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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 502033생성일: 2026년 10월 25일

1-Hydroxybenzotriazole → N-[2-(4-chlorophenoxy)ethyl]-3-(3,4-dimethoxybenzamido)-4-methylbenzamide

https://huagongshe.com/reaction/502033

반응식

참여 물질

역할이름HCID투입량
반응물1-HydroxybenzotriazoleHCID 75771—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
반응물2-(4-Chlorophenoxy)ethylamineHCID 2794191—
반응물3-[(3,4-Dimethoxybenzoyl)amino]-4-methylbenzoic acidHCID 3600179—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매DichloromethaneHCID 6344—
생성물N-[2-(4-chlorophenoxy)ethyl]-3-(3,4-dimethoxybenzamido)-4-methylbenzamideHCID 2263610267.7%

반응 단계

A solution of 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (0.095 g) in methylene chloride (5 ml) was added to a stirred mixture of 3-(3,4-dimethoxybenzamido)-4-methylbenzoic acid (0.157 g), 2-(4-chlorophenoxy)ethylamine (C. Chim. Ther., 1973, 8, 259; 0.086 g), 4-dimethylaminopyridine (0.007 g), 1-hydroxybenzotriazole (0.074 g) and methylene chloride (5 ml). The resultant mixture was stirred at ambient temperature for 16 hours. The mixture was evaporated and the residue was partitioned between ethyl acetate and a saturated aqueous sodium bicarbonate solution. The organic phase was washed with an aqueous citric acid solution, dried over magnesium sulphate and evaporated. There was thus obtained the title compound as a solid (0.158 g); Mass Spectrum: M+H+ 469.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07772432B2
출처 데이터셋uspto-grants-2010_08
ORD IDord-d534d7fcd7fa4f299534f054646de1cd
출처 메모uspto-grants-2010_08