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HRID 2222904作成日:2026年10月27日

Triethylamine → Methyl trans-2-{[(cyanomethyl)amino]carbonyl}cyclopentanecarboxylate

https://huagongshe.com/reaction/2222904

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Aminoacetonitrile hydrochlorideHCID 11491918—
反応物2-(Methoxycarbonyl)cyclopentane-1-carboxylic acidHCID 13239030—
反応物Tripyrrolidinophosphonium hexafluorophosphateHCID 22226026—
溶媒DimethylformamideHCID 6228—
生成物Methyl trans-2-{[(cyanomethyl)amino]carbonyl}cyclopentanecarboxylateHCID 86596126—

反応条件

温度0 °C

反応手順

Cyclopentane-1,2-dicarboxylic acid monomethyl ester (2.21 g, 12.8 mmol), 2-aminoacetonitrile hydrochloride (1.48 g, 16.0 mmol) and benzotriazol-1-yloxy)tripyrrolidinophosphonium hexafluorophosphate (PyBOP) (7.34 g, 14.1 mmol) were dissolved in dimethylformamide (26 mL) and the reaction mixture was cooled to 0° C. Triethylamine (4.9 mL, 35 mmol) was added and the reaction mixture was stirred at ambient temperature for 3 h. The reaction mixture was partitioned between water (150 mL) and ethyl acetate (100 mL). The product was extracted into ethyl acetate, washed with saturated sodium chloride aqueous solution, dried over anhydrous sodium sulfate and concentrated. The residue was chromatographed on silica gel with 3:2 ethyl acetate:hexanes eluent to give methyl trans-2-{[(cyanomethyl)amino]carbonyl}cyclopentanecarboxylate as a colorless solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07371747B2
出典データセットuspto-grants-2008_05
ORD IDord-00527ddaf1df475ca700b359b698bed5
出典メモuspto-grants-2008_05