Preparation method of Ticagrelor and intermediates thereof
AssigneeSuzhou Miracpharma Technology Co., Ltd.
InventorXuenong Xu
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AssigneeSuzhou Miracpharma Technology Co., Ltd.
InventorXuenong Xu
Estimating the term…
Disclosed in the present invention is a method for preparing Ticagrelor (I), comprising the following steps: a cyclization reaction of 5-amino-1,4-di-substituted-1,2,3-triazole (II) and dialkyl carbonate (HI), to obtain 9-substituted-2,6-dihydroxy-8-azapurine (IV); chlorination of intermediate (IV), to obtain 9-substituted-2,6-dichloro-8-azapurine (V); an amination reaction of intermediate (V) and trans-(1R,2S)-2-(3,4-difluorophenyl)cyclopropanamine (VI) generates 9-substituted-6-amino-substituted-2-chloro-8-azapurine (VII); and a propanethiolation reaction of intermediate (VII) and propanethiol (VIII), to obtain Ticagrelor (I). The preparation method is simple in process, has a high chemical and chiral purity and provides a new preparation method for industrializing Ticagrelor. In addition, also provided in the present invention are intermediates of Ticagrelor and a preparation method thereof, wherein raw materials of the preparation method are easily available, the conditions thereof are mild, and the yield thereof is high.
A method for preparing Ticagrelor (I),
A azide compound (IX), wherein its chemical name is 1-alkoxy-substituted-2,3-acetone protected o-hydroxy-4-azido-cyclopentane, and its chemical formula is shown as formula (IX) below:
A Ticagrelor intermediate (II), wherein its chemical name is 5-amino-1,4-di-substituted-1,2,3-triazole (II), and its chemical formula is shown in formula (II),
Dependencies are inferred from the claim text.