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Home > Encyclopedia > ethyl 5-ethyl-1H-iMidazole-2-carboxylate

ethyl 5-ethyl-1H-iMidazole-2-carboxylate

ethyl 5-ethyl-1H-iMidazole-2-carboxylate structure

ethyl 5-ethyl-1H-iMidazole-2-carboxylate 

structure
  • CAS No:

    1171124-65-4

  • Formula:

    C8H12N2O2

  • Chemical Name:

    ethyl 5-ethyl-1H-iMidazole-2-carboxylate

  • Synonyms:

    Ethyl 5-ethyl-1H-imidazole-2-carboxylate;1H-Imidazole-2-carboxylic acid, 5-ethyl-, ethyl ester;ethyl 4-ethyl-1H-imidazole-2-carboxylate;SCHEMBL2823105;SCHEMBL19358702;DTXSID60566632;KS-00000R5Y;MFCD24386911;ZINC91301331;AKOS016012283

  • Categories:

    Pharmaceutical Intermediates  >  Bulk Drug Intermediates

ethyl 5-ethyl-1H-iMidazole-2-carboxylate Basic Attributes

168.19308

168.089874

-0

DTXSID60566632

2933290090

Characteristics

55

1.4

1.134±0.06 g/cm3(Predicted)

298.1±33.0 °C(Predicted)

134.1±25.4 °C

1.516

ethyl 5-ethyl-1H-iMidazole-2-carboxylate Use and Manufacturing

(1b) Ethyl 5-ethyl-1H-imidazole-2-carboxylate Sodium acetate (9.3 g, 113.4 mmol) was added to a solution of 1-amino-butan-2-one hydrochloride (3.41 g, 27.60 mmol) and ethyl imino(methylthio)acetate tetrafluoroborate (7.45 g, 31.84 mmol) synthesized according to the method described in the document (J. Med. Chem., 38, 1995, 2196-2201) in acetic acid (120 mL), and the mixture was stirred at 100°C for four hours. The reaction solution was concentrated under reduced pressure and then saturated aqueous sodium bicarbonate solution was added to the reaction solution, followed by extraction with ethyl acetate. Then, the organic layer was washed with brine and dried over anhydrous sodium sulfate. Following concentration under reduced pressure, the residue was purified by silica gel column chromatography (elution solvent: hexane/ethyl acetate = 5/1, 2/1, 1/2) to obtain 3.35 g of the title compound as a pale yellow solid (72percent). (1b) Ethyl 5-ethyl-1H-imidazole-2-carboxylate Sodium acetate (9.3 g, 113.4 mmol) was added to a solution of 1-amino-butan-2-one hydrochloride (3.41 g, 27.60 mmol) and ethyl imino(methylthio)acetate tetrafluoroborate (7.45 g, 31.84 mmol) synthesized according to the method described in the document (J. Med. Chem., 38, 1995, 2196-2201) in acetic acid (120 mL), and the mixture was stirred at 100°C for four hours. The reaction solution was concentrated under reduced pressure and then saturated aqueous sodium bicarbonate solution was added to the reaction solution, followed by extraction with ethyl acetate. Then, the organic layer was washed with brine and dried over anhydrous sodium sulfate. Following concentration under reduced pressure, the residue was purified by silica gel column chromatography (elution solvent: hexane/ethyl acetate = 5/1, 2/1, 1/2) to obtain 3.35 g of the title compound as a pale yellow solid (72percent).

Computed Properties

Molecular Weight:168.19
XLogP3:1.4
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:4
Exact Mass:168.089877630
Monoisotopic Mass:168.089877630
Topological Polar Surface Area:55
Heavy Atom Count:12
Complexity:161
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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