ChemicalBook--->CAS DataBase List--->79128-68-0

79128-68-0

79128-68-0 Structure

79128-68-0 Structure
IdentificationBack Directory
[Name]

3-(2,2,2-trifluoro-acetylaMino)-thiophene-2-carboxylicacidMethylester
[CAS]

79128-68-0
[Synonyms]

methyl 3-[(trifluoroacetyl)amino]thiophene-2-carboxylate
Methyl 3-(2,2,2-trifluoroacetaMido)thiophene-2-carboxylate
3-(N-TrifluoroacetylaMino)thiophene-2-carboxylic acid Methyl ester
3-(2,2,2-trifluoro-acetylaMino)-thiophene-2-carboxylicacidMethylester
3-(N-Trifluoroacetylamino)thiophene-2-carboxylic acid methyl ester, 97.5%
2-Thiophenecarboxylic acid, 3-[(2,2,2-trifluoroacetyl)amino]-, methyl ester
[EINECS(EC#)]

201-215-5
[Molecular Formula]

C8H6F3NO3S
[MDL Number]

MFCD00103374
[MOL File]

79128-68-0.mol
[Molecular Weight]

253.2
Chemical PropertiesBack Directory
[storage temp. ]

2-8°C(protect from light)
[Appearance]

Light yellow to yellow Solid
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P280-P301+P312-P302+P352-P305+P351+P338
[Safety Statements ]

24/25
[HS Code ]

29349990
Spectrum DetailBack Directory
[Spectrum Detail]

3-(2,2,2-trifluoro-acetylaMino)-thiophene-2-carboxylicacidMethylester(79128-68-0)1HNMR
Hazard InformationBack Directory
[Synthesis]

Methyl 3-amino-2-thiophenecarboxylate

22288-78-4

Trifluoroacetic anhydride

407-25-0

3-(2,2,2-trifluoro-acetylaMino)-thiophene-2-carboxylicacidMethylester

79128-68-0

To a stirred solution of methyl 3-amino-2-thiophenecarboxylate (25.0 g, 159 mmol) in acetonitrile (325 mL) was added sequentially pyridine (15.5 mL) and trifluoroacetic anhydride (29.3 mL) at 0 °C. After 5 minutes of reaction, the reaction mixture was slowly warmed to room temperature and stirring was continued for 20 minutes. Subsequently, the reaction mixture was slowly poured into ice water (3.0 L) and stirred for 15 minutes to quench the reaction. The resulting precipitate was collected by filtration, washed with cold water and dried under vacuum to afford methyl 3-(2,2,2-trifluoroacetamido)-2-thiophenecarboxylate (37.3 g, 93% yield) as a pink solid. Its 1H NMR (300 MHz, DMSO-d6) data were as follows: δ 3.86 (3H, s), 7.72 (1H, d, J = 5.4 Hz), 8.03 (1H, d, J = 5.4 Hz), 11.17 (1H, br s).

[References]

[1] Bioorganic and Medicinal Chemistry Letters, 2007, vol. 17, # 9, p. 2535 - 2539
[2] Journal of Medicinal Chemistry, 2016, vol. 59, # 13, p. 6293 - 6302
[3] Patent: WO2010/101302, 2010, A1. Location in patent: Page/Page column 129-130
[4] Patent: WO2005/47293, 2005, A1. Location in patent: Page/Page column 28
[5] Patent: WO2007/71434, 2007, A1. Location in patent: Page/Page column 27
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