JP2014015483A5 - - Google Patents

Download PDF

Info

Publication number
JP2014015483A5
JP2014015483A5 JP2013219880A JP2013219880A JP2014015483A5 JP 2014015483 A5 JP2014015483 A5 JP 2014015483A5 JP 2013219880 A JP2013219880 A JP 2013219880A JP 2013219880 A JP2013219880 A JP 2013219880A JP 2014015483 A5 JP2014015483 A5 JP 2014015483A5
Authority
JP
Japan
Prior art keywords
compound
formula
compound according
complex
triethylenediamine
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
JP2013219880A
Other languages
English (en)
Japanese (ja)
Other versions
JP2014015483A (ja
JP6148594B2 (ja
Filing date
Publication date
Application filed filed Critical
Publication of JP2014015483A publication Critical patent/JP2014015483A/ja
Publication of JP2014015483A5 publication Critical patent/JP2014015483A5/ja
Application granted granted Critical
Publication of JP6148594B2 publication Critical patent/JP6148594B2/ja
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

JP2013219880A 2007-08-02 2013-10-23 E1活性化酵素阻害剤の合成のためのプロセス Expired - Fee Related JP6148594B2 (ja)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US96300807P 2007-08-02 2007-08-02
US60/963,008 2007-08-02
US6237808P 2008-01-25 2008-01-25
US61/062,378 2008-01-25

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
JP2010519947A Division JP5479336B2 (ja) 2007-08-02 2008-08-01 E1活性化酵素阻害剤の合成のためのプロセス

Related Child Applications (1)

Application Number Title Priority Date Filing Date
JP2014215250A Division JP2015025009A (ja) 2007-08-02 2014-10-22 E1活性化酵素阻害剤の合成のためのプロセス

Publications (3)

Publication Number Publication Date
JP2014015483A JP2014015483A (ja) 2014-01-30
JP2014015483A5 true JP2014015483A5 (cg-RX-API-DMAC7.html) 2014-12-04
JP6148594B2 JP6148594B2 (ja) 2017-06-14

Family

ID=40225413

Family Applications (3)

Application Number Title Priority Date Filing Date
JP2010519947A Expired - Fee Related JP5479336B2 (ja) 2007-08-02 2008-08-01 E1活性化酵素阻害剤の合成のためのプロセス
JP2013219880A Expired - Fee Related JP6148594B2 (ja) 2007-08-02 2013-10-23 E1活性化酵素阻害剤の合成のためのプロセス
JP2014215250A Pending JP2015025009A (ja) 2007-08-02 2014-10-22 E1活性化酵素阻害剤の合成のためのプロセス

Family Applications Before (1)

Application Number Title Priority Date Filing Date
JP2010519947A Expired - Fee Related JP5479336B2 (ja) 2007-08-02 2008-08-01 E1活性化酵素阻害剤の合成のためのプロセス

Family Applications After (1)

Application Number Title Priority Date Filing Date
JP2014215250A Pending JP2015025009A (ja) 2007-08-02 2014-10-22 E1活性化酵素阻害剤の合成のためのプロセス

Country Status (14)

Country Link
US (3) US8933225B2 (cg-RX-API-DMAC7.html)
EP (4) EP2540726B1 (cg-RX-API-DMAC7.html)
JP (3) JP5479336B2 (cg-RX-API-DMAC7.html)
KR (2) KR101925902B1 (cg-RX-API-DMAC7.html)
CN (3) CN106243111B (cg-RX-API-DMAC7.html)
AU (1) AU2008305767B2 (cg-RX-API-DMAC7.html)
CA (2) CA2949336C (cg-RX-API-DMAC7.html)
ES (4) ES2655028T3 (cg-RX-API-DMAC7.html)
IL (2) IL203590A (cg-RX-API-DMAC7.html)
MX (1) MX2010001126A (cg-RX-API-DMAC7.html)
RU (2) RU2553476C2 (cg-RX-API-DMAC7.html)
TW (2) TWI426077B (cg-RX-API-DMAC7.html)
WO (1) WO2009042013A1 (cg-RX-API-DMAC7.html)
ZA (1) ZA201000482B (cg-RX-API-DMAC7.html)

