ChemicalBook--->CAS DataBase List--->14080-51-4

14080-51-4

14080-51-4 Structure

14080-51-4 Structure
IdentificationMore
[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 PropertiesBack 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)
Safety DataBack Directory
[Hazard Codes ]

Xi
[Risk Statements ]

22-36-43
[Safety Statements ]

26-36/37
[HazardClass ]

IRRITANT
[HS Code ]

2934999090
Spectrum DetailBack Directory
[Spectrum Detail]

2-AMINO-THIOPHENE-3-CARBOXYLIC ACID AMIDE(14080-51-4)1HNMR
Hazard InformationBack Directory
[Synthesis]

2,5-Dihydroxy-1,4-dithiane

40018-26-6

2-Cyanoacetamide

107-91-5

2-AMINO-THIOPHENE-3-CARBOXYLIC ACID AMIDE

14080-51-4

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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