JP2013512954A - 置換インダゾール及びアザインダゾール化合物の生成に有効な中間体の合成方法 - Google Patents
置換インダゾール及びアザインダゾール化合物の生成に有効な中間体の合成方法 Download PDFInfo
- Publication number
- JP2013512954A JP2013512954A JP2012543154A JP2012543154A JP2013512954A JP 2013512954 A JP2013512954 A JP 2013512954A JP 2012543154 A JP2012543154 A JP 2012543154A JP 2012543154 A JP2012543154 A JP 2012543154A JP 2013512954 A JP2013512954 A JP 2013512954A
- Authority
- JP
- Japan
- Prior art keywords
- formula
- metal catalyst
- hydrogen
- compound
- compounds
- 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.)
- Pending
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/62—Oxygen or sulfur atoms
- C07D213/70—Sulfur atoms
- C07D213/71—Sulfur atoms to which a second hetero atom is attached
-
- 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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
-
- 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]
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
- B01J23/38—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals
- B01J23/40—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals of the platinum group metals
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Epidemiology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Rheumatology (AREA)
- Pain & Pain Management (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Catalysts (AREA)
- Plural Heterocyclic Compounds (AREA)
- Steroid Compounds (AREA)
- Pyridine Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US26753809P | 2009-12-08 | 2009-12-08 | |
| US61/267,538 | 2009-12-08 | ||
| PCT/US2010/058594 WO2011071730A1 (en) | 2009-12-08 | 2010-12-01 | Process for synthesis of intermediates useful for making substituted indazole and azaindazole compounds |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JP2013512954A true JP2013512954A (ja) | 2013-04-18 |
Family
ID=43416915
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2012543154A Pending JP2013512954A (ja) | 2009-12-08 | 2010-12-01 | 置換インダゾール及びアザインダゾール化合物の生成に有効な中間体の合成方法 |
Country Status (17)
| Country | Link |
|---|---|
| US (1) | US20110137042A1 (enExample) |
| EP (1) | EP2509952A1 (enExample) |
| JP (1) | JP2013512954A (enExample) |
| KR (1) | KR20120101667A (enExample) |
| CN (1) | CN102596908A (enExample) |
| AR (1) | AR079324A1 (enExample) |
| AU (1) | AU2010328480A1 (enExample) |
| BR (1) | BR112012013582A2 (enExample) |
| CA (1) | CA2782384A1 (enExample) |
| CL (1) | CL2012001300A1 (enExample) |
| EA (1) | EA201200820A1 (enExample) |
| IL (1) | IL219274A0 (enExample) |
| IN (1) | IN2012DN05081A (enExample) |
| MX (1) | MX2012006524A (enExample) |
| PH (1) | PH12012501153A1 (enExample) |
| TW (1) | TW201144282A (enExample) |
| WO (1) | WO2011071730A1 (enExample) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2722923C (en) | 2008-04-29 | 2016-08-02 | Boehringer Ingelheim International Gmbh | Indazole compounds as ccr1 receptor antagonists |
| EP2297112B1 (en) * | 2008-05-06 | 2013-04-03 | Boehringer Ingelheim International GmbH | Pyrazole compounds as ccr1 antagonists |
| AP2739A (en) | 2008-09-26 | 2013-09-30 | Boehringer Ingelheim Int | Azaindazole compounds as CCRI receptor antagonists |
| PL2491028T3 (pl) | 2009-10-21 | 2014-05-30 | Boehringer Ingelheim Int | Związki indazolowe i pirazolopirydynowe jako antagoniści receptora CCR1 |
