Basic information Safety Supplier Related

N-Ethyl-N-3-((3-dimethylamino-1-oxo-2-propenyl)phenyl)acetamide

Basic information Safety Supplier Related

N-Ethyl-N-3-((3-dimethylamino-1-oxo-2-propenyl)phenyl)acetamide Basic information

Product Name:
N-Ethyl-N-3-((3-dimethylamino-1-oxo-2-propenyl)phenyl)acetamide
Synonyms:
  • Zaleplon Related Compound A CIV (15 mg) ((E)-N-(3-[3-(dimethylamino)acryloyl]phenyl)-N-ethylacetamide)
  • N-Ethyl-N-3-[(3-diMethylaMine-1-oxo-2-propene)phen
  • 3-DiMethylaMino-1-(3-N-ethyl-N-acetylaMinophenyl)-2-propen-1-one
  • N-[3-[3-(DiMethylaMino)-1-oxo-2-propen-1-yl]phenyl]-N-ethyl-acetaMide
  • Zaleplon related coMpound A
  • Zaleplon Related CoMpound A CIV
  • N-[3-[(E)-3-(dimethylamino)prop-2-enoyl]phenyl]-N-ethyl-acetamide
  • N-[3-[3-(Dimethylamino)acryloyl]phenyl]-N-ethylacetamide
CAS:
96605-66-2
MF:
C15H20N2O2
MW:
260.33
EINECS:
619-229-8
Product Categories:
  • Intermediates of Zaleplon
  • Amines
  • Aromatics
  • Impurities
  • Intermediates & Fine Chemicals
  • Pharmaceuticals
  • Acetics acid and esters
  • (intermediate of zaleplon)
Mol File:
96605-66-2.mol
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N-Ethyl-N-3-((3-dimethylamino-1-oxo-2-propenyl)phenyl)acetamide Chemical Properties

Melting point:
111.0 to 115.0 °C
Boiling point:
400.7±45.0 °C(Predicted)
Density 
1.087±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
solubility 
Chloroform, Dichloromethane
form 
powder to crystal
pka
6.40±0.70(Predicted)
color 
Light orange to Yellow to Green
CAS DataBase Reference
96605-66-2(CAS DataBase Reference)
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Safety Information

HS Code 
29242990
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N-Ethyl-N-3-((3-dimethylamino-1-oxo-2-propenyl)phenyl)acetamide Usage And Synthesis

Uses

An impurity and intermediate of Zaleplon production.It is used as a reagent in the preparation of immunogens for immunodetection and quantification of pyrazolopyrimidine sedatives.

Synthesis

4637-24-5

200630-96-2

96605-66-2

1. Acetamidoacetophenone (0.2 g, 1.13 mmol) was dissolved in acetone (2 mL), potassium hydroxide (63 mg, 1.13 mmol) was added, followed by ethyl iodide (0.45 mL, 5.64 mmol). After stirring at room temperature overnight, the reaction mixture was concentrated to dryness. The residue was redissolved in ethyl acetate, washed sequentially with water and brine and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure to give N-(3-acetylphenyl)-N-ethylacetamide as an orange powder (0.23 g, 100%) with a melting point of 203-204 °C. 2. The above product (0.23 g, 1.13 mmol) was dissolved in acetonitrile (2 mL), N,N-dimethylformamide dimethyl acetal (150 μL, 0.12 mmol) was added, and the reaction was carried out in a microwave reactor at 180 °C for 10 min. After evaporation of the solvent, the residue was filtered and washed with ethyl acetate/petroleum ether (1:3) to afford N-[3-(3-dimethylaminopropenoyl)phenyl]-N-ethylacetamide as an orange solid (0.30 g, 100%). 3. The above substance (0.228 g, 0.88 mmol), 4-hydroxyphenylguanidine nitrate (0.188 g, 0.88 mmol) and sodium hydroxide (35 mg, 0.88 mmol) were mixed in acetonitrile (2 mL), and heated in a microwave reactor for 15 min at 190 °C. After evaporation of the solvent, the residue was purified by silica gel column chromatography (ethyl acetate/petroleum ether, 1:1) to afford N-ethyl-N-3-[(3-dimethylamino-1-oxo-2-propenyl)phenyl]-acetamide as a yellow solid (117 mg, 38%).

References

[1] Patent: WO2005/12262, 2005, A1. Location in patent: Page/Page column 45-46
[2] Patent: CN105622615, 2016, A. Location in patent: Paragraph 0128; 0129; 0130; 0131

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