CN1303374A - 取代的吲哚满酮,其制法及其作为药物组合物的用途 - Google Patents

取代的吲哚满酮,其制法及其作为药物组合物的用途 Download PDF

Info

Publication number
CN1303374A
CN1303374A CN99806884A CN99806884A CN1303374A CN 1303374 A CN1303374 A CN 1303374A CN 99806884 A CN99806884 A CN 99806884A CN 99806884 A CN99806884 A CN 99806884A CN 1303374 A CN1303374 A CN 1303374A
Authority
CN
China
Prior art keywords
methyl
amino
phenyl
alkyl
methylene radical
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
CN99806884A
Other languages
English (en)
Chinese (zh)
Inventor
阿明·赫克尔
雷纳·沃尔特
沃尔夫冈·格雷尔
雅各布斯·C·A·范米尔
诺伯特·里德曼
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.)
Boehringer Ingelheim GmbH
Original Assignee
Boehringer Ingelheim GmbH
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 Boehringer Ingelheim GmbH filed Critical Boehringer Ingelheim GmbH
Publication of CN1303374A publication Critical patent/CN1303374A/zh
Pending legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D209/00Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/02Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
    • C07D209/04Indoles; Hydrogenated indoles
    • C07D209/30Indoles; Hydrogenated indoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to carbon atoms of the hetero ring
    • 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
    • C07D209/00Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/02Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
    • C07D209/04Indoles; Hydrogenated indoles
    • C07D209/30Indoles; Hydrogenated indoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to carbon atoms of the hetero ring
    • C07D209/32Oxygen atoms
    • C07D209/34Oxygen atoms in position 2

Landscapes

  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Animal Behavior & Ethology (AREA)
  • Medicinal Chemistry (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Indole Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
CN99806884A 1998-06-04 1999-05-28 取代的吲哚满酮,其制法及其作为药物组合物的用途 Pending CN1303374A (zh)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE19824922.5 1998-06-04
DE19824922A DE19824922A1 (de) 1998-06-04 1998-06-04 Neue substituierte Indolinone, ihre Herstellung und ihre Verwendung als Arzneimittel

Publications (1)

Publication Number Publication Date
CN1303374A true CN1303374A (zh) 2001-07-11

Family

ID=7869856

Family Applications (1)

Application Number Title Priority Date Filing Date
CN99806884A Pending CN1303374A (zh) 1998-06-04 1999-05-28 取代的吲哚满酮,其制法及其作为药物组合物的用途

Country Status (23)

Country Link
EP (1) EP1100779A1 (ru)
JP (1) JP2002516906A (ru)
KR (1) KR20010043973A (ru)
CN (1) CN1303374A (ru)
AU (1) AU764782B2 (ru)
BG (1) BG104938A (ru)
BR (1) BR9910898A (ru)
CA (1) CA2328291A1 (ru)
CO (1) CO5050294A1 (ru)
DE (1) DE19824922A1 (ru)
EA (1) EA003514B1 (ru)
EE (1) EE200000723A (ru)
HR (1) HRP20000831A2 (ru)
HU (1) HUP0102210A3 (ru)
ID (1) ID27035A (ru)
IL (1) IL138702A0 (ru)
NO (1) NO20006138L (ru)
PL (1) PL344467A1 (ru)
SK (1) SK18222000A3 (ru)
TR (1) TR200003515T2 (ru)
WO (1) WO1999062882A1 (ru)
YU (1) YU73900A (ru)
ZA (1) ZA200005435B (ru)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN100338036C (zh) * 1998-04-15 2007-09-19 贝林格尔英格海姆法玛两合公司 对激酶及细胞周期蛋白复合物具有抑制作用的取代的吲哚满酮
CN100455568C (zh) * 1999-10-13 2009-01-28 贝林格尔英格海姆法玛两合公司 6-位取代的吲哚满酮,其制备及其作为药物组合物的用途
CN101735071A (zh) * 2009-12-04 2010-06-16 大连凯飞精细化工有限公司 一种生产4-n,n-二甲胺基甲基苯胺的方法
CN103102352A (zh) * 2011-11-15 2013-05-15 山东亨利医药科技有限责任公司 酪氨酸激酶抑制剂吲哚满酮衍生物
CN103130775A (zh) * 2011-11-22 2013-06-05 山东亨利医药科技有限责任公司 作为酪氨酸激酶抑制剂的吲哚满酮衍生物
CN103848814A (zh) * 2012-12-06 2014-06-11 山东亨利医药科技有限责任公司 作为酪氨酸激酶抑制剂的取代吲哚满酮衍生物

