PL2900675T3 - Sposób wytwarzania pochodnej tienopirymidyny - Google Patents
Sposób wytwarzania pochodnej tienopirymidynyInfo
- Publication number
- PL2900675T3 PL2900675T3 PL13779938T PL13779938T PL2900675T3 PL 2900675 T3 PL2900675 T3 PL 2900675T3 PL 13779938 T PL13779938 T PL 13779938T PL 13779938 T PL13779938 T PL 13779938T PL 2900675 T3 PL2900675 T3 PL 2900675T3
- Authority
- PL
- Poland
- Prior art keywords
- production method
- thienopyrimidine derivative
- thienopyrimidine
- derivative
- production
- Prior art date
Links
- 238000004519 manufacturing process Methods 0.000 title 1
- RBNBDIMXFJYDLQ-UHFFFAOYSA-N thieno[3,2-d]pyrimidine Chemical class C1=NC=C2SC=CC2=N1 RBNBDIMXFJYDLQ-UHFFFAOYSA-N 0.000 title 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
- C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D495/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D333/00—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
- C07D333/02—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
- C07D333/04—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
- C07D333/26—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D333/38—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Heterocyclic Compounds Containing Sulfur Atoms (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2012217679 | 2012-09-28 | ||
| EP13779938.3A EP2900675B1 (en) | 2012-09-28 | 2013-09-27 | Production method of thienopyrimidine derivative |
| PCT/JP2013/077013 WO2014051164A2 (en) | 2012-09-28 | 2013-09-27 | Production method of thienopyrimidine derivative |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PL2900675T3 true PL2900675T3 (pl) | 2019-08-30 |
Family
ID=49448235
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PL13779938T PL2900675T3 (pl) | 2012-09-28 | 2013-09-27 | Sposób wytwarzania pochodnej tienopirymidyny |
| PL18185835T PL3415517T3 (pl) | 2012-09-28 | 2013-09-27 | Postać krystaliczna 1-(4-1-(2,6-difluorobenzylo)-5-dimetyloaminometylo-3-(6-metoksypirydazyn-3-ylo)-2,4-diokso-1,2,3,4-tetrahydrotieno(2,3-d)-pirymidyn-6-ylo)fenylo)-3-metoksymocznika |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PL18185835T PL3415517T3 (pl) | 2012-09-28 | 2013-09-27 | Postać krystaliczna 1-(4-1-(2,6-difluorobenzylo)-5-dimetyloaminometylo-3-(6-metoksypirydazyn-3-ylo)-2,4-diokso-1,2,3,4-tetrahydrotieno(2,3-d)-pirymidyn-6-ylo)fenylo)-3-metoksymocznika |
Country Status (21)
| Country | Link |
|---|---|
| US (10) | US9758528B2 (pl) |
| EP (3) | EP2900675B1 (pl) |
| JP (1) | JP6250564B2 (pl) |
