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ChemicalBook >  Product Catalog >  Biochemical Engineering >  Amino Acids and Derivatives >  Amino acid esters >  ETHYL 5-AMINOBENZOFURAN-2-CARBOXYLATE

ETHYL 5-AMINOBENZOFURAN-2-CARBOXYLATE

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ETHYL 5-AMINOBENZOFURAN-2-CARBOXYLATE Basic information

Product Name:
ETHYL 5-AMINOBENZOFURAN-2-CARBOXYLATE
Synonyms:
  • ETHYL 5-AMINOBENZOFURAN-2-CARBOXYLATE
  • 2-Benzofurancarboxylicacid,5-amino-,ethylester(9CI)
  • Ethyl 5-aminobenzo[b]furan-2-carboxylate
  • Ethyl 5-amino-1-benzofuran-2-carboxylate (en)
  • 5-Amino-2-(ethoxycarbonyl)-1-benzofuran
  • 5-Amino-2-(ethoxycarbonyl)-1-benzofuran, Ethyl 5-amino-1-benzofuran-2-carboxylate
  • ethyle5-aminobenzo[b]furan-2-carboxylate
  • 5-Amino-2-(ethoxycarbonyl)-1-benzofura
CAS:
174775-48-5
MF:
C11H11NO3
MW:
205.21
EINECS:
1806241-263-5
Product Categories:
  • Esters
  • Furans, Benzofurans & Dihydrobenzofurans
  • AMINOACID
Mol File:
174775-48-5.mol
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ETHYL 5-AMINOBENZOFURAN-2-CARBOXYLATE Chemical Properties

Melting point:
54-56°C
Boiling point:
348.1±22.0 °C(Predicted)
Density 
1.258±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2–8 °C
solubility 
soluble in Chloroform, DMSO
form 
Powder
pka
3.32±0.10(Predicted)
color 
Beige
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Safety Information

Hazard Codes 
Xi
HazardClass 
IRRITANT
HS Code 
2932990090
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ETHYL 5-AMINOBENZOFURAN-2-CARBOXYLATE Usage And Synthesis

Chemical Properties

Brown Solid

Uses

Ethyl 5-amino-1-benzofuran-2-carboxylate is used as an synthetic intermediate in the preparation of indolebutylpiperazines, a class of dual 5-HT1A receptor agonists and serotonin reuptake inhibitors. Ethyl 5-amino-1-benzofuran-2-carboxylate was also used as a potential radiolabelled analog for melanoma imaging and targeted radiotherapy.

Uses

Ethyl 5-aminobenzofuran-2-carboxylate is used as an synthetic intermediate in the preparation of indolebutylpiperazines, a class of dual 5-HT1A receptor agonists and serotonin reuptake inhibitors. Ethyl 5-amino-1-benzofuran-2-carboxylate was also used as a potential radiolabelled analog for melanoma imaging and targeted radiotherapy.

Synthesis

69604-00-8

174775-48-5

General procedure for the synthesis of ethyl 5-aminobenzofuran-2-carboxylate from ethyl 5-nitrobenzofuran-2-carboxylate: 20.0 g of ethyl 5-nitrobenzofuran-2-carboxylate was placed in a reaction flask and 300 mL of ethanol was added as a solvent. Subsequently, 2 g of 5% Pd/C catalyst was added. The reaction system was replaced twice with hydrogen to ensure that the reaction environment was a hydrogen atmosphere. The hydrogenation reaction was carried out for 3 hours by adjusting the hydrogen pressure to 0.3-0.5 MPa and controlling the reaction temperature in the range of 10-30°C. The reaction was carried out by filtration. Upon completion of the reaction, the catalyst was removed by filtration. The filtrate was concentrated under reduced pressure and dried to give 17.1 g of ethyl 5-aminobenzofuran-2-carboxylate in 98% yield.

References

[1] Patent: WO2013/153492, 2013, A2. Location in patent: Page/Page column 23
[2] Patent: US2015/87835, 2015, A1. Location in patent: Paragraph 0125
[3] ChemCatChem, 2014, vol. 6, # 11, p. 3153 - 3159
[4] Patent: CN107674052, 2018, A. Location in patent: Paragraph 0035-0037
[5] Patent: CN107540646, 2018, A. Location in patent: Paragraph 0041; 0042; 0043

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