JP2016512831A - 重水素化されたパルボシクリブ - Google Patents

重水素化されたパルボシクリブ Download PDF

Info

Publication number
JP2016512831A
JP2016512831A JP2016501574A JP2016501574A JP2016512831A JP 2016512831 A JP2016512831 A JP 2016512831A JP 2016501574 A JP2016501574 A JP 2016501574A JP 2016501574 A JP2016501574 A JP 2016501574A JP 2016512831 A JP2016512831 A JP 2016512831A
Authority
JP
Japan
Prior art keywords
same
compound
compound according
hydrogen
disease
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.)
Pending
Application number
JP2016501574A
Other languages
English (en)
Japanese (ja)
Other versions
JP2016512831A5 (enExample
Inventor
アダム ジェイ. モーガン
アダム ジェイ. モーガン
Original Assignee
コンサート ファーマシューティカルズ インコーポレイテッド
コンサート ファーマシューティカルズ インコーポレイテッド
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 コンサート ファーマシューティカルズ インコーポレイテッド, コンサート ファーマシューティカルズ インコーポレイテッド filed Critical コンサート ファーマシューティカルズ インコーポレイテッド
Publication of JP2016512831A publication Critical patent/JP2016512831A/ja
Publication of JP2016512831A5 publication Critical patent/JP2016512831A5/ja
Pending legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/14Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04Ortho-condensed systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic 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
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/519Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/66Phosphorus compounds
    • A61K31/675Phosphorus compounds having nitrogen as a ring hetero atom, e.g. pyridoxal phosphate
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/14Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing three or more hetero rings
    • 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
    • C07D487/04Ortho-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/02Phosphorus compounds
    • C07F9/06Phosphorus compounds without P—C bonds
    • C07F9/062Organo-phosphoranes without P-C bonds

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Public Health (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • Epidemiology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Biochemistry (AREA)
  • Molecular Biology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
JP2016501574A 2013-03-15 2014-03-12 重水素化されたパルボシクリブ Pending JP2016512831A (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201361787540P 2013-03-15 2013-03-15
US61/787,540 2013-03-15
PCT/US2014/024564 WO2014150925A2 (en) 2013-03-15 2014-03-12 Deuterated palbociclib

Publications (2)

Publication Number Publication Date
JP2016512831A true JP2016512831A (ja) 2016-05-09
JP2016512831A5 JP2016512831A5 (enExample) 2017-10-12

Family

ID=51581623

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2016501574A Pending JP2016512831A (ja) 2013-03-15 2014-03-12 重水素化されたパルボシクリブ

Country Status (8)

Country Link
US (3) US20160024084A1 (enExample)
EP (2) EP3492470A1 (enExample)
JP (1) JP2016512831A (enExample)
AU (1) AU2014235462C1 (enExample)
CA (1) CA2904054A1 (enExample)
EA (2) EA032094B1 (enExample)
MX (1) MX2015012741A (enExample)
WO (1) WO2014150925A2 (enExample)

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20170032244A (ko) 2014-07-26 2017-03-22 선샤인 레이크 파르마 컴퍼니 리미티드 Cdk 저해제로서 2-아미노-피리도[2,3-d]피리미딘-7(8h)-온 유도체 및 그 용도
CN105111201B (zh) * 2014-10-16 2017-01-11 上海页岩科技有限公司 5-甲基-2-(吡啶-2-基氨基)-8H-吡啶并[2,3-d]嘧啶-7-酮化合物
WO2016092442A1 (en) * 2014-12-08 2016-06-16 Sun Pharmaceutical Industries Limited Processes for the preparation of crystalline forms of palbociclib acetate
CN104892604B (zh) * 2015-06-19 2016-08-24 北京康立生医药技术开发有限公司 一种cdk4抑制剂的合成方法
CN105153149B (zh) * 2015-07-29 2017-09-19 江苏中邦制药有限公司 一种选择性激酶抑制剂Palbociclib的制备方法
EP3386981B1 (en) * 2015-12-13 2021-10-13 Hangzhou Innogate Pharma Co., Ltd. Heterocycles useful as anti-cancer agents
CN106986871B (zh) * 2017-03-29 2019-02-26 浙江同源康医药股份有限公司 一种氘代Palbociclib的晶型及其制备方法和应用
CN106967064B (zh) * 2017-03-29 2018-03-23 郑州泰基鸿诺医药股份有限公司 氘代Palbociclib的衍生物、制备方法及其应用
MX2021000895A (es) 2018-07-27 2021-08-24 California Inst Of Techn Inhibidores de cinasas dependientes de ciclinas (cdk) y usos de los mismos.
US12358911B2 (en) 2018-12-07 2025-07-15 Hangzhou Innogate Pharma Co., Ltd. Heterocyclic comipound as CDK-HDAC dual pathway inhibitor
WO2021113595A1 (en) * 2019-12-06 2021-06-10 Beta Pharma, Inc. Phosphorus derivatives as kras inhibitors
LV15575A (lv) 2019-12-20 2021-06-20 Latvijas Organiskās Sintēzes Institūts Selenofēnhromēnu deiterēti analogi, to iegūšana un izmantošana

