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SG10201907576SA - Salts of pi3k inhibitor and processes for their preparation - Google Patents

Salts of pi3k inhibitor and processes for their preparation

Info

Publication number
SG10201907576SA
SG10201907576SA SG10201907576SA SG10201907576SA SG10201907576SA SG 10201907576S A SG10201907576S A SG 10201907576SA SG 10201907576S A SG10201907576S A SG 10201907576SA SG 10201907576S A SG10201907576S A SG 10201907576SA SG 10201907576S A SG10201907576S A SG 10201907576SA
Authority
SG
Singapore
Prior art keywords
processes
salts
preparation
pi3k inhibitor
inhibitor
Prior art date
Application number
SG10201907576SA
Inventor
Lei Qiao
Lingkai Weng
Chongsheng Eric Shi
David Meloni
Qiyan Lin
Michael Xia
Vaqar Sharief
William Frietze
Zhongjiang Jia
Yongchun Pan
Pingli Liu
Tai-Yuen Yue
Jiacheng Zhou
Original Assignee
Incyte Corp
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=55854770&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=SG10201907576S(A) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Incyte Corp filed Critical Incyte Corp
Publication of SG10201907576SA publication Critical patent/SG10201907576SA/en

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    • 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
    • A61K31/395—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
    • A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • A—HUMAN NECESSITIES
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    • A61P13/00—Drugs for disorders of the urinary system
    • A61P13/08—Drugs for disorders of the urinary system of the prostate
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    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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    • A61P13/12—Drugs for disorders of the urinary system of the kidneys
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    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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    • A61P7/06—Antianaemics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • 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
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    • A61P9/14—Vasoprotectives; Antihaemorrhoidals; Drugs for varicose therapy; Capillary stabilisers
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D207/18—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member
    • C07D207/22—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member 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
    • C07D207/24—Oxygen or sulfur atoms
    • C07D207/26—2-Pyrrolidones
    • C07D207/263—2-Pyrrolidones with only hydrogen atoms or radicals containing only hydrogen and carbon atoms directly attached to other ring carbon atoms
    • C07D207/267—2-Pyrrolidones with only hydrogen atoms or radicals containing only hydrogen and carbon atoms directly attached to other ring carbon atoms with only hydrogen atoms or radicals containing only hydrogen and carbon atoms directly attached to the ring nitrogen atom
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/10—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a carbon chain containing aromatic rings
    • 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

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  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Immunology (AREA)
  • Hematology (AREA)
  • Pulmonology (AREA)
  • Rheumatology (AREA)
  • Diabetes (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Urology & Nephrology (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Pain & Pain Management (AREA)
  • Oncology (AREA)
  • Epidemiology (AREA)
  • Vascular Medicine (AREA)
  • Transplantation (AREA)
  • Cardiology (AREA)
  • Dermatology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Neurology (AREA)
  • Ophthalmology & Optometry (AREA)
  • Obesity (AREA)
  • Emergency Medicine (AREA)
  • Endocrinology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Pyrrole Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)

Abstract

The present application provides processes for preparing (R)-4-(3-((S)-1-(4- amino-3-methyl-1H-pyrazolo[3,4-d]pyrimidin-1-yl)ethyl)-5-chloro-2-ethoxy-6- fluorophenyl)pyrrolidin-2-one, which is useful as an inhibitor phosphoinositide 3-kinase- delta (PI3Kδ), a s well as a salt form and intermediates related thereto. 5 N O FIGURE
SG10201907576SA 2015-02-27 2016-02-26 Salts of pi3k inhibitor and processes for their preparation SG10201907576SA (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US201562121697P 2015-02-27 2015-02-27

Publications (1)

Publication Number Publication Date
SG10201907576SA true SG10201907576SA (en) 2019-09-27

Family

ID=55854770

Family Applications (3)

Application Number Title Priority Date Filing Date
SG10201907576SA SG10201907576SA (en) 2015-02-27 2016-02-26 Salts of pi3k inhibitor and processes for their preparation
SG11201706917WA SG11201706917WA (en) 2015-02-27 2016-02-26 Salts of pi3k inhibitor and processes for their preparation
SG10201912302VA SG10201912302VA (en) 2015-02-27 2016-02-26 Salts of pi3k inhibitor and processes for their preparation

Family Applications After (2)

Application Number Title Priority Date Filing Date
SG11201706917WA SG11201706917WA (en) 2015-02-27 2016-02-26 Salts of pi3k inhibitor and processes for their preparation
SG10201912302VA SG10201912302VA (en) 2015-02-27 2016-02-26 Salts of pi3k inhibitor and processes for their preparation

