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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1427154생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1427154

반응식

참여 물질

역할이름HCID투입량
반응물PropynalHCID 12222—
반응물Bis(1,1-Dimethylethyl) 2-[(1Z)-1-amino-3-(ethyloxy)-3-oxo-1-propen-1-yl]-1,4-piperazinedicarboxylateHCID 70556570—
용매TolueneHCID 1140—
생성물2-(3-Ethoxycarbonyl-pyridin-2-yl)-piperazine-1,4-dicarboxylic acid di-tert-butyl esterHCID 70556643—

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08933132B2
출처 데이터셋uspto-grants-2015_01
ORD IDord-69007446e09a45529f316b58907815fc
출처 메모uspto-grants-2015_01