CA2648369A1 - Formes polymorphes de (2r,z)-2-amino-2-cyclohexyl-n-(5-(1-methyl-1h-pyrazol-4?l)-1-oxo-2,6-dihydro-1h-[1,2]diazepino[4,5,6-cd]indol-8-yl)acetamide - Google Patents

Formes polymorphes de (2r,z)-2-amino-2-cyclohexyl-n-(5-(1-methyl-1h-pyrazol-4?l)-1-oxo-2,6-dihydro-1h-[1,2]diazepino[4,5,6-cd]indol-8-yl)acetamide Download PDF

Info

Publication number
CA2648369A1
CA2648369A1 CA002648369A CA2648369A CA2648369A1 CA 2648369 A1 CA2648369 A1 CA 2648369A1 CA 002648369 A CA002648369 A CA 002648369A CA 2648369 A CA2648369 A CA 2648369A CA 2648369 A1 CA2648369 A1 CA 2648369A1
Authority
CA
Canada
Prior art keywords
crystalline form
compound
peaks
methyl
indol
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.)
Abandoned
Application number
CA002648369A
Other languages
English (en)
Inventor
Sacha Ninkovic
Raymond Rynberg
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Pfizer Products Inc
Original Assignee
Pfizer Products Inc.
Sacha Ninkovic
Raymond Rynberg
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
Application filed by Pfizer Products Inc., Sacha Ninkovic, Raymond Rynberg filed Critical Pfizer Products Inc.
Publication of CA2648369A1 publication Critical patent/CA2648369A1/fr
Abandoned legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic 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
    • C07D487/06Peri-condensed systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00Drugs for disorders of the urinary system
    • A61P13/08Drugs for disorders of the urinary system of the prostate
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00Drugs for disorders of the urinary system
    • A61P13/10Drugs for disorders of the urinary system of the bladder
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • A61P35/02Antineoplastic agents specific for leukemia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • A61P35/04Antineoplastic agents specific for metastasis

Landscapes

  • Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • Oncology (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Urology & Nephrology (AREA)
  • Hematology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
CA002648369A 2006-04-04 2007-03-26 Formes polymorphes de (2r,z)-2-amino-2-cyclohexyl-n-(5-(1-methyl-1h-pyrazol-4?l)-1-oxo-2,6-dihydro-1h-[1,2]diazepino[4,5,6-cd]indol-8-yl)acetamide Abandoned CA2648369A1 (fr)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US78935106P 2006-04-04 2006-04-04
US60/789,351 2006-04-04
PCT/IB2007/000859 WO2007113647A1 (fr) 2006-04-04 2007-03-26 Formes polymorphes de (2r,z)-2-amino-2-cyclohexyl-n-(5-(1-méthyl-1h-pyrazol-4υl)-1-oxo-2,6-dihydro-1h-[1,2]diazépino[4,5,6-cd]indol-8-yl)acétamide

Publications (1)

Publication Number Publication Date
CA2648369A1 true CA2648369A1 (fr) 2007-10-11

Family

ID=38294083

Family Applications (1)

Application Number Title Priority Date Filing Date
CA002648369A Abandoned CA2648369A1 (fr) 2006-04-04 2007-03-26 Formes polymorphes de (2r,z)-2-amino-2-cyclohexyl-n-(5-(1-methyl-1h-pyrazol-4?l)-1-oxo-2,6-dihydro-1h-[1,2]diazepino[4,5,6-cd]indol-8-yl)acetamide

Country Status (6)

Country Link
EP (1) EP2004655A1 (fr)
JP (1) JP2007277241A (fr)
AR (1) AR060348A1 (fr)
CA (1) CA2648369A1 (fr)
TW (1) TW200806671A (fr)
WO (1) WO2007113647A1 (fr)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
TWI548630B (zh) * 2011-04-06 2016-09-11 Lg生命科學有限公司 1-(3-氰基-1-異丙基-吲哚-5-基)吡唑-4-羧酸結晶型及其製造方法
EP2797919B1 (fr) 2011-12-31 2017-03-29 BeiGene, Ltd. Pyridophthalazinones tétra ou pentacycliques fusionnés à utiliser en tant qu'inhibiteurs de parp
EA027533B1 (ru) 2011-12-31 2017-08-31 Бейджен, Лтд. Конденсированные тетра- или пентациклические дигидродиазепинокарбазолоны в качестве ингибиторов parps
CN102746211B (zh) * 2012-06-27 2015-05-27 上海泰坦化学有限公司 一种取代吲哚-3-甲醛类化合物的制备方法