| EP2493875B1 (en) | 2009-10-27 | 2014-08-06 | Boehringer Ingelheim International GmbH | Heterocyclic compounds as ccr1 receptor antagonists |
| US8871786B2 (en) | 2010-04-30 | 2014-10-28 | Boehringer Ingelheim International Gmbh | Azaindazole amide compounds as CCR1 receptor antagonists |
| US8546442B2 (en) | 2010-12-23 | 2013-10-01 | Boehringer Ingelheim International Gmbh | Pyrazolopiperidine compounds as CCR1 receptor antagonists |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2007505902A (ja) * | 2003-09-18 | 2007-03-15 | アストラゼネカ・アクチエボラーグ | 好中球エラスターゼ阻害剤としての2−ピリドン誘導体およびその使用 |
| JP2007505901A (ja) * | 2003-09-18 | 2007-03-15 | アストラゼネカ・アクチエボラーグ | 好中球エラスターゼ阻害剤としての2−ピリドン誘導体およびそれらの使用 |
| WO2010036632A1 (en) * | 2008-09-26 | 2010-04-01 | Boehringer Ingelheim International Gmbh | Azaindazole compounds as ccr1 receptor antagonists |
Family Cites Families (44)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5242931A (en) * | 1988-06-09 | 1993-09-07 | Kyowa Hakko Kogyo Co., Ltd. | Tricyclic compounds as TXA2 antagonists |
| US4999363A (en) * | 1988-06-09 | 1991-03-12 | Kyowa Hakko Kogyo Co., Ltd. | Tricyclic compounds |
| US5750542A (en) * | 1993-09-28 | 1998-05-12 | Pfizer | Benzisoxazole and benzisothizole derivatives as cholinesterase inhibitors |
| US5612360A (en) * | 1992-06-03 | 1997-03-18 | Eli Lilly And Company | Angiotensin II antagonists |
| WO1994001415A1 (fr) * | 1992-07-03 | 1994-01-20 | Kumiai Chemical Industry Co., Ltd. | Derive heterocyclique condense et desherbant |
| GB9304919D0 (en) * | 1993-03-10 | 1993-04-28 | Celltech Ltd | Chemical compounds |
| EP0657450B1 (en) * | 1993-06-25 | 1998-09-09 | KumaiI Chemical Industry Co., Ltd. | Indazolesulfonylurea derivative, use thereof, and intermediate for production thereof |
| CA2207201A1 (en) * | 1994-12-06 | 1996-06-13 | Caroline Henry | Azetidine, pyrrolidine and piperidine derivatives as 5ht1 receptor agonists |
| GB9519563D0 (en) * | 1995-09-26 | 1995-11-29 | Merck Sharp & Dohme | Therapeutic agents |
| GB9523583D0 (en) * | 1995-11-17 | 1996-01-17 | Merck Sharp & Dohme | Therapeutic agents |
| US5760028A (en) * | 1995-12-22 | 1998-06-02 | The Dupont Merck Pharmaceutical Company | Integrin receptor antagonists |
| GB9615449D0 (en) * | 1996-07-23 | 1996-09-04 | Merck Sharp & Dohme | Therapeutic agents |
| NZ503995A (en) * | 1997-11-04 | 2003-02-28 | Pfizer Prod Inc | Indazole compounds, and pharmaceutical compositions and uses thereof, based on indazole bioisostere replacement of catechol in PDE4 inhibitors |
| US6331640B1 (en) * | 1998-10-13 | 2001-12-18 | Hoffmann-La Roche Inc. | Diaminopropionic acid derivatives |
| CA2375920A1 (en) * | 1999-06-14 | 2000-12-21 | Eli Lilly And Company | Compounds |
| AU5895500A (en) * | 1999-06-29 | 2001-01-31 | Cor Therapeutics, Inc. | Novel indazole peptidomimetics as thrombin receptor antagonists |
| GB0030303D0 (en) * | 2000-12-13 | 2001-01-24 | Lilly Co Eli | Compounds |
| GB0030304D0 (en) * | 2000-12-13 | 2001-01-24 | Lilly Co Eli | Compounds |
| GB0030305D0 (en) * | 2000-12-13 | 2001-01-24 | Lilly Co Eli | Compounds |
| GB0030306D0 (en) * | 2000-12-13 | 2001-01-24 | Lilly Co Eli | Compounds |
| US7211594B2 (en) * | 2000-07-31 | 2007-05-01 | Signal Pharmaceuticals, Llc | Indazole compounds and compositions thereof as JNK inhibitors and for the treatment of diseases associated therewith |