| CN (3) | CN109053766B (pl) |
| AR (1) | AR092707A1 (pl) |
| CA (1) | CA2881132C (pl) |
| CY (2) | CY1121641T1 (pl) |
| DK (2) | DK2900675T3 (pl) |
| ES (2) | ES2913753T3 (pl) |
| HR (2) | HRP20220622T1 (pl) |
| HU (2) | HUE044048T2 (pl) |
| LT (2) | LT2900675T (pl) |
| PL (2) | PL2900675T3 (pl) |
| PT (2) | PT2900675T (pl) |
| RS (2) | RS58703B1 (pl) |
| SI (2) | SI3415517T1 (pl) |
| SM (2) | SMT202200255T1 (pl) |
| TR (1) | TR201906318T4 (pl) |
| TW (3) | TWI663171B (pl) |
| UY (1) | UY35058A (pl) |
| WO (1) | WO2014051164A2 (pl) |
Families Citing this family (58)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| SMT202200255T1 (it) | 2012-09-28 | 2022-07-21 | Takeda Pharmaceuticals Co | Forma cristallina di 1-(4-1-(2,6-difluorobenzil)-5-dimetilamminometil-3-(6-metossipiridazin-3-il)-2,4-diosso-1,2,3,4-tetraidrotieno(2,3-d)-pirimidin-6il)fenil)-3-metossiurea |
| FI4233847T3 (fi) | 2015-02-26 | 2024-09-24 | Takeda Pharmaceuticals Co | Metoksiureajohdannaista ja mannitolihiukkasia käsittävä tabletti |
| DK3518932T3 (da) | 2016-09-30 | 2025-01-27 | Takeda Pharmaceuticals Co | Behandling af prostatacancer |
| SMT202200254T1 (it) | 2016-09-30 | 2022-07-21 | Takeda Pharmaceuticals Co | Metodi di trattamento di fibromi uterini ed endometriosi |
| JP2019535712A (ja) * | 2016-11-14 | 2019-12-12 | ジエンス ヘンルイ メデイシンカンパニー リミテッドＪｉａｎｇｓｕ Ｈｅｎｇｒｕｉ Ｍｅｄｉｃｉｎｅ Ｃｏ．，Ｌｔｄ． | ＧｎＲＨ受容体アンタゴニストの結晶体およびその製造方法 |
| EP3634418A1 (en) | 2017-06-05 | 2020-04-15 | ObsEva S.A. | Gonadotropin-releasing hormone antagonist dosing regimens for the treatment of endometriosis |
| CN107188855A (zh) * | 2017-07-14 | 2017-09-22 | 常州工程职业技术学院 | 一种3‑氨基‑6甲氧基哒嗪的制备方法 |
| EP3765464A1 (en) | 2018-03-14 | 2021-01-20 | Teva Pharmaceuticals USA, Inc. | Solid state forms of relugolix |
| US12441738B2 (en) | 2018-03-14 | 2025-10-14 | Assia Chemical Industries Ltd. | Solid state forms of Relugolix |
| EP3666776A1 (en) | 2018-12-11 | 2020-06-17 | Sandoz AG | Hydrate of a gonadotropin-releasing hormone receptor antagonist |
| EP3969455A4 (en) * | 2019-05-15 | 2023-07-05 | Dr. Reddy's Laboratories Limited | AMORPHOUS AND CRYSTALLINE FORMS OF RELUGOLIX |
| CN110194776B (zh) * | 2019-06-27 | 2021-05-28 | 四川伊诺达博医药科技有限公司 | 一种瑞卢戈利的合成方法 |
| CN111943960B (zh) * | 2019-07-29 | 2022-02-15 | 广东东阳光药业有限公司 | 取代的嘧啶二酮类化合物及其用途 |
| WO2021026011A1 (en) * | 2019-08-02 | 2021-02-11 | Johnson Matthey Public Limited Company | Solid-state forms of relugolix |
| CN112321602A (zh) * | 2019-08-05 | 2021-02-05 | 苏州鹏旭医药科技有限公司 | 一种瑞卢戈利药物中间体的制备方法 |
