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HRID 963031作成日:2026年10月27日

Phenylacetyl chloride → N-(4-(3-(2-chlorobenzoyl)-5-ethylthiophen-2-yl)-5-methyl[1,2,4]triazol-3-ylmethyl)-2-phenylacetamide

https://huagongshe.com/reaction/963031

反応式

関与物質

役割名称HCID仕込み量
反応物Phenylacetyl chlorideHCID 7679—
反応物TriethylamineHCID 8471—
反応物Sodium BicarbonateHCID 516892—
反応物3-Aminomethyl-4-(3-(2-chlorobenzoyl)-5-ethylthiophen-2-yl)-5-methyl[1,2,4]triazole ditosylateHCID 19085095—
溶媒DimethylformamideHCID 6228—
生成物N-(4-(3-(2-chlorobenzoyl)-5-ethylthiophen-2-yl)-5-methyl[1,2,4]triazol-3-ylmethyl)-2-phenylacetamideHCID 19085277—

反応手順

3-Aminomethyl-4-(3-(2-chlorobenzoyl)-5-ethylthiophen-2-yl)-5-methyl[1,2,4]triazole di-p-toluenesulfonate (4.0 g) was dissolved in dimethylformamide (20 ml). Phenylacetyl chloride (0.9 ml) and triethylamine (3.2 ml) were added under ice-cooling, and the mixture was stirred at room temperature for 1.5 hours. A saturated aqueous sodium hydrogencarbonate solution was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with an aqueous citric acid solution and saturated brine, and dried over magnesium sulfate. The solvent was evaporated, and the residue was recrystallized from ethyl acetate to give 1.56 g of N-(4-(3-(2-chlorobenzoyl)-5-ethylthiophen-2-yl)-5-methyl[1,2,4]triazol-3-ylmethyl)-2-phenylacetamide.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05760032
出典データセットuspto-grants-1998_06
ORD IDord-31956222ffb948fd8527f78d2b9f3887
出典メモuspto-grants-1998_06