JP2000517291A - 4―アニリノキナゾリン誘導体 - Google Patents
4―アニリノキナゾリン誘導体Info
- Publication number
- JP2000517291A JP2000517291A JP09531552A JP53155297A JP2000517291A JP 2000517291 A JP2000517291 A JP 2000517291A JP 09531552 A JP09531552 A JP 09531552A JP 53155297 A JP53155297 A JP 53155297A JP 2000517291 A JP2000517291 A JP 2000517291A
- Authority
- JP
- Japan
- Prior art keywords
- methoxy
- formula
- quinazoline
- compound
- chloro
- 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.)
- Granted
Links
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/70—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings condensed with carbocyclic rings or ring systems
- C07D239/72—Quinazolines; Hydrogenated quinazolines
- C07D239/86—Quinazolines; Hydrogenated quinazolines with hetero atoms directly attached in position 4
- C07D239/94—Nitrogen atoms
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- 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
- A61K31/517—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with carbocyclic ring systems, e.g. quinazoline, perimidine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/02—Drugs for dermatological disorders for treating wounds, ulcers, burns, scars, keloids, or the like
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/06—Antipsoriatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- 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
Abstract
Description
Claims (1)
- 【特許請求の範囲】 1.式Iのキナゾリン誘導体: (式中: R1は、水素またはメトキシを表し; R2は、メトキシ、エトキシ、2−メトキシエトキシ、3−メトキシプロポキ シ、2−エトキシエトキシ、トリフルオロメトキシ、2.2,2−トリフルオロ エトキシ、2−ヒドロキシエトキシ、3−ヒドロキシプロポキシ、2−(N,N −ジメチルアミノ)エトキシ、3−(N,N−ジメチルアミノ)プロポキシ、2 −モルホリノエトキシ、3−モルホリノプロポキシ、4−モルホリノブトキシ、 2−ピペリジノエトキシ、3−ピペリジノプロポキシ、4−ピペリジノブトキシ 、2−(ピペラジン−1−イル)エトキシ、3−(ピペラジン−1−イル)プロ ポキシ、4−(ピペラジン−1−イル)ブトキシ、2−(4−メチルピペラジン −1−イル)エトキシ、3−(4−メチルピペラジン−1−イル)プロポキシま たは4−(4−メチルピペラジン−1−イル)ブトキシを表し; (R3)2を保有するフェニル基は以下のものから選択される:2−フルオロ− 5−ヒドロキシフェニル、4−ブロモ−2−フルオロフェニル、2,4−ジフル オロフェニル、4−クロロ−2−フルオロフェニル、2−フルオロ−4−メチル フェニル、2−フルオロ−4−メトキシフェニル、4−ブロモ−3−ヒドロキシ フェニル、4−フルオロ−3−ヒドロキシフェニル、4−クロロ−3−ヒドロキ シフェニル、3−ヒドロキシ−4−メチルフェニル、3−ヒドロキシ−4−メト キシフェニルおよび4−シアノ−2−フルオロフェニル); およびその塩類。 2.R1がメトキシである、請求項1記載のキナゾリン誘導体。 3.(R3)2を保有するフェニル基が4−クロロ−2−フルオロフェニルまた は4−ブロモ−2−フルオロフェニルである、請求項1または2記載のキナゾリ ン誘導体。 4.R2がメトキシ、エトキシ、2−メトキシエトキシ、3−メトキシプロポ キシ、トリフルオロメトキシ、2,2,2−トリフルオロエトキシ、2−ヒドロ キシエトキシ、3−ヒドロキシプロポキシ、2−(N,N−ジメチルアミノ)エ トキシ、3−(N,N−ジメチルアミノ)プロポキシ、2−モルホリノエトキシ 、3−モルホリノプロポキシ、2−ピペリジノエトキシ、3−ピペリジノプロポ キシ、2−(ピペラジン−1−イル)エトキシ、3−(ピペラジン−1−イル) プロポキシ、2−(4−メチルピペラジン−1−イル)エトキシまたは3−(4 −メチルピペラジン−1−イル)プロポキシである、請求項1〜3のいずれか1 項記載のキナゾリン誘導体。 5.R2が2−メトキシエトキシ、2−モルホリノエトキシ、3−モルホリノ プロポキシまたは2−(4−メチルピペラジン−1−イル)エトキシである、請 求項4記載のキナゾリン誘導体。 