首页> 外国专利> Enantioselective synthesis of 6-amino-7-hydroxy-4, 5, 6, 7-tetrahydro-imidazo 4, 5, 1-JK 1-benzazepin-2 1H-one and zilpaterol

Enantioselective synthesis of 6-amino-7-hydroxy-4, 5, 6, 7-tetrahydro-imidazo 4, 5, 1-JK 1-benzazepin-2 1H-one and zilpaterol

机译:对映选择性合成6-氨基-7-羟基-4、5、6、7-四氢咪唑并[4、5、1-JK] [1]-苯并ze庚因2 [1H] -one和齐帕特罗

摘要

This invention relates to a process for the hydrogenation of a ketooxime to selectively form an aminoalcohol stereoisomer, and, in particular, to a process for the hydrogenation of 4,5-dihydro-imidazo[4,5,1-jk][1]benzazepin-2,6,7[1H]-trione-6-oxime or a salt thereof to selectively form a stereoisomer of 6-amino-7-hydroxy-4,5,6,7-tetrahydro-imidazo[4,5,1-jk][1]-benzazepin-2[1H]-one or a salt thereof. This invention also relates to the use of the 6-amino-7-hydroxy-4,5,6,7-tetrahydro-imidazo[4,5,1-jk][1]-benzazepin-2[1H]-one hydrogenation product or a salt thereof to selectively make a stereoisomer of zilpaterol or a salt thereof, as well as the use of such a zilpaterol stereoisomer or salt in methods of treatment and medicaments for animals.
机译:酮肟加氢选择性形成氨基醇立体异构体的方法技术领域本发明涉及酮肟肟加氢选择性地形成氨基醇立体异构体的方法,尤其涉及4,5-二氢咪唑并[4,5,1-jk] [1]的氢化方法。苯并ze庚因-2,6,7 [1H]-三酮-6-肟或其盐可选择性地形成6-氨基-7-羟基-4,5,6,7-四氢咪唑并[4,5, 1-jk] [1]-苯并ze庚因-2 [1H]-之一或其盐。本发明还涉及6-氨基-7-羟基-4,5,6,7-四氢咪唑并[4,5,1-jk] [1]-苯并ze庚因-2 [1H]-一氢化的用途。产物或其盐以选择性地制备齐帕特罗的立体异构体或其盐,以及此类齐帕特罗立体异构体或盐在动物的治疗方法和药物中的用途。

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