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ChemicalBook >  Product Catalog >  Pharmaceutical intermediates >  Heterocyclic compound >  Thiophene compounds >  2-AMINO-4,5-DIMETHYL-THIOPHENE-3-CARBOXYLIC ACID METHYL ESTER

2-AMINO-4,5-DIMETHYL-THIOPHENE-3-CARBOXYLIC ACID METHYL ESTER

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2-AMINO-4,5-DIMETHYL-THIOPHENE-3-CARBOXYLIC ACID METHYL ESTER Basic information

Product Name:
2-AMINO-4,5-DIMETHYL-THIOPHENE-3-CARBOXYLIC ACID METHYL ESTER
Synonyms:
  • SPECS AK-968/37166326
  • ART-CHEM-BB B000679
  • METHYL 2-AMINO-4,5-DIMETHYL-3-THIOPHENECARBOXYLATE
  • METHYL 2-AMINO-4,5-DIMETHYLTHIOPHENE-3-CARBOXYLATE
  • 2-AMINO-4,5-DIMETHYL-THIOPHENE-3-CARBOXYLIC ACID METHYL ESTER
  • AKOS B000679
  • AKOS 92456
  • AKOS NCG-0059
CAS:
4651-93-8
MF:
C8H11NO2S
MW:
185.24
Product Categories:
  • Thiophene&Benzothiophene
  • Thiophene
Mol File:
4651-93-8.mol
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2-AMINO-4,5-DIMETHYL-THIOPHENE-3-CARBOXYLIC ACID METHYL ESTER Chemical Properties

Melting point:
123-125 °C
Boiling point:
287.8±35.0 °C(Predicted)
Density 
1?+-.0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2–8 °C
pka
0.55±0.10(Predicted)
Appearance
Light yellow to yellow Solid
InChIKey
MZBOBUPJGXDOFT-UHFFFAOYSA-N
CAS DataBase Reference
4651-93-8(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
HazardClass 
IRRITANT
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2-AMINO-4,5-DIMETHYL-THIOPHENE-3-CARBOXYLIC ACID METHYL ESTER Usage And Synthesis

Synthesis

78-93-3

105-34-0

4651-93-8

The general procedure for the synthesis of methyl 2-amino-3,5-dimethylthiophene-3-carboxylate from 2-butanone and methyl cyanoacetate was as follows: sulfur powder (160.0 mg, 5.0 mmol) was placed in a single-necked flask and 1.5 mL of DMF was added to dissolve it. Methyl cyanoacetate (495.4 mg, 5.0 mmol) and morpholine (435.6 mg, 5.0 mmol) were then added sequentially, and the reaction solution immediately changed to dark brown color. Then 2-butanone (901.4 mg, 12.5 mmol) was added and the reaction mixture was stirred at 50 °C overnight. After completion of the reaction, the mixture was cooled to room temperature, diluted with an appropriate amount of water and extracted three times with ethyl acetate. The organic phases were combined, washed with saturated sodium chloride solution and dried over anhydrous magnesium sulfate. The solvent was removed by distillation under reduced pressure to give the crude product. Finally, the crude product was separated and purified by column chromatography to give a light yellow solid target compound in 40.7% yield.

References

[1] Patent: CN106167497, 2016, A. Location in patent: Paragraph 0414; 0415; 0416
[2] ChemMedChem, 2018,
[3] European Journal of Medicinal Chemistry, 2019, vol. 161, p. 239 - 251

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