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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Glycol monoethyl ether | HCID 8076 | — |
| 반응물 | 2,4-Dichloro-5-methoxyaniline | HCID 1476636 | — |
| 반응물 | Pyridinium chloride | HCID 10176127 | — |
| 반응물 | 4-Chloro-7-methoxy-8-(2-chloroethoxy)benzo[g]quinoline-3-carbonitrile | HCID 11515773 | — |
| 반응물 | 4-Chloro-8-methoxy-7-(2-chloroethoxy)benzo[g]quinoline-3-carbonitrile | HCID 11617183 | — |
| 생성물 | 4-(2,4-Dichloro-5-methoxyanilino)-7-methoxy-8-(chloroethoxy)benzo[g]quinoline-3-carbonitrile | HCID 11569639 | 48% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06638929B2 |
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| 출처 데이터셋 | uspto-grants-2003_10 |
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| ORD ID | ord-74b21ec7a4f74e91a6bed0248c332ccb |
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| 출처 메모 | uspto-grants-2003_10 |
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