ChemicalBook--->CAS DataBase List--->82454-61-3

82454-61-3

82454-61-3 Structure

82454-61-3 Structure
IdentificationBack Directory
[Name]

5-ethynyl-2-pyridinaMine
[CAS]

82454-61-3
[Synonyms]

5-ethynyl-2-pyridinaMine
5-Ethynylpyridin-2-aMine
2-aMino-5-ethynylpyridine
2-Pyridinamine, 5-ethynyl-
5-Ethynyl-pyridin-2-ylamine
[Molecular Formula]

C7H6N2
[MDL Number]

MFCD13175209
[MOL File]

82454-61-3.mol
[Molecular Weight]

118.14
Chemical PropertiesBack Directory
[Melting point ]

127-129 °C
[Boiling point ]

246.5±25.0 °C(Predicted)
[density ]

1.13±0.1 g/cm3(Predicted)
[storage temp. ]

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

5.13±0.13(Predicted)
[Appearance]

Yellow to orange Solid
Safety DataBack Directory
[Symbol(GHS) ]

Corrosion (GHS05)Exclamation Mark (GHS07)Health Hazard (GHS08)Environment (GHS09)
GHS05,GHS07,GHS08,GHS09
[Signal word ]

Danger
[Hazard statements ]

H302-H314-H361-H410
[Precautionary statements ]

P501-P273-P270-P202-P201-P264-P280-P391-P308+P313-P303+P361+P353-P301+P330+P331-P363-P301+P312+P330-P304+P340+P310-P305+P351+P338+P310-P405
Hazard InformationBack Directory
[Uses]

5-Ethynyl-2-pyridinamine (CAS:82454-61-3) is a useful research compound.
[Synthesis]

2-amino-5-trimethylsilanylethynylpyridine

457628-40-9

5-ethynyl-2-pyridinaMine

82454-61-3

General procedure for the synthesis of 5-alkynylpyridin-2-amines from 2-amino-5-[(trimethylsilyl)ethynyl]pyridines: To a mixed solution of 5-trimethylsilyl ethynyl-pyridin-2-ylamine (26 mg, 137 μmol) described in Preparation Example 28-1-2 in tetrahydrofuran (1 mL) and methanol (1 mL) was added potassium carbonate (37.9 mg, 274 μ mol). The reaction mixture was stirred at room temperature for 1 hour. Upon completion of the reaction, the reaction solution was partitioned into water and ethyl acetate at 0 °C for extraction. The organic layer was washed with saturated aqueous sodium chloride solution and dried with anhydrous magnesium sulfate. The solvent was removed by concentration under reduced pressure and the residue was purified by silica gel column chromatography (eluent: heptane/ethyl acetate=1:1) to afford the target product 5-alkynylpyridin-2-amines (16 mg, 99% yield).1H-NMR (CDCl3) δ (ppm): 3.07 (1H, s), 4.73 (2H, brs), 6.46 (1H, d, J=8.6 Hz). 7.53 (1H, dd, J=2.2,8.6 Hz), 8.21 (1H, s).

[References]

[1] Patent: US2009/82403, 2009, A1. Location in patent: Page/Page column 76-77
[2] Patent: US2007/105904, 2007, A1. Location in patent: Page/Page column 74
[3] Dalton Transactions, 2006, vol. 6, # 13, p. 1627 - 1635
[4] Patent: WO2005/90333, 2005, A1. Location in patent: Page/Page column 71
[5] Patent: US2007/287739, 2007, A1. Location in patent: Page/Page column 7
Spectrum DetailBack Directory
[Spectrum Detail]

5-ethynyl-2-pyridinaMine(82454-61-3)1HNMR
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