ChemicalBook--->CAS DataBase List--->159724-40-0

159724-40-0

159724-40-0 Structure

159724-40-0 Structure
IdentificationBack Directory
[Name]

3-(4-Morpholinyl)aniline
[CAS]

159724-40-0
[Synonyms]

AKOS BB-8950
3-Morpholinoaniline
3-MORPHOLIN-4-YLANILINE
3-morpholinobenzenamine
3-(4-Morpholinyl)aniline
3-Morpholin-4ylaniline 97%
4-(3-Aminophenyl)morpholine
3-Morpholin-4-yl-phenylamine
3-(Morpholin-4-yl)aniline 97+%
Benzenamine, 3-(4-morpholinyl)-
[Molecular Formula]

C10H14N2O
[MDL Number]

MFCD03197165
[MOL File]

159724-40-0.mol
[Molecular Weight]

178.23
Chemical PropertiesBack Directory
[Melting point ]

118 °C
[Boiling point ]

0°C
[density ]

1.149±0.06 g/cm3(Predicted)
[Fp ]

0°C
[storage temp. ]

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

Chloroform (Slightly), DMSO (Slightly, Heated, Sonicated)
[form ]

Solid
[pka]

5.27±0.10(Predicted)
[color ]

Pale Brown to Brown
Safety DataBack Directory
[Hazard Codes ]

Xn
[Risk Statements ]

20/21/22-36/37/38-22
[Safety Statements ]

22-36/37/39-26
[RIDADR ]

UN2811
[Hazard Note ]

Harmful
[HazardClass ]

IRRITANT
[HS Code ]

2934999090
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Ethanol-->Ethyl acetate-->Methanol-->N,N-Dimethylformamide-->Potassium carbonate-->Palladium-->Hydrogen-->Dimethyl sulfoxide-->Morpholine-->Ammonium formate-->1-Fluoro-3-nitrobenzene
Hazard InformationBack Directory
[Uses]

3-Morpholin-4-ylaniline can be used to prevent and treat influenza.
[Definition]

ChEBI: 3-Morpholin-4-ylaniline is a member of morpholines.
[Synthesis]

4-(3-Nitrophenyl)morpholine

116922-22-6

3-(4-Morpholinyl)aniline

159724-40-0

To a solution of 4-(3-nitrophenyl)morpholine (43) (4.16 g, 20 mmol) in methanol (50 mL) cooled to 0 °C in an ice water bath was added 10% palladium/carbon catalyst (460 mg). The reaction mixture was stirred at room temperature and under hydrogen atmosphere (1 atm) for 16 hours. Upon completion of the reaction, the catalyst was removed by filtration through diatomaceous earth (Celite?). The filtrate was dried with anhydrous magnesium sulfate, filtered and concentrated under reduced pressure to give 3-(4-morpholinyl)aniline (3.39 g, 95.2%) as an orange solid. The product was analyzed by LC-MS showing m/z(ESP): 179 [M+H]? and retention time (R/T) of 1.69 min, which is sufficiently pure to be used in subsequent reactions without further purification.

[References]

[1] Journal of Medicinal Chemistry, 2005, vol. 48, # 26, p. 8261 - 8269
[2] Patent: US2006/199804, 2006, A1. Location in patent: Page/Page column 31
[3] Journal of Medicinal Chemistry, 2008, vol. 51, # 3, p. 407 - 416
[4] Patent: WO2007/339, 2007, A1. Location in patent: Page/Page column 52
[5] Patent: WO2003/90912, 2003, A1. Location in patent: Page/Page column 76
Spectrum DetailBack Directory
[Spectrum Detail]

3-(4-Morpholinyl)aniline(159724-40-0)1HNMR
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