Families Citing this family (22)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB9904933D0 (en) 1999-03-04 1999-04-28 Glaxo Group Ltd Compounds
US6624171B1 (en) 1999-03-04 2003-09-23 Smithkline Beecham Corporation Substituted aza-oxindole derivatives
US6762180B1 (en) 1999-10-13 2004-07-13 Boehringer Ingelheim Pharma Kg Substituted indolines which inhibit receptor tyrosine kinases
EP1339680A1 (en) * 2000-09-01 2003-09-03 Glaxo Group Limited Substituted oxindole derivatives as tyrosine kinase inhibitors
AU8664701A (en) * 2000-09-01 2002-03-22 Glaxo Group Ltd Oxindole derivatives
DE10117204A1 (de) * 2001-04-06 2002-10-10 Boehringer Ingelheim Pharma In 6-Stellung substituierte Indolinone, ihre Herstellung und ihre Verwendung als Arzneimittel
DK1401415T3 (da) * 2001-06-29 2006-10-16 Ab Science Anvendelse af N-phenyl-2-pyrimidinamin-derivater til behandling af inflammatoriske sygdomme
JP2004537542A (ja) 2001-06-29 2004-12-16 アブ サイエンス 炎症性腸疾患(ibd)を治療するための、チロシンキナーゼ阻害剤の使用
US7727731B2 (en) 2001-06-29 2010-06-01 Ab Science Potent, selective and non toxic c-kit inhibitors
CA2452371A1 (en) 2001-06-29 2003-01-09 Ab Science Use of tyrosine kinase inhibitors for treating allergic diseases
US20050176687A1 (en) * 2001-06-29 2005-08-11 Alain Moussy Use of tyrosine kinase inhibitors for treating autoimmune diseases
AU2002341881B2 (en) 2001-09-27 2008-05-08 Allergan, Inc. 3-(arylamino)methylene-1, 3-dihydro-2h-indol-2-ones as kinase inhibitors
US7169936B2 (en) 2002-07-23 2007-01-30 Boehringer Ingelheim Pharma Gmbh & Co. Kg Indolinone derivatives substituted in the 6-position, their preparation and their use as medicaments
JP4879492B2 (ja) * 2002-11-27 2012-02-22 アラーガン、インコーポレイテッド 疾患の治療のためのキナーゼ阻害剤
DE102004012070A1 (de) * 2004-03-12 2005-09-29 Boehringer Ingelheim Pharma Gmbh & Co. Kg Neue cycloalkyl-haltige 5-Acylindolinone, deren Herstellung und deren Verwendung als Arzneimittel
PE20060777A1 (es) * 2004-12-24 2006-10-06 Boehringer Ingelheim Int Derivados de indolinona para el tratamiento o la prevencion de enfermedades fibroticas
SG177128A1 (en) * 2006-12-05 2012-01-30 Arena Pharm Inc Processes for preparing (r)-8-chloro-1-methyl-2,3,4,5-tetrahydro-1h-3-benzazepine and intermediates thereof
GB0706072D0 (en) * 2007-03-28 2007-05-09 Sterix Ltd Compound
US20170065529A1 (en) 2015-09-09 2017-03-09 Boehringer Ingelheim International Gmbh Pharmaceutical dosage form for immediate release of an indolinone derivative
GB201208775D0 (en) 2012-05-18 2012-07-04 Uni I Oslo Chemical compounds
EP3966207B1 (en) 2019-05-10 2023-11-01 Deciphera Pharmaceuticals, LLC Phenylaminopyrimidine amide autophagy inhibitors and methods of use thereof
US20240150368A1 (en) * 2022-09-02 2024-05-09 Deciphera Pharmaceuticals, Llc Ulk inhibitors and methods of use thereof

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BE838623A (fr) * 1976-02-16 1976-06-16 Derives de 3-hydroxymethylene-2-indolinone et procede pour leur production
US4145422A (en) * 1977-09-06 1979-03-20 Abbott Laboratories Aminomethylene oxindoles
US5880141A (en) * 1995-06-07 1999-03-09 Sugen, Inc. Benzylidene-Z-indoline compounds for the treatment of disease
AU4155697A (en) * 1996-08-23 1998-03-06 Sugen, Inc. Indolinone combinatorial libraries and related products and methods for the treatment of disease
GB9718913D0 (en) * 1997-09-05 1997-11-12 Glaxo Group Ltd Substituted oxindole derivatives

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN100338036C (zh) * 1998-04-15 2007-09-19 贝林格尔英格海姆法玛两合公司 对激酶及细胞周期蛋白复合物具有抑制作用的取代的吲哚满酮
CN100455568C (zh) * 1999-10-13 2009-01-28 贝林格尔英格海姆法玛两合公司 6-位取代的吲哚满酮,其制备及其作为药物组合物的用途
CN101735071A (zh) * 2009-12-04 2010-06-16 大连凯飞精细化工有限公司 一种生产4-n,n-二甲胺基甲基苯胺的方法
CN103102352A (zh) * 2011-11-15 2013-05-15 山东亨利医药科技有限责任公司 酪氨酸激酶抑制剂吲哚满酮衍生物
CN103102352B (zh) * 2011-11-15 2015-08-12 山东亨利医药科技有限责任公司 酪氨酸激酶抑制剂吲哚满酮衍生物
CN103130775A (zh) * 2011-11-22 2013-06-05 山东亨利医药科技有限责任公司 作为酪氨酸激酶抑制剂的吲哚满酮衍生物
CN103130775B (zh) * 2011-11-22 2015-09-30 山东亨利医药科技有限责任公司 作为酪氨酸激酶抑制剂的吲哚满酮衍生物
CN103848814A (zh) * 2012-12-06 2014-06-11 山东亨利医药科技有限责任公司 作为酪氨酸激酶抑制剂的取代吲哚满酮衍生物
CN103848814B (zh) * 2012-12-06 2016-08-17 山东亨利医药科技有限责任公司 作为酪氨酸激酶抑制剂的取代吲哚满酮衍生物