Country Status (36)

Country Link
US (4) US10336759B2 (en)
EP (3) EP4183789A1 (en)
JP (2) JP6816005B2 (en)
KR (2) KR102698327B1 (en)
CN (4) CN117777139A (en)
AR (1) AR103804A1 (en)
AU (3) AU2016222556B2 (en)
BR (1) BR122021004509B1 (en)
CA (1) CA3285092A1 (en)
CL (2) CL2017002179A1 (en)
CO (1) CO2017008924A2 (en)
CR (2) CR20210055A (en)
CY (1) CY1123729T1 (en)
DK (2) DK3262046T3 (en)
EA (1) EA201791923A1 (en)
EC (2) ECSP17064131A (en)
ES (2) ES2933694T3 (en)
HR (2) HRP20210036T1 (en)
HU (2) HUE060953T2 (en)
IL (1) IL254093B (en)
LT (2) LT3262046T (en)
MA (2) MA55193B1 (en)
MD (2) MD3262046T2 (en)
MX (2) MX373232B (en)
MY (1) MY187502A (en)
PE (2) PE20230156A1 (en)
PH (3) PH12017501538B1 (en)
PL (2) PL3831833T3 (en)
PT (2) PT3262046T (en)
RS (2) RS63963B1 (en)
SG (3) SG10201907576SA (en)
SI (2) SI3831833T1 (en)
SM (2) SMT202100015T1 (en)
TW (2) TWI748941B (en)
UA (1) UA122332C2 (en)
WO (1) WO2016138363A1 (en)

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PL2448938T3 (en) 2009-06-29 2014-11-28 Incyte Holdings Corp Pyrimidinones as pi3k inhibitors
CA2822070C (en) 2010-12-20 2019-09-17 Incyte Corporation N-(1-(substituted-phenyl)ethyl)-9h-purin-6-amines as pi3k inhibitors
PH12021552978A1 (en) 2011-09-02 2022-08-22 Incyte Holdings Corp Heterocyclylamines as pi3k inhibitors
AR090548A1 (en) 2012-04-02 2014-11-19 Incyte Corp BICYCLIC AZAHETEROCICLOBENCILAMINS AS PI3K INHIBITORS
TW202214254A (en) * 2013-03-01 2022-04-16 美商英塞特控股公司 USE OF PYRAZOLOPYRIMIDINE DERIVATIVES FOR THE TREATMENT OF PI3Kδ RELATED DISORDERS
NZ763326A (en) 2014-04-08 2023-04-28 Incyte Holdings Corp Treatment of b-cell malignancies by a combination jak and pi3k inhibitor
US10077277B2 (en) 2014-06-11 2018-09-18 Incyte Corporation Bicyclic heteroarylaminoalkyl phenyl derivatives as PI3K inhibitors
LT3262046T (en) 2015-02-27 2021-01-11 Incyte Corporation Salts of pi3k inhibitor and processes for their preparation
WO2016183060A1 (en) 2015-05-11 2016-11-17 Incyte Corporation Process for the synthesis of a phosphoinositide 3-kinase inhibitor
US9988401B2 (en) 2015-05-11 2018-06-05 Incyte Corporation Crystalline forms of a PI3K inhibitor
ES2830446T3 (en) 2015-12-11 2021-06-03 Sichuan Kelun Biotech Biopharmaceutical Co Ltd Azetidine derivative, method of preparation and use of the same
PE20251292A1 (en) 2018-03-08 2025-05-14 Incyte Corp DIOLIC AMINOPYRAZINE COMPOUNDS AS PI3K-GAMMA INHIBITORS
CA3101323A1 (en) * 2018-06-01 2019-12-05 Incyte Corporation Dosing regimen for the treatment of pi3k related disorders
WO2020010003A1 (en) 2018-07-02 2020-01-09 Incyte Corporation AMINOPYRAZINE DERIVATIVES AS PI3K-γ INHIBITORS
CA3203587A1 (en) 2020-11-30 2022-06-02 Incyte Corporation Combination therapy with an anti-cd19 antibody and parsaclisib
WO2022115120A1 (en) 2020-11-30 2022-06-02 Incyte Corporation Combination therapy with an anti-cd19 antibody and parsaclisib
AR127966A1 (en) 2021-12-16 2024-03-13 Incyte Corp TOPICAL FORMULATIONS OF PI3K-DELTA INHIBITORS
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