CN102596908A - 用于制备取代的吲唑和氮杂吲唑化合物的中间体的合成方法 - Google Patents

用于制备取代的吲唑和氮杂吲唑化合物的中间体的合成方法 Download PDF

Info

Publication number
CN102596908A
CN102596908A CN2010800504234A CN201080050423A CN102596908A CN 102596908 A CN102596908 A CN 102596908A CN 2010800504234 A CN2010800504234 A CN 2010800504234A CN 201080050423 A CN201080050423 A CN 201080050423A CN 102596908 A CN102596908 A CN 102596908A
Authority
CN
China
Prior art keywords
formula
metal catalyst
compounds
hydrogen
solvent
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
Application number
CN2010800504234A
Other languages
English (en)
Chinese (zh)
Inventor
H.拉扎维
J.T.里夫斯
S.罗德里古兹
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Boehringer Ingelheim International GmbH
Original Assignee
Boehringer Ingelheim International GmbH
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Boehringer Ingelheim International GmbH filed Critical Boehringer Ingelheim International GmbH
Publication of CN102596908A publication Critical patent/CN102596908A/zh
Pending legal-status Critical Current

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)
  • Materials Engineering (AREA)
  • Rheumatology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Epidemiology (AREA)
  • Engineering & Computer Science (AREA)
  • Pain & Pain Management (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Catalysts (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Steroid Compounds (AREA)
  • Pyridine Compounds (AREA)
CN2010800504234A 2009-12-08 2010-12-01 用于制备取代的吲唑和氮杂吲唑化合物的中间体的合成方法 Pending CN102596908A (zh)

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
CN102596908A true CN102596908A (zh) 2012-07-18

Family

ID=43416915

Family Applications (1)

Application Number Title Priority Date Filing Date
CN2010800504234A Pending CN102596908A (zh) 2009-12-08 2010-12-01 用于制备取代的吲唑和氮杂吲唑化合物的中间体的合成方法

Country Status (17)

Country Link
US (1) US20110137042A1 (https=)
EP (1) EP2509952A1 (https=)
JP (1) JP2013512954A (https=)
KR (1) KR20120101667A (https=)
CN (1) CN102596908A (https=)
AR (1) AR079324A1 (https=)
AU (1) AU2010328480A1 (https=)
BR (1) BR112012013582A2 (https=)
CA (1) CA2782384A1 (https=)
CL (1) CL2012001300A1 (https=)
EA (1) EA201200820A1 (https=)
IL (1) IL219274A0 (https=)
IN (1) IN2012DN05081A (https=)
MX (1) MX2012006524A (https=)
PH (1) PH12012501153A1 (https=)
TW (1) TW201144282A (https=)
WO (1) WO2011071730A1 (https=)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
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
CA2722811C (en) * 2008-05-06 2016-07-05 Boehringer Ingelheim International Gmbh Pyrazole compounds as ccr1 antagonists
NZ591115A (en) 2008-09-26 2012-10-26 Boehringer Ingelheim Int Azaindazole compounds as ccr1 receptor antagonists
PH12012500775A1 (en) 2009-10-21 2012-11-26 Boehringer Ingelheim Int Indazole and pyrazolopyridine compounds as ccr1 receptor antagonists
US8927550B2 (en) 2009-10-27 2015-01-06 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
WO2012087782A1 (en) 2010-12-23 2012-06-28 Boehringer Ingelheim International Gmbh Pyrazolopiperidine compounds as ccr1 receptor antagonists

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1671700A (zh) * 2001-01-12 2005-09-21 安姆根有限公司 取代的烷基胺衍生物和使用方法
CN101141878A (zh) * 2005-03-16 2008-03-12 巴斯福股份公司 联苯-n-（4-吡啶基）甲基磺酰胺
CN101258131A (zh) * 2005-09-01 2008-09-03 伊莱利利公司 作为5－HT<sub>2c</sub>受体激动剂的6－芳烷基氨基－2,3,4,5－四氢－1H－苯并[d]氮杂䓬
CN101410397A (zh) * 2006-03-31 2009-04-15 诺瓦提斯公司 有机化合物
WO2009057827A1 (en) * 2007-10-31 2009-05-07 Nissan Chemical Industries, Ltd. Pyridazinone derivatives and use thereof as p2x7 receptor inhibitors
US20100093724A1 (en) * 2008-09-26 2010-04-15 Boehringer Ingelheim International Gmbh Azaindazole Compounds As CCR1 Receptor Antagonists

Family Cites Families (41)

