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ChemicalBook--->CAS DataBase List--->15889-32-4

15889-32-4

15889-32-4 Structure

15889-32-4 Structure
IdentificationBack Directory
[Name]

2-(3-AMINOPHENYL)PYRIDINE
[CAS]

15889-32-4
[Synonyms]

p60068
3-(2-Pyridinyl)aniline
3-(Pyridin-2-yl)aniline
2-(3-AMINOPHENYL)PYRIDINE
2-(m-Aminophenyl)pyridine
3-(2-Pyridinyl)benzenamine
3-Pyridin-2-yl-phenylaMine
Benzenamine, 3-(2-pyridinyl)-
[Molecular Formula]

C11H10N2
[MDL Number]

MFCD00956760
[MOL File]

15889-32-4.mol
[Molecular Weight]

170.21
Chemical PropertiesBack Directory
[Melting point ]

72-73℃
[Boiling point ]

145-147 °C(Press: 0.1 Torr)
[density ]

1.133±0.06 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Sealed in dry,Room Temperature
[pka]

4.81±0.12(Predicted)
[Appearance]

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


GHS06
[Signal word ]

Danger
[Hazard statements ]

H335-H315-H319-H301
[Precautionary statements ]

P264-P270-P301+P310-P321-P330-P405-P501-P264-P280-P305+P351+P338-P337+P313P-P264-P280-P302+P352-P321-P332+P313-P362
[Hazard Codes ]

T
[Risk Statements ]

25-36/37/38
[Safety Statements ]

26-45
Spectrum DetailBack Directory
[Spectrum Detail]

2-(3-AMINOPHENYL)PYRIDINE(15889-32-4)1HNMR
Hazard InformationBack Directory
[Synthesis]

2-Bromopyridine

109-04-6

3-Aminobenzeneboronic acid

30418-59-8

2-(3-AMINOPHENYL)PYRIDINE

15889-32-4

General procedure for the synthesis of 3-(2-pyridyl)aniline from 2-bromopyridine and 3-aminophenylboronic acid: cf. Example 31; to a suspension of 2-bromopyridine (0.5 g, 3.2 mmol), 3-aminophenylboronic acid (0.49 g, 3.2 mmol), anhydrous K2CO3 (0.87 g, 6.3 mmol) and Pd(PPh3)4 (0.36 g, 0.32 mmol) in a suspension of 1,2-dimethoxyethane (50 mL) and water (0.66 mL) under argon protection. The reaction mixture was heated at 80 °C under argon atmosphere overnight. After completion of the reaction, it was cooled to room temperature and extracted by adding water and EtOAc. The organic and aqueous phases were separated, and the combined organic phase was dried with Na2SO4 and concentrated under reduced pressure to remove the solvent. The crude product was purified by silica gel column chromatography using a mixed solvent of gradient polarity hexane-EtOAc as eluent to give 0.22 g of 3-(2-pyridinyl)aniline (Yield: 42%). LC-MS (Method 1): tR = 1.46 min; m/z = 171.2 [M + H]+.

[References]

[1] Molecular Crystals and Liquid Crystals, 2006, vol. 458, # 1, p. 227 - 235
[2] Journal of Medicinal Chemistry, 2000, vol. 43, # 6, p. 1123 - 1134
[3] Patent: WO2007/339, 2007, A1. Location in patent: Page/Page column 52
[4] Tetrahedron, 2006, vol. 62, # 49, p. 11483 - 11498
[5] Patent: US2006/94644, 2006, A1. Location in patent: Page/Page column 23
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