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HRID 1427154作成日:2026年10月27日

Propynal → 2-(3-Ethoxycarbonyl-pyridin-2-yl)-piperazine-1,4-dicarboxylic acid di-tert-butyl ester

https://huagongshe.com/reaction/1427154

反応式

関与物質

役割名称HCID仕込み量
反応物PropynalHCID 12222—
反応物Bis(1,1-Dimethylethyl) 2-[(1Z)-1-amino-3-(ethyloxy)-3-oxo-1-propen-1-yl]-1,4-piperazinedicarboxylateHCID 70556570—
溶媒TolueneHCID 1140—
生成物2-(3-Ethoxycarbonyl-pyridin-2-yl)-piperazine-1,4-dicarboxylic acid di-tert-butyl esterHCID 70556643—

反応手順

To a solution of bis(1,1-Dimethylethyl) 2-[(1Z)-1-amino-3-(ethyloxy)-3-oxo-1-propen-1-yl]-1,4-piperazinedicarboxylate (may be prepared as described in Intermediate 4; 500 mg) in toluene (100 mL), propiolaldehyde (1.0 eq) was added at room temperature. After completion of addition, the reaction mixture was stirred for 2 h at room temperature and then heated to 90° C. Completion of reaction was followed by TLC. TLC showed disappearance of starting material in 5 h. Toluene was removed by vacuo then the residue was diluted with ethyl acetate (100 mL) and washed with water (2×50 mL) followed by brine solution (50 mL) and dried over anhydrous sodium sulphate, concentrated under vacuum to get 600 mg of crude product. The crude product was purified by column chromatography over 100-200 mesh silica gel by using 10%-30% ethyl acetate in pet ether as solvent, which yielded the title compound (200 mg).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08933132B2
出典データセットuspto-grants-2015_01
ORD IDord-69007446e09a45529f316b58907815fc
出典メモuspto-grants-2015_01