Also Published As

Publication number Publication date
SK18222000A3 (sk) 2001-08-06
DE19824922A1 (de) 1999-12-09
JP2002516906A (ja) 2002-06-11
ZA200005435B (en) 2002-01-07
CA2328291A1 (en) 1999-12-09
EP1100779A1 (de) 2001-05-23
ID27035A (id) 2001-02-22
IL138702A0 (en) 2001-10-31
EA200100001A1 (ru) 2001-08-27
AU764782B2 (en) 2003-08-28
TR200003515T2 (tr) 2001-06-21
CO5050294A1 (es) 2001-06-27
KR20010043973A (ko) 2001-05-25
HRP20000831A2 (en) 2001-12-31
YU73900A (sh) 2003-04-30
BR9910898A (pt) 2001-02-13
EA003514B1 (ru) 2003-06-26
NO20006138D0 (no) 2000-12-01
HUP0102210A2 (hu) 2001-11-28
WO1999062882A1 (de) 1999-12-09
PL344467A1 (en) 2001-11-05
EE200000723A (et) 2002-04-15
HUP0102210A3 (en) 2002-12-28
BG104938A (en) 2001-06-29
NO20006138L (no) 2001-02-01
AU4370799A (en) 1999-12-20

Similar Documents

Publication Publication Date Title
CN1303374A (zh) 取代的吲哚满酮,其制法及其作为药物组合物的用途
CN100338036C (zh) 对激酶及细胞周期蛋白复合物具有抑制作用的取代的吲哚满酮
CN1257891C (zh) 含氮五员环化合物
CN1150171C (zh) 二环杂环,含这些化合物的药物组合物,及其制备方法
CN1224623C (zh) 1-苯基磺酰基-1,3-二氢-2h-吲哚-2-酮衍生物,其制备及其治疗应用
CN1279023C (zh) 吲哚-3-硫衍生物
CN1192773C (zh) 环胺ccr3拮抗剂
CN1198825C (zh) 8-苯基-6,9-二氢-[1,2,4]三唑并[3,4-i]嘌呤-5-酮衍生物
CN100343237C (zh) 酰胺衍生物及医药品
CN1642552A (zh) 作为酪氨酸激酶抑制剂的4-(n-苯氨基)-喹唑啉/喹啉
CN1286810C (zh) 2-酰基吲哚衍生物及它们作为抗肿瘤剂的用途
CN1184471A (zh) 氨基噻唑衍生物、含有它们的药物及制备该化合物的中间体
CN1157619A (zh) 嘧啶并[5,4-d]嘧啶,含该化合物的药物,其用途及其制备方法
CN1422268A (zh) 5-烷基吡啶并[2,3-d]嘧啶酪氨酸激酶抑制剂
CN1079464A (zh) 治疗包括胆碱能功能降低的病症有价值的吲哚酮和吲哚二酮的衍生物的制备方法
CN1087904A (zh) 羧酸衍生物,含有这些化合物的药物组合物以及其制备方法
CN1087086A (zh) 噻唑基乙烯基苯基衍生物
CN1319090A (zh) 新的取代的二氢吲哚酮、它们的制备方法和它们作为药物的用途
CN1890218A (zh) 微管蛋白抑制剂
CN1282743A (zh) 新颖的β-咔啉化合物、它们的制备方法和含有它们的药物组合物
CN1921848A (zh) 新型氮杂双环衍生物、其制备方法及包含其的药物组合物
CN1059908A (zh) 嘧啶衍生物及其药物
CN1352644A (zh) 抑制磷酸二酯酶IV的1-氨基三唑并[4,3-α]喹唑啉-5酮类化合物和/或-5-硫酮类化合物
CN1250542C (zh) 具有抗肿瘤活性的2-(1h-吲哚-3-基)-2-氧代-乙酰胺
CN1208318C (zh) 环胺ccr5受体拮抗剂

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C02 Deemed withdrawal of patent application after publication (patent law 2001)
WD01 Invention patent application deemed withdrawn after publication
REG Reference to a national code

Ref country code: HK

Ref legal event code: WD

Ref document number: 1035727

Country of ref document: HK