JP2006316058A5 - - Google Patents

Download PDF

Info

Publication number
JP2006316058A5
JP2006316058A5 JP2006132110A JP2006132110A JP2006316058A5 JP 2006316058 A5 JP2006316058 A5 JP 2006316058A5 JP 2006132110 A JP2006132110 A JP 2006132110A JP 2006132110 A JP2006132110 A JP 2006132110A JP 2006316058 A5 JP2006316058 A5 JP 2006316058A5
Authority
JP
Japan
Prior art keywords
ethoxyethyl
ethyl
pyrazolo
methylamino
pyrimidine
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
Application number
JP2006132110A
Other languages
English (en)
Japanese (ja)
Other versions
JP4271695B2 (ja
JP2006316058A (ja
Filing date
Publication date
Application filed filed Critical
Publication of JP2006316058A publication Critical patent/JP2006316058A/ja
Publication of JP2006316058A5 publication Critical patent/JP2006316058A5/ja
Application granted granted Critical
Publication of JP4271695B2 publication Critical patent/JP4271695B2/ja
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

JP2006132110A 2005-05-12 2006-05-11 無水結晶形態のN−[1−(2−エトキシエチル)−5−(N−エチル−N−メチルアミノ)−7−(4−メチルピリジン−2−イル−アミノ)−1H−ピラゾロ[4,3−d]ピリミジン−3−カルボニル]メタンスルホンアミド Expired - Fee Related JP4271695B2 (ja)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US68044505P 2005-05-12 2005-05-12
US68171105P 2005-05-17 2005-05-17

Related Child Applications (1)

Application Number Title Priority Date Filing Date
JP2009001627A Division JP4996631B2 (ja) 2005-05-12 2009-01-07 無水結晶形態のN−[1−(2−エトキシエチル)−5−(N−エチル−N−メチルアミノ)−7−(4−メチルピリジン−2−イル−アミノ)−1H−ピラゾロ[4,3−d]ピリミジン−3−カルボニル]メタンスルホンアミド

Publications (3)

Publication Number Publication Date
JP2006316058A JP2006316058A (ja) 2006-11-24
JP2006316058A5 true JP2006316058A5 (https=) 2008-12-11
JP4271695B2 JP4271695B2 (ja) 2009-06-03

Family

ID=37106941

Family Applications (2)

Application Number Title Priority Date Filing Date
JP2006132110A Expired - Fee Related JP4271695B2 (ja) 2005-05-12 2006-05-11 無水結晶形態のN−[1−(2−エトキシエチル)−5−(N−エチル−N−メチルアミノ)−7−(4−メチルピリジン−2−イル−アミノ)−1H−ピラゾロ[4,3−d]ピリミジン−3−カルボニル]メタンスルホンアミド
JP2009001627A Expired - Fee Related JP4996631B2 (ja) 2005-05-12 2009-01-07 無水結晶形態のN−[1−(2−エトキシエチル)−5−(N−エチル−N−メチルアミノ)−7−(4−メチルピリジン−2−イル−アミノ)−1H−ピラゾロ[4,3−d]ピリミジン−3−カルボニル]メタンスルホンアミド

Family Applications After (1)

Application Number Title Priority Date Filing Date
JP2009001627A Expired - Fee Related JP4996631B2 (ja) 2005-05-12 2009-01-07 無水結晶形態のN−[1−(2−エトキシエチル)−5−(N−エチル−N−メチルアミノ)−7−(4−メチルピリジン−2−イル−アミノ)−1H−ピラゾロ[4,3−d]ピリミジン−3−カルボニル]メタンスルホンアミド

Country Status (23)

Country Link
US (3) US8227475B2 (https=)
EP (1) EP1881985B1 (https=)
JP (2) JP4271695B2 (https=)
KR (1) KR100939890B1 (https=)
AT (1) ATE493413T1 (https=)
AU (1) AU2006245416B2 (https=)
BR (1) BRPI0609225A2 (https=)
CA (1) CA2608018C (https=)
CR (1) CR9505A (https=)
CY (1) CY1111171T1 (https=)
DE (1) DE602006019231D1 (https=)
DK (1) DK1881985T3 (https=)
EA (1) EA012577B1 (https=)
IL (1) IL186693A (https=)
MA (1) MA29447B1 (https=)
MX (1) MX2007013215A (https=)
NO (1) NO20075258L (https=)
NZ (1) NZ564187A (https=)
PL (1) PL1881985T3 (https=)
PT (1) PT1881985E (https=)
TN (1) TNSN07414A1 (https=)
TW (1) TWI380986B (https=)
WO (1) WO2006120552A2 (https=)

