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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1610629생성일: 2026년 10월 27일

5-Chloro-1-naphthoic acid → N-[(1RS,2SR)-1-(4-tert-butylbenzyl)-2-(3-chlorophenyl)-2-hydroxyethyl]-5-chloro-1-naphthamide

https://huagongshe.com/reaction/1610629

반응식

참여 물질

역할이름HCID투입량
반응물5-Chloro-1-naphthoic acidHCID 937057—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
반응물1-Hydroxybenzotriazole hydrateHCID 2796029—
반응물(1RS,2SR)-2-amino-3-(4-tert-butylphenyl)-1-(3-chlorophenyl)propan-1-olHCID 22261970—
용매WaterHCID 962—
용매AcetonitrileHCID 6342—
생성물N-[(1RS,2SR)-1-(4-tert-butylbenzyl)-2-(3-chlorophenyl)-2-hydroxyethyl]-5-chloro-1-naphthamideHCID 22262327—

반응 단계

To a solution of (1RS,2SR)-2-amino-3-(4-tert-butylphenyl)-1-(3-chlorophenyl)propan-1-ol (1.0 g, 3.15 mmol) in acetonitrile (40 ml) were added 5-chloronaphthalenecarboxylic acid (651 mg, 3.15 mmol), 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (725 mg, 3.78 mmol) and 1-hydroxybenzotriazole hydrate (482 mg, 3.15 mmol), and the mixture was stirred overnight at room temperature. The reaction solution was diluted with water (200 ml), and the mixture was extracted with ethyl acetate (200 ml×2). The extract was washed successively with water and saturated brine, dried (anhydrous magnesium sulfate) and evaporated under reduced pressure. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=4:1-1:1). Recrystallization from ethyl acetate-hexane gave the objective substance (1.04 g, 66%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06982348B2
출처 데이터셋uspto-grants-2006_01
ORD IDord-13c2814ca7f9434bbeda66598ba33fd4
출처 메모uspto-grants-2006_01