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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1948868생성일: 2026년 10월 25일

2-Pyridinamine, 5-iodo- → 2-(4'-Hydroxy-3'-methoxyphenyl)-6-iodoimidazo[1,2-a]pyridine hydrobromide salt

https://huagongshe.com/reaction/1948868

반응식

참여 물질

역할이름HCID투입량
반응물2-Pyridinamine, 5-iodo-HCID 88579—
반응물2-Bromo-1-(4-hydroxy-3-methoxyphenyl)ethan-1-oneHCID 13542258—
용매AcetonitrileHCID 6342—
생성물2-(4'-Hydroxy-3'-methoxyphenyl)-6-iodoimidazo[1,2-a]pyridine hydrobromide saltHCID 68719556—

반응 단계

First, 2-bromo-4′-hydroxy-3′-methoxyacetophenone and 2-amino-5-iodopyridine are dissolved in an inactive solvent such as acetonitrile, and are allowed to react with each other at a reflux temperature for 2 to 6 hours to produce 2-(4′-hydroxy-3′-methoxyphenyl)-6-iodoimidazo[1,2-a]pyridine hydrobromide salt as white precipitates. The solvent used in this instance may be acetonitrile or another solvent that is usually employed in a similar reaction, for example, methanol and acetone. The reaction temperature may be a temperature allowing refluxing, for example, 110° C. when the solvent is acetonitrile. The amount of the solvent to be used may be an amount sufficient to effect the reaction, however, it should be noted that if the solvent is too much, it will become difficult to obtain precipitates of reaction products. For example, when 2-bromo-4′-hydroxy-3′-methoxyacetophenone in an amount corresponding to 2 mmol is used for the reaction, the amount of a solvent to be used can be about 15 to 30 mL.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08399672B2
출처 데이터셋uspto-grants-2013_03
ORD IDord-be4bb38fcbb84033ad4506e283d659ad
출처 메모uspto-grants-2013_03