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HRID 5404作成日:2026年10月23日

Triethylamine → 10-(Acetylthiomethyl)-3-t-butoxycarbonylmethyl-2-oxo-1-azacyclodecane

https://huagongshe.com/ja/reaction/5404

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物2-Thiopheneacetic acidHCID 15970—
反応物2-Fluoro-1-methylpyridinium p-toluenesulfonateHCID 171631—
反応物3-t-Butoxycarbonylmethyl-10-hydroxymethyl-2-oxo-1-azacyclodecaneHCID 19930843—
溶媒AcetoneHCID 180—
溶媒BenzeneHCID 241—
生成物10-(Acetylthiomethyl)-3-t-butoxycarbonylmethyl-2-oxo-1-azacyclodecaneHCID 19930829—

反応手順

3-t-Butoxycarbonylmethyl-10-hydroxymethyl-2-oxo-1-azacyclodecane (0.50 g, 1.67 mmol) is dissolved in acetone (5.0 mL) and benzene (5.0 mL). Triethylamine (0.26 mL, 1.9 mmol) is added, followed by 2-fluoro-1-methylpyridinium toluene-4-sulfonate (0.54 g, 1.9 mmol), and the reaction is stirred at room temperature for 90 minutes. Thiolacetic acid (0.14 mL, 1.9 mmol) and more triethylamine (0.26 mL, 1.9 mmol) are added, and the reaction is heated to reflux for 2 hours. The solvent is then removed, the crude product is partitioned between methylene chloride and water, and the aqueous phase is extracted several times with methylene chloride. The combined organic layers are dried (MgSO4) and the solvent is evaporated. The crude product is purified by silica gel chromatography (15% ethyl acetate/hexane) to give 10-(acetylthiomethyl)-3-t-butoxycarbonylmethyl-2-oxo-1-azacyclodecane, MS: M+1=358.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05244889
出典データセットuspto-grants-1993_09
ORD IDord-b0cbfac023104194ba68e11d16883fb1
出典メモuspto-grants-1993_09