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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 842763생성일: 2026년 10월 25일

Acetic Acid → 5-[3,4-Dichlorophenoxy]-6-methoxy-8-[4-phthalimido-1-methyl-butylamino]lepidine

https://huagongshe.com/reaction/842763

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물Sodium HydroxideHCID 14798—
반응물2-(4-Oxopentyl)-1H-isoindole-1,3(2H)-dioneHCID 236270—
반응물8-Amino-5-[3,4-dichlorophenoxy]-6-methoxylepidineHCID 609014—
반응물Sodium borohydrideHCID 4311764—
생성물5-[3,4-Dichlorophenoxy]-6-methoxy-8-[4-phthalimido-1-methyl-butylamino]lepidineHCID 633117—
생성물5-(3,4-Dichlorophenoxy)-6-methoxy-1methyl-8-[(4-phthalimido-1-methylbutyl)amino]quinolineHCID 69464197—

반응 조건

온도30 °C

반응 단계

A mixture of 12.4 g of 8-amino-5-(3,4-dichlorophenoxy)-6-methoxy-4-methylquinoline (36 mM) and 11.6 g of 4-oxo-1-phthalimidopentane (50 mM), in glacial acetic acid was stirred for 15 min under nitrogen and 2.6 g of sodium borohydride (70 mM) was added portionwise maintaining the temperature 25-35° C. After the addition, the reaction mixture was stirred for 30 min and then poured into ice cold solution of concentrated sodium hydroxide. The resulting precipitate was filtered and chromatographed over silica gel. Elution with hexanes:ethyl acetate 90:10 yielded the expected product of 5-(3,4-dichlorophenoxy)-6-methoxy-4-methyl-8-[(4-phthalimido-1-methylbutyl)amino]quino line which was crystallized from ether to give 12.4 g (22 mM) of yellow crystalline product.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06376511B2
출처 데이터셋uspto-grants-2002_04
ORD IDord-21095a23d393418fbcba0e1d862ca66b
출처 메모uspto-grants-2002_04