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198821-79-3

198821-79-3 Structure

198821-79-3 Structure
IdentificationBack Directory
[Name]

3-METHOXY-4-(1,3-OXAZOL-5-YL)ANILINE
[CAS]

198821-79-3
[Synonyms]

3-Methoxy-4-(oxazol-5-yl)
3-Methoxy-4-(oxazol-5-yl)aniline
5-(4-Amino-2-methoxyphenyl)oxazole
3-Methoxy-4-(5-oxazolyl)benzenamine
3-Methoxy-4-(5-oxazolyl)aniline, 97%
3-METHOXY-4-(1,3-OXAZOL-5-YL)ANILINE
BenzenaMine, 3-Methoxy-4-(5-oxazolyl)-
[Molecular Formula]

C10H10N2O2
[MDL Number]

MFCD03844645
[MOL File]

198821-79-3.mol
[Molecular Weight]

190.2
Chemical PropertiesBack Directory
[Boiling point ]

318.7±27.0 °C(Predicted)
[density ]

1.211±0.06 g/cm3(Predicted)
[storage temp. ]

under inert gas (nitrogen or Argon) at 2–8 °C
[pka]

3.03±0.10(Predicted)
[Appearance]

Off-white to yellow Solid
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H332-H335
[Precautionary statements ]

P261-P280-P305+P351+P338
[HS Code ]

2934999090
Hazard InformationBack Directory
[Synthesis]

5-(2-METHOXY-4-NITROPHENYL)OXAZOLE

198821-78-2

3-METHOXY-4-(1,3-OXAZOL-5-YL)ANILINE

198821-79-3

The general procedure for the synthesis of 3-methoxy-4-(1,3-oxazolyl)aniline from 5-(2-methoxy-4-nitrophenyl)oxazole was as follows: 5-(2-methoxy-4-nitrophenyl)oxazole (10 g, 45.4 mmol) was dissolved in a solvent mixture of tetrahydrofuran (185 ml) and ethanol (37 ml). Palladium-carbon catalyst (Pd/C, 2.0 g, 1.88 mmol) was added to the reaction system under argon protection. After displacing the gas in the reaction system with hydrogen, the reaction mixture was stirred vigorously at room temperature overnight. Upon completion of the reaction, the catalyst was removed by filtration and washed with tetrahydrofuran and ethanol. The filtrate was concentrated to give an oil, which was allowed to stand for several hours and then crystallized. 3-Methoxy-4-(1,3-oxazole)aniline was finally obtained as a yellow solid (8.54 g, 97% yield); mass spectrum (ISN) m/z = 191.08 [(M + H)+].

[References]

[1] Patent: WO2014/79850, 2014, A1. Location in patent: Page/Page column 53; 54
[2] Bioorganic and Medicinal Chemistry Letters, 2002, vol. 12, # 9, p. 1323 - 1326
[3] Bioorganic and Medicinal Chemistry Letters, 2002, vol. 12, # 20, p. 2879 - 2882
[4] Heterocycles, 2006, vol. 68, # 1, p. 167 - 173
[5] Patent: WO2004/214, 2003, A2. Location in patent: Page 42
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