JP2014015483A5 - - Google Patents
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- 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
Links
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 (enExample) | 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 (enExample) |
| EP (4) | EP2178880B1 (enExample) |
| JP (3) | JP5479336B2 (enExample) |
| KR (2) | KR101925902B1 (enExample) |
| CN (3) | CN101868461B (enExample) |
| AU (1) | AU2008305767B2 (enExample) |
| CA (2) | CA2695193C (enExample) |
| ES (4) | ES2655028T3 (enExample) |
| IL (2) | IL203590A (enExample) |
| MX (1) | MX2010001126A (enExample) |
| RU (2) | RU2015108944A (enExample) |
| TW (2) | TWI426077B (enExample) |
| WO (1) | WO2009042013A1 (enExample) |
| ZA (1) | ZA201000482B (enExample) |
Families Citing this family (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR101925902B1 (ko) | 2007-08-02 | 2018-12-06 | 밀레니엄 파머슈티컬스 인코퍼레이티드 | E1 활성화 효소 억제제의 합성 방법 |
| SG10201402148SA (en) | 2009-05-14 | 2014-07-30 | Millennium Pharm Inc | 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 |
| JP2013541587A (ja) * | 2010-11-05 | 2013-11-14 | ミレニアム ファーマシューティカルズ, インコーポレイテッド | Nedd8活性化酵素阻害剤の投与 |
| EP3173413B1 (en) | 2012-02-17 | 2019-05-01 | Millennium Pharmaceuticals, Inc. | Pyrazolopyrimidinyl inhibitors of ubiquitin-activating enzyme |
| 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 |
| JP6556701B2 (ja) | 2013-05-14 | 2019-08-07 | ミレニアム ファーマシューティカルズ, インコーポレイテッドMillennium Pharmaceuticals, Inc. | Nedd8活性化酵素阻害剤及び化学療法剤の投与 |
| EP3901159A1 (en) | 2014-07-01 | 2021-10-27 | Millennium Pharmaceuticals, Inc. | Heteroaryl compounds useful as inhibitors of sumo activating enzyme |
| TW201628621A (zh) | 2014-10-29 | 2016-08-16 | 千禧製藥公司 | 泛素活化酶抑制劑及輻射之施用 |
| 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 |
| WO2019060536A1 (en) | 2017-09-21 | 2019-03-28 | Millennium Pharmaceuticals, Inc. | CO-CRYSTALLINE FORMS OF ((1S, 2S, 4R) -4- {4 - [(1S) -2,3-DIHYDRO-1H-INDEN-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 |
| CN114072407A (zh) | 2019-04-02 | 2022-02-18 | 阿里戈斯治疗公司 | 靶向prmt5的化合物 |
| US12520610B2 (en) * | 2020-05-26 | 2026-01-06 | Sony Semiconductor Solutions Corporation | Ranging device |
| US20240368165A1 (en) | 2020-11-25 | 2024-11-07 | 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)
| 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 |
| CN1164855A (zh) | 1994-09-09 | 1997-11-12 | 惠尔康基金会集团公司 | 含有连接碳环的取代苯并咪唑碱的抗病毒核苷类似物 |
| US5912356A (en) * | 1995-09-11 | 1999-06-15 | Glaxo Wellcome Inc. | Antiviral nucleoside analogues containing a substituted benzimidazole base attached to a carbocyclic ring |
| SI1040094T1 (sl) * | 1997-12-17 | 2009-10-31 | Biocryst Pharm Inc | Substituirane ciklopentanske in ciklopentenske spojine, uporabne kot inhibitorji nevraminidaze |
| 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 |
| EP1235834A1 (en) | 1999-12-10 | 2002-09-04 | Glaxo Group Limited | (1r,cis)-4-(4-amino-7h-pyrr0l0[2,3- i(d)]pyrimidine-7-yl)-2-cyclopentene-1-methanol derivatives as antiviral |
| EP1250128A2 (en) * | 1999-12-16 | 2002-10-23 | Alcon, Inc. | Inhibitors of adenosine kinase for the treatment of optic nerve and retinal damage |
| ATE317369T1 (de) * | 2001-12-21 | 2006-02-15 | Schering Ag | Industriell anwendbares verfahren zur sulfamoylation von alkoholen und von phenolen |
| AU2003248708A1 (en) * | 2002-06-17 | 2003-12-31 | Isis Pharmaceuticals, Inc. | Oligomeric compounds that include carbocyclic nucleosides and their use in gene modulation |
