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标题标题2专利权人发明人附图摘要摘要2优先权号IPC专利类型
首页123456下页尾页134 条记录, 当前第1/14页。
公开号 公开日 申请号 申请日
1. US2014073816A1 2014/3/13 US201214005123 2012/3/14
专利标题:PROCESS FOR THE PREPARATION OF A STABLE POLYMORPHIC FORM OF ATOVAGUONE 法律状态
The present invention provides a process for the preparation of a stable polymorph III of Atovaquone exhibiting characteristic peaks (expressed in degrees 2theta+-0.2 DEG theta) at about 6.9, 9.6, 14.1, 14.7, 17.0, 18.5, 19.1, 19.9, 20.3, 22.0, 22.6, 23.2, 24.2, 26.8, and 28.5, which comprises: (a) providing a sample of Atovaquone particles


2. CN103570521A 2014/2/12
专利标题:A kind of preparation method of atovaquone 法律状态
专利权人


3. WO2013098832A4 2013/12/5
专利标题:Novel process for selective isolation and purification of 2-[4-(4-chlorophenyl) cyclohexyl]-3-chloro-1, 4-naphthoquinone and atovaquone 法律状态
The present invention relates to an improved method for preparation and purification of atovaquone and its intermediate product. The present invention claims for an improved method for preparation and purification of the intermediate trans-2-[4-(4-chlorophenyl)cyclohexyl]-3-chloro-14-naphthoquinone(II) of formula-II and also preparation of stable form of 2-[trans-4-(4-chlorophenyl)cyclohexyl]-3-hydroxy-14-naphthoquinone(I) Atovaquone of formula - I and selective purification of trans-2-[4-(4-chl...


4. US8598387B2 2013/12/3
专利标题:Process for the preparation of atovaquone 法律状态
专利权人GLAXO GROUP LIMITED;
Disclosed herein is novel process for preparation of atovaquone which process includes reacting 1H-2-benzopyran-14(3H)-dione with 4-(4-chlorophenyl)cyclohexanecarbaldehyde. The invention further discloses novel intermediates useful in the preparation of atovaquone.


5. EP2651868A2 2013/10/23 EP20110805451 2011/12/13
专利标题:PROCESS FOR THE PREPARATION OF ATOVAQUONE 法律状态
专利权人GLAXO GROUP LTD [GB];


6. US2013267717A1 2013/10/10 US201113993683 2011/12/13
专利标题:PROCESS FOR THE PREPARATION OF ATOVAQUONE 法律状态
Disclosed herein is novel process for preparation of atovaquone, which process includes reacting 1H-2-benzopyran-1,4(3H)-dione with 4-(4-chlorophenyl)cyclohexanecarbaldehyde. The invention further discloses novel intermediates useful in the preparation of atovaquone.


7. US20130267717A1 2013/10/10
专利标题:Process for the preparation of atovaquone 法律状态
专利权人GLAXO GROUP LIMITED;
Disclosed herein is novel process for preparation of atovaquone which process includes reacting 1H-2-benzopyran-14(3H)-dione with 4-(4-chlorophenyl)cyclohexanecarbaldehyde. The invention further discloses novel intermediates useful in the preparation of atovaquone.


8. WO2013098832A3 2013/10/10
专利标题:Novel process for selective isolation and purification of 2-[4-(4-chlorophenyl) cyclohexyl]-3-chloro-1, 4-naphthoquinone and atovaquone 法律状态
The present invention relates to an improved method for preparation and purification of atovaquone and its intermediate product. The present invention claims for an improved method for preparation and purification of the intermediate trans-2-[4-(4-chlorophenyl)cyclohexyl]-3-chloro-14-naphthoquinone(II) of formula-II and also preparation of stable form of 2-[trans-4-(4-chlorophenyl)cyclohexyl]-3-hydroxy-14-naphthoquinone(I) Atovaquone of formula - I and selective purification of trans-2-[4-(4-chl...


9. WO2013093937A3 2013/8/15
专利标题:''3-(5-methyl-2-oxo-l, 3-dioxol-4-yl) methyloxy-2- trans-[(4-chloro phenyl) cyclohexyl] [1,4]naphthaquinone"-atovaquone prodrug 法律状态
专利权人Alkem Laboratories Ltd.;
The present invention relates to atovaquone prodrug compound of formula (I). Accordingly present invention provides a process involving condensation of Atovaquone (II) with 5-methyl-4- chloromethyl dioxalone (III) in suitable solvent system and optionally followed by distillation and crystallization to provide Atovaquone prodrug compound of formula (I) in high yields purity and suitable for large-scale manufacture.


10. WO2013093937A2 2013/6/27 WO2012IN00613 2012/9/14
专利标题:''3-(5-METHYL-2-OXO-L, 3-DIOXOL-4-YL) METHYLOXY-2- TRANS-[(4-CHLORO PHENYL) CYCLOHEXYL] [1,4]NAPHTHAQUINONE"-ATOVAQUONE PRODRUG 法律状态
The present invention relates to atovaquone prodrug compound of formula (I). Accordingly, present invention provides a process involving condensation of Atovaquone (II) with 5-methyl-4- chloromethyl dioxalone (III) in suitable solvent system and optionally followed by distillation and crystallization to provide Atovaquone prodrug compound of formula (I) in high yields, purity, and suitable for large-scale manufacture.



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