Families Citing this family (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA2949336C (en) 2007-08-02 2018-11-06 Lei Zhu Process for the synthesis of e1 activating enzyme inhibitors
UA108986C2 (uk) 2009-05-14 2015-07-10 Мілленніум Фармасьютікалз, Інк. Кристалічна форма гідрохлориду ((1s,2s,4r)-4-{4-[(1s)-2,3-дигідро-1h-інден-1-іламіно]-7h-піроло[2,3-d]піримідин-7іл}-2-гідроксициклопентил)метилсульфамату (варіанти)
US20120115892A1 (en) * 2010-11-05 2012-05-10 Millennium Pharmaceuticals, Inc. Administration of nedd8-activating enzyme inhibitor
MX352963B (es) 2012-02-17 2017-12-15 Millennium Pharm Inc Inhibidores de pirazolopirimidinilo en enzima activadora de ubiquitina.
CN104072381B (zh) * 2013-03-26 2017-04-12 安徽贝克联合制药有限公司 光学纯氨基醇盐酸盐的制备方法
WO2014186388A2 (en) 2013-05-14 2014-11-20 Millennium Pharmaceutcals, Inc. Administration of nedd8-activating enzyme inhibitor and chemotherapeutic agents
CN106999479B (zh) 2014-07-01 2021-07-16 米伦纽姆医药公司 可用作sumo活化酶抑制剂的杂芳基化合物
US10335411B2 (en) 2014-10-29 2019-07-02 Millennium Pharmaceuticals, Inc. Administration of ubiquitin-activating enzyme inhibitor and radiation
CN104974051A (zh) * 2015-06-30 2015-10-14 苏州开元民生科技股份有限公司 (1S,4R)-cis-4-氨基-2-环戊烯-1-甲醇盐酸盐的合成方法
CN106854208B (zh) * 2016-11-25 2019-04-09 成都柏睿泰生物科技有限公司 肿瘤抑制剂mln4924的合成方法
EP3684363A4 (en) 2017-09-21 2021-05-12 Millennium Pharmaceuticals, Inc. CO-CRYSTALLINE FORMS OF ((1S, 2S, 4R) -4- {4 - [(1S) -2,3-DIHYDRO-1H-INDÉN-1-YLAMINO] -7H-PYRROLO [2,3-D] PYRIMIDIN -7-YL} -2-HYDROXYCYCLOPENTYL) METHYLSULFAMATE, THEIR FORMULATIONS AND USES
KR102018341B1 (ko) * 2018-06-21 2019-09-04 성균관대학교산학협력단 RNF170 및 pUL50을 유효성분으로 포함하는 암 예방 또는 치료용 약학적 조성물
EP3947388A4 (en) 2019-04-02 2022-12-21 Aligos Therapeutics, Inc. PRMT5 TARGETING COMPOUNDS
DE112021002937T5 (de) * 2020-05-26 2023-03-30 Sony Semiconductor Solutions Corporation Entfernungsmessvorrichtung
WO2022112951A1 (en) 2020-11-25 2022-06-02 Takeda Pharmaceutical Company Limited Solid state forms of hydrochloride salt of ((1s,2s,4r)-4-{4-[(1s)-2,3-dihydro-1h-inden-1-ylamino]-7h-pyrrolo[2,3-d]pyrimidin-7-yl}-2-hydroxycyclopentyl)methyl sulfamate

