戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 20233作成日:2026年10月24日

Triethylamine → Benzyl 4-(4-methyl-2-oxotetrahydropyrimidin-1(2H)-yl)piperidin-1-carboxylate

https://huagongshe.com/ja/reaction/20233

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Benzyl 4-isocyanatopiperidine-1-carboxylateHCID 2776273—
反応物4-Bromobutan-2-amine hydrobromideHCID 13555988—
反応物Potassium tert-butoxideHCID 23665647—
溶媒AcetonitrileHCID 6342—
溶媒TetrahydrofuranHCID 8028—
生成物Benzyl 4-(4-methyl-2-oxotetrahydropyrimidin-1(2H)-yl)piperidin-1-carboxylateHCID 6842047962%

反応手順

A solution of benzyl 4-isocyanatopiperidin-1-carboxylate (0.26 g) in acetonitrile (10 mL) was added to a solution of 4-bromobutan-2-amine hydrobromide (0.17 g) and triethylamine (0.10 g) in acetonitrile (10 mL), followed by stirring at room temperature for one hour. Potassium tert-butoxide (0.29 g) and THF (20 mL) were added thereto, and the mixture was further stirred at room temperature for 15 hours. The reaction mixture was concentrated under reduced pressure, and the residue was diluted with water, and extracted with ethyl acetate. The extract was washed with water and saturated saline solution and dried over anhydrous sodium sulfate, and the solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate to ethyl acetate/methanol=10/1) to obtain the title compound (0.15 g, 45%) as a light brown solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07745623B2
出典データセットuspto-grants-2010_06
ORD IDord-dd0ca6057de441808d4ef09f4c6f81e1
出典メモuspto-grants-2010_06