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HRID 276786作成日:2026年10月26日

4-ethoxymethylene-2-(1)-naphthyl-5(4H)-oxazolone → [1-(2-Naphthalen-1-yl-5-oxo-oxazol-4-ylidenemethyl)-piperidin-4-yl]-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/276786

反応式

関与物質

役割名称HCID仕込み量
反応物4-ethoxymethylene-2-(1)-naphthyl-5(4H)-oxazoloneHCID 356930—
反応物4-(N-Boc-amino)piperidineHCID 723833—
溶媒TetrahydrofuranHCID 8028—
生成物[1-(2-Naphthalen-1-yl-5-oxo-oxazol-4-ylidenemethyl)-piperidin-4-yl]-carbamic acid tert-butyl esterHCID 54409055—

反応手順

To a solution of 4-ethoxymethylene-2-naphthalen-1-yl-4H-oxazol-5-one (6.30 g, 23.7 mmol) in tetrahydrofuran, piperidin-4-yl-carbamic acid tert-butyl ester (4.70 g, 23.7 mmol) was added, and the mixture was stirred at room temperature for 24 h. The reaction mixture was concentrated under reduced pressure to yield [1-(2-naphthalen-1-yl-5-oxo-oxazol-4-ylidenemethyl)-piperidin-4-yl]-carbamic acid tert-butyl ester.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06355641B1
出典データセットuspto-grants-2002_03
ORD IDord-70c55eef495c4922a9fbdecab2bff985
出典メモuspto-grants-2002_03