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2005519909A (ja) * 2002-01-22 2005-07-07 ワーナー−ランバート・カンパニー、リミテッド、ライアビリティ、カンパニー 2−(ピリジン−2−イルアミノ)−ピリド[2,3−d]ピリミジン−7−オン
JP2007530425A (ja) * 2003-07-11 2007-11-01 ワーナー−ランバート カンパニー リミテッド ライアビリティー カンパニー 選択的cdk4阻害剤のイセチオン酸塩
JP2008094834A (ja) * 2006-09-08 2008-04-24 Pfizer Prod Inc 2−(ピリジンー2−イルアミノ)−ピリド[2,3−d]ピリミジン−7−オン類の合成
CN101948467A (zh) * 2010-05-17 2011-01-19 苏州波锐生物医药科技有限公司 噻唑酰胺类化合物及其在制备抗恶性肿瘤药物中的用途
JP2011510079A (ja) * 2008-01-22 2011-03-31 コンサート ファーマシューティカルズ インコーポレイテッド ゲフィチニブ誘導体
WO2011101417A1 (en) * 2010-02-19 2011-08-25 Novartis Ag Deuterated pyrrolopyrimidine compounds as inhibitors of cdk4/6

Family Cites Families (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5304121A (en) 1990-12-28 1994-04-19 Boston Scientific Corporation Drug delivery system making use of a hydrogel polymer coating
US5994341A (en) 1993-07-19 1999-11-30 Angiogenesis Technologies, Inc. Anti-angiogenic Compositions and methods for the treatment of arthritis
US6099562A (en) 1996-06-13 2000-08-08 Schneider (Usa) Inc. Drug coating with topcoat
TW354293B (en) 1995-06-06 1999-03-11 Bristol Myers Squibb Co Prodrugs of paclitaxel derivatives
GB9925962D0 (en) 1999-11-02 1999-12-29 Novartis Ag Organic compounds
EP1390063B1 (en) 2001-05-03 2004-11-17 F. Hoffmann-La Roche Ag Pharmaceutical dosage form of amorphous nelfinavir mesylate
CA2446904A1 (en) 2001-05-24 2003-04-03 Alexza Molecular Delivery Corporation Delivery of drug esters through an inhalation route
CA2581169A1 (en) 2004-09-29 2006-04-13 Cordis Corporation Pharmaceutical dosage forms of stable amorphous rapamycin like compounds
CN102516176A (zh) 2005-10-28 2012-06-27 雅培制药有限公司 抑制trpv1受体的吲唑衍生物
US20080182853A1 (en) 2006-12-14 2008-07-31 Inna Kruman Methods of neuroprotection by cyclin-dependent kinase inhibition
US20090030005A1 (en) 2007-07-19 2009-01-29 Amgen Inc. Combinations for the treatment of cancer
WO2009061345A2 (en) 2007-11-07 2009-05-14 Cornell Research Foundation, Inc. Targeting cdk4 and cdk6 in cancer therapy
JP2012504645A (ja) 2008-10-01 2012-02-23 ザ ユニバーシティ オブ ノース カロライナ アット チャペル ヒル 健康な細胞に対する電離放射線の影響を低下させる又は防止するための医薬組成物
CN102231984A (zh) 2008-10-01 2011-11-02 北卡罗来纳大学查珀尔希尔分校 使用选择性细胞周期蛋白依赖性激酶4/6抑制剂对抗化疗化合物的造血防护
WO2010132725A2 (en) 2009-05-13 2010-11-18 The University Of North Carolina At Chapel Hill Cyclin dependent kinase inhibitors and methods of use
ES2689177T3 (es) 2010-04-13 2018-11-08 Novartis Ag Combinación que comprende un inhibidor de cinasa 4 dependiente de ciclina o cinasa dependiente de ciclina (CDK4/6) y un inhibidor de mTOR para tratar cáncer
CN103501789A (zh) 2010-11-17 2014-01-08 北卡罗来纳大学查珀尔希尔分校 通过抑制增殖性激酶cdk4和cdk6保护肾组织免于局部缺血

