Basic information Safety Supplier Related

3-(3-CYANO-PHENYL)-3-OXO-PROPIONIC ACID ETHYL ESTER

Basic information Safety Supplier Related

3-(3-CYANO-PHENYL)-3-OXO-PROPIONIC ACID ETHYL ESTER Basic information

Product Name:
3-(3-CYANO-PHENYL)-3-OXO-PROPIONIC ACID ETHYL ESTER
Synonyms:
  • ETHYL 3-(3-CYANOPHENYL)-3-OXOPROPANOATE
  • 3-(3-CYANO-PHENYL)-3-OXO-PROPIONIC ACID ETHYL ESTER
  • 3-(3-Cyanophenyl)-3-oxopropanoic acid ethyl ester
  • Ethyl (m-cyanobenzoyl)acetate
  • 3-Cyano-b-oxo-benzenepropanoic acid ethyl ester
  • Ethyl 3-(3-Cyanophenyl)-3-oxopropionate
  • Benzenepropanoic acid, 3-cyano-β-oxo-, ethyl ester
CAS:
62088-13-5
MF:
C12H11NO3
MW:
217.22
Mol File:
62088-13-5.mol
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3-(3-CYANO-PHENYL)-3-OXO-PROPIONIC ACID ETHYL ESTER Chemical Properties

Boiling point:
338.0±22.0 °C(Predicted)
Density 
1.19
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
pka
9.57±0.46(Predicted)
Appearance
White to yellow Solid
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3-(3-CYANO-PHENYL)-3-OXO-PROPIONIC ACID ETHYL ESTER Usage And Synthesis

Uses

Ethyl 3-(3-cyanophenyl)-3-oxopropanoate is used in the synthetic preparation of benzamidine factor Xa inhibitors containing a vicinally-substituted heterocyclic core towards the discovery of novel antithrombotic agents.

Synthesis

6136-68-1

105-58-8

62088-13-5

Part A. Preparation of ethyl 3-(3-cyanophenyl)-3-oxopropanoate. To a hexane-washed suspension of sodium hydride (1.2 g, 60% mineral oil suspension, 30.3 mmol) in 40 mL of tetrahydrofuran, diethyl carbonate (3.7 mL, 30.3 mmol) and 3-acetylbenzonitrile (2.2 g, 15.2 mmol) were added sequentially. The resulting suspension was stirred at 65 °C for 1 h and then cooled to room temperature. 40 mL of 10% HCl aqueous solution was added and the reaction mixture was diluted with ethyl acetate and layered. The organic layer was washed with brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure to afford 3.2 g (96% yield) of ethyl 3-(4-cyanophenyl)-oxopropanoate, which was pure enough to be used directly in subsequent reactions without further purification. Mass spectrum (NH3-Cl) m/z: 218.3 ([M+H]+).

References

[1] Journal of Medicinal Chemistry, 2006, vol. 49, # 6, p. 1910 - 1915
[2] Bioorganic and Medicinal Chemistry Letters, 2001, vol. 11, # 5, p. 641 - 645
[3] Patent: WO2011/46774, 2011, A1. Location in patent: Page/Page column 16
[4] Patent: EP946528, 2003, B1
[5] Patent: US6187797, 2001, B1

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