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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2371800생성일: 2026년 10월 26일

2-Methylbenzenesulfonamide → 4-[7-(2-Ethylbutylcarbamoyl)naphth-1-ylmethyl]-3-methoxy-N-(2-methylphenylsulfonyl)benzamide

https://huagongshe.com/reaction/2371800

반응식

참여 물질

역할이름HCID투입량
반응물2-MethylbenzenesulfonamideHCID 6924—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
반응물4-[7-(2-Ethylbutylcarbamoyl)naphth-1-ylmethyl]-3-methoxybenzoic acidHCID 19906369—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매DichloromethaneHCID 6344—
생성물4-[7-(2-Ethylbutylcarbamoyl)naphth-1-ylmethyl]-3-methoxy-N-(2-methylphenylsulfonyl)benzamideHCID 1990639270%

반응 단계

A mixture of 4-[7-(2-ethylbutylcarbamoyl)naphth-1-ylmethyl]-3-methoxybenzoic acid (189 mg), 4-dimethylaminopyridine (110 mg), 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (172 mg), and o-toluenesulfonamide (96 mg) in methylene chloride (2 ml) was stirred for 18 h. Methylene chloride (25 ml) was added, and the solution was washed (1N hydrochloric acid, brine), dried (MgSO4) and evaporated. The residue was recrystallized from 21 ml of 1:0.5:1 methylene chloride:methanol:hexane, ground to a powder and vacuum dried at 100° C. to give the title compound (179 mg, 70%) as a colorless solid; mp 126.0°-128.0° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05095038
출처 데이터셋uspto-grants-1992_03
ORD IDord-3be7c6496fb94d648eacc92bff9b613d
출처 메모uspto-grants-1992_03