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HRID 354151作成日:2026年10月25日

Potassium Iodide → 2-(4-Methoxyphenyl)-N-(4-methylbenzyl)-N-[1-(2-methylthiazol-4-ylmethyl)piperidin-4-yl]acetamide

https://huagongshe.com/reaction/354151

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium IodideHCID 4875—
反応物Potassium CarbonateHCID 11430—
反応物4-(Chloromethyl)-2-methyl-1,3-thiazole--hydrogen chloride (1/1)HCID 2734203—
反応物2-(4-Methoxyphenyl)-N-(4-methylbenzyl)-N-(piperidin-4-yl)acetamideHCID 9946526—
溶媒AcetonitrileHCID 6342—
生成物2-(4-Methoxyphenyl)-N-(4-methylbenzyl)-N-[1-(2-methylthiazol-4-ylmethyl)piperidin-4-yl]acetamideHCID 68952697—

反応条件

温度82 °C

反応手順

50ELH87 (0.3 g, 0.852 mmol, 1.0 eq) and 4-(chloromethyl)-2-methylthiazole hydrochloride (0.235 g, 1.5 eq) were added to a 7 ml vial and dissolved in acetonitrile (3 ml). Potassium carbonate (141.3 g, 1.2 eq) and a crystal of potassium iodide were added and the vial was sealed and shaken for 20 h at 82° C. The reaction mixture was extracted with distilled water (made basic by potassium carbonate, pH 10) and dichloromethane. The crude product was dried with sodium sulfate and concentrated. After purification by HPLC the product was converted into the hydrochloride salt by dissolving the free base in 1 ml dichloromethane and adding 1 eq. HCl in ether (2M). This mixture was added drop-wise to an excess of heptane where the product precipitated. The solvent was removed by evaporation leaving a white powder as the product. yield 83.8 mg (21%), UV/MS 100/90 (M+ 463), rt (B, MS) 11.82.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06756393B2
出典データセットuspto-grants-2004_06
ORD IDord-f76ba16408f648aeaacc679366b45b0e
出典メモuspto-grants-2004_06