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2-(4,5-DIHYDRO-1H-IMIDAZOL-2-YL)PYRIDINE

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Products Intro: Product Name:2-(4,5-DIHYDRO-1H-IMIDAZOL-2-YL)PYRIDINE
CAS:7471-05-8
Purity:0.99 Package:5KG;1KG
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Products Intro: Product Name:2-(4,5-Dihydro-1H-imidazol-2-yl)pyridine
CAS:7471-05-8
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Products Intro: Product Name:2-(4,5-DIHYDRO-1H-IMIDAZOL-2-YL)PYRIDINE
CAS:7471-05-8
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Products Intro: CAS:7471-05-8
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2-(4,5-DIHYDRO-1H-IMIDAZOL-2-YL)PYRIDINE manufacturers

2-(4,5-DIHYDRO-1H-IMIDAZOL-2-YL)PYRIDINE Basic information
Product Name:2-(4,5-DIHYDRO-1H-IMIDAZOL-2-YL)PYRIDINE
Synonyms:2-(4,5-DIHYDRO-1H-IMIDAZOL-2-YL)PYRIDINE;4,5-Dihydro-2-(pyridin-2-yl)-1H-imidazole;NSC 403538;Pyridine, 2-(4,5-dihydro-1H-imidazol-2-yl)-;2-(4,5-DIHYDRO-1H-IMIDAZOL-2-YL)PYRIDINE ISO 9001:2015 REACH;2-(4,5-Dihydro-2-imidazolyl)pyridine
CAS:7471-05-8
MF:C8H9N3
MW:147.18
EINECS:
Product Categories:
Mol File:Mol File
2-(4,5-DIHYDRO-1H-IMIDAZOL-2-YL)PYRIDINE Structure
2-(4,5-DIHYDRO-1H-IMIDAZOL-2-YL)PYRIDINE Chemical Properties
Melting point 104-105℃
Boiling point 172-173℃ (6 Torr)
density 1.24±0.1 g/cm3 (20 ºC 760 Torr)
Fp 121.8±25.1℃
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
solubility Chloroform (Slightly), Methanol (Slightly)
pka8.92±0.40(Predicted)
form Solid
color Pale Yellow to Light Beige
Safety Information
MSDS Information
2-(4,5-DIHYDRO-1H-IMIDAZOL-2-YL)PYRIDINE Usage And Synthesis
Uses2-(4,5-Dihydro-1H-imidazol-2-yl)pyridine is used in preparation of γ-lactam and δ-lactam by C-H amination.
Synthesis
2-Cyanopyridine

100-70-9

Ethylenediamine

107-15-3

2-(4,5-DIHYDRO-1H-IMIDAZOL-2-YL)PYRIDINE

7471-05-8

Typical reactions were carried out under microwave radiation conditions. A mixture of 2-cyanopyridine (10 mmol), ethylenediamine (40 mmol) and Cu(II)-(IAA)2 (2.0 mmol) was placed in a microwave reactor and irradiated with pulses at a power of 1000 W for 5-20 min. The reaction process was monitored by thin layer chromatography (TLC) with an eluent ratio of ethyl acetate/methanol (3:1). Upon completion of the reaction, the mixture was cooled to room temperature and diluted by addition of dichloromethane (CH2Cl2), followed by filtration to remove the catalyst. The solvent was removed by rotary evaporation to give almost pure 2-(4,5-dihydro-1H-imidazol-2-yl)pyridine. For further purification, the standard method for the synthesis of imidazolines under reflux conditions can be used. The structure of the product was confirmed by melting point (mp), nuclear magnetic resonance hydrogen spectroscopy (1H NMR), mass spectrometry (MS) and infrared spectroscopy (IR) data.

References[1] Journal of the Serbian Chemical Society, 2012, vol. 77, # 9, p. 1181 - 1189,9
[2] Canadian Journal of Chemistry, 2010, vol. 88, # 2, p. 135 - 141
[3] Monatshefte fur Chemie, 2007, vol. 138, # 6, p. 579 - 583
[4] Tetrahedron Letters, 2011, vol. 52, # 14, p. 1578 - 1582
[5] Tetrahedron Letters, 2006, vol. 47, # 13, p. 2129 - 2132
2-(4,5-DIHYDRO-1H-IMIDAZOL-2-YL)PYRIDINE Preparation Products And Raw materials
Raw materials2-Cyanopyridine-->Ethylenediamine
Tag:2-(4,5-DIHYDRO-1H-IMIDAZOL-2-YL)PYRIDINE(7471-05-8) Related Product Information
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