| US20050009876A1 (en) * | 2000-07-31 | 2005-01-13 | Bhagwat Shripad S. | Indazole compounds, compositions thereof and methods of treatment therewith |
| US7058826B2 (en) * | 2000-09-27 | 2006-06-06 | Amphus, Inc. | System, architecture, and method for logical server and other network devices in a dynamically configurable multi-server network environment |
| US20020052373A1 (en) * | 2000-10-26 | 2002-05-02 | Zorn Stevin H. | Combination treatment for dementia or cognitive deficits associated with alzheimer's disease and parkinson's disease |
| US6995162B2 (en) * | 2001-01-12 | 2006-02-07 | Amgen Inc. | Substituted alkylamine derivatives and methods of use |
| ATE455104T1 (de) * | 2001-11-01 | 2010-01-15 | Icagen Inc | Pyrazolamide zur anwendung in der behandlung von schmerz |
| TW200406385A (en) * | 2002-05-31 | 2004-05-01 | Eisai Co Ltd | Pyrazole compound and pharmaceutical composition containing the same |
| TW200500341A (en) * | 2002-11-12 | 2005-01-01 | Astrazeneca Ab | Novel compounds |
| SE0203825D0 (sv) * | 2002-12-20 | 2002-12-20 | Astrazeneca Ab | Novel fused heterocycles and uses thereof |
| MXPA05009595A (es) * | 2003-03-12 | 2005-11-04 | Celgene Corp | Compuestos 7-amino-isoindolilo y sus usos farmaceuticos. |
| US7129264B2 (en) * | 2003-04-16 | 2006-10-31 | Bristol-Myers Squibb Company | Biarylmethyl indolines and indoles as antithromboembolic agents |
| US20040220170A1 (en) * | 2003-05-01 | 2004-11-04 | Atkinson Robert N. | Pyrazole-amides and sulfonamides as sodium channel modulators |
| EP1664052B1 (en) * | 2003-08-15 | 2009-02-18 | AstraZeneca AB | Fused heterocycles as inhibitors of glutamate racemase (muri) |
| GB0504828D0 (en) * | 2005-03-09 | 2005-04-13 | Merck Sharp & Dohme | Therapeutic agents |
| PT1860941E (pt) * | 2005-03-16 | 2008-12-22 | Basf Se | Bifenil-n-(4-piridil)metilsulfonamidas |
| AU2006247136C1 (en) * | 2005-05-17 | 2020-01-16 | Bausch + Lomb Ireland Limited | Compositions and methods for treatment of eye disorders |
| JP5155864B2 (ja) * | 2005-09-01 | 2013-03-06 | イーライ リリー アンド カンパニー | 5−HT2C受容体アゴニストとしての6−アリールアルキルアミノ−2,3,4,5−テトラヒドロ−1H−ベンゾ[d]アゼピン |
| JP2009513677A (ja) * | 2005-10-25 | 2009-04-02 | スミスクライン・ビーチャム・コーポレイション | 化合物 |
| WO2007113226A1 (en) * | 2006-03-31 | 2007-10-11 | Novartis Ag | Organic compounds |
| PE20081775A1 (es) * | 2006-12-20 | 2008-12-18 | Bristol Myers Squibb Co | Compuestos macrociclicos como inhibidores del factor viia |
| GB0716292D0 (en) * | 2007-08-21 | 2007-09-26 | Biofocus Dpi Ltd | Imidazopyrazine compounds |
| CA2699631A1 (en) * | 2007-10-31 | 2009-05-07 | Nissan Chemical Industries, Ltd. | Pyridazinone compounds and p2x7 receptor inhibitors |
| CA2722923C (en) * | 2008-04-29 | 2016-08-02 | Boehringer Ingelheim International Gmbh | Indazole compounds as ccr1 receptor antagonists |
| EP2297112B1 (en) * | 2008-05-06 | 2013-04-03 | Boehringer Ingelheim International GmbH | Pyrazole compounds as ccr1 antagonists |
-
2010
- 2010-12-01 PH PH1/2012/501153A patent/PH12012501153A1/en unknown
- 2010-12-01 EA EA201200820A patent/EA201200820A1/ru unknown
- 2010-12-01 AU AU2010328480A patent/AU2010328480A1/en not_active Abandoned
- 2010-12-01 WO PCT/US2010/058594 patent/WO2011071730A1/en not_active Ceased
- 2010-12-01 BR BR112012013582A patent/BR112012013582A2/pt not_active IP Right Cessation
- 2010-12-01 IN IN5081DEN2012 patent/IN2012DN05081A/en unknown
- 2010-12-01 JP JP2012543154A patent/JP2013512954A/ja active Pending
