Preparation method of Ticagrelor intermediate
A technology for ticagrelor and intermediates, which is applied in the field of preparation of ticagrelor intermediates, can solve the problems of unsuitability for large-scale industrial production, column purification of products, and many side reactions, and achieve high product yields and excellent reaction conditions. Gentle and easy to control, easy to operate effect
Patent Information
- Authority / Receiving Office
- CN · China
- Patent Type
- Applications(China)
- Current Assignee / Owner
- Publication Date
- 2012-11-28
Smart Images
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Abstract
Description
(1) Technical field
[0001] The invention relates to the field of pharmaceutical chemical synthesis, in particular to a preparation method of a ticagrelor intermediate. (2) Background technology
[0002] Ticagrelor, English name ticagrelor, chemical name (1S, 2S, 3R, 5s)-3-[7-[(1R, 2S)-2-(3,4-difluorophenyl) cyclopropylamino]- 5-(thiopropyl)-3H-[1,2,3]triazol[4,5-d]pyrimidin-3-yl]-5-(2-hydroxyethoxy)cyclopentane-1,2 -diol is a novel, selective small molecule anticoagulant drug developed by AstraZeneca. The drug has obvious inhibitory effect on platelet aggregation caused by ADP, and the effect is rapid after oral administration, so it can effectively improve the symptoms of patients with acute coronary heart disease.
[0003] Trans-(1R,2S)-2-(3,4-difluorophenyl)-cyclopropylamine is an important intermediate for the synthesis of ticagrelor, and its structural formula is
[0004]
[0005] The preparation method of currently announced trans-(1R, 2S)-2-(3,4-difluorophenyl)-...
Examples
Embodiment Construction
[0051] The present invention is further illustrated by the following examples, which are only for illustration and not for limiting the present invention.
[0052] The preparation method of this ticagrelor intermediate adopts the following steps:
[0053] (1) Preparation of ethyl 3,4-difluorocinnamate:
[0054] a) Preparation of phosphorus ylide feed liquid:
[0055] Add 16.6g of triethyl phosphite, 80ml of tetrahydrofuran, and 12.2ml of ethyl α-bromoacetate to the first reaction flask in sequence, stir, heat, and reflux for 2 hours, stop heating, cool down to room temperature naturally, and then control the temperature in an ice-water bath Add 12.5 g of sodium tert-butoxide in batches to the first reaction flask at around 0°C, stir for 1 hour, and use it directly for the reaction of preparing ethyl 3,4-difluorocinnamate;
[0056] b) Preparation of ethyl 3,4-difluorocinnamate:
[0057] Add 12.8g of 3,4-difluorobenzaldehyde (I) and 60ml of tetrahydrofuran to the second react...