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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 276858생성일: 2026년 10월 25일

Trifluoroacetic acid → 6-Amino-4-(3-bromo-phenylamino)-[1,7]naphthyridine-3-carbonitrile

https://huagongshe.com/reaction/276858

반응식

참여 물질

역할이름HCID투입량
반응물Trifluoroacetic acidHCID 6422—
반응물4-MethoxybenzylamineHCID 75452—
반응물4-(3-Bromo-phenylamino)-6-fluoro-[1,7]naphthyridine-3-carbonitrileHCID 18548979—
반응물Chloroform methanolHCID 21584188—
용매EthanolHCID 702—
용매TolueneHCID 1140—
용매ChloroformHCID 6212—
생성물6-Amino-4-(3-bromo-phenylamino)-[1,7]naphthyridine-3-carbonitrileHCID 9798006—

반응 단계

To 1.3 g of 4-(3-bromo-phenylamino)-6-fluoro-[1.7]naphthyridine-3-carbonitrile in 20 mL of absolute ethanol was added 5 ml of 4-methoxy-benzylamine. The reaction was refluxed for six days, stripped of solvents, and passed through a plug of silica gel with 5% methanol/chloroform. This crude product was dissolved in 10 mL of chloroform containing 5% anisole and 10 mL of trifluoroacetic acid was added. After stirring under an inert atmosphere for 20 hours, 10 mL of toluene was added and the solvents stripped on a rotary evaporator. The product was purified by flash chromatography with a gradient of 0-10% methanol/chloroform. The solid was extracted with hot, 5% methanol/isopropyl ether and then cooled, filtered, and dried to give 250 mg of 6-amino-4-(3-bromo-phenylamino)-[1.7]naphthyridine-3-carbonitrile as an off-white solid. mass spectrum (m/e): M+H 306.2.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06355636B1
출처 데이터셋uspto-grants-2002_03
ORD IDord-6d2ad1b6640247b58f8e221f0e4a0ebf
출처 메모uspto-grants-2002_03