CN111132983A - 一种异喹啉磺酰衍生物的晶型及其制备方法 - Google Patents
一种异喹啉磺酰衍生物的晶型及其制备方法 Download PDFInfo
- Publication number
- CN111132983A CN111132983A CN201880062448.2A CN201880062448A CN111132983A CN 111132983 A CN111132983 A CN 111132983A CN 201880062448 A CN201880062448 A CN 201880062448A CN 111132983 A CN111132983 A CN 111132983A
- Authority
- CN
- China
- Prior art keywords
- degrees
- compound
- formula
- crystal form
- preparation
- Prior art date
- Legal status (The legal status 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 status listed.)
- Granted
Links
Images
Classifications
-
- 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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/47—Quinolines; Isoquinolines
- A61K31/472—Non-condensed isoquinolines, e.g. papaverine
- A61K31/4725—Non-condensed isoquinolines, e.g. papaverine containing further heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
- A61P27/06—Antiglaucoma agents or miotics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/12—Antihypertensives
-
- 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
Abstract
本发明公开了一种Rho蛋白激酶抑制剂的盐型、晶型、制备方法及其医药用途。
Description
PCT国内申请,说明书已公开。
Claims (13)
- PCT国内申请,权利要求书已公开。
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201710874795 | 2017-09-25 | ||
CN2017108747952 | 2017-09-25 | ||
PCT/CN2018/106745 WO2019057121A1 (zh) | 2017-09-25 | 2018-09-20 | 一种异喹啉磺酰衍生物的晶型及其制备方法 |
Publications (2)
Publication Number | Publication Date |
---|---|
CN111132983A true CN111132983A (zh) | 2020-05-08 |
CN111132983B CN111132983B (zh) | 2022-05-17 |
Family
ID=65810677
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201880062448.2A Active CN111132983B (zh) | 2017-09-25 | 2018-09-20 | 一种异喹啉磺酰衍生物的晶型及其制备方法 |
Country Status (2)
Country | Link |
---|---|
CN (1) | CN111132983B (zh) |
WO (1) | WO2019057121A1 (zh) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN114746431A (zh) * | 2019-10-18 | 2022-07-12 | 贵州伊诺其尼科技有限公司 | 一种lrrk2抑制剂的晶型及其制备方法 |
Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS61227581A (ja) * | 1985-04-02 | 1986-10-09 | Asahi Chem Ind Co Ltd | 血管拡張剤 |
CN1210521A (zh) * | 1996-02-02 | 1999-03-10 | 日本新药株式会社 | 异喹啉衍生物及医药 |
WO2004106325A1 (en) * | 2003-05-29 | 2004-12-09 | Schering Aktiengesellschaft | Prodrugs of 1-(1-hydroxy-5-isoquinolinesulfonyl)homopiperazine |
US20050272751A1 (en) * | 2004-02-24 | 2005-12-08 | Bioaxone Therapeutique Inc. | 4-Substituted piperidine derivatives |
CN101622243A (zh) * | 2007-02-28 | 2010-01-06 | 旭化成制药株式会社 | 磺酰胺衍生物 |
CN105085525A (zh) * | 2014-04-28 | 2015-11-25 | 南京明德新药研发股份有限公司 | 作为rho激酶抑制剂的异喹啉磺酰衍生物 |
-
2018
- 2018-09-20 CN CN201880062448.2A patent/CN111132983B/zh active Active
- 2018-09-20 WO PCT/CN2018/106745 patent/WO2019057121A1/zh active Application Filing
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS61227581A (ja) * | 1985-04-02 | 1986-10-09 | Asahi Chem Ind Co Ltd | 血管拡張剤 |
