ETHYL 5-AMINOBENZOFURAN-2-CARBOXYLATE
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
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
Safety Information
- Hazard Codes
- Xi
- HazardClass
- IRRITANT
- HS Code
- 2932990090
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
ETHYL 5-AMINOBENZOFURAN-2-CARBOXYLATESupplier
- Tel
- 18210857532; 18210857532
- jkinfo@jkchemical.com
- Tel
- 4006356688 18621169109
- market03@meryer.com
- Tel
- 021-67121386
- Sales-CN@TCIchemicals.com
- Tel
- 0757-86329057 18934348241
- sales4.gd@hwrkchemical.com
- Tel
- 021-021-58432009 400-005-6266
- sales8178@energy-chemical.com