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 |
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