MX2020002046A - Forma cristalina del inhibidor de parp-1 y método de preparación de ésta. - Google Patents
Forma cristalina del inhibidor de parp-1 y método de preparación de ésta.Info
- Publication number
- MX2020002046A MX2020002046A MX2020002046A MX2020002046A MX2020002046A MX 2020002046 A MX2020002046 A MX 2020002046A MX 2020002046 A MX2020002046 A MX 2020002046A MX 2020002046 A MX2020002046 A MX 2020002046A MX 2020002046 A MX2020002046 A MX 2020002046A
- Authority
- MX
- Mexico
- Prior art keywords
- preparation
- crystal form
- method therefor
- parp
- inhibitor
- Prior art date
Links
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/50—Pyridazines; Hydrogenated pyridazines
- A61K31/502—Pyridazines; Hydrogenated pyridazines ortho- or peri-condensed with carbocyclic ring systems, e.g. cinnoline, phthalazine
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
- A61K31/35—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom
- A61K31/351—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom not condensed with another ring
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/4164—1,3-Diazoles
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K33/00—Medicinal preparations containing inorganic active ingredients
- A61K33/24—Heavy metals; Compounds thereof
- A61K33/243—Platinum; Compounds thereof
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B2200/00—Indexing scheme relating to specific properties of organic compounds
- C07B2200/13—Crystalline forms, e.g. polymorphs
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Epidemiology (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Saccharide Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
Se divulgan en la presente invención una forma cristalina de un inhibidor de PARP-1 y un método de preparación de ésta; específicamente, se divulgan en la presente invención una forma cristalina A de 4-[[3-[[2-(trifluorometil)-5,6,7,8-tetrahidro-[1,2 ,4]triazolo[1,5-a]pirazina-7-il]carbonil]-4-fluorofenil]metil-1(2 H)-ftalazinona (fórmula I) y un método de preparación de ésta. (ver fórmula).
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201710737513 | 2017-08-24 | ||
PCT/CN2018/101875 WO2019037753A1 (zh) | 2017-08-24 | 2018-08-23 | 一种parp-1抑制剂的晶型及其制备方法 |
Publications (1)
Publication Number | Publication Date |
---|---|
MX2020002046A true MX2020002046A (es) | 2020-09-17 |
Family
ID=65439965
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MX2020002046A MX2020002046A (es) | 2017-08-24 | 2018-08-23 | Forma cristalina del inhibidor de parp-1 y método de preparación de ésta. |
Country Status (11)
Country | Link |
---|---|
US (1) | US11180505B2 (es) |
EP (1) | EP3674304B1 (es) |
JP (1) | JP2020531522A (es) |
CN (1) | CN110914272A (es) |
AU (1) | AU2018320562B2 (es) |
CA (1) | CA3073613A1 (es) |
ES (1) | ES2915830T3 (es) |
MX (1) | MX2020002046A (es) |
MY (1) | MY197303A (es) |
TW (1) | TWI765086B (es) |
WO (1) | WO2019037753A1 (es) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN115650988A (zh) * | 2022-10-27 | 2023-01-31 | 江苏恒瑞医药股份有限公司 | 一种parp抑制剂的制备方法 |
WO2024109871A1 (zh) * | 2022-11-23 | 2024-05-30 | 江苏恒瑞医药股份有限公司 | 一种含氮杂环类化合物的可药用盐、晶型及制备方法 |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
TWI404716B (zh) * | 2006-10-17 | 2013-08-11 | Kudos Pharm Ltd | 酞嗪酮(phthalazinone)衍生物 |
US8653059B2 (en) | 2007-08-21 | 2014-02-18 | Merck Sharp & Dohme Corp. | Heterocyclic compounds as dipeptidyl peptidase-IV inhibitors for the treatment or prevention of diabetes |
CN102372706A (zh) | 2010-08-09 | 2012-03-14 | 江苏恒瑞医药股份有限公司 | 酞嗪酮类衍生物、其制备方法及其在医药上的应用 |
CN102372716A (zh) * | 2010-08-09 | 2012-03-14 | 江苏恒瑞医药股份有限公司 | 酞嗪酮类衍生物、其制备方法及其在医药上的应用 |
EP2643314B1 (en) | 2010-11-25 | 2016-07-13 | ratiopharm GmbH | Novel salts and polymorphic forms of afatinib |
CN105461697A (zh) * | 2014-04-29 | 2016-04-06 | 中国医学科学院药物研究所 | 喹唑啉酮类parp-1抑制剂及含有它们的组合物和抗肿瘤用途 |
US20170204067A1 (en) * | 2016-01-14 | 2017-07-20 | Scinopharm Taiwan, Ltd. | Crystalline forms of olaparib and manufacturing processes therefor |
-
2018
- 2018-08-23 WO PCT/CN2018/101875 patent/WO2019037753A1/zh unknown
- 2018-08-23 AU AU2018320562A patent/AU2018320562B2/en not_active Ceased
- 2018-08-23 ES ES18849247T patent/ES2915830T3/es active Active
- 2018-08-23 US US16/639,898 patent/US11180505B2/en active Active
- 2018-08-23 EP EP18849247.4A patent/EP3674304B1/en active Active
- 2018-08-23 MY MYPI2020000891A patent/MY197303A/en unknown
- 2018-08-23 CA CA3073613A patent/CA3073613A1/en active Pending
- 2018-08-23 TW TW107129448A patent/TWI765086B/zh active
- 2018-08-23 JP JP2020511304A patent/JP2020531522A/ja active Pending
- 2018-08-23 CN CN201880047608.6A patent/CN110914272A/zh active Pending
- 2018-08-23 MX MX2020002046A patent/MX2020002046A/es unknown
Also Published As
Publication number | Publication date |
---|---|
TWI765086B (zh) | 2022-05-21 |
EP3674304A4 (en) | 2020-12-16 |
US20200291031A1 (en) | 2020-09-17 |
RU2020110106A3 (es) | 2021-12-24 |
EP3674304B1 (en) | 2022-04-13 |
AU2018320562A1 (en) | 2020-03-12 |
MY197303A (en) | 2023-06-12 |
ES2915830T3 (es) | 2022-06-27 |
EP3674304A1 (en) | 2020-07-01 |
CN110914272A (zh) | 2020-03-24 |
TW201912646A (zh) | 2019-04-01 |
RU2020110106A (ru) | 2021-09-14 |
WO2019037753A1 (zh) | 2019-02-28 |
AU2018320562B2 (en) | 2022-09-01 |
US11180505B2 (en) | 2021-11-23 |
CA3073613A1 (en) | 2019-02-28 |
JP2020531522A (ja) | 2020-11-05 |
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