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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 989361생성일: 2026년 10월 24일

Glycol monoethyl ether → 4-(2,4-Dichloro-5-methoxyanilino)-7-methoxy-8-(chloroethoxy)benzo[g]quinoline-3-carbonitrile

https://huagongshe.com/ko/reaction/989361

반응식

참여 물질

역할이름HCID투입량
반응물Glycol monoethyl etherHCID 8076—
반응물2,4-Dichloro-5-methoxyanilineHCID 1476636—
반응물Pyridinium chlorideHCID 10176127—
반응물4-Chloro-7-methoxy-8-(2-chloroethoxy)benzo[g]quinoline-3-carbonitrileHCID 11515773—
반응물4-Chloro-8-methoxy-7-(2-chloroethoxy)benzo[g]quinoline-3-carbonitrileHCID 11617183—
생성물4-(2,4-Dichloro-5-methoxyanilino)-7-methoxy-8-(chloroethoxy)benzo[g]quinoline-3-carbonitrileHCID 1156963948%

반응 조건

온도135 °C

반응 단계

A mixture of 1.10 g (3.17 mmol) of 4-chloro-7-methoxy-8-(2-chloroethoxy)benzo[g]quinoline-3-carbonitrile and 4-chloro-8-methoxy-7-(2-chloroethoxy)benzo[g]quinoline-3-carbonitrile (1:1 mixture), 50 mg of pyridine hydrochloride, 742 mg (3.86 mmol) of 2,4-dichloro-5-methoxyaniline and 25 mL of 2-ethoxyethanol is stirred and heated to 135° C. After 1 hour, the reaction is cooled to room temperature, quenched with 1.0 mL of triethylamine and concentrated in vacuo. The residue is dissolved in 95:5 methylene chloride/methanol and chromatographed on silica gel, eluting with 1:1 hexane/ethyl acetate. The product is precipitated from ethyl acetate to provide 0.760 g (48%) of 4-(2,4-dichloro-5-methoxyanilino)-7-methoxy-8-(chloroethoxy)benzo[g]quinoline-3-carbonitrile and 4-(2,4-dichloro-5-methoxyanilino)-8-methoxy-7(chloroethoxy)benzo[g]quinoline-3-carbonitrile (1:1 mixture) as a dull yellow solid, m.p. 239-55° C. dec.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06638929B2
출처 데이터셋uspto-grants-2003_10
ORD IDord-74b21ec7a4f74e91a6bed0248c332ccb
출처 메모uspto-grants-2003_10