SG10201906517VA - Synthesis of a bruton's tyrosine kinase inhibitor - Google Patents

Synthesis of a bruton's tyrosine kinase inhibitor

Info

Publication number
SG10201906517VA
SG10201906517VA SG10201906517VA SG10201906517VA SG10201906517VA SG 10201906517V A SG10201906517V A SG 10201906517VA SG 10201906517V A SG10201906517V A SG 10201906517VA SG 10201906517V A SG10201906517V A SG 10201906517VA SG 10201906517V A SG10201906517V A SG 10201906517VA
Authority
SG
Singapore
Prior art keywords
bruton
synthesis
tyrosine kinase
kinase inhibitor
inhibitor
Prior art date
Application number
SG10201906517VA
Other languages
English (en)
Inventor
Cyril Benhaim
Wei Chen
Erick Goldman
Andras Horvath
Philip Pye
Mark Smyth
Erik Verner
Original Assignee
Pharmacyclics Llc
Janssen Pharmaceutica Nv
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 Pharmacyclics Llc, Janssen Pharmaceutica Nv filed Critical Pharmacyclics Llc
Publication of SG10201906517VA publication Critical patent/SG10201906517VA/en

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
    • C07D487/04Ortho-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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Epidemiology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
SG10201906517VA 2015-01-14 2016-01-14 Synthesis of a bruton's tyrosine kinase inhibitor SG10201906517VA (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US201562103507P 2015-01-14 2015-01-14

Publications (1)

Publication Number Publication Date
SG10201906517VA true SG10201906517VA (en) 2019-08-27

Family

ID=56406389

Family Applications (2)

Application Number Title Priority Date Filing Date
SG11201705678YA SG11201705678YA (en) 2015-01-14 2016-01-14 Synthesis of a bruton's tyrosine kinase inhibitor
SG10201906517VA SG10201906517VA (en) 2015-01-14 2016-01-14 Synthesis of a bruton's tyrosine kinase inhibitor

Family Applications Before (1)

Application Number Title Priority Date Filing Date
SG11201705678YA SG11201705678YA (en) 2015-01-14 2016-01-14 Synthesis of a bruton's tyrosine kinase inhibitor

Country Status (16)

Country Link
US (5) US20180009814A1 (fr)
EP (1) EP3245208A4 (fr)
JP (2) JP2018502077A (fr)
KR (1) KR20170102887A (fr)
CN (2) CN113816962A (fr)
AU (2) AU2016206693A1 (fr)
BR (1) BR112017015206B1 (fr)
CA (2) CA2971460C (fr)
HK (1) HK1246293A1 (fr)
IL (3) IL308276A (fr)
MA (1) MA41350A (fr)
MX (2) MX366827B (fr)
RU (1) RU2017128308A (fr)
SG (2) SG11201705678YA (fr)
WO (1) WO2016115356A1 (fr)
ZA (1) ZA201704338B (fr)

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP3257855B1 (fr) * 2015-02-12 2020-04-22 Shanghai Dude Medical Science and Technology Co., Ltd. Procédé de préparation d'ibrutinib
US11883404B2 (en) 2016-03-04 2024-01-30 Taiho Pharmaceuticals Co., Ltd. Preparation and composition for treatment of malignant tumors
EP3424505A4 (fr) 2016-03-04 2019-10-16 Taiho Pharmaceutical Co., Ltd. Préparation et composition de traitement de tumeurs malignes
CN109206426B (zh) * 2017-07-06 2021-10-08 上海复星星泰医药科技有限公司 吡唑并嘧啶类化合物的制备方法
US20200369611A1 (en) 2017-08-01 2020-11-26 Boehringer Ingelheim International Gmbh Intermediate compounds and methods
CN107814804A (zh) * 2017-10-27 2018-03-20 广州科锐特生物科技有限公司 依鲁替尼的制备方法
WO2019181876A1 (fr) 2018-03-19 2019-09-26 大鵬薬品工業株式会社 Composition pharmaceutique comprenant du sulfate d'alkyle de sodium
EP3787751A1 (fr) 2018-05-03 2021-03-10 Juno Therapeutics, Inc. Polythérapie d'une thérapie par lymphocytes t à récepteur antigénique chimérique (car) et d'un inhibiteur de btk
JP6944496B2 (ja) * 2018-10-22 2021-10-06 ファイザー・インク ピロロ[2,3−d]ピリミジントシル酸塩、その結晶形態、ならびにその製造方法および中間体
WO2020095452A1 (fr) 2018-11-09 2020-05-14 大鵬薬品工業株式会社 Procédé de fabrication de composé diméthoxybenzène
CN109988175A (zh) * 2019-04-28 2019-07-09 梯尔希(南京)药物研发有限公司 一种依鲁替尼-d5的制备方法
BR112021022646A2 (pt) 2019-05-21 2022-03-29 Janssen Pharmaceutica Nv Processos e intermediários para a preparação de um inibidor de btk
KR20220011668A (ko) 2019-05-21 2022-01-28 얀센 파마슈티카 엔.브이. Btk 억제제 제조를 위한 방법 및 중간체
US20240092785A1 (en) 2021-01-21 2024-03-21 Synthon B.V. Process for making ibrutinib
CN114853662B (zh) * 2021-02-05 2024-01-12 四川青木制药有限公司 手性肼基哌啶衍生物的制备方法
WO2023220655A1 (fr) 2022-05-11 2023-11-16 Celgene Corporation Méthodes pour surmonter la résistance aux médicaments par ré-sensibilisation de cellules cancéreuses à un traitement avec une thérapie antérieure par l'intermédiaire d'un traitement avec une thérapie par lymphocytes t
WO2023242384A1 (fr) 2022-06-17 2023-12-21 Krka, D.D., Novo Mesto Formes cristallines d'ibrutinib

