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Home > Encyclopedia > 8-METHYLIMIDAZO[1,2-A]PYRIDINE

8-METHYLIMIDAZO[1,2-A]PYRIDINE

8-METHYLIMIDAZO[1,2-A]PYRIDINE structure

8-METHYLIMIDAZO[1,2-A]PYRIDINE 

structure
  • CAS No:

    874-10-2

  • Formula:

    C8H8N2

  • Chemical Name:

    8-METHYLIMIDAZO[1,2-A]PYRIDINE

  • Synonyms:

    8-methylimidazo[1,2-a]pyridine;8-methyl-imidazo[1,2-a]pyridine;Imidazo[1,2-a]pyridine, 8-methyl-;NSC305206;SCHEMBL259019;CTK5F8336;DTXSID60316598;ZINC170147;Imidazo[1,2-a]pyridine,8-methyl-;3834AC

  • Categories:

    Pharmaceutical Intermediates  >  Heterocyclic Compound

8-METHYLIMIDAZO[1,2-A]PYRIDINE Basic Attributes

132.166

132.06900

305206

DTXSID60316598

2933990090

Characteristics

17.3

2.1

1.11 g/cm3

69ºC 0,1mm

1.609

Safety Information

36/37

8-METHYLIMIDAZO[1,2-A]PYRIDINE Use and Manufacturing

2-amino-3-methylpyridine (10 g, 92.5 mmol) and 2-bromo-1, 1-diethoxyethane (36.4 g, 185 mmol) were dissolved in ethanol (100 mL) Then, 48percent aqueous hydrogen bromide solution (9 mL) was slowly added dropwise to the reaction solution. After the reaction system was heated to 90 ° C for 26 hours, LC-MS detection reaction has ended, And then cooled to room temperature. The first reaction in the system of ethanol decompression distillation, The excess hydrobromic acid in the reaction was neutralized with excess saturated sodium bicarbonate water (100 mL) and sodium bicarbonate solids (15 g). The remaining mixture was extracted with ethyl acetate (200 mL x 3) All organic phases were then mixed and washed once with deionized water (100 mL) and saturated brine (100 mL) Dried over anhydrous sodium sulfate, Press the steam to remove the solvent. The remaining mixture was purified by silica gel column chromatography (eluent: dichloromethane / methanol = 0-10percent), To give 8-methyl-imidazo [1, 2-a] pyridine (12 g, yield 98percent).EXAMPLE IV Preparation of ethyl imidazopyridine propenoate (According to the Literature Method: Chezal, J. M. and al. J. Org. Chem. 2001, 66, 6576-6584).Ethyl azidoacetate (1.81 g, 14.0 mmol) was added dropwise at -30° C. to a stirred solution containing sodium (0.20 g, 8.70 mmol) in dry ethanol (10 mL). To this solution was added dropwise a solution of aldehyde 4 (1.00 mmol) in dry ethanol (8 mL). The reaction mixture was returned back room temperature and stirred for 3 h (CAUTION: an exothermic reaction can take place, with gas expansion). The solution was poured into aqueous saturated ammonium chloride solution (30 mL) and then extracted with CH

Computed Properties

Molecular Weight:132.16
XLogP3:2.1
Hydrogen Bond Acceptor Count:1
Exact Mass:132.068748264
Monoisotopic Mass:132.068748264
Topological Polar Surface Area:17.3
Heavy Atom Count:10
Complexity:124
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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