Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1178633생성일: 2026년 10월 25일
Pyridinium chloride → 4-[(3-chloro-4-[(1-methyl-1H-imidazol-2-yl)thio]phenyl)amino]thieno[2,3-b]pyridine-5-carbonitrile
https://huagongshe.com/reaction/1178633
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Pyridinium chloride | HCID 10176127 | — |
| 반응물 | 4-Chlorothieno[2,3-b]pyridine-5-carbonitrile | HCID 11412907 | — |
| 반응물 | 3-chloro-4-(1-methyl-1H-imidazol-2-ylsulfanyl)phenylamine | HCID 11459088 | — |
| 용매 | Glycol monoethyl ether | HCID 8076 | — |
| 생성물 | 4-[(3-chloro-4-[(1-methyl-1H-imidazol-2-yl)thio]phenyl)amino]thieno[2,3-b]pyridine-5-carbonitrile | HCID 11741550 | 26.6% |
반응 단계
A mixture of (3-chloro-4-[(1-methyl-1H-imidazol-2-yl)sulfanyl]aniline (135 mg, 0.57 mmol), pyridine hydrochloride (66 mg, 0.57 mmol) and 4-chlorothieno[2,3-b]pyridine-5-carbonitrile (0.1 g, 0.52 mmol) in 4 mL of 2-ethoxyethanol is heated at reflux for 24 hours. The solution is cooled and the solvent is evaporated. The resultant residue is treated with a minimum amount of methanol and the product is purified by flash column chromatography eluting with 3% methanol in dichloromethane. The fractions containing product are combined and concentrated. Ethyl acetate is added and the insoluble material collected by filtration to provide 55 mg of 4-[(3-chloro-4-[(1-methyl-1H-imidazol-2-yl)thio]phenyl)amino]thieno[2,3-b]pyridine-5-carbonitrile as a tan solid, mp>240° C.; 1H NMR (DMSO-d6) δ 3.61 (s, 3H), 6.53 (d, J=9 Hz, 1H), 7.15 (m, 1H), 7.17 (s, 1H), 7.44 (m, 1H), 7.52 (s, 1H), 7.54 (s, 1H), 7.81 (d, J=6 Hz, 1H), 8.53 (s, 1H), 9.76 (s, 1H); MS 396.2 (M−H)−.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07276519B2 |
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| 출처 데이터셋 | uspto-grants-2007_10 |
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| ORD ID | ord-d2fc971d491549a488fa423a93f6e543 |
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| 출처 메모 | uspto-grants-2007_10 |
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