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HRID 1935186생성일: 2026년 10월 27일

Methanol → 6-Amino-4-(3-chloro-4-fluoroanilino)-3-cyano-7-ethyloxyquinoline

https://huagongshe.com/reaction/1935186

반응식

참여 물질

역할이름HCID투입량
반응물MethanolHCID 887—
반응물Ammonium ChlorideHCID 25517—
반응물4-((3-Chloro-4-fluorophenyl)amino)-7-ethoxy-6-nitroquinoline-3-carbonitrile hydrochlorideHCID 22466579—
촉매IronHCID 23925—
용매WaterHCID 962—
생성물6-Amino-4-(3-chloro-4-fluoroanilino)-3-cyano-7-ethyloxyquinolineHCID 11035685—

반응 단계

4-(3-Chloro-4-fluoro-phenylamino)-7-ethoxy-6-nitro-quinoline-3-carbonitrile hydrochloride (38.6 g 91.2 mmol) was mixed with 35.7 g (638 mmol) of iron powder. A solution of 43.9 g (820 mmol) of ammonium chloride in 280 ml of water was added followed by 985 ml of methanol. The mixture was reflux with mechanical stirring under nitrogen for 4 hr at which time TLC indicated complete reduction. The reaction mixture was filtered hot and solids were washed with 500 ml of boiling methanol. After the combined filtrate was evaporated, the residue was partitioned between 1.5L of warm ethyl acetate and 700 ml of saturated sodium bicarbonate solution. The organic layer was dried over magnesium sulfate, treated with Norite, filtered and evaporated to give a solid which was recrystallized from CHCl3-hexanes giving 29.0 g (89%) of 6-amino-4-(3-chloro-4-fluoro-phenylamino)-7-ethoxy-quinoline-3-carbonitrile as a light green solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06384051B1
출처 데이터셋uspto-grants-2002_05
ORD IDord-b1e8a7058d5246a3bd22db9d1866d7c9
출처 메모uspto-grants-2002_05