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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 374795생성일: 2026년 10월 26일

Triethylamine → N-[3-[4-(2-Methoxyphenyl)-1-piperazinyl]propyl]-2-benzofurancarboxamide Dihydrochloride

https://huagongshe.com/reaction/374795

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물2-Benzofurancarbonyl chlorideHCID 38949—
반응물1-(3-Aminopropyl)-4-(2-methoxyphenyl)piperazineHCID 10467259—
용매DichloromethaneHCID 6344—
생성물N-[3-[4-(2-Methoxyphenyl)-1-piperazinyl]propyl]-2-benzofurancarboxamide DihydrochlorideHCID 18995783—

반응 단계

To a stirred solution of [4-(2-methoxyphenyl)piperazinyl]propylamine (1.0 g, 0.04 mol) in 50 mL of methylene dichloride, benzofurane-2-carboxylic acid chloride (1.01 g, 0.0056 mol) and triethylamine (1 g, 0.01 mol) were added. Stirring was continued at room temperature overnight. The methylene chloride solution was washed with water, dried over anhydrous sodium sulfate and evaporated under reduced pressure. The remaining residue was subjected to preparative HPLC using silica gel column and ethyl acetate as the eluent. The title compound was separated and converted to the dihydrochloride salt with ethanolic HCl (0.9 g), m.p. 228°-232° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05482940
출처 데이터셋uspto-grants-1996_01
ORD IDord-5237be46d3504ae4a458eac030c49b0c
출처 메모uspto-grants-1996_01