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HRID 267082作成日:2026年10月27日

Triethylamine → N-Methoxy-N-methyl-1-(2-naphthylmethyl)-1H-imidazol-5-ylacetamide

https://huagongshe.com/reaction/267082

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物3-hydroxy-1,2,3-benzotriazin-4(3H)-oneHCID 73026—
反応物Sodium BicarbonateHCID 516892—
反応物1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
反応物1-(2-naphthylmethyl)-1H-imidazol-5-ylacetic acid hydrochlorideHCID 70206205—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物N-Methoxy-N-methyl-1-(2-naphthylmethyl)-1H-imidazol-5-ylacetamideHCID 86751125—

反応手順

To a solution of 1-(2-naphthylmethyl)-1H-imidazol-5-ylacetic acid hydrochloride (prepared in Example 4, 0.819 mg, 2.70 mmol) in dimethylformamide (15 ml) was added sequentially N, O-dimethylhydroxylamine hydrochloride (293 mg, 3.0 mmol), 3-hydroxy-1,2,3-benzotriazin-4(3H)-one (HOOBT, 489 mg, 3.0 mmol), 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (EDC, 575 mg, 3.0 mmol) and triethylamine (1.67 ml, 12.0 mmol) and the resulting mixture stirred at room temperature for 18 h. Saturated aq. sodium bicarbonate (30 ml) and water (30 ml) were added and the mixture was extracted with methylene chloride (2×50 ml). The combined organic extracts were washed with brine (50 ml) and the solvent evaporated in vacuo. The residue was purified by flash chromatography (2-4% methanol/methylene chloride gradient elution) to provide the title compound as an oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05652257
出典データセットuspto-grants-1997_07
ORD IDord-b1467f2bd5694d53a51470721eae605e
出典メモuspto-grants-1997_07