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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1906438생성일: 2026년 10월 27일

1-(2-Methoxyphenyl)piperazine → 2-Carbamoyl-7-{2-hydroxy-3-[4-(2-methoxyphenyl)piperazinyl]propoxy}benzofuran

https://huagongshe.com/reaction/1906438

반응식

참여 물질

역할이름HCID투입량
반응물1-(2-Methoxyphenyl)piperazineHCID 1346—
반응물2-Carbamoyl-7-(2,3-epoxypropoxy)benzofuranHCID 13729403—
용매EthanolHCID 702—
생성물2-Carbamoyl-7-{2-hydroxy-3-[4-(2-methoxyphenyl)piperazinyl]propoxy}benzofuranHCID 13729383—

반응 단계

There was suspended 1.2 g (0.005 mole) of 2-carbamoyl-7-(2,3-epoxypropoxy)benzofuran in 15 ml of ethanol, and thereto 1.1 g (0.0055 mole) of 1-(2-methoxyphenyl)piperazine was added. Thereafter, the mixture was refluxed with heating for 2 hours. After completion of the reaction, the solvent was distilled away from the reaction mixture under reduced pressure, and then the resultant residue was crystallized from chloroform and petroleum ether.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04652566
출처 데이터셋uspto-grants-1987_03
ORD IDord-b04fffa17ff647cf8475d77b2c6e1a69
출처 메모uspto-grants-1987_03