1,3]THIAZOLE-6-CARBOXYLATE Chemical Properties

Melting point:
87 °C
CAS DataBase Reference
64951-04-8
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Safety Information

Hazard Note 
Harmful
HS Code 
2934999090
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ETHYL IMIDAZO[2,1-B][1,3]THIAZOLE-6-CARBOXYLATE Usage And Synthesis

Synthesis

96-50-4

70-23-5

64951-04-8

General procedure for the synthesis of ethylimidazo[2,1-b]thiazole-6-carboxylic acid from 2-aminothiazole (0.500 g, 5 mmol) and ethyl 3-bromopyruvate (90%, 1.625 g, 7.5 mmol): firstly, 2-amino thiazole was dissolved in tetrahydrofuran, followed by the addition of ethyl 3-bromopyruvate dropwise. The reaction mixture was stirred at room temperature for 8 hours before the precipitate was collected by filtration. The resulting filter cake was dissolved in hot ethanol and refluxed at 80°C for 8 hours. After completion of the reaction, the mixture was cooled and the solvent was removed by distillation. The residual solid was washed with cold water and filtered. After drying under vacuum, the intermediate (0.375 g) was obtained, which was dissolved in tetrahydrofuran. The yield of this step was 38.27%.

References

[1] Journal of Medicinal Chemistry, 2003, vol. 46, # 18, p. 3914 - 3929
[2] Journal of Medicinal Chemistry, 2015, vol. 58, # 6, p. 2764 - 2778
[3] Patent: CN105985356, 2016, A. Location in patent: Paragraph 0117; 0118
[4] Farmaco, Edizione Scientifica, 1977, vol. 32, # 10, p. 735 - 746
[5] Patent: US2010/249071, 2010, A1. Location in patent: Page/Page column 45

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