Families Citing this family (35)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7676953B2 (en) * 2006-12-29 2010-03-16 Signature Control Systems, Inc. Calibration and metering methods for wood kiln moisture measurement
WO2009050554A2 (en) * 2007-10-19 2009-04-23 Pfizer Inc. Treatment of central nervous system disorders
WO2012048330A2 (en) * 2010-10-08 2012-04-12 The Mclean Hospital Corporation Treatment of motor neuron disease
CA2830027C (en) 2011-03-31 2016-04-26 Pfizer Inc. Novel bicyclic pyridinones
AP2013007253A0 (en) 2011-04-21 2013-11-30 Origenis Gmbh Pyrazolo [4,3-D] pyrimidines useful as kinase inhibitors
WO2012172449A1 (en) 2011-06-13 2012-12-20 Pfizer Inc. Lactams as beta secretase inhibitors
CN102952138B (zh) * 2011-08-17 2016-07-06 上海特化医药科技有限公司 一种吡唑并嘧啶酮化合物的盐、多晶型物及其药物组合物、制备方法和应用
JP6043355B2 (ja) 2011-08-31 2016-12-14 ファイザー・インク ヘキサヒドロピラノ[3,4−d][1,3]チアジン−2−アミン化合物
WO2013164730A1 (en) 2012-05-04 2013-11-07 Pfizer Inc. Heterocyclic substituted hexahydropyrano [3,4-d] [1,3] thiazin- 2 -amine compounds as inhibitors of app, bace1 and bace 2.
EP2897964A1 (en) 2012-09-20 2015-07-29 Pfizer Inc. Alkyl-substituted hexahydropyrano [3,4-d][1,3]thiazin-2-amine compounds
UA110688C2 (uk) 2012-09-21 2016-01-25 Пфайзер Інк. Біциклічні піридинони
WO2014060112A1 (en) 2012-10-19 2014-04-24 Origenis Gmbh Pyrazolo[4,3-d]pyrimidines as kinase inhibitors
MX2015005004A (es) * 2012-10-23 2015-07-17 Pfizer Uso de un compuesto de pirazolo[4,3-d]pirimidina tetrasubstituida para tratar la nefropatia diabetica.
EP2931731A1 (en) 2012-12-11 2015-10-21 Pfizer Inc. Hexahydropyrano [3,4-d][1,3]thiazin-2-amine compounds as inhibitors of bace1
US9403846B2 (en) 2012-12-19 2016-08-02 Pfizer Inc. Carbocyclic- and heterocyclic-substituted hexahydropyrano[3,4-d][1,3]thiazin-2-amine compounds
EP2956458B1 (en) 2013-02-13 2017-08-09 Pfizer Inc Heteroaryl-substituted hexahydropyrano[3,4-d][1,3]thiazin-2-amine compounds
US9233981B1 (en) 2013-02-15 2016-01-12 Pfizer Inc. Substituted phenyl hexahydropyrano[3,4-d][1,3]thiazin-2-amine compounds
BR112015019276A2 (pt) 2013-02-19 2017-07-18 Pfizer compostos de azabenzimidazol como inibidores de isoenzimas de pde4 para o tratamento de distúrbios do snc e outros distúrbios
JP6425717B2 (ja) 2013-10-04 2018-11-21 ファイザー・インク ガンマセクレターゼモジュレーターとしての新規二環式ピリジノン
AP2016009465A0 (en) 2014-04-01 2016-09-30 Pfizer Chromene and 1,1 a,2,7b-tetrahydrocyclopropa[c]chromene pyridopyrazinediones as gamma-secretase modulators
CN106459088A (zh) 2014-04-10 2017-02-22 辉瑞公司 2‑氨基‑6‑甲基‑4,4a,5,6‑四氢吡喃并[3,4‑d][1,3]噻嗪‑8a(8H)‑基‑1,3‑噻唑‑4‑基酰胺
WO2016012896A1 (en) 2014-07-24 2016-01-28 Pfizer Inc. Pyrazolopyrimidine compounds
MD20170011A2 (ro) 2014-08-06 2017-08-31 Pfizer Inc. Compuşi imidazopiridazinici
MX368391B (es) 2015-02-03 2019-09-30 Pfizer Ciclopropabenzofuranil-piridopirazindionas novedosas.
CN107787322B (zh) 2015-06-17 2023-07-07 辉瑞大药厂 三环化合物以及它们作为磷酸二酯酶抑制剂的用途
JP2018534251A (ja) 2015-09-24 2018-11-22 ファイザー・インク Bace阻害剤として有用なn−[2−(3−アミノ−2,5−ジメチル−1,1−ジオキシド−5,6−ジヒドロ−2h−1,2,4−チアジアジン−5−イル)−1,3−チアゾール−4−イル]アミド
WO2017051303A1 (en) 2015-09-24 2017-03-30 Pfizer Inc. Tetrahydropyrano[3,4-d][1,3]oxazin derivatives and their use as bace inhibitors
JP2018531923A (ja) 2015-09-24 2018-11-01 ファイザー・インク N−[2−(2−アミノ−6,6−二置換−4,4a,5,6−テトラヒドロピラノ[3,4−d][1,3]チアジン−8a(8H)−イル)−1,3−チアゾール−4−イル]アミド
CN113332292A (zh) 2016-02-23 2021-09-03 辉瑞公司 6,7-二氢-5H-吡唑并[5,1-b][1,3]噁嗪-2-甲酰胺化合物
PT3478679T (pt) 2016-07-01 2021-06-30 Pfizer Derivados de 5,7-dihidro-pirrolo-piridina para o tratamento de doenças neurológicas e neurodegenerativas
IL271290B2 (en) 2017-06-22 2023-11-01 Pfizer Dihydro-pyrrolo-pyridine derivatives
PT3768669T (pt) 2018-03-23 2023-04-24 Pfizer Derivados de piperazina azaspiro
US12144815B2 (en) 2021-02-23 2024-11-19 Hoth Therapeutics, Inc. Use of aprepitant for treating Alzheimer's disease
WO2024118524A1 (en) 2022-11-28 2024-06-06 Cerevel Therapeutics, Llc Azaindole compounds and their use as phosphodiesterase inhibitors
WO2025145091A1 (en) 2023-12-29 2025-07-03 Pfizer Inc. Crystalline forms of a muscarinic m4 receptor modulator and methods of treating diseases