| CN112390812A (zh) * | 2019-08-14 | 2021-02-23 | 苏州鹏旭医药科技有限公司 | 瑞卢戈利化合物的晶型和无定型固体及其制备方法 |
| WO2021031148A1 (zh) * | 2019-08-21 | 2021-02-25 | 深圳仁泰医药科技有限公司 | 促性腺素释放激素拮抗剂的晶型及其制备方法和用途 |
| JP7713934B2 (ja) * | 2019-10-10 | 2025-07-28 | スミトモ ファーマ スウィッツァーランド ゲーエムベーハー | Ｎ－（４－（１－（２，６－ジフルオロベンジル）－５－（（ジメチルアミノ）メチル）－３－（６－メトキシ－３－ピリダジニル）－２，４－ジオキソ－１，２，３，４－テトラヒドロチエノ［２，３－ｄ］ピリミジン－６－イル）フェニル）－Ｎ’－メトキシ尿素の結晶溶媒和形 |
| WO2021069711A1 (en) * | 2019-10-10 | 2021-04-15 | Myovant Sciences Gmbh | Crystalline forms of n-(4-(1-(2,6-difluorobenzyl)-5- ((dimethylamino)methyl)-3-(6-methoxy-3-pyridazinyl)-2,4-dioxo- 1,2,3,4-tetrahydrothieno[2,3-d]pyrimidin-6-yl)phenyl)-n'- methoxyurea |
| CN112745304A (zh) * | 2019-10-29 | 2021-05-04 | 上海度德医药科技有限公司 | 一种Relugolix的制备方法及中间体化合物 |
| CN111423452B (zh) * | 2020-03-26 | 2023-08-22 | 江西青峰药业有限公司 | 瑞卢戈利的中间体及其制备方法和应用 |
| CN113444105A (zh) * | 2020-03-27 | 2021-09-28 | 南京海润医药有限公司 | 一种Relugolix的制备方法 |
| CN111333633B (zh) * | 2020-04-01 | 2023-10-20 | 江西科睿药业有限公司 | 一种瑞卢戈利的中间体化合物及其制备方法和用途 |
| CN111574534B (zh) * | 2020-05-25 | 2021-06-04 | 东莞市东阳光新药研发有限公司 | 苯基取代的噻吩并[2,3-d]嘧啶-2,4(1H,3H)-二酮类化合物及其用途 |
| MX2022015003A (es) | 2020-05-29 | 2023-03-03 | Myovant Sciences Gmbh | Formas de dosificacion oral solidas de combinacion de antagonistas de la hormona liberadora de gonadotropina. |
| US11655256B1 (en) | 2020-11-06 | 2023-05-23 | Macfarlan Smith Limited | Processes for making a solid-state form of relugolix |
| WO2022101303A1 (en) | 2020-11-11 | 2022-05-19 | Myovant Sciences Gmbh | Methods of administering relugolix |
| CN112552312B (zh) * | 2020-12-07 | 2022-08-05 | 杭州科巢生物科技有限公司 | 一种瑞卢戈利或其盐的合成方法 |
| CN114685468A (zh) * | 2020-12-25 | 2022-07-01 | 成都硕德药业有限公司 | 用于治疗子宫肌瘤的药物的中间体化合物及其制备方法 |
| CN113620972A (zh) * | 2021-02-02 | 2021-11-09 | 奥锐特药业(天津)有限公司 | 瑞卢戈利新晶型及其制备方法 |
| CN114907370B (zh) | 2021-02-10 | 2023-11-03 | 奥锐特药业(天津)有限公司 | 高纯度的噻吩并嘧啶化合物及其制备方法 |
| CN115073491A (zh) * | 2021-03-12 | 2022-09-20 | 上海医药工业研究院 | 一种瑞卢戈利中间体、其制备方法及其应用 |
| WO2022214645A1 (en) | 2021-04-09 | 2022-10-13 | Farmhispania Group, S.L. | Processes and intermediates for the preparation of relugolix |
| CA3217608A1 (en) * | 2021-06-15 | 2022-12-22 | Yuli Xie | Idh mutant inhibitor and use thereof |
| CN115594688B (zh) * | 2021-06-28 | 2023-11-17 | 成都倍特药业股份有限公司 | 瑞卢戈利中间体的制备方法 |
| US20240287090A1 (en) * | 2021-09-15 | 2024-08-29 | Cipla Limited | Solid state forms of relugolix |
| CN118451082A (zh) | 2021-10-18 | 2024-08-06 | 住友制药瑞士有限公司 | N-(4-(1-(2,6-二氟苄基)-5-((二甲基氨基)甲基)-3-(6-甲氧基-3-哒嗪基)-2,4-二氧代-1,2,3,4-四氢噻吩并[2,3-d]嘧啶-6-基)苯基)-N'-甲氧基脲的乙醇溶剂化物的结晶形式 |
