Basic information Safety Supplier Related

5-Amino-thiophene-2-carboxylic acid methyl ester

Basic information Safety Supplier Related

5-Amino-thiophene-2-carboxylic acid methyl ester Basic information

Product Name:
5-Amino-thiophene-2-carboxylic acid methyl ester
Synonyms:
  • 2-Thiophenecarboxylicacid, 5-aMino-, Methyl ester
  • 5-Amino-thiophene-2-carboxylic acid methyl ester
  • 5-aminothiophene-2-carboxylic methyl ester
CAS:
14597-58-1
MF:
C6H7NO2S
MW:
157.19
EINECS:
200-110-4
Mol File:
14597-58-1.mol
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5-Amino-thiophene-2-carboxylic acid methyl ester Chemical Properties

Melting point:
81 °C
Boiling point:
304.8±22.0 °C(Predicted)
Density 
1.319±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2–8 °C
pka
0.38±0.10(Predicted)
Appearance
Light brown to brown Solid
InChI
InChI=1S/C6H7NO2S/c1-9-6(8)4-2-3-5(7)10-4/h2-3H,7H2,1H3
InChIKey
NNQTUMGJWXJMIR-UHFFFAOYSA-N
SMILES
C1(C(OC)=O)SC(N)=CC=1
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5-Amino-thiophene-2-carboxylic acid methyl ester Usage And Synthesis

Synthesis

5832-01-9

14597-58-1

General procedure for the synthesis of methyl 5-amino-2-thiophenecarboxylate from methyl 5-nitro-2-thiophenecarboxylate: Methyl 5-nitro-2-thiophenecarboxylate (11.55 mmol) was dissolved in ethanol (20 mL), and 10% palladium carbon catalyst (1 g) was added. The reaction mixture was hydrogenated overnight with stirring under hydrogen atmosphere. Upon completion of the reaction, the catalyst was removed by filtration and the filtrate was subsequently concentrated to afford the target product methyl 5-amino-2-thiophenecarboxylate (1.67 g, 92% yield). The product was detected by LCMS (ESI) and showed a molecular ion peak of 157 [M+H]+.

References

[1] Patent: WO2006/65788, 2006, A2. Location in patent: Page/Page column 10
[2] Patent: US2007/43045, 2007, A1. Location in patent: Page/Page column 59
[3] Bioorganic and Medicinal Chemistry Letters, 2002, vol. 12, # 10, p. 1379 - 1382
[4] Patent: WO2004/108683, 2004, A1. Location in patent: Page 564-565
[5] Patent: WO2004/18480, 2004, A1. Location in patent: Page 156

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