反应 #4131892
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openreactiondata ↗doi:10.1039/C8SC04228D
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-a496083cb8de42c888ea221002165337暂无可渲染的结构数据
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12 条反应 · 12 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-a496083cb8de42c888ea221002165337反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-568154a3dfce4b55a3e5ea850f635714反应条件: temp:0.00; pressure:0.00; stir:
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来源 ID: ord-e439c155dff44e10b71f31c7da3f918e反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-e795f2349f2a46cbb04c0b03d8e75179反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-8ef34c43512147e28b3fd61bb20a29fb反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-705f4db1a1fc4670ab004025b9494ef7反应条件: temp:80.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: According to the general protocol described in J. Heterocyclic. Chem., 1988, 25, 129-137, to solution of 5-fluoropyridin-2-amine (1.80 g, 16 mmol) in EtOH (24 mL) was added 1,3-dichloropropan-2-one (2.03 g, 16 mmol) and the resulting mixture was stirred overnight at 80° C. The solvent was evaporated, and the residue was dissolved in a minimum volume of water. The solution was neutralized (pH=8) with saturated NaHCO3. The aqueous layer was extracted with AcOEt and the organic layer was washed with saturated NaCl. The solvent was evaporated and The crude product was purified by chromatography (prepacked 25 g silicagel column, DCM as eluent) to afford 1.7 g of 2-(chloromethyl)-6-fluoro-imidazo[1,2-a]pyridine (Yield: 57%) as a beige solid. The solvent was evaporated the residue was dissolved in a minimum volume of water The aqueous layer was extracted with AcOEt the organic layer was washed with saturated NaCl The solvent was evaporated The crude product was purified by chromatography (prepacked 25 g silicagel column, DCM as eluent)
来源 ID: ord-690a45c177a745c7aacb7183f3a0c928PubChem References
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