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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 989397생성일: 2026년 10월 25일

Potassium Phosphate, Tribasic → HCID 10164661, 화합물

https://huagongshe.com/reaction/989397

반응식

참여 물질

역할이름HCID투입량
반응물Potassium Phosphate, TribasicHCID 62657—
반응물2-(Dicyclohexylphosphino)-2'-(dimethylamino)biphenylHCID 2734217—
반응물8-(Benzyloxy)-4-chloro-7-methoxybenzo[g]quinoline-3-carbonitrileHCID 21956464—
반응물2-Chloro-4-fluoro-5-methoxybenzenamineHCID 21956478—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
용매1,2-DimethoxyethaneHCID 8071—
생성물HCID 10164661HCID 1016466136%

반응 조건

온도80 °C

반응 단계

A mixture of 8-(benzyloxy)-4-chloro-7-methoxybenzo[g]quinoline-3-carbonitrile (1.00 g, 2.7 mmol), 2-chloro-4-fluoro-5-methoxyaniline (560 mg, 3.2 mmol), tris(dibenzylideneacetone)dipalladium(0) (240 mg, 0.26 mmol), 2-dicyclohexylphosphino-2′-(N,N-dimethylamino)biphenyl (330 mg, 0.84 mmol) and K3PO4 (860 mg, 4.1 mmol) in 15 mL of ethylene glycol dimethyl ether is heated at 80° C. for 3 hours. An additional 5% of all reagents is added and the mixture is heated at 80° C. for 2 hours then cooled to room temperature and partitioned between aqueous sodium bicarbonate and methylene chloride. The organic layer is dried over magnesium sulfate, filtered and concentrated in vacuo. Purification by column chromatography eluting with 1:1 hexane/ethyl acetate yields 500 mg (36%) of 8-(benzyloxy)-4-[(2-chloro-4-fluoro-5-methoxyphenyl)amino]-7-methoxybenzo[g]quinoline-3-carbonitrile as a yellow solid, mp 248-250° C. dec.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06638929B2
출처 데이터셋uspto-grants-2003_10
ORD IDord-aecfa2c0a67a4253a009600be570a396
출처 메모uspto-grants-2003_10