EE200200669A - Uued triasolopürimidiini ühendid - Google Patents

Uued triasolopürimidiini ühendid

Info

Publication number
EE200200669A
EE200200669A EEP200200669A EEP200200669A EE200200669A EE 200200669 A EE200200669 A EE 200200669A EE P200200669 A EEP200200669 A EE P200200669A EE P200200669 A EEP200200669 A EE P200200669A EE 200200669 A EE200200669 A EE 200200669A
Authority
EE
Estonia
Prior art keywords
triazolopyrimidine compounds
novel triazolopyrimidine
novel
compounds
triazolopyrimidine
Prior art date
Application number
EEP200200669A
Other languages
English (en)
Inventor
Larsson Ulf
Magnusson Mattias
Musil Tibor
Palmgren Andreas
Original Assignee
Astrazeneca Ab
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=26244413&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=EE200200669(A) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Astrazeneca Ab filed Critical Astrazeneca Ab
Publication of EE200200669A publication Critical patent/EE200200669A/et
Publication of EE05223B1 publication Critical patent/EE05223B1/et

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
    • C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
    • C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
    • C07D239/47—One nitrogen atom and one oxygen or sulfur atom, e.g. cytosine
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D317/00—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms
    • C07D317/08—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3
    • C07D317/44—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 ortho- or peri-condensed with carbocyclic rings or ring systems
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04—Ortho-condensed systems
EEP200200669A 2000-06-02 2001-05-31 Triasoloprimidiini hendid, meetod nende valmistamiseks ning nende kasutamine EE05223B1 (et)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
GBGB0013488.2A GB0013488D0 (en) 2000-06-02 2000-06-02 Chemical compound
SE0002102A SE0002102D0 (sv) 2000-06-02 2000-06-06 Chemical compound
PCT/SE2001/001241 WO2001092263A1 (en) 2000-06-02 2001-05-31 Novel triazolo pyrimidine compounds

Publications (2)

Publication Number Publication Date
EE200200669A true EE200200669A (et) 2004-06-15
EE05223B1 EE05223B1 (et) 2009-10-15

Family

ID=26244413

Family Applications (1)

Application Number Title Priority Date Filing Date
EEP200200669A EE05223B1 (et) 2000-06-02 2001-05-31 Triasoloprimidiini hendid, meetod nende valmistamiseks ning nende kasutamine

Country Status (36)

Country Link
US (6) US7067663B2 (et)
EP (1) EP1299390B1 (et)
JP (1) JP4947870B2 (et)
KR (2) KR100814229B1 (et)
CN (3) CN1200940C (et)
AR (1) AR028605A1 (et)
AT (1) ATE386039T1 (et)
AU (4) AU2001262876B2 (et)
BG (1) BG65866B1 (et)
BR (1) BR0111319A (et)
CA (1) CA2408914C (et)
CY (1) CY1108101T1 (et)
CZ (3) CZ302645B6 (et)
DE (1) DE60132776T2 (et)
DK (1) DK1299390T3 (et)
EE (1) EE05223B1 (et)
ES (1) ES2299487T3 (et)
GB (1) GB0013488D0 (et)
HK (1) HK1053122A1 (et)
HU (1) HU229281B1 (et)
IL (3) IL152776A0 (et)
IS (1) IS2600B (et)
MX (2) MXPA02011793A (et)
MY (1) MY131942A (et)
NO (1) NO324266B1 (et)
NZ (1) NZ522637A (et)
PL (3) PL210375B1 (et)
PT (1) PT1299390E (et)
RU (1) RU2295526C2 (et)
SE (1) SE0002102D0 (et)
SI (1) SI1299390T1 (et)
SK (1) SK286845B6 (et)
TW (1) TWI285203B (et)
UA (1) UA73182C2 (et)
WO (1) WO2001092263A1 (et)
ZA (1) ZA200209068B (et)

Families Citing this family (85)

