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PROCESS FOR BIOREDUCTION OF BISARYL KETONE TO BISARYL ALCOHOL

机译:双SARAL基酮生物还原为双SARAL基醇的方法

摘要

The present invention is directed to an improved process for making PDE IV inhibitors. Specifically, this application describes a process for making and purifying a chiral bisaryl alcohol, an intermediate compound necessary for the preparation of PDE IV inhibitors such as CDP 840, by asymmetric bioreduction of a pro-chiral ketone. Furthermore, the bioprocess provides for production of each enantiomer of a bisaryl alcohol at elevated optical purity. This invention takes advantage of a microorganism's ability to reduce a pro-chiral bisaryl ketone to the chiral bisaryl alcohol. The alcohol is readily isolated from the media by solvent extraction, crystallography, or other purification method known to the skilled artisan. The chiral alcohol can then be converted to a PDE IV inhibitor, such as CDP 840, by methods well known in the art.
机译:本发明涉及制备PDE IV抑制剂的改进方法。具体地,本申请描述了一种通过手性前酮的不对称生物还原来制备和纯化手性双芳基醇的方法,该手性双芳基醇是制备PDE IV抑制剂如CDP 840所必需的中间化合物。此外,该生物过程提供了在提高的光学纯度下双芳基醇的每个对映体的生产。本发明利用了微生物将手性双芳基酮还原为手性双芳基醇的能力。可通过溶剂萃取,晶体学或本领域技术人员已知的其他纯化方法容易地从介质中分离出醇。然后可以通过本领域众所周知的方法将手性醇转化为PDE IV抑制剂,例如CDP 840。

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