Family Cites Families (31)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4138433A (en) * 1975-06-26 1979-02-06 Hoechst Aktiengesellschaft Process for preparing 1,2-oxa-phospholanes
US4081455A (en) * 1976-06-02 1978-03-28 Pfizer Inc. 6-Amino-2,2-dimethyl-3-cyanopenams
US4803272A (en) * 1987-02-24 1989-02-07 E. I. Du Pont De Nemours And Company S-modified adenosyl-1,8-diamino-3-thiooctane derivatives
US4927830A (en) 1988-04-08 1990-05-22 The Regents Of The University Of Michigan Acyclic pyrrolo[2,3-D]pyrimidine analogs as antiviral agents
GB9204015D0 (en) * 1992-02-25 1992-04-08 Wellcome Found Therapeutic nucleosides
GB9205071D0 (en) 1992-03-09 1992-04-22 Wellcome Found Therapeutic nucleosides
AU3692895A (en) 1994-09-09 1996-03-27 Regents Of The University Of Michigan, The Antiviral nucleoside analogues containing a substituted benzimidazole base attached to a carbocyclic ring
US5912356A (en) 1995-09-11 1999-06-15 Glaxo Wellcome Inc. Antiviral nucleoside analogues containing a substituted benzimidazole base attached to a carbocyclic ring
CN1282316A (zh) 1997-12-17 2001-01-31 生物晶体药品股份有限公司 用作神经氨酸酶抑制剂的取代环戊烷和环戊烯化合物
US6878716B1 (en) 1998-06-02 2005-04-12 Osi Pharmaceuticals, Inc. Compounds specific to adenosine A1 receptor and uses thereof
US6379552B1 (en) 1998-07-06 2002-04-30 Toray Industries, Inc. Method for resolving optical isomers
JP2000290201A (ja) * 1998-07-06 2000-10-17 Toray Ind Inc 光学異性体の分割方法
GB9907082D0 (en) 1999-03-26 1999-05-19 Chirotech Technology Ltd The preparation of carboxylic acid derivatives
CO5261573A1 (es) * 1999-11-19 2003-03-31 Novartis Ag Derivados de benzoxa y bezotiazol, compuesto y composicion farmaceutica que los contiene y proceso para la preparacion de la mencionada composicion
JP2003516408A (ja) 1999-12-10 2003-05-13 グラクソ グループ リミテッド 抗ウィルス薬としての(1R,シス)−4−[4−アミノ−7H−ピロロ(2,3−d)ピリミジン−7−イル]−2−シクロペンテン−1−メタノール類縁物
AU1929801A (en) 1999-12-16 2001-06-25 Alcon Inc. Inhibitors of adenosine kinase for the treatment of optic nerve and retinal damage
JP4347696B2 (ja) 2001-12-21 2009-10-21 ステリックス リミティド アルコール及びフェノールのスルファモイル化のための産業的適用方法
WO2003106477A1 (en) * 2002-06-01 2003-12-24 Isis Pharmaceuticals, Inc. Oligomeric compounds that include carbocyclic nucleosides and their use in gene modulation
WO2003105770A2 (en) 2002-06-17 2003-12-24 Merck & Co., Inc. Carbocyclic nucleoside derivatives as inhibitors of rna-dependent rna viral polymerase
GB0225986D0 (en) * 2002-11-07 2002-12-11 Astrazeneca Ab Chemical compounds
US7429596B2 (en) 2003-06-20 2008-09-30 The Regents Of The University Of California 1H-pyrrolo [2,3-D] pyrimidine derivatives and methods of use thereof
US7338957B2 (en) * 2003-08-28 2008-03-04 Irm Llc Compounds and compositions as protein kinase inhibitors
WO2005095357A2 (en) 2004-03-30 2005-10-13 Taisho Pharmaceutical Co., Ltd. Pyrimidine derivatives and methods of treatment related to the use thereof
WO2005097738A1 (ja) * 2004-04-06 2005-10-20 Dainippon Sumitomo Pharma Co., Ltd. 新規スルホンアミド誘導体
CA2471666C (en) 2004-06-18 2009-10-13 Apotex Pharmachem Inc. An improved process for the preparation of oxcarbazepine and related intermediates
SI1848718T1 (sl) * 2005-02-04 2012-12-31 Millennium Pharmaceuticals, Inc. Inhibitorji E1 aktivacijskih enzimov
ES2593433T3 (es) * 2006-02-02 2016-12-09 Millennium Pharmaceuticals, Inc. Inhibidores de las enzimas activadoras E1
DE602007009998D1 (de) * 2006-08-08 2010-12-02 Millennium Pharm Inc Heteroarylverbindungen als hemmer der e1-aktivierenden enzyme
US8008307B2 (en) 2006-08-08 2011-08-30 Millennium Pharmaceuticals, Inc. Heteroaryl compounds useful as inhibitors of E1 activating enzymes
CA2949336C (en) 2007-08-02 2018-11-06 Lei Zhu Process for the synthesis of e1 activating enzyme inhibitors
UA108986C2 (uk) 2009-05-14 2015-07-10 Мілленніум Фармасьютікалз, Інк. Кристалічна форма гідрохлориду ((1s,2s,4r)-4-{4-[(1s)-2,3-дигідро-1h-інден-1-іламіно]-7h-піроло[2,3-d]піримідин-7іл}-2-гідроксициклопентил)метилсульфамату (варіанти)