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SE0401001D0 (sv) * 2004-03-31 2004-03-31 Astrazeneca Ab Chemical process
SE0400873D0 (sv) * 2004-03-31 2004-03-31 Astrazeneca Ab Chemical process
GB0615619D0 (en) 2006-08-05 2006-09-13 Astrazeneca Ab Chemical process for preparation of intermediates
GB0615620D0 (en) 2006-08-05 2006-09-13 Astrazeneca Ab A process for the preparation of optically active intermediates
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US8563755B2 (en) 2008-09-09 2013-10-22 Astrazeneca Ab Process for preparing [1S-[1-α, 2-α, 3-β(1S*,2R*) 5-β]]-3-[7-[2-(3,4-difluorophenyl)-cyclopropylamino]-5-(propylthio)-3H-1,2,3-triazolo [4,5-d] pyrimidin-3-yl]-5-(2-hydroxyethoxy) cyclopentane-1,2-diol and to its intermediates
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AU2011244023A1 (en) 2010-04-20 2012-10-25 Actavis Group Ptc Ehf Novel process for preparing phenylcyclopropylamine derivatives using novel intermediates
CA2803354A1 (en) * 2010-06-30 2012-01-05 Actavis Group Ptc Ehf Novel processes for the preparation of phenylcyclopropylamine derivatives and use thereof for preparing ticagrelor
WO2012063126A2 (en) 2010-11-09 2012-05-18 Actavis Group Ptc Ehf Improved processes for preparing pure (3ar,4s,6r,6as)-6-amino-2,2-dimethyltetrahdro-3ah-cyclopenta[d] [1,3]-dioxol-4-ol and its key starting material
US20130317220A1 (en) 2010-12-20 2013-11-28 Actavis Group Ptc Ehf NOVEL PROCESSES FOR PREPARING TRIAZOLO[4, 5-d]PYRIMIDINE DERIVATIVES AND INTERMEDIATES THEREOF
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CN103534245B (zh) * 2011-05-13 2015-08-19 阿斯利康(瑞典)有限公司 [(3aS,4R,6S,6aR)-6-羟基-2,2-二甲基四氢-3aH-环戊二烯并[d][1,3]二氧戊环-4-基]氨基甲酸苄酯的制备方法和该方法中的中间体
US20140206867A1 (en) 2011-06-15 2014-07-24 Actavis Group Ptc Ehf Process for Preparing Cyclopentylamine Derivatives and Intermediates Thereof
EP2570405A1 (en) 2011-09-14 2013-03-20 LEK Pharmaceuticals d.d. Synthesis of Triazolopyrimidine Compounds
CA2848621C (en) 2011-09-14 2019-10-01 Lek Pharmaceuticals D.D. Synthesis of triazolopyrimidine compounds
EP2586773A1 (en) 2011-10-27 2013-05-01 LEK Pharmaceuticals d.d. Synthesis of Triazolopyrimidine Compounds
CA2852652A1 (en) 2011-10-27 2013-05-02 Lek Pharmaceuticals D.D. Synthesis of triazolopyrimidine compounds
CN104039792A (zh) 2011-11-30 2014-09-10 阿特维斯集团公司 替格瑞洛的新结晶形式及其制备方法
IN2014KN01491A (et) 2011-12-23 2015-10-23 Lek Pharmaceuticals
EP2628721A1 (en) 2012-02-20 2013-08-21 LEK Pharmaceuticals d.d. Synthesis of 2-(3,4-difluorophenyl)cyclopropanecarboxylic acid
CN104603098B (zh) * 2012-03-30 2016-06-29 桑多斯股份公司 2-(3,4-二氟苯基)环丙胺衍生物和盐的合成
EP2644590A1 (en) 2012-03-30 2013-10-02 LEK Pharmaceuticals d.d. Synthesis of 2-(3,4-difluorophenyl)cyclopropanamine derivatives and salts
US9233966B2 (en) 2012-04-05 2016-01-12 Dr. Reddy's Laboratories Limited Preparation of ticagrelor
WO2013163892A1 (en) * 2012-05-02 2013-11-07 Sunshine Lake Pharma Co., Ltd. Novel triazolo pyrimidine compounds and a process of preparation thereof
CN102659815B (zh) * 2012-05-04 2013-07-17 开原亨泰制药股份有限公司 一种制备选择性抗凝血药替卡格雷及其中间体的方法
CN102675321B (zh) * 2012-05-11 2014-12-10 上海皓元化学科技有限公司 一种替卡格雷的制备方法
EP2666771A1 (en) 2012-05-24 2013-11-27 LEK Pharmaceuticals d.d. Synthesis of Aminocyclopentanetriol Derivatives
WO2014023681A1 (en) * 2012-08-06 2014-02-13 Enantia, S.L. A process for the preparation of an intermediate for a triazolopyrimidine carbonucleoside
CN103588674B (zh) * 2012-08-14 2015-02-11 上海医药工业研究院 一种具有光学活性的环丙烷酰阱化合物、其制备和应用
CN103626743B (zh) * 2012-08-23 2018-06-08 广东东阳光药业有限公司 替卡格雷的新型中间体及其制备方法
CN102875537A (zh) * 2012-09-10 2013-01-16 常州制药厂有限公司 一种新的抗血栓药物的制备方法