CN1210521A (zh) * | 1996-02-02 | 1999-03-10 | 日本新药株式会社 | 异喹啉衍生物及医药 |
WO2004106325A1 (en) * | 2003-05-29 | 2004-12-09 | Schering Aktiengesellschaft | Prodrugs of 1-(1-hydroxy-5-isoquinolinesulfonyl)homopiperazine |
US20050272751A1 (en) * | 2004-02-24 | 2005-12-08 | Bioaxone Therapeutique Inc. | 4-Substituted piperidine derivatives |
CN101622243A (zh) * | 2007-02-28 | 2010-01-06 | 旭化成制药株式会社 | 磺酰胺衍生物 |
CN105085525A (zh) * | 2014-04-28 | 2015-11-25 | 南京明德新药研发股份有限公司 | 作为rho激酶抑制剂的异喹啉磺酰衍生物 |
Non-Patent Citations (1)
Title |
---|
吕扬 等: "《晶型药物》", 31 October 2009, 人民卫生出版社 * |
Also Published As
Publication number | Publication date |
---|---|
WO2019057121A1 (zh) | 2019-03-28 |
CN111132983B (zh) | 2022-05-17 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP5702396B2 (ja) | ベンゾジアゼピンブロモドメイン阻害剤 | |
ES2648288T3 (es) | Formas cristalinas de sulfato de 4-metil-N-[3-(4-metil-imidazol-1-il)-5-trifluoro-metil-fenil]-3-(4-piridin-3-il-pirimidin-2-il-amino)-benzamida y su forma amorfa | |
US11629153B2 (en) | Forms and compositions of a MK2 inhibitor | |
AU2014239995A1 (en) | Salt of omecamtiv mecarbil and process for preparing salt | |
WO2014093583A2 (en) | Synthetic methods for preparing 3-(imidazo[1,2-b]pyridazin-3-ylethynyl)-4-methyl-n-{4-[(4-methylpiperazin-1-yl)methyl]-3-(trifluoromethyl)phenyl}benzamide mono hydrochloride, other salt forms of this compound and intermediates thereof | |
AU2019303777B2 (en) | Salt of LSD1 inhibitor and a polymorph thereof | |
CN111132983B (zh) | 一种异喹啉磺酰衍生物的晶型及其制备方法 | |
KR20230061444A (ko) | Rho-연관 단백질 인산화효소 억제제의 염, 염의 고체 형태, 이의 제조 방법 및 이의 용도 | |
JP2020535193A (ja) | 結晶のリナグリプチン中間体およびリナグリプチンの調製のためのプロセス | |
US20220242873A1 (en) | Method for synthesizing furoimidazopyridine compound, polymorphic substance and polymorphic substance of salt | |
KR101446789B1 (ko) | 1-((2S)-2-아미노-4-(2,4-비스(트리플루오로메틸)-5,8-디히드로피리도(3,4-d)피리미딘-7(6H)-일)-4-옥소부틸)-5,5-디플루오로피페리딘-2-온 타트레이트염의 수화물 | |
WO2022199591A1 (zh) | 一种氟取代的吡啶并吡唑类化合物的晶型及其制备方法 | |
CN109721531B (zh) | 一种新型的脂质体激酶抑制剂 | |
CN111448185A (zh) | 一种作为fgfr和vegfr抑制剂化合物的盐型、晶型及其制备方法 | |
KR102183356B1 (ko) | Fgfr 억제제를 제조하기 위한 방법 | |
CN109563097A (zh) | 一种7H-吡咯并[2,3-d]嘧啶类化合物的晶型、盐型及其制备方法 | |
WO2013181251A9 (en) | Crizotinib hydrochloride salt in crystalline | |
JP7076565B2 (ja) | Fgfr4阻害剤として用いられる化合物の塩形態、結晶形及びその製造方法 | |
JPH0357895B2 (zh) | ||
JP2022523035A (ja) | 1,2,3-トリアゾロ[1,5-a]ピラジン誘導体の結晶形および結晶形の調製方法 | |
WO2023138681A1 (zh) | 含氮并环类衍生物抑制剂的酸式盐或晶型及其制备方法和应用 | |
CN108864063A (zh) | 一种治疗癌症的药物溶剂合物及其制备方法 | |
BR112020006051A2 (pt) | formas cristalinas de lenalidomida | |
CN111757871B (zh) | 一种Caspase抑制剂的结晶 | |
RU2787767C2 (ru) | Кристалл производного бензоксазола |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PB01 | Publication | ||
PB01 | Publication | ||
SE01 | Entry into force of request for substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
GR01 | Patent grant | ||
GR01 | Patent grant |