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US4550214A (en) * 1981-01-05 1985-10-29 Polaroid Corporation Blocked vinyl biphenyl compounds
US4874822A (en) * 1988-04-07 1989-10-17 Minnesota Mining And Manufacturing Company Process for the acrylamidoacylation of alcohols
PL1706385T3 (pl) * 2003-12-23 2011-03-31 Astex Therapeutics Ltd Pochodne pirazolu jako modulatory kinazy białkowej
EP2526933B1 (fr) * 2006-09-22 2015-02-25 Pharmacyclics, Inc. Inhibiteurs de la tyrosine kinase de Bruton
SG10201508035TA (en) * 2007-03-28 2015-10-29 Pharmacyclics Inc Inhibitors of bruton's tyrosine kinase
US7741330B1 (en) * 2009-10-12 2010-06-22 Pharmacyclics, Inc. Pyrazolo-pyrimidine inhibitors of Bruton's tyrosine kinase
AU2013296627C9 (en) * 2012-07-30 2018-03-22 Concert Pharmaceuticals, Inc. Deuterated ibrutinib
CN103121999A (zh) * 2012-08-29 2013-05-29 苏州迪飞医药科技有限公司 一种酪氨酸激酶抑制剂pci-32765的合成方法
US9156847B2 (en) * 2013-03-15 2015-10-13 Janssen Pharmaceutica Nv Processes and intermediates for preparing a medicament
US8957080B2 (en) * 2013-04-09 2015-02-17 Principia Biopharma Inc. Tyrosine kinase inhibitors
CN103626774B (zh) * 2013-11-20 2015-11-04 苏州明锐医药科技有限公司 伊鲁替尼的制备方法
CN105471823B (zh) * 2014-09-03 2018-10-26 阿里巴巴集团控股有限公司 一种敏感信息处理方法、装置、服务器及安全判定***
WO2016115869A1 (fr) * 2015-01-21 2016-07-28 中国科学院合肥物质科学研究院 Nouvel inhibiteur de la kinase flt3 et utilisation de ce dernier

Also Published As

Publication number Publication date
SG11201705678YA (en) 2017-08-30
IL253020A0 (en) 2017-08-31
IL308276A (en) 2024-01-01
MX2017009154A (es) 2017-10-12
CA2971460C (fr) 2023-10-10
CN107108640A (zh) 2017-08-29
JP2018502077A (ja) 2018-01-25
CA3210320A1 (fr) 2016-07-21
MX2019008815A (es) 2019-09-26
HK1246293A1 (zh) 2018-09-07
ZA201704338B (en) 2023-10-25
RU2017128308A3 (fr) 2019-10-24
EP3245208A4 (fr) 2018-10-17
RU2017128308A (ru) 2019-02-14
JP2021035947A (ja) 2021-03-04
BR112017015206A2 (pt) 2018-06-19
WO2016115356A1 (fr) 2016-07-21
CN113816962A (zh) 2021-12-21
US20180009814A1 (en) 2018-01-11
CA2971460A1 (fr) 2016-07-21
AU2016206693A1 (en) 2017-07-13
MX366827B (es) 2019-07-25
US20240158400A1 (en) 2024-05-16
BR112017015206B1 (pt) 2023-04-11
US20220098200A1 (en) 2022-03-31
EP3245208A1 (fr) 2017-11-22
IL274716A (en) 2020-07-30
US20190367518A1 (en) 2019-12-05
US20200347064A1 (en) 2020-11-05
AU2020230323A1 (en) 2020-10-01
KR20170102887A (ko) 2017-09-12
MA41350A (fr) 2017-11-21

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