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发明公开
CN101260110A α－(8－喹啉氧基)单取代酞菁锌及其制备方法 有权 许可

α－(8－喹啉氧基)单取代酞菁锌及其制备方法
摘要：
本发明提供一种α－(8－喹啉氧基)单取代酞菁锌及其合成方法，其分子式为：C41H21N9OZn；其制备方法为：以8－羟基喹啉和3－硝基邻苯二甲腈为起始物，合成得到3－(8－喹啉氧基)邻苯二甲腈；然后，以3－(8－喹啉氧基)邻苯二甲腈、邻苯二甲腈及相应的锌盐为起始物，在DBU催化下合成得到酞菁锌配合物经HPLC分离，得到产物。本发明的该配合物结构单一，不存在异构体，该配合物具有结构确定、易于分离等特点。该类配合物可以应用于制备新型抗癌药物等高科技领域。
摘要（英）：

The invention provided an alpha-(8-quinoly) single substituted zinc phthalocyanine and a preparation method thereof, with the molecular formula of C41H21N9OZn; the preparation method is as follows: 8-hydroxyl quinoly and 3- nitrophthalonitrile are adopted as the original substances to synthesize 3-(8- quinoly) phthalonitrile; then 3-(8- quinoly) phthalonitrile, phthalonitrile, and the corresponding zinc salt are adopted as the original substances to synthesize a coordination compound of Phthalocyanine-zinc under the DBU catalysis, and then the coordination compound of Phthalocyanine-zinc is separated to obtain the final product. The coordination compound provided by the invention has a single structure without any isomer, and is characterized in defined structure and easy separation. The coordination compound can be applied in the high-tech fields such as the preparation of novel anti-cancer drugs.

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