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HRID 1883956생성일: 2026년 10월 27일

Chloroacetamide → Tert-butyl 4-(2-carbamoylbenzofuran-5-yl)piperazine-1-carboxylate

https://huagongshe.com/reaction/1883956

반응식

참여 물질

역할이름HCID투입량
반응물ChloroacetamideHCID 6580—
반응물Potassium CarbonateHCID 11430—
반응물tert-Butyl 4-(3-formyl-4-hydroxyphenyl)piperazine-1-carboxylateHCID 23508726—
용매N-methyl-2-pyrrolidoneHCID 13387—
생성물Tert-butyl 4-(2-carbamoylbenzofuran-5-yl)piperazine-1-carboxylateHCID 11244883—

반응 조건

온도60 °C

반응 단계

5 ml of 1-methyl-2-pyrrolidone, 0.16 g of chloroacetamide and 0.25 g of potassium carbonate are added at 20° C. with stirring/under nitrogen to 0.5 g of 5-(4-tert-butoxycarbonylpiperazin-1-yl)-2-hydroxybenzaldehyde. The mixture is stirred at 60° C. for 16 hours, cooled and then filtered, and the solvent is removed under reduced pressure. The residue is taken up in MTB ether, re-filtered and concentrated, and the residue is crystallized from toluene. The isolated yield is 0.34 g (60%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06762300B2
출처 데이터셋uspto-grants-2004_07
ORD IDord-18960a06f803452e8e3f8345adf75c2b
출처 메모uspto-grants-2004_07