WO2014083139A1 (en) 2012-11-29 2014-06-05 Actavis Group Ptc Ehf Novel amorphous form of ticagrelor
CN103848834B (zh) * 2012-12-06 2017-09-22 博瑞生物医药（苏州）股份有限公司 一种制备替卡格雷的方法及其中间体
US20150322071A1 (en) * 2012-12-06 2015-11-12 Brightgene Bio-Medical Technology (Suzhou) Co., Ltd Process for preparing triazole pyrimidine compounds and intermediates thereof
CN104341402B (zh) * 2013-07-23 2018-04-27 博瑞生物医药（苏州）股份有限公司 一种制备替卡格雷中间体的方法
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CN103936767B (zh) * 2013-01-23 2016-08-03 上海医药工业研究院 一种制备化合物(1r,2s,6s,7s)-4,4-二甲基-9-苯甲基-3,5,8-三氧杂-9-氮杂三环[5.2.1.02.6]葵烷的方法
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CN103275056B (zh) * 2013-05-24 2015-06-17 浙江普洛医药科技有限公司 一种替卡格雷中间体的制备方法
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CN104230818B (zh) * 2013-06-06 2018-01-12 郝聪梅 替卡格雷中间体的改进制备方法
WO2014206187A1 (zh) * 2013-06-24 2014-12-31 苏州明锐医药科技有限公司 替卡格雷及其中间体的制备方法
CN103275087A (zh) * 2013-06-28 2013-09-04 南京工业大学 一种三氮唑并嘧啶类衍生物及其制备方法
CN104059069B (zh) * 2013-08-22 2016-08-10 北京康立生医药技术开发有限公司 一种替卡格雷的制备方法
CN104592237A (zh) * 2013-10-31 2015-05-06 徐州万邦金桥制药有限公司 一种抗凝血药替格瑞洛的合成方法
CN103588750B (zh) * 2013-11-07 2014-11-26 苏州明锐医药科技有限公司 替卡格雷中间体的制备方法
CN103588712B (zh) * 2013-11-08 2016-06-08 南京欧信医药技术有限公司 一种嘧啶类化合物及其制备方法、和应用
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CN104710425B (zh) * 2013-12-16 2019-06-14 石药集团中奇制药技术（石家庄）有限公司 一种替格瑞洛新结晶及其制备方法
CN104744424B (zh) * 2013-12-27 2018-12-25 博瑞生物医药（苏州）股份有限公司 一种替卡格雷中间体的制备方法
CN103923020A (zh) * 2014-04-02 2014-07-16 黄河三角洲京博化工研究院有限公司 一种2-丙硫基-4,6-二氯-5-氨基嘧啶的制备方法
CN103992323B (zh) * 2014-04-18 2017-03-29 南通常佑药业科技有限公司 一种替格瑞洛的制备方法
WO2015162630A1 (en) 2014-04-25 2015-10-29 Anlon Chemical Research Organization Novel processes for preparing triazolo [4,5-d]- pyrimidines, including ticagrelor, vianew intermediates and new route of synthesis.
US10011605B2 (en) 2014-06-18 2018-07-03 Flamma Spa Process for the preparation of triazolo[4,5-D] pyrimidine cyclopentane compounds
WO2016001851A1 (en) * 2014-07-02 2016-01-07 Dr. Reddy's Laboratories Limited Preparation of ticagrelor
CN104193748A (zh) * 2014-08-14 2014-12-10 严白双 一种替卡格雷的合成方法
WO2016030704A1 (en) * 2014-08-30 2016-03-03 Cipla Limited Solid form of intermediate of ticagrelor
CN105801583A (zh) * 2014-12-31 2016-07-27 徐州万邦金桥制药有限公司 一种替格瑞洛的纯化方法
WO2016116942A1 (en) 2015-01-20 2016-07-28 Anlon Chemical Research Organization Novel pharmaceutical compounds comprising ticagrelor with salts of aspirin
WO2016117852A2 (ko) * 2015-01-22 2016-07-28 동아에스티 주식회사 티카그렐러 제조방법 및 이를 위한 신규한 중간체
CN105968113B (zh) * 2015-03-12 2019-06-07 四川海思科制药有限公司 一种三唑并嘧啶衍生物及其应用
CN105153167B (zh) * 2015-09-06 2017-09-19 惠州信立泰药业有限公司 一种替格瑞洛结晶及含有该结晶的药物组合物
CN105198864B (zh) * 2015-10-21 2018-11-06 华仁药业股份有限公司 一种环戊基嘧啶化合物的无溶剂制备方法
WO2017072790A1 (en) * 2015-10-26 2017-05-04 Avra Laboratories Pvt. Ltd. An improved process for synthesis of ticagrelor
CN105669681A (zh) * 2016-04-11 2016-06-15 成都华宇制药有限公司 一种替格瑞洛的合成方法
CN106543191B (zh) * 2016-10-28 2019-03-01 天津红日药业股份有限公司 一种替格瑞洛制备工艺
CN107337675A (zh) * 2017-06-03 2017-11-10 湖南天济草堂制药股份有限公司 一种制备替格瑞洛的改进方法
CN107382953A (zh) * 2017-07-25 2017-11-24 安徽诺全药业有限公司 一种制备多取代环戊烷衍生物的方法
CN108689984B (zh) * 2018-05-02 2019-09-20 淮阴工学院 一种替格瑞洛中间体的生物合成方法及其中间体
CN110894184B (zh) * 2019-11-25 2022-02-18 安徽一帆香料有限公司 一种基于绿色环保的替格瑞洛中间体的制备方法
EP3919497A1 (en) 2020-06-04 2021-12-08 Zaklady Farmaceutyczne Polpharma S.A. Process for the preparation of ticagrelor
CN112457316B (zh) * 2020-11-05 2022-04-12 南通常佑药业科技有限公司 一种应用连续流反应技术制备替卡格雷高级中间体的方法
CN112724119B (zh) * 2020-12-30 2022-05-03 江苏恒沛药物科技有限公司 一种替卡格雷关键中间体的合成方法
CN115160320A (zh) * 2022-06-27 2022-10-11 南通常佑药业科技有限公司 一种手性嘧啶并三唑类替格瑞洛的制备方法
CN115785058A (zh) * 2022-12-09 2023-03-14 广州康瑞泰药业有限公司 一种合成替格瑞洛五元环中间体的方法