6.R2が2−メトキシエトキシまたは3−モルホリノプロポキシである、請 求項5記載のキナゾリン誘導体。 7.4−(4−クロロ−2−フルオロアニリノ)−6−メトキシ−7−(2− メトキシエトキシ)キナゾリン、 4−(4−クロロ−2−フルオロアニリノ)−6−メトキシ−7−(2−モルホ リノエトキシ)キナゾリン、 4−(4−クロロ−2−フルオロアニリノ)−6−メトキシ−7−(3−モルホ リノプロポキシ)キナゾリン、 4−(4−クロロ−2−フルオロアニリノ)−6−メトキシ−7−(2−(4− メチルピペラジン−1−イル)エトキシ)キナゾリン、 4−(4−ブロモ−2−フルオロアニリノ)−6−メトキシ−7−(3−モルホ リノプロポキシ)キナゾリン およびその塩類から選択される、請求項1記載のキナゾリン誘導体。 8.4−(4−ブロモ−2−フルオロアニリノ)−6−メトキシ−7−(2− メトキシエトキシ)キナゾリン、 4−(4−ブロモ−2−フルオロアニリノ)−6−メトキシ−7−(2−(4− メチルピベラジン−1−イル)エトキシ)キナゾリン、 4−(4−ブロモ−2−フルオロアニリノ)−6−メトキシ−7−(2−モルホ リノエトキシ)キナゾリン およびその塩類から選択される、請求項1記載のキナゾリン誘導体。 9.薬剤学的に許容しうる塩の形である、請求項1〜8のいずれか1項記載の キナゾリン誘導体。 10.式Iのキナゾリン誘導体またはその塩(請求項1に定義したとおり)を 製造するための、以下を含む方法: (a)式IIIの化合物: (式中、R1およびR2は請求項1に定義したとおりであり、L1は置換可能な部 分である)を、式IVの化合物: (式中、R3は請求項1に定義したとおりである)と反応させ、これにより式I の化合物およびその塩類を得る; (b)式IIの基:(式中、R3は請求項1に定義したとおりである)がヒドロキシ基を保有するフ ェニル基を表す式Iの化合物およびその塩類を製造するためには、式Vの化合物 : (式中、R1、R2およびR3は請求項1に定義したとおりであり、Pはフェノー ル性ヒドロキシの保護基である)を脱保護する; (c)式VIの化合物: (式中、R1およびR3は請求項1に定義したとおりである)を、式VIIの化合 物: R4−L1 (VII) (式中、L1は前記に定義したとおりであり、R4はメチル、エチル、2−メトキ シエチル、3−メトキシプロピル、2−エトキシエチル、トリフルオロメチル、 2,2,2−トリフルオロエチル、2−ヒドロキシエチル、3−ヒドロキシプロ ピル、2−(N,N−ジメチルアミノ)エチル、3−(N,N−ジメチルアミノ )プロピル、2−モルホリノエチル、3−モルホリノプロピル、4−モルホリノ ブチル、2−ピペリジノエチル、3−ピペリジノプロピル、4−ピペリジノブチ ル、2−(ピペラジン−1−イル)エチル、3−(ピペラジン−1−イル)プロ ピル、4−(ピペラジン−1−イル)ブチル、2−(4−メチルピペラジン−1 −イル)エチル、3−(4−メチルピペラジン−1−イル)プロピルまたは4− (4−メチルピペラジン−1−イル)ブチルである)と反応させる; (d)式VIIIの化合物: を、式IXの化合物: R2−H (IX) (これらの式中、L1は前記に定義したとおりであり、R1、R2およびR3は請求 項1に定義したとおりである)と反応させる; (e)R2がR5C1 〜4アルコキシ(ここでR5はメトキシ、エトキシ、ヒドロ キシ、N,N−ジメチルアミノ、モルホリノ、ピペリジノ、ピペラジン−1−イ ルまたは4−メチルピペラジン−1−イルから選択される)である式Iの化合物 およびその塩類を製造するためには、式Xの化合物: (式中、L1は前記に定義したとおりであり、R1およびR3は請求項1に定義し たとおりであり、R6はC1 〜4アルコキシである)を、式XIの化合物: R5−H (XI) (式中、R5は前記に定義したとおりである)と反応させる; かつ、式Iのキナゾリン誘導体の塩が必要である場合、得られた化合物を酸また は塩基と反応させ、これにより目的とする塩を得る。 11.有効成分としての請求項1〜9のいずれか1項記載の式Iのキナゾリン 誘導体またはその薬剤学的に許容しうる塩を、薬剤学的に許容しうる賦形剤また はキャリヤーと一緒に含む、薬剤組成物。 12.抗脈管形成作用および/または脈管透過性低下作用を、その処置を必要 とする温血動物において生じる方法であって、該動物に有効量の請求項1〜9の いずれか1項記載の式Iの化合物またはその薬剤学的に許容しうる塩を投与する ことを含む方法。 13.医薬として使用するための、請求項1〜9のいずれか1項記載のキナゾ リン誘導体。
Applications Claiming Priority (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP96400468.3 | 1996-03-05 | ||
EP96400468 | 1996-03-05 | ||
EP96401499.7 | 1996-07-08 | ||
EP96401499 | 1996-07-08 | ||
PCT/GB1997/000550 WO1997032856A1 (en) | 1996-03-05 | 1997-02-28 | 4-anilinoquinazoline derivatives |
Related Child Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2009171068A Division JP2010013450A (ja) | 1996-03-05 | 2009-07-22 | 4−アニリノキナゾリン誘導体 |
Publications (2)
Publication Number | Publication Date |
---|---|
JP2000517291A true JP2000517291A (ja) | 2000-12-26 |