Family Cites Families (22)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB9119704D0 (en) 1991-09-14 1991-10-30 Pfizer Ltd Therapeutic agents
GB9121028D0 (en) 1991-10-03 1991-11-13 Pfizer Ltd Therapeutic agents
GB9126260D0 (en) 1991-12-11 1992-02-12 Pfizer Ltd Therapeutic agents
GB9213623D0 (en) 1992-06-26 1992-08-12 Pfizer Ltd Therapeutic agents
GB9218322D0 (en) 1992-08-28 1992-10-14 Pfizer Ltd Therapeutic agents
GB9401090D0 (en) 1994-01-21 1994-03-16 Glaxo Lab Sa Chemical compounds
US6723719B1 (en) 1997-04-25 2004-04-20 Pfizer Inc Pyrazolopyrimidinones which inhibit type 5 cyclic guanosine 3′,5′—monophosphate phosphodiesterase (cGMP PDE5) for the treatment of sexual dysfunction
CA2395558C (en) 1997-11-12 2007-07-17 Bayer Aktiengesellschaft Intermediates for 2-phenyl substituted imidazotriazinones as phosphodiesterase inhibitors
RS50011B (sr) 1998-04-20 2008-09-29 Pfizer Inc., Derivati piridin-3-karboksilne kiseline i njihova upotreba kao intermedijera
BR9915532A (pt) 1998-10-23 2001-08-14 Pfizer Inibidores de cgmp pde5 de pirazolopirimidinona para tratamento da disfunção sexual
DE19942474A1 (de) 1999-09-06 2001-03-15 Merck Patent Gmbh Pyrazolo[4,3-d]pyrimidine
TWI265925B (en) 1999-10-11 2006-11-11 Pfizer Pyrazolo[4,3-d]pyrimidin-7-ones useful in inhibiting type 5 cyclic guanosine 3',5'-monophosphate phosphodiesterases(cGMP PDE5), process and intermediates for their preparation, their uses and composition comprising them
HK1049834A1 (zh) 1999-10-11 2003-05-30 辉瑞大药厂 用作磷酸二酯酶抑制剂的5-(2-取代的-5-杂环基磺酰基吡啶-3-基)-二氢吡唑并[4,3-d]嘧啶-7-酮类化合物
DE10031584A1 (de) 2000-06-29 2002-01-10 Merck Patent Gmbh 5-Aminoalkyl-pyrazolo[4,3-d]pyrimidine
PT1305314E (pt) 2000-07-28 2005-04-29 Pfizer Agente terapeutico cristalino
ATE478872T1 (de) * 2002-03-28 2010-09-15 Ustav Ex Botan Av Cr V V I I O Pyrazoloä4,3-düpyrimidine, verfahren zu ihrer herstellung und therapeutische anwendung
OA13050A (en) 2003-04-29 2006-11-10 Pfizer Ltd 5,7-diaminopyrazolo [4,3-D] pyrimidines useful in the treatment of hypertension.
US7572799B2 (en) * 2003-11-24 2009-08-11 Pfizer Inc Pyrazolo[4,3-d]pyrimidines as Phosphodiesterase Inhibitors
GB0327323D0 (en) 2003-11-24 2003-12-31 Pfizer Ltd Novel pharmaceuticals
GB0327319D0 (en) * 2003-11-24 2003-12-24 Pfizer Ltd Novel pharmaceuticals
CA2562251C (en) 2004-04-07 2009-04-28 Pfizer Inc. Pyrazolo'4,3-d pyrimidines
EP1809632A2 (en) 2004-10-28 2007-07-25 Pharmacia & Upjohn Company LLC Pyrazolo[4,3-d]pyrimidine derivatives useful as pde-5 inhibitors

