JP2005528363A5 - - Google Patents

Download PDF

Info

Publication number
JP2005528363A5
JP2005528363A5 JP2003578334A JP2003578334A JP2005528363A5 JP 2005528363 A5 JP2005528363 A5 JP 2005528363A5 JP 2003578334 A JP2003578334 A JP 2003578334A JP 2003578334 A JP2003578334 A JP 2003578334A JP 2005528363 A5 JP2005528363 A5 JP 2005528363A5
Authority
JP
Japan
Prior art keywords
hydroxyl
alkyl
formula
atom
halogen
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.)
Withdrawn
Application number
JP2003578334A
Other languages
English (en)
Japanese (ja)
Other versions
JP2005528363A (ja
Filing date
Publication date
Priority claimed from SE0200920A external-priority patent/SE0200920D0/xx
Application filed filed Critical
Publication of JP2005528363A publication Critical patent/JP2005528363A/ja
Publication of JP2005528363A5 publication Critical patent/JP2005528363A5/ja
Withdrawn legal-status Critical Current

Links

JP2003578334A 2002-03-25 2003-03-24 新規アダマンタン誘導体 Withdrawn JP2005528363A (ja)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
SE0200920A SE0200920D0 (sv) 2002-03-25 2002-03-25 Novel compounds
PCT/SE2003/000481 WO2003080579A1 (en) 2002-03-25 2003-03-24 Novel adamantane derivatives

Publications (2)

Publication Number Publication Date
JP2005528363A JP2005528363A (ja) 2005-09-22
JP2005528363A5 true JP2005528363A5 (https=) 2006-05-18

Family

ID=20287392

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2003578334A Withdrawn JP2005528363A (ja) 2002-03-25 2003-03-24 新規アダマンタン誘導体

Country Status (8)

Country Link
US (2) US20050090524A1 (https=)
EP (1) EP1490341A1 (https=)
JP (1) JP2005528363A (https=)
AR (1) AR039124A1 (https=)
AU (1) AU2003216013A1 (https=)
SE (1) SE0200920D0 (https=)
TW (1) TW200306800A (https=)
WO (1) WO2003080579A1 (https=)