JP4464466B2 JP4464466B2 (ja) | 2010-05-19 |
Family
ID=26144020
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP53155297A Expired - Fee Related JP4464466B2 (ja) | 1996-03-05 | 1997-02-28 | 4―アニリノキナゾリン誘導体 |
JP2009171068A Pending JP2010013450A (ja) | 1996-03-05 | 2009-07-22 | 4−アニリノキナゾリン誘導体 |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2009171068A Pending JP2010013450A (ja) | 1996-03-05 | 2009-07-22 | 4−アニリノキナゾリン誘導体 |
Country Status (18)
Country | Link |
---|---|
US (1) | US6291455B1 (ja) |
EP (1) | EP0885198B1 (ja) |
JP (2) | JP4464466B2 (ja) |
KR (1) | KR100489174B1 (ja) |
CN (1) | CN1116286C (ja) |
AT (1) | ATE211134T1 (ja) |
AU (1) | AU719327B2 (ja) |
CA (1) | CA2244897C (ja) |
DE (1) | DE69709319T2 (ja) |
DK (1) | DK0885198T3 (ja) |
ES (1) | ES2169355T3 (ja) |
IL (1) | IL125954A (ja) |
MY (1) | MY125675A (ja) |
NO (1) | NO311427B1 (ja) |
NZ (1) | NZ331191A (ja) |
PT (1) | PT885198E (ja) |
TW (1) | TW542826B (ja) |
WO (1) | WO1997032856A1 (ja) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2010524909A (ja) * | 2007-04-16 | 2010-07-22 | シプラ・リミテッド | ゲフィチニブの製造方法 |
JP2017526668A (ja) * | 2014-08-11 | 2017-09-14 | 石薬集団中奇制薬技術(石家庄)有限公司 | キナゾリン誘導体 |
Families Citing this family (442)
Publication number | Priority date | Publication date | Assignee | Title |
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US5747498A (en) | 1996-05-28 | 1998-05-05 | Pfizer Inc. | Alkynyl and azido-substituted 4-anilinoquinazolines |
US6184225B1 (en) | 1996-02-13 | 2001-02-06 | Zeneca Limited | Quinazoline derivatives as VEGF inhibitors |
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GB9718972D0 (en) * | 1996-09-25 | 1997-11-12 | Zeneca Ltd | Chemical compounds |
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JP2002523403A (ja) * | 1998-08-21 | 2002-07-30 | パーカー ヒューズ インスティテュート | キナゾリン誘導体 |
SK12112001A3 (sk) | 1999-02-27 | 2001-12-03 | Boehringer Ingelheim Pharma Kg | 4-amino-chinazolínové a chinolínové deriváty, spôsob ich prípravy, farmaceutický prostriedok s ich obsahom a ich použitie |
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US6258820B1 (en) | 1999-03-19 | 2001-07-10 | Parker Hughes Institute | Synthesis and anti-tumor activity of 6,7-dialkoxy-4-phenylamino-quinazolines |
YU13200A (sh) | 1999-03-31 | 2002-10-18 | Pfizer Products Inc. | Postupci i intermedijeri za dobijanje anti-kancernih jedinjenja |
CA2384291A1 (en) | 1999-09-21 | 2001-03-29 | Astrazeneca Ab | Quinazoline derivatives and their use as pharmaceuticals |
CZ20021010A3 (cs) * | 1999-09-21 | 2002-06-12 | Astrazeneca Ab | Nové sloučeniny chinazolinu a farmaceutické kompozice, které je obsahují |