Similar Documents

Publication Publication Date Title
JP2006316058A5 (https=)
CA2608018A1 (en) Anhydrous crystalline forms of n-[1-(2-ethoxyethyl)-5-(n-ethyl-n-methylamino)-7-(4-methylpyridin-2-yl-amino)-1h-pyrazolo[4,3-d]pyrimidine-3-carbonyl]methanesulfonamide
ES2299501T3 (es) Compuestos heterociclicos utiles como inhibidores de tirosina-quinasas.
JP2014518266A5 (https=)
IL210071A (en) Derivatives of {3– (pyrid – 2 – illmethyl) –3 h– [1, 2, 3] triazolo [4, 5 – d] pyrimidine-5-amine}, their pharmaceutical preparations and their use in drug preparation
NZ601754A (en) Pyrrolopyrimidine compounds as inhibitors of cdk4/6
NZ591712A (en) Imidazopyridazinecarbonitriles useful as kinase inhibitors
JP2019501865A5 (https=)
FI2134702T4 (fi) 6-[2-(metyylikarbamoyyli)fenyylisulfanyyli]-3-E-[2-(pyridiini-2-yyli)etenyyli]indatsolin kidemuotoja jotka soveltuvat nisäkkäiden poikkeavan solukasvun hoitamiseen
JP2012502067A5 (https=)
MX2007006497A (es) Nuevos derivados de pirrolo [3,2-d] pirimidin-4-ona y su uso en terapia.
JP2016539156A5 (https=)
JP2009537498A5 (https=)
RU2015132371A (ru) Твердые формы селективного ингибитора CDK4/6
AU2016298962B2 (en) Compounds and pharmaceutical composition associated with ubiquitination-proteasome system
WO2006130160A3 (en) Furanopyridine derivatives as ack1 and lck modulators
RU2018101363A (ru) Кристаллическая форма свободного основания лорлатиниба
JP2012512158A5 (https=)
JP2017039702A5 (https=)
RU2022109286A (ru) Кристаллическая форма гидрата свободного основания лорлатиниба
FI3894411T3 (fi) 7-fenoksi-n-(3-atsabisyklo[3.2.1]oktan-8-yyli)-6,7-dihydro-5h-pyrrolo[1,2-b][1,2,4]triatsoli-2-amiinijohdannaisia ja niihin liittyviä yhdisteitä gammasekretaasin modulaattoreina alzheimerin taudin hoitoon
JP2020524148A (ja) 置換5−シアノインドール化合物及びその使用
JP2021515015A5 (https=)
JP2007527913A5 (https=)
WO2004041794A8 (en) Antiinflammatory 3-arylthio-3-thiazolyl-alkylamines