Families Citing this family (45)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
TWI258462B (en) 1999-12-17 2006-07-21 Astrazeneca Ab Adamantane derivative compounds, process for preparing the same and pharmaceutical composition comprising the same
GB0013737D0 (en) 2000-06-07 2000-07-26 Astrazeneca Ab Novel compounds
SE0103836D0 (sv) 2001-11-16 2001-11-16 Astrazeneca Ab Novel compounds
SE0200920D0 (sv) * 2002-03-25 2002-03-25 Astrazeneca Ab Novel compounds
SE0300480D0 (sv) * 2003-02-21 2003-02-21 Astrazeneca Ab Novel compounds
EP1644042A1 (en) * 2003-05-29 2006-04-12 AstraZeneca AB A pharmaceutical composition containing a p2x7 receptor antagonist and methotrexate
WO2004105797A1 (en) * 2003-05-29 2004-12-09 Astrazeneca Ab A pharmaceutical composition comprising a p2x7 antagonist and sulfasalazine
TW200507829A (en) * 2003-05-29 2005-03-01 Astrazeneca Ab New combination
GB0312609D0 (en) * 2003-06-02 2003-07-09 Astrazeneca Ab Novel compounds
SE0302192D0 (sv) * 2003-08-08 2003-08-08 Astrazeneca Ab Novel compounds
SE0302488D0 (sv) * 2003-09-18 2003-09-18 Astrazeneca Ab New combination
SA05260265A (ar) * 2004-08-30 2005-12-03 استرازينيكا ايه بي مركبات جديدة
EP2287301A3 (en) * 2004-08-31 2011-11-02 Sylentis S.A.U. Methods and compositions to inhibit P2X7 receptor expression
SE0402925D0 (sv) * 2004-11-30 2004-11-30 Astrazeneca Ab Novel Compounds
US7297700B2 (en) * 2005-03-24 2007-11-20 Renovis, Inc. Bicycloheteroaryl compounds as P2X7 modulators and uses thereof
GB0506133D0 (en) * 2005-03-24 2005-05-04 Sterix Ltd Compound
WO2006110516A1 (en) * 2005-04-11 2006-10-19 Abbott Laboratories Acylhydrazide p2x7 antagonists and uses thereof
WO2006136791A1 (en) * 2005-06-21 2006-12-28 Astrazeneca Ab Polymorphisms and haplotypes in p2x7 gene and their use in determining susceptibility for atherosclerosis-mediated diseases
WO2007028022A2 (en) * 2005-09-01 2007-03-08 Renovis, Inc. Novel compounds as p2x7 modulators and uses thereof
TWI464148B (zh) * 2006-03-16 2014-12-11 Evotec Us Inc 作為ｐ２ｘ7調節劑之雙環雜芳基化合物與其用途
BRPI0709596A2 (pt) 2006-03-16 2011-07-19 Renovis Inc compostos bicicloeteroarila como moduladores de p2x7 e seus usos
JP2009541205A (ja) * 2006-03-16 2009-11-26 レノビス， インコーポレイテッド Ｐ２ｘ７調節因子としてのビシクロへテロアリール化合物およびその使用
WO2007109172A2 (en) * 2006-03-16 2007-09-27 Renovis, Inc. Bicycloheteroaryl compounds as p2x7 modulators and uses thereof
EA201300152A1 (ru) 2006-11-27 2013-07-30 Х. Лундбекк А/С Гетероариламидные производные
AU2007329064C1 (en) 2006-12-07 2013-01-17 F. Hoffmann-La Roche Ag 2-Aminoquinolines as 5-HT(5A) receptor antagonists
BRPI0809106A2 (pt) 2007-03-22 2014-08-26 Astrazeneca Ab Derivados de quinolina para o tratamento de doenças inflamatórias
BRPI0809567A2 (pt) 2007-04-10 2014-09-23 Lundbeck & Co As H Composto, composição farmacêutica, método para modular a atividade de um receptor de p2x7, para tratar uma condição responsiva à modulação do receptor de p2x7 em um paciente, para inibir a morte de células do gânglio retinal em um paciente, e para determinar a presença ou ausência do receptor de p2x7 em uma amostra, preparação farmacêutica acondiciaonada, e, uso de um composto
US8106073B2 (en) 2007-11-30 2012-01-31 Astrazeneca Ab Quinoline derivatives 057
CN102015650A (zh) * 2008-03-07 2011-04-13 弗·哈夫曼-拉罗切有限公司 作为5-ht5a受体拮抗剂的2-氨基喹啉衍生物
CN101959864A (zh) * 2008-03-07 2011-01-26 弗·哈夫曼-拉罗切有限公司 2-氨基喹啉衍生物
CN102046240B (zh) 2008-03-25 2014-06-25 阿费克蒂斯药品公司 新的p2x7r拮抗剂及其应用
WO2010118921A1 (en) 2009-04-14 2010-10-21 Affectis Pharmaceuticals Ag Novel p2x7r antagonists and their use
EP2569281A1 (en) 2010-05-14 2013-03-20 Affectis Pharmaceuticals AG Novel methods for the preparation of p2x7r antagonists
CN102464631B (zh) * 2010-11-08 2016-08-10 中国科学院上海药物研究所 哌嗪取代的1,3-二取代脲类化合物及哌嗪取代的酰胺类化合物及其制备方法和用途
WO2012110190A1 (en) 2011-02-17 2012-08-23 Affectis Pharmaceuticals Ag Novel p2x7r antagonists and their use
WO2012163456A1 (en) 2011-05-27 2012-12-06 Affectis Pharmaceuticals Ag Novel p2x7r antagonists and their use
WO2012163792A1 (en) 2011-05-27 2012-12-06 Affectis Pharmaceuticals Ag Novel p2x7r antagonists and their use
CN103687860B (zh) 2011-07-22 2016-06-08 埃科特莱茵药品有限公司 作为p2x7受体拮抗剂的杂环酰胺衍生物
EA024204B1 (ru) 2012-01-20 2016-08-31 Актелион Фармасьютиклз Лтд. Производные гетероциклических амидов в качестве антагонистов p2xрецептора
AR093921A1 (es) 2012-12-12 2015-06-24 Actelion Pharmaceuticals Ltd Derivados de indol carboxamida como antagonistas del receptor p2x7
KR102232744B1 (ko) 2012-12-18 2021-03-26 이도르시아 파마슈티컬스 리미티드 Ｐ２ｘ７ 수용체 길항제로서의 인돌 카르복사미드 유도체
KR102222220B1 (ko) 2013-01-22 2021-03-03 이도르시아 파마슈티컬스 리미티드 Ｐ2ｘ7 수용체 길항제로서의 헤테로시클릭 아미드 유도체
ES2616883T3 (es) 2013-01-22 2017-06-14 Actelion Pharmaceuticals Ltd. Derivados amida heterocíclicos como antagonistas del receptor P2X7
WO2015187905A1 (en) * 2014-06-05 2015-12-10 Merck Patent Gmbh Novel quinoline derivatives and their use in neurodegenerative diseases
KR102035463B1 (ko) * 2018-02-14 2019-11-26 연세대학교 산학협력단 암 줄기세포의 치료용 약학 조성물

