돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 276863생성일: 2026년 10월 25일

(4-Aminophenoxy)benzene → 6-Fluoro-4-(4-phenoxyanilino)-1,7-naphthyridine-3-carbonitrile

https://huagongshe.com/reaction/276863

반응식

참여 물질

역할이름HCID투입량
반응물(4-Aminophenoxy)benzeneHCID 8764—
반응물Sodium BicarbonateHCID 516892—
반응물4-Chloro-6-fluoro-1,7-naphthyridine-3-carbonitrileHCID 18548960—
용매MethanolHCID 887—
용매Sodium chloride; waterHCID 57417360—
생성물6-Fluoro-4-(4-phenoxyanilino)-1,7-naphthyridine-3-carbonitrileHCID 1854895669%

반응 단계

To 2.0 g of 4-chloro-6-fluoro-[1.7]naphthyridine-3-carbonitrile in 50 mL of methanol was added 2.2 g of 4-phenoxyaniline. After stirring the reaction under an inert atmosphere for 18 hr, the reaction mixture was poured into a mixture of brine and saturated aqueous sodium bicarbonate and the resultant crystals filtered and washed with water. The product was then recrystallized from chloroformhexanes. Drying in vacuo yielded 2.35 g (69%) of 6-fluoro-4-(4-phenoxy-phenylamino)-[1.7]naphthyridine-3-carbonitrile as yellow needles: melting point 211-213° C.; mass spectrum (m/e): M+H 356.9.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06355636B1
출처 데이터셋uspto-grants-2002_03
ORD IDord-d0aa85005d3e41988f68ffd694a1f31c
출처 메모uspto-grants-2002_03