| CN114230576A (zh) * | 2021-12-21 | 2022-03-25 | 伊诺药物研究(南京)有限公司 | 一种瑞卢戈利的制备方法 |
| WO2023119333A1 (en) * | 2021-12-25 | 2023-06-29 | Dr. Reddy’S Laboratories Limited | Process for preparation of relugolix and its intermediates |
| CN114409629B (zh) * | 2022-02-22 | 2023-12-29 | 浙江科聚生物医药有限公司 | 一种高纯度Relugolix关键中间体的制备方法及应用 |
| CN114790189B (zh) * | 2022-02-24 | 2023-06-09 | 海化生命(厦门)科技有限公司 | 瑞卢戈利中间体的制备方法 |
| CN114755320B (zh) * | 2022-03-17 | 2024-10-01 | 南京方生和医药科技有限公司 | 一种3-氨基-6-甲氧基哒嗪有关物质的检测方法 |
| IN202221021078A (pl) * | 2022-04-08 | 2023-10-13 | ||
| CN114621249B (zh) * | 2022-04-27 | 2024-01-26 | 江苏慧聚药业股份有限公司 | 瑞卢戈利关键中间体的制备 |
| CN119546611A (zh) * | 2022-05-05 | 2025-02-28 | 台湾神隆股份有限公司 | 瑞卢戈利的制备工艺及其中间体 |
| CN117069735A (zh) * | 2022-05-10 | 2023-11-17 | 北京海美源医药科技有限公司 | 一种高效合成瑞卢戈利的方法和其应用 |
| CN117285506A (zh) * | 2022-07-14 | 2023-12-26 | 江西同和药业股份有限公司 | 一种瑞卢戈利中间体及其制备方法 |
| CN115594689B (zh) * | 2022-07-14 | 2024-03-19 | 江西同和药业股份有限公司 | 一种瑞卢戈利中间体、一种瑞卢戈利的合成方法 |
| CN115417883B (zh) * | 2022-09-16 | 2024-08-27 | 浙江科聚生物医药有限公司 | 一种瑞卢戈利的晶型及其制备方法 |
| WO2024069492A1 (en) | 2022-09-29 | 2024-04-04 | Macfarlan Smith Limited | Processes for the preparation and manufacture of relugolix |
| CN115650950A (zh) * | 2022-11-03 | 2023-01-31 | 江西同和药业股份有限公司 | 一种瑞卢戈利中间体及其制备方法以及一种酰胺缩合方法 |
| EP4634195A1 (en) | 2022-12-15 | 2025-10-22 | Medichem, S.A. | Process for the preparation of relugolix |
| CN115650965B (zh) * | 2022-12-26 | 2023-03-31 | 南京威凯尔生物医药科技有限公司 | 一种瑞卢戈利关键中间体的制备方法 |
| WO2025037218A1 (en) * | 2023-08-11 | 2025-02-20 | Glenmark Life Sciences Limited | Crystalline solvate of relugolix and a process for its preparation |
| CN117327091A (zh) * | 2023-09-28 | 2024-01-02 | 浙江天宇药业股份有限公司 | 一种瑞卢戈利的合成方法 |
| CN119859136A (zh) * | 2023-10-19 | 2025-04-22 | 诚达药业股份有限公司 | 一种瑞卢戈利关键中间体化合物g及其制备方法 |
| CN119859135B (zh) * | 2023-10-19 | 2025-12-02 | 浙江工业大学 | 一种瑞卢戈利中间体及其制备方法 |
| WO2025127790A1 (ko) | 2023-12-12 | 2025-06-19 | 주식회사 와이에스생명과학 | 렐루골릭스의 제조방법 |
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| DK3518932T3 (da) | 2016-09-30 | 2025-01-27 | Takeda Pharmaceuticals Co | Behandling af prostatacancer |
-
2013
- 2013-09-27 SM SM20220255T patent/SMT202200255T1/it unknown
- 2013-09-27 EP EP13779938.3A patent/EP2900675B1/en active Active
- 2013-09-27 CN CN201811130716.8A patent/CN109053766B/zh active Active
- 2013-09-27 TW TW107136006A patent/TWI663171B/zh active
- 2013-09-27 SI SI201331988T patent/SI3415517T1/sl unknown
- 2013-09-27 AR ARP130103480A patent/AR092707A1/es unknown
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