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公开(公告)号:EP2651857A1
公开(公告)日:2013-10-23
申请号:EP11802893.5
申请日:2011-12-14
IPC分类号: C07B59/00
CPC分类号: C07D209/84 , C07B59/002
摘要: The present invention provides a method to prepare an
18 F-labelled tricyclic indole compound comprising a solid-phase extraction (SPE) purification step. This method is particularly suitable for carrying out the radiofluorination method on an automated synthesiser. In addition to the radiofluorination method, the present invention provides a cassette designed to carry out the method on an automated synthesiser.摘要翻译: 本发明提供一种制备包含固相萃取(SPE)纯化步骤的18F-标记的三环吲哚化合物的方法。 该方法特别适用于在自动合成器上进行放射性氟化方法。 除了放射性氟化法之外,本发明还提供了一种设计用于在自动合成器上执行该方法的盒。
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公开(公告)号:EP2766325B1
公开(公告)日:2020-03-18
申请号:EP12781295.6
申请日:2012-10-15
发明人: BHALLA, Rajiv , WILSON, Anthony , KHAN, Imtiaz , BROWN, Jane
IPC分类号: A61K51/04 , C07C303/30 , C07D451/02 , C07C227/16 , C07C67/10 , C07C319/14 , C07B59/00
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公开(公告)号:EP2651857B1
公开(公告)日:2017-02-15
申请号:EP11802893.5
申请日:2011-12-14
IPC分类号: C07B59/00
CPC分类号: C07D209/84 , C07B59/002
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公开(公告)号:EP2766325A1
公开(公告)日:2014-08-20
申请号:EP12781295.6
申请日:2012-10-15
发明人: BHALLA, Rajiv , WILSON, Anthony , KHAN, Imtiaz , BROWN, Jane
IPC分类号: C07B59/00 , C07C67/10 , C07C213/08 , C07C227/16 , C07C229/36 , C07C269/06 , C07C271/18 , C07C271/34 , C07C319/14 , C07C323/03 , C07C323/44 , C07C323/58
摘要: The present invention provides a method for the synthesis of 18F-labelled biomolecules, which is amenable to automation. The present invention also provides a cassette for automating the method of the invention. The method of the present invention provides numerous advantages over the prior art methods. One less purification step is required as compared with known methods. Also, one less reagent is required as a particular reagent is employed in two different steps. The chemistry process is thereby simplified, the cost of goods is reduced and the burden of validation and documentation of reagents required for GMP clinical production is minimized.
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公开(公告)号:EP2766326B1
公开(公告)日:2019-11-27
申请号:EP12781296.4
申请日:2012-10-15
发明人: NAIRNE, Robert, James, Domett , BHALLA, Rajiv , KHAN, Imtiaz , BROWN, Jane , WILSON, Anthony , BLACK, Andrew
IPC分类号: C07C319/20 , C07C319/14 , C07C303/30 , C07C227/16 , C07C67/10 , C07D451/02 , C07B59/00 , B01L3/00 , A61K51/04
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公开(公告)号:EP3448835A1
公开(公告)日:2019-03-06
申请号:EP17720506.9
申请日:2017-05-02
IPC分类号: C07C319/06 , C07C319/14
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公开(公告)号:EP2681177A1
公开(公告)日:2014-01-08
申请号:EP12707289.0
申请日:2012-03-01
IPC分类号: C07B59/00 , C07D213/61
CPC分类号: C07B59/002 , C07D213/61 , C07D213/81 , C07D295/135
摘要: Provided by the present invention is a novel method for obtaining an 18F-labelled compound wherein said compound comprises an 18F-labelled pyridyl ring. The method of the invention is advantageous over the prior art methods as it provides these compounds in higher radiochemical yields than have been possible with previous methods. Also provided by the present invention is an 18F-labelled synthon useful in the method of the invention.
摘要翻译: 本发明提供了一种获得18 F-标记的化合物的新方法,其中所述化合物包含18 F-标记的吡啶基环。 本发明的方法优于现有技术方法,因为它提供的这些化合物的放射化学产率比以前的方法所能达到的要高。 本发明还提供了用于本发明方法的18 F-标记的合成子。
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