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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 499104생성일: 2026년 10월 25일

Pyridinium chloride → 4-[3-chloro-4-(1-methyl-1H-imidazole-2-ylsulfanyl)phenylamino]-7-fluoro-6-methoxyquinoline-3-carbonitrile

https://huagongshe.com/reaction/499104

반응식

참여 물질

역할이름HCID투입량
반응물Pyridinium chlorideHCID 10176127—
반응물3-chloro-4-(1-methyl-1H-imidazol-2-ylsulfanyl)phenylamineHCID 11459088—
반응물4-Chloro-7-fluoro-6-methoxy-3-quinolinecarbonitrileHCID 12150703—
용매Glycol monoethyl etherHCID 8076—
생성물4-[3-chloro-4-(1-methyl-1H-imidazole-2-ylsulfanyl)phenylamino]-7-fluoro-6-methoxyquinoline-3-carbonitrileHCID 23498074—

반응 조건

온도120 °C

반응 단계

A mixture of 1.0 g (4.23 mmol) of 4-chloro-7-fluoro-6-methoxyquinoline-3-carbonitrile (AM100856), 1.114 g (4.65 mmol) of 3-chloro-4-(1-methyl-1H-imidazole-2-ylsulfanyl)phenylamine and 0.489 g (4.23 mmol) of pyridine hydrochloride in 10 mL of 2-ethoxyethanol is heated at 120° C. for 1.5 hours, then cooled to room temperature. The resulting solid is filtered, washed with cold 2-ethoxyethanol, then ethyl acetate. After drying in vacuo, the solid is suspended in a saturated solution of sodium bicarbonate, stirred for 45 minutes and collected by filtration. The reaction product is washed with water and dried in vacuo, to provide 4-[3-chloro-4-(1-methyl-1H-imidazole-2-ylsulfanyl)-phenylamino]-7-fluoro-6-methoxyquinoline-3-carbonitrile as a tan solid, mp 295-297° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07767671B2
출처 데이터셋uspto-grants-2010_08
ORD IDord-44ce814751b34bbb98a256c830e2b2c7
출처 메모uspto-grants-2010_08