Family Cites Families (25)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3471491A (en) * 1967-08-28 1969-10-07 Squibb & Sons Inc Adamantyl-s-triazines
US3464998A (en) * 1968-03-04 1969-09-02 Searle & Co Adamantyl esters and amides of pyridinecarboxylic acids
US4349552A (en) * 1978-10-30 1982-09-14 Fujisawa Pharmaceutical Company, Ltd. 5-Fluorouracil derivatives, and their pharmaceutical compositions
US4751292A (en) * 1985-07-02 1988-06-14 The Plant Cell Research Institute, Inc. Adamantyl purines
US5399564A (en) * 1991-09-03 1995-03-21 Dowelanco N-(4-pyridyl or 4-quinolinyl) arylacetamide and 4-(aralkoxy or aralkylamino) pyridine pesticides
PL181782B1 (pl) * 1993-08-10 2001-09-28 Black James Foundation Nowe zwiazki i sposób wytwarzania nowych zwiazków PL
EP0952832B1 (en) * 1996-05-20 2008-08-27 Darwin Discovery Limited Quinoline carboxamides as tnf inhibitors and as pde-iv inhibitors
SE9704545D0 (sv) * 1997-12-05 1997-12-05 Astra Pharma Prod Novel compounds
SE9704544D0 (sv) * 1997-12-05 1997-12-05 Astra Pharma Prod Novel compounds
CN1147483C (zh) * 1999-04-09 2004-04-28 阿斯特拉曾尼卡有限公司 金刚烷衍生物
SE9904505D0 (sv) * 1999-12-09 1999-12-09 Astra Pharma Prod Novel compounds
TWI258462B (en) * 1999-12-17 2006-07-21 Astrazeneca Ab Adamantane derivative compounds, process for preparing the same and pharmaceutical composition comprising the same
GB0013737D0 (en) * 2000-06-07 2000-07-26 Astrazeneca Ab Novel compounds
US8058441B2 (en) * 2001-07-02 2011-11-15 N.V. Organon Tetrahydroquinoline derivatives
WO2003042190A1 (en) * 2001-11-12 2003-05-22 Pfizer Products Inc. N-alkyl-adamantyl derivatives as p2x7-receptor antagonists
SE0103836D0 (sv) * 2001-11-16 2001-11-16 Astrazeneca Ab Novel compounds
US6908939B2 (en) * 2001-12-21 2005-06-21 Galderma Research & Development S.N.C. Biaromatic ligand activators of PPARγ receptors
SE0200920D0 (sv) * 2002-03-25 2002-03-25 Astrazeneca Ab Novel compounds
SE0300445D0 (sv) * 2003-02-18 2003-02-18 Astrazeneca Ab New combination
SE0300480D0 (sv) * 2003-02-21 2003-02-21 Astrazeneca Ab Novel compounds
WO2004105797A1 (en) * 2003-05-29 2004-12-09 Astrazeneca Ab A pharmaceutical composition comprising a p2x7 antagonist and sulfasalazine
TW200507829A (en) * 2003-05-29 2005-03-01 Astrazeneca Ab New combination
EP1644042A1 (en) * 2003-05-29 2006-04-12 AstraZeneca AB A pharmaceutical composition containing a p2x7 receptor antagonist and methotrexate
SE0302192D0 (sv) * 2003-08-08 2003-08-08 Astrazeneca Ab Novel compounds
SE0302488D0 (sv) * 2003-09-18 2003-09-18 Astrazeneca Ab New combination

Similar Documents

Publication Publication Date Title
JP2005528363A5 (https=)
EP3105220B1 (en) Process for manufacturing pyrimidine sulfamide derivatives
EP2186808A1 (en) Salts of 4-methyl-n-[3-(4-methyl-imidazol-1-yl)-5-trifluoromethyl-phenyl]-3-(4-pyridin-3-yl-pyrimidin-2-ylamino)-benzamide
AU637015B2 (en) Dideoxydidehydrocarbocyclic pyrimidines
EP3473625B1 (en) Preparation method for chiral pyrrolopyrimidine compound
CN107771178A (zh) 杂环化合物的合成
CN101541818A (zh) 4’-叠氮基胞苷衍生物的制备方法
MX2008008447A (es) Proceso para la preparacion de imatinib.
AU2006258051B2 (en) Process for the synthesis of 5- (methyl-1H-imidazol-1-yl) -3- (tri fluorome th yl) -benzeneamine
KR20180038460A (ko) 세포독성 벤조다이아제핀 유도체의 제조 방법
CN119954804B (zh) 嘧啶并[6,1-a]异喹啉-4-酮衍生物及其用途
CN114728923B (zh) 用于制备氧杂环丁烷-2-基甲胺的方法和中间体
AU2021300294A1 (en) Methods and intermediates for preparing JAK inhibitors
JP2010513410A (ja) アバカビルの調製方法
US7507738B2 (en) 5-protected aminopyrimidine compound, production method thereof and intermediate therefor
US20220064205A1 (en) Process for the preparation of a cyclic dinucleotide
KR100273823B1 (ko) 5-치환된 사이토신 및 다른 4,5-이치환된 피리미딘-2(1h)-온의 제조방법
US7875722B2 (en) Method for producing quinolone carboxylic acid derivative
ES2955554T3 (es) Proceso para producir un derivado de purinona
RU2187504C2 (ru) Четвертичная триметиламмонийная соль 1,3,5-триазина в качестве промежуточного продукта в синтезе модификатора-соотвердителя эпоксиолигомеров в композициях ангидридного отверждения
JP5420549B2 (ja) エピポドフィロトキシンの（ポリ）アミノアルキルアミノアセトアミドの抗腫瘍性誘導体の合成方法
KR101012135B1 (ko) 발사르탄 메틸 에스테르의 제조방법
JP7145802B2 (ja) ２－アミノ－１，３，５－トリアジン化合物の製造方法
WO2025219939A1 (en) Salts and polymorphs of cx3cr1 modulators
WO2025131978A1 (en) Drug-linker reagents for conjugation