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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Pyridinium chloride | HCID 10176127 | — |
| 반응물 | 3-chloro-4-(1-methyl-1H-imidazol-2-ylsulfanyl)phenylamine | HCID 11459088 | — |
| 반응물 | 4-Chloro-7-fluoro-6-methoxy-3-quinolinecarbonitrile | HCID 12150703 | — |
| 용매 | Glycol monoethyl ether | HCID 8076 | — |
| 생성물 | 4-[3-chloro-4-(1-methyl-1H-imidazole-2-ylsulfanyl)phenylamino]-7-fluoro-6-methoxyquinoline-3-carbonitrile | HCID 23498074 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07767671B2 |
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| 출처 데이터셋 | uspto-grants-2010_08 |
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| ORD ID | ord-44ce814751b34bbb98a256c830e2b2c7 |
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| 출처 메모 | uspto-grants-2010_08 |
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