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Also Published As

Publication number Publication date
US7067663B2 (en) 2006-06-27
BG107333A (bg) 2003-07-31
KR20030007828A (ko) 2003-01-23
NO20025719L (no) 2003-02-03
IL152776A (en) 2013-06-27
AU2001262876B2 (en) 2007-03-01
US20030148888A1 (en) 2003-08-07
AU6287601A (en) 2001-12-11
CZ303162B6 (cs) 2012-05-09
IL225893A (en) 2015-08-31
NO20025719D0 (no) 2002-11-28
BR0111319A (pt) 2003-06-03
CY1108101T1 (el) 2014-02-12
MXPA02011793A (es) 2003-04-10
PL359183A1 (en) 2004-08-23
HUP0302345A3 (en) 2007-10-29
SI1299390T1 (sl) 2008-06-30
KR20080003458A (ko) 2008-01-07
EE05223B1 (et) 2009-10-15
PL210375B1 (pl) 2012-01-31
US20110218330A1 (en) 2011-09-08
AU2007200776A1 (en) 2007-03-15
SK16832002A3 (sk) 2003-06-03
CZ302644B6 (cs) 2011-08-10
KR100802884B1 (ko) 2008-02-13
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RU2295526C2 (ru) 2007-03-20
PT1299390E (pt) 2008-04-17
CZ302645B6 (cs) 2011-08-10
CN100354268C (zh) 2007-12-12
NZ522637A (en) 2004-09-24
IL152776A0 (en) 2003-06-24
WO2001092263A1 (en) 2001-12-06
AU2010200461B2 (en) 2011-08-18
CN1200940C (zh) 2005-05-11
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US8273879B2 (en) 2012-09-25
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CN101143864A (zh) 2008-03-19
PL392726A1 (pl) 2010-12-06
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AR028605A1 (es) 2003-05-14

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