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU2004203977B2 (en) * 2003-01-09 2010-06-17 Pfizer Inc. Diazepinoindole derivatives as kinase inhibitors

Also Published As

Publication number Publication date
TW200806671A (en) 2008-02-01
AR060348A1 (es) 2008-06-11
JP2007277241A (ja) 2007-10-25
WO2007113647A1 (fr) 2007-10-11
EP2004655A1 (fr) 2008-12-24

Similar Documents

Publication Publication Date Title
RU2344138C2 (ru) Способ получения ингибиторов поли(адф-рибоза)полимераз
WO2014134774A1 (fr) Composés inhibant l'activité enzymatique de la kinase à séquence répétée riche en leucine
WO2014093583A2 (fr) Procédés de synthèse pour la préparation de monochlorhydrate de 3-(imidazo [1,2-b] pyridazin-3-yléthynyl) -4-méthyl-n-{4-[(4-méthylpipérazin-1-yl) méthyl]-3-(trifluorométhyl) phényl}benzamide, d'autres formes de sels de ce composé, et d'intermédiaires de ceux-ci
JP6937828B2 (ja) ピロロ6員複素芳香環誘導体の製造方法、および中間体
CN110678178A (zh) Mk2抑制剂的形式和组合物
EP2184283A1 (fr) Procédé de préparation de composants utiles en tant qu'intermédiaires pour la préparation de modulateurs de l'activité de récepteur de chimiokine
WO2022228576A1 (fr) Composé ciblant un régulateur de protéine et son application
CA2648369A1 (fr) Formes polymorphes de (2r,z)-2-amino-2-cyclohexyl-n-(5-(1-methyl-1h-pyrazol-4?l)-1-oxo-2,6-dihydro-1h-[1,2]diazepino[4,5,6-cd]indol-8-yl)acetamide
CN109937200B (zh) 一种苯并呋喃类衍生物游离碱的晶型及制备方法
US9255063B2 (en) Colchicine solid-state forms; methods of making; and methods of use thereof
KR20230061444A (ko) Rho-연관 단백질 인산화효소 억제제의 염, 염의 고체 형태, 이의 제조 방법 및 이의 용도
EP3964505A1 (fr) Forme solide de composé de diaminopyrimidine ou d'un hydrate de celui-ci, son procédé de préparation et son application
CN112142747B (zh) 一种吡唑酮并嘧啶类化合物、其制备方法及应用
CN113278012B (zh) 用作激酶抑制剂的化合物及其应用
CN115175902A (zh) 一类用作激酶抑制剂的化合物及其应用
AU2017341999A1 (en) Inhibitors of mutant isocitrate dehydrogenases and compositions and methods thereof
KR20220008285A (ko) 디아미노피리미딘 화합물의 염, 이의 고체, 이의 제조 방법 및 이의 용도
EP3830091A1 (fr) Nouveaux polymorphes d'acalabrutinib, un inhibiteur de la tyrosine kinase de bruton
CA3111527A1 (fr) Procede de fabrication d'une forme solide d'un inhibiteur de bromodomaine bet
CN108484640B (zh) 一种抗肿瘤的细胞凋亡蛋白抑制剂
CA2972746A1 (fr) Procede de production d'un derive thiazole
TW202024087A (zh) 四氫哌喃基胺基-吡咯并嘧啶酮化合物的固體形式
US20240150300A1 (en) S-configuration-containing amino benzamide pyridazinone compound, preparation method therefor, and pharmaceutical composition and application thereof
WO2017186147A1 (fr) Composé indole lié au benzimidazole agissant comme nouvel antagoniste d'iap divalent
KR20240063968A (ko) Rho 관련 단백질 키나아제 억제제 또는 이의 용매화물의 고체 형태, 이의 제조 방법 및 용도

Legal Events

Date Code Title Description
EEER Examination request
FZDE Dead