SE9903544D0 (sv) | 1999-10-01 | 1999-10-01 | Astra Pharma Prod | Novel compounds |
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1997
- 1997-02-28 DE DE69709319T patent/DE69709319T2/de not_active Expired - Lifetime
- 1997-02-28 WO PCT/GB1997/000550 patent/WO1997032856A1/en active IP Right Grant
- 1997-02-28 AU AU18664/97A patent/AU719327B2/en not_active Ceased
- 1997-02-28 KR KR10-1998-0706632A patent/KR100489174B1/ko not_active IP Right Cessation
- 1997-02-28 IL IL12595497A patent/IL125954A/xx not_active IP Right Cessation
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- 1997-02-28 DK DK97906814T patent/DK0885198T3/da active
- 1997-02-28 US US09/142,339 patent/US6291455B1/en not_active Expired - Fee Related
- 1997-02-28 CN CN97192807A patent/CN1116286C/zh not_active Expired - Fee Related
- 1997-02-28 NZ NZ331191A patent/NZ331191A/xx unknown
- 1997-02-28 EP EP97906814A patent/EP0885198B1/en not_active Expired - Lifetime
- 1997-02-28 PT PT97906814T patent/PT885198E/pt unknown
- 1997-02-28 ES ES97906814T patent/ES2169355T3/es not_active Expired - Lifetime
- 1997-03-04 TW TW086102593A patent/TW542826B/zh active
- 1997-03-04 MY MYPI97000873A patent/MY125675A/en unknown
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1998
- 1998-09-04 NO NO19984085A patent/NO311427B1/no not_active IP Right Cessation
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Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2010524909A (ja) * | 2007-04-16 | 2010-07-22 | シプラ・リミテッド | ゲフィチニブの製造方法 |
JP2017526668A (ja) * | 2014-08-11 | 2017-09-14 | 石薬集団中奇制薬技術(石家庄)有限公司 | キナゾリン誘導体 |
Also Published As
Publication number | Publication date |
---|---|
ATE211134T1 (de) | 2002-01-15 |
KR19990087234A (ko) | 1999-12-15 |
AU1866497A (en) | 1997-09-22 |
CA2244897C (en) | 2006-04-11 |
NO311427B1 (no) | 2001-11-26 |
NO984085D0 (no) | 1998-09-04 |
KR100489174B1 (ko) | 2005-09-30 |
AU719327B2 (en) | 2000-05-04 |
IL125954A (en) | 2003-06-24 |
EP0885198A1 (en) | 1998-12-23 |
EP0885198B1 (en) | 2001-12-19 |
TW542826B (en) | 2003-07-21 |
ES2169355T3 (es) | 2002-07-01 |
CA2244897A1 (en) | 1997-09-12 |
NZ331191A (en) | 2000-03-27 |
NO984085L (no) | 1998-09-04 |
CN1212684A (zh) | 1999-03-31 |
CN1116286C (zh) | 2003-07-30 |
DK0885198T3 (da) | 2002-03-25 |
PT885198E (pt) | 2002-06-28 |
JP4464466B2 (ja) | 2010-05-19 |
DE69709319T2 (de) | 2002-08-14 |
DE69709319D1 (de) | 2002-01-31 |
IL125954A0 (en) | 1999-04-11 |
JP2010013450A (ja) | 2010-01-21 |
US6291455B1 (en) | 2001-09-18 |
MY125675A (en) | 2006-08-30 |
WO1997032856A1 (en) | 1997-09-12 |
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