| JP2005533777A (ja) | 2002-06-17 | 2005-11-10 | メルク エンド カムパニー インコーポレーテッド | Rna抗ウイルス剤としての炭素環ヌクレオシドアナログ |
| 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 |
| RU2373197C2 (ru) * | 2004-03-30 | 2009-11-20 | Тайсо Фармасьютикал Ко., Лтд. | Пиримидиновые производные, обладающие активностью в отношении мсн |
| 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 |
| AU2006210422B2 (en) * | 2005-02-04 | 2012-09-13 | Takeda Pharmaceutical Company Limited | Inhibitors of E1 activating enzymes |
| CN106008512B (zh) * | 2006-02-02 | 2019-03-12 | 千禧药品公司 | E1活化酶抑制剂 |
| HRP20110017T1 (hr) | 2006-08-08 | 2011-02-28 | Millennium Pharmaceuticals | Spojevi heteroarila korisni kao inhibitori e1 aktivirajućih enzima |
| US8008307B2 (en) * | 2006-08-08 | 2011-08-30 | Millennium Pharmaceuticals, Inc. | Heteroaryl compounds useful as inhibitors of E1 activating enzymes |
| KR101925902B1 (ko) | 2007-08-02 | 2018-12-06 | 밀레니엄 파머슈티컬스 인코퍼레이티드 | E1 활성화 효소 억제제의 합성 방법 |
| SG10201402148SA (en) * | 2009-05-14 | 2014-07-30 | Millennium Pharm Inc | 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 |
-
2008
- 2008-08-01 KR KR1020157014228A patent/KR101925902B1/ko not_active Expired - Fee Related
- 2008-08-01 CA CA2695193A patent/CA2695193C/en not_active Expired - Fee Related
- 2008-08-01 RU RU2015108944/04A patent/RU2015108944A/ru not_active Application Discontinuation
- 2008-08-01 KR KR1020107004735A patent/KR20100066475A/ko not_active Ceased
- 2008-08-01 TW TW097129447A patent/TWI426077B/zh not_active IP Right Cessation
- 2008-08-01 EP EP08832973.5A patent/EP2178880B1/en active Active
- 2008-08-01 ES ES08832973.5T patent/ES2655028T3/es active Active
- 2008-08-01 ES ES12172365.4T patent/ES2684309T3/es active Active
- 2008-08-01 CN CN2008801015257A patent/CN101868461B/zh not_active Expired - Fee Related
- 2008-08-01 ES ES12172364T patent/ES2758027T3/es active Active
- 2008-08-01 AU AU2008305767A patent/AU2008305767B2/en not_active Ceased
- 2008-08-01 JP JP2010519947A patent/JP5479336B2/ja not_active Expired - Fee Related
- 2008-08-01 EP EP12172364.7A patent/EP2540726B1/en active Active
- 2008-08-01 EP EP12172365.4A patent/EP2540727B1/en active Active
- 2008-08-01 CN CN201610622354.9A patent/CN106243111B/zh not_active Expired - Fee Related
- 2008-08-01 TW TW102143875A patent/TW201434851A/zh unknown
- 2008-08-01 CN CN201310356726.4A patent/CN103483342B/zh not_active Expired - Fee Related
- 2008-08-01 EP EP12172363.9A patent/EP2546256B1/en active Active
- 2008-08-01 CA CA2949336A patent/CA2949336C/en not_active Expired - Fee Related
- 2008-08-01 MX MX2010001126A patent/MX2010001126A/es active IP Right Grant
- 2008-08-01 WO PCT/US2008/009338 patent/WO2009042013A1/en not_active Ceased
- 2008-08-01 ES ES12172363T patent/ES2757928T3/es active Active
- 2008-08-01 RU RU2010107471/04A patent/RU2553476C2/ru active
- 2008-08-01 US US12/221,399 patent/US8933225B2/en not_active Expired - Fee Related
-
2010
- 2010-01-21 ZA ZA2010/00482A patent/ZA201000482B/en unknown
- 2010-01-28 IL IL203590A patent/IL203590A/en active IP Right Grant
-
2013
- 2013-10-23 JP JP2013219880A patent/JP6148594B2/ja not_active Expired - Fee Related
-
2014
- 2014-10-22 JP JP2014215250A patent/JP2015025009A/ja active Pending
- 2014-11-25 US US14/552,883 patent/US9802938B2/en not_active Expired - Fee Related
-
2017
- 2017-03-23 IL IL251372A patent/IL251372B/en active IP Right Grant
- 2017-09-22 US US15/713,293 patent/US10745404B2/en not_active Expired - Fee Related
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