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2005519909A (ja) * 2002-01-22 2005-07-07 ワーナー−ランバート・カンパニー、リミテッド、ライアビリティ、カンパニー 2−(ピリジン−2−イルアミノ)−ピリド[2,3−d]ピリミジン−7−オン
JP2007530425A (ja) * 2003-07-11 2007-11-01 ワーナー−ランバート カンパニー リミテッド ライアビリティー カンパニー 選択的cdk4阻害剤のイセチオン酸塩
JP2008094834A (ja) * 2006-09-08 2008-04-24 Pfizer Prod Inc 2−(ピリジンー2−イルアミノ)−ピリド[2,3−d]ピリミジン−7−オン類の合成
JP2011510079A (ja) * 2008-01-22 2011-03-31 コンサート ファーマシューティカルズ インコーポレイテッド ゲフィチニブ誘導体
WO2011101417A1 (en) * 2010-02-19 2011-08-25 Novartis Ag Deuterated pyrrolopyrimidine compounds as inhibitors of cdk4/6
CN101948467A (zh) * 2010-05-17 2011-01-19 苏州波锐生物医药科技有限公司 噻唑酰胺类化合物及其在制备抗恶性肿瘤药物中的用途

Non-Patent Citations (5)

* Cited by examiner, † Cited by third party
Title
ADVANCES IN DRUG RESEARCH, vol. 14, JPN6010015673, 1985, pages 1 - 40, ISSN: 0003972546 *
CAN. J. PHYSIOL. PHARMACOL., vol. 77, JPN6010015668, 1999, pages 79 - 88, ISSN: 0003972547 *
FINN, R. S. ET AL: "PD 0332991, a selective cyclin D kinase 4/6 inhibitor, preferentially inhibits proliferation of lumi", BREAST CANCER RESEARCH, vol. 11(5), JPN7018000872, 2009, pages 77, ISSN: 0003972544 *
FRY D. W. ET AL: "Specific inhibition of cyclin-dependent kinase 4/6 by PD 0332991 and associated antitumor activity i", MOLECULAR CANCER THERAPEUTICS, vol. 3(11), JPN7018000871, 2004, pages 1427 - 1438, ISSN: 0003972543 *
LING, C. ET AL: "A deuterated analog of dasatinib disrupts cell cycle progression and displays anti-non-small cell lu", INTERNATIONAL JOURNAL OF CANCER, vol. 131(10), JPN6018010034, 2012, pages 2411 - 2419, ISSN: 0003972545 *

Also Published As

Publication number Publication date
EP2970209A4 (en) 2016-08-31
AU2014235462B2 (en) 2018-05-17
EP3492470A1 (en) 2019-06-05
CA2904054A1 (en) 2014-09-25
US20180051022A1 (en) 2018-02-22
EP2970209A2 (en) 2016-01-20
US20160024084A1 (en) 2016-01-28
AU2014235462A1 (en) 2015-09-17
WO2014150925A3 (en) 2014-12-04
MX2015012741A (es) 2016-02-19
US20190225605A1 (en) 2019-07-25
AU2014235462C1 (en) 2018-11-01
EA201892726A1 (ru) 2019-04-30
EP2970209B1 (en) 2018-12-26
WO2014150925A2 (en) 2014-09-25
EA032094B1 (ru) 2019-04-30
EA201591628A1 (ru) 2016-03-31

Similar Documents

Publication Publication Date Title
US10842792B2 (en) Deuterated baricitinib
JP2016512831A (ja) 重水素化されたパルボシクリブ
JP6261580B2 (ja) 重水素化イブルチニブ
US9776973B2 (en) Deuterated momelotinib
WO2012151361A1 (en) Carbamoylpyridone derivatives
WO2014011971A2 (en) Deuterated carfilzomib
WO2018005328A1 (en) Deuterated bictegravir
US9199986B2 (en) Deuterated pyrazino[2,1-a]isoquinolines for the treatment of diseases and/or conditions
US9676790B2 (en) Substituted thienotriazolodiazapines
WO2012129381A1 (en) Deuterated preladenant
JP2016512530A (ja) 重水素化されたパクリチニブ
WO2015009889A1 (en) Deuterated intedanib derivatives and their use for the treatment of proliferative disorders

Legal Events

Date Code Title Description
A621 Written request for application examination

Free format text: JAPANESE INTERMEDIATE CODE: A621

Effective date: 20170303

A521 Request for written amendment filed

Free format text: JAPANESE INTERMEDIATE CODE: A523

Effective date: 20170830

A977 Report on retrieval

Free format text: JAPANESE INTERMEDIATE CODE: A971007

Effective date: 20180222

A131 Notification of reasons for refusal

Free format text: JAPANESE INTERMEDIATE CODE: A131

Effective date: 20180322

A601 Written request for extension of time

Free format text: JAPANESE INTERMEDIATE CODE: A601

Effective date: 20180618

A521 Request for written amendment filed

Free format text: JAPANESE INTERMEDIATE CODE: A523

Effective date: 20180920

A02 Decision of refusal

Free format text: JAPANESE INTERMEDIATE CODE: A02

Effective date: 20190206