| | Identification | More |  | [Name] 
 2-AMINO-THIOPHENE-3-CARBOXYLIC ACID AMIDE
 |  | [CAS] 
 14080-51-4
 |  | [Synonyms] 
 2-AMINO-3-THIOPHENECARBOXAMIDE
 2-AMINOTHIOPHENE-3-CARBOXAMIDE
 2-AMINO-THIOPHENE-3-CARBOXYLIC ACID AMIDE
 AKOS 93830
 AKOS B014696
 ART-CHEM-BB B014696
 CHEMBRDG-BB 3014696
 TIMTEC-BB SBB007065
 |  | [Molecular Formula] 
 C5H6N2OS
 |  | [MDL Number] 
 MFCD00706455
 |  | [Molecular Weight] 
 142.18
 |  | [MOL File] 
 14080-51-4.mol
 | 
 | Chemical Properties | Back Directory |  | [Melting point ] 
 153-155°C
 |  | [Boiling point ] 
 321.8±22.0 °C(Predicted)
 |  | [density ] 
 1.423±0.06 g/cm3(Predicted)
 |  | [storage temp. ] 
 under inert gas (nitrogen or Argon) at 2–8 °C
 |  | [form ] 
 powder to crystal
 |  | [pka] 
 15.58±0.50(Predicted)
 |  | [color ] 
 White to Orange to Green
 |  | [InChI] 
 InChI=1S/C5H6N2OS/c6-4(8)3-1-2-9-5(3)7/h1-2H,7H2,(H2,6,8)
 |  | [InChIKey] 
 WHZIZZOTISTHCT-UHFFFAOYSA-N
 |  | [SMILES] 
 C1(N)SC=CC=1C(N)=O
 |  | [CAS DataBase Reference] 
 14080-51-4(CAS DataBase Reference)
 | 
 | Hazard Information | Back Directory |  | [Synthesis] 
 
 General procedure for the synthesis of 2-aminothiophene-3-amides from 1,4-dithio-2,5-diol and cyanoacetamide: Triethylamine (36 mL, 256 mmol) was added to a solution of ethanol (400 mL) containing 2-cyanoacetamide (10.8 g, 128 mmol) and 1,4-dithiazan-2,5-diol (19.5 g, 128 mmol). The reaction mixture was stirred at room temperature for 5 minutes and then heated to reflux for 2 hours. After completion of the reaction, the mixture was cooled to room temperature, filtered and concentrated in vacuum. The residue was dissolved in ethyl acetate (400 mL) and washed sequentially with 1 M aqueous sodium hydroxide (200 mL), water (2 x 200 mL) and brine (200 mL). The organic layer was dried over anhydrous sodium sulfate and concentrated in vacuo to give 2-aminothiophene-3-amide (16 g, 113 mmol, 88% yield) as a light yellow solid.LC-MS [M+H]+ m/z 143. |  | [References] 
 [1] Patent: WO2003/104218,  2003,  A1. Location in patent: Page 13
 [2] Synthesis (Germany),  2013,  vol. 45,  # 1,  p. 45 - 52
 [3] Patent: WO2012/30894,  2012,  A1. Location in patent: Page/Page column 87
 [4] Tetrahedron Letters,  2007,  vol. 48,  # 30,  p. 5261 - 5264
 [5] Journal of Medicinal Chemistry,  2011,  vol. 54,  # 19,  p. 6734 - 6750
 | 
 |  |