Similar Documents

Publication Publication Date Title
JP2014015483A5 (cg-RX-API-DMAC7.html)
JP2016512563A5 (cg-RX-API-DMAC7.html)
JP2017509689A5 (cg-RX-API-DMAC7.html)
JP2012041365A5 (cg-RX-API-DMAC7.html)
PE20161475A1 (es) Pirazolopiridinas y pirazolopirimidinas
JP2013529196A5 (cg-RX-API-DMAC7.html)
JP2009542613A5 (cg-RX-API-DMAC7.html)
JP2016525135A5 (cg-RX-API-DMAC7.html)
MX363327B (es) Materiales zeoliticos de tipo cha y metodos para su preparacion usando compuestos de cicloalquilamonio.
JP2017535555A5 (cg-RX-API-DMAC7.html)
JP2014500870A5 (cg-RX-API-DMAC7.html)
AR068057A1 (es) Esteres de 1-fenil-2-(3,5-dicloro)-piridina, metodo de preparacion de los mismos, composiciones farmaceuticas que los contienen y usos de los mismos para el tratamiento de enfermedades del tracto respiratorio.
JP2017535614A5 (cg-RX-API-DMAC7.html)
JP2015520143A5 (cg-RX-API-DMAC7.html)
JP2011511835A5 (cg-RX-API-DMAC7.html)
MY165730A (en) Process for preparing heterocyclic compounds including trans-7-oxo-6-(sulphooxy)-1,6-diazabicyclo[3,2,1]octane-2-carboxamide and salts thereof
JP2018531941A5 (cg-RX-API-DMAC7.html)
MY150289A (en) Derivatives of indole-2-carboxamides and of azaindole-2-carboxamides substituted with a silanyl group, preparation thereof and therapeutic use thereof
JP2017504635A5 (cg-RX-API-DMAC7.html)
WO2010007318A3 (fr) NOUVEAUX DERIVES IMIDAZO[1,2-a]PYRIMIDINE, LEUR PROCEDE DE PREPARATION, LEUR APPLICATION A TITRE DE MEDICAMENTS, COMPOSITIONS PHARMACEUTIQUES ET NOUVELLE UTILISATION NOTAMMENT COMME INHIBITEURS DE MET
JP2017503030A5 (cg-RX-API-DMAC7.html)
JP2016513122A5 (cg-RX-API-DMAC7.html)
DE602006010775D1 (de) Verfahren zur Herstellung von Siliziumscheiben
EP3676249C0 (en) PROCESS FOR THE PREPARATION OF ARYLSULFONYLPROPENENITRILES BY PHOTOCATALYTIC REACTIONS
AR074866A1 (es) 2-amino-pirimidinas 4,6-disustituidas como modulador del receptor h4 de histamina