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公开(公告)号:US20190023681A1
公开(公告)日:2019-01-24
申请号:US16070658
申请日:2016-01-18
发明人: Mingxing Yin , Dongdong Wu , Weijiang Wen
IPC分类号: C07D315/00
CPC分类号: C07D315/00 , C07H1/00 , C07H1/06 , C07H17/00
摘要: A method and an intermediate for preparing a tulathromycin. The method includes the following step: in an organic solvent, subjecting a compound represented by formula (II) and an n-propylamine to a ring-opening addition shown below to obtain a tulathromycin represented by formula (I), wherein the organic solvent is a 1,2-propandiol. Tulathromycin obtained using the method has a high purity, with an HPLC purity being 95% and above, and up to 99% and above, satisfying a required purity for preparing a tulathromycin as a pharmaceutical formulation. The method has a high yield, is simple to operate, and is more suitable for industrial production.
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公开(公告)号:US10414746B2
公开(公告)日:2019-09-17
申请号:US16070658
申请日:2016-01-18
发明人: Mingxing Yin , Dongdong Wu , Weijiang Wen
IPC分类号: C07D315/00 , C07H1/00 , C07H17/00 , C07H17/08
摘要: A method and an intermediate for preparing a tulathromycin. The method includes the following step: in an organic solvent, subjecting a compound represented by formula (II) and an n-propylamine to a ring-opening addition shown below to obtain a tulathromycin represented by formula (I), wherein the organic solvent is a 1,2-propandiol. Tulathromycin obtained using the method has a high purity, with an HPLC purity being 95% and above, and up to 99% and above, satisfying a required purity for preparing a tulathromycin as a pharmaceutical formulation. The method has a high yield, is simple to operate, and is more suitable for industrial production.
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