- 2010-12-01 CA CA2782384A patent/CA2782384A1/en not_active Abandoned
- 2010-12-01 US US12/957,483 patent/US20110137042A1/en not_active Abandoned
- 2010-12-01 MX MX2012006524A patent/MX2012006524A/es not_active Application Discontinuation
- 2010-12-01 CN CN2010800504234A patent/CN102596908A/zh active Pending
- 2010-12-01 KR KR1020127014239A patent/KR20120101667A/ko not_active Withdrawn
- 2010-12-01 EP EP10787651A patent/EP2509952A1/en not_active Withdrawn
- 2010-12-07 AR ARP100104528A patent/AR079324A1/es unknown
- 2010-12-07 TW TW099142648A patent/TW201144282A/zh unknown
-
2012
- 2012-04-19 IL IL219274A patent/IL219274A0/en unknown
- 2012-05-18 CL CL2012001300A patent/CL2012001300A1/es unknown
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2007505902A (ja) * | 2003-09-18 | 2007-03-15 | アストラゼネカ・アクチエボラーグ | 好中球エラスターゼ阻害剤としての2−ピリドン誘導体およびその使用 |
| JP2007505901A (ja) * | 2003-09-18 | 2007-03-15 | アストラゼネカ・アクチエボラーグ | 好中球エラスターゼ阻害剤としての2−ピリドン誘導体およびそれらの使用 |
| WO2010036632A1 (en) * | 2008-09-26 | 2010-04-01 | Boehringer Ingelheim International Gmbh | Azaindazole compounds as ccr1 receptor antagonists |
Non-Patent Citations (1)
| Title |
|---|
| JPN6013062888; 第5版実験化学講座14 有機化合物の合成II , 2005, 352-356 * |
Also Published As
| Publication number | Publication date |
|---|---|
| CN102596908A (zh) | 2012-07-18 |
| KR20120101667A (ko) | 2012-09-14 |
| IL219274A0 (en) | 2012-06-28 |
| BR112012013582A2 (pt) | 2016-07-05 |
| TW201144282A (en) | 2011-12-16 |
| CL2012001300A1 (es) | 2012-09-07 |
| EP2509952A1 (en) | 2012-10-17 |
| IN2012DN05081A (enExample) | 2015-10-09 |
| AU2010328480A1 (en) | 2012-05-17 |
| PH12012501153A1 (en) | 2012-10-22 |
| US20110137042A1 (en) | 2011-06-09 |
| CA2782384A1 (en) | 2011-06-16 |
| EA201200820A1 (ru) | 2013-01-30 |
| WO2011071730A1 (en) | 2011-06-16 |
| MX2012006524A (es) | 2012-07-17 |
| AR079324A1 (es) | 2012-01-18 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP2013512954A (ja) | 置換インダゾール及びアザインダゾール化合物の生成に有効な中間体の合成方法 | |
| EP2300431B1 (en) | Process for the manufacture of an intermediate in the synthesis of dabigatran | |
| JP5667576B2 (ja) | トランス4−アミノ−シクロヘキシル酢酸エチル・エステルHClの製法 | |
| JP2014501719A (ja) | キラルスピロ−ピリジルアミドフォスフィン配位子化合物、その合成方法及びその利用 | |
| TW499409B (en) | Method for preparing of L-phenylephrine hydrochloride | |
| CN102285891A (zh) | 一种由芳香硝基化合物催化加氢制备芳胺的方法 | |
| WO2016055015A1 (zh) | 一种不对称还原法制备西他列汀中间体的方法 | |
| CN105934430B (zh) | 制备1‑烷基‑3‑二氟甲基‑5‑氟‑1h‑吡唑‑4‑甲醛和1‑烷基‑3‑二氟甲基‑5‑氟‑1h‑吡唑‑4‑甲酸酯的方法 | |
| CN110028436B (zh) | 一种沃诺拉赞关键中间体的制备方法 | |
| CN114181077B (zh) | 一种合成氨甲环酸的方法 | |
| KR101413877B1 (ko) | 펙소페나딘의 제조 방법 | |
| JP3890452B2 (ja) | アミノメチルピリジン化合物の製造法 | |
| JP6182507B2 (ja) | 2,3−ジハロゲノアニリンの製造方法 | |
| CN102766147B (zh) | 一种芬司匹利及其氢卤酸盐的制备方法 | |
| JP4769464B2 (ja) | アルコール化合物の製造方法 | |
| JP4896476B2 (ja) | メチルオキシメチルアミノピリジン誘導体及びその製造方法 | |
| JP5797108B2 (ja) | 2−インダノールの製造方法 | |
| JP2005170848A (ja) | 2,3−ジアミノピリジン類の製造方法 | |
| CN102584609B (zh) | 一种沙美特罗的制备方法 | |
| CN114875434A (zh) | 一种亚胺类化合物胺化的电化学方法 | |
| JP2004067592A (ja) | アミノ−フェニルピペリジンの製造法 | |
| CN101993413A (zh) | 一种制备4-吡啶丙醇的方法 | |
| JP2003192667A (ja) | 光学活性3−ヒドロキシピロリジン誘導体の製造方法 | |
| JP2008297259A (ja) | シス−アミノシクロヘキサンカルボン酸の製造方法 | |
| JP2002326978A (ja) | 4−アミノシクロヘキシル酢酸またはそのエステルの製造法 |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20131224 |
|
| A02 | Decision of refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A02 Effective date: 20140908 |