* Cited by examiner, † Cited by third party
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
BR9305569A (pt) * 1992-07-03 1995-12-26 Kumiai Chemical Industry Co Derivados heterocíclicos condensados e herbicidas
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
US6025374A (en) * 1994-12-06 2000-02-15 Merck Sharp & Dohme, Ltd. 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
IL135714A0 (en) * 1997-11-04 2001-05-20 Pfizer Prod Inc Therapeutically active compounds 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
JP2003502314A (ja) * 1999-06-14 2003-01-21 イーライ・リリー・アンド・カンパニー 化合物
WO2001000656A2 (en) * 1999-06-29 2001-01-04 Ortho-Mcneil Pharmaceutical, Inc. Novel indazole peptidomimetics as thrombin receptor antagonists
GB0030304D0 (en) * 2000-12-13 2001-01-24 Lilly Co Eli Compounds
GB0030303D0 (en) * 2000-12-13 2001-01-24 Lilly Co Eli Compounds
GB0030306D0 (en) * 2000-12-13 2001-01-24 Lilly Co Eli Compounds
GB0030305D0 (en) * 2000-12-13 2001-01-24 Lilly Co Eli Compounds
US20050009876A1 (en) * 2000-07-31 2005-01-13 Bhagwat Shripad S. Indazole compounds, compositions thereof and methods of treatment therewith
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
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
WO2003037274A2 (en) * 2001-11-01 2003-05-08 Icagen, Inc. Pyrazole-amides and-sulfonamides
US7429609B2 (en) * 2002-05-31 2008-09-30 Eisai R & D Management Co., Ltd. Pyrazole compound and medicinal 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
JP4713465B2 (ja) * 2003-03-12 2011-06-29 セルジーン コーポレイション ７−アミド−イソインドリル化合物およびその薬学的使用
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
ATE423122T1 (de) * 2003-08-15 2009-03-15 Astrazeneca Ab Kondensierte heterocyclen als inhibitoren von glutamatracemase (muri)
SE0302487D0 (sv) * 2003-09-18 2003-09-18 Astrazeneca Ab Novel compounds
SE0302486D0 (sv) * 2003-09-18 2003-09-18 Astrazeneca Ab Novel compounds
GB0504828D0 (en) * 2005-03-09 2005-04-13 Merck Sharp & Dohme Therapeutic agents
DK2444079T3 (en) * 2005-05-17 2017-01-30 Sarcode Bioscience Inc Compositions and Methods for the Treatment of Eye Diseases
WO2007102883A2 (en) * 2005-10-25 2007-09-13 Smithkline Beecham Corporation Chemical 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
CA2722923C (en) * 2008-04-29 2016-08-02 Boehringer Ingelheim International Gmbh Indazole compounds as ccr1 receptor antagonists
CA2722811C (en) * 2008-05-06 2016-07-05 Boehringer Ingelheim International Gmbh Pyrazole compounds as ccr1 antagonists

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1671700A (zh) * 2001-01-12 2005-09-21 安姆根有限公司 取代的烷基胺衍生物和使用方法
CN101141878A (zh) * 2005-03-16 2008-03-12 巴斯福股份公司 联苯-n-（4-吡啶基）甲基磺酰胺
CN101258131A (zh) * 2005-09-01 2008-09-03 伊莱利利公司 作为5－HT<sub>2c</sub>受体激动剂的6－芳烷基氨基－2,3,4,5－四氢－1H－苯并[d]氮杂䓬
CN101410397A (zh) * 2006-03-31 2009-04-15 诺瓦提斯公司 有机化合物
WO2009057827A1 (en) * 2007-10-31 2009-05-07 Nissan Chemical Industries, Ltd. Pyridazinone derivatives and use thereof as p2x7 receptor inhibitors
US20100093724A1 (en) * 2008-09-26 2010-04-15 Boehringer Ingelheim International Gmbh Azaindazole Compounds As CCR1 Receptor Antagonists

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
蔡可迎,等: "吲唑的简便合成", 《化学试剂》, vol. 29, no. 1, 31 January 2007 (2007-01-31), pages 53 - 54 *

Also Published As

Publication number Publication date
AR079324A1 (es) 2012-01-18
IL219274A0 (en) 2012-06-28
EP2509952A1 (en) 2012-10-17
WO2011071730A1 (en) 2011-06-16
CL2012001300A1 (es) 2012-09-07
CA2782384A1 (en) 2011-06-16
KR20120101667A (ko) 2012-09-14
IN2012DN05081A (https=) 2015-10-09
MX2012006524A (es) 2012-07-17
JP2013512954A (ja) 2013-04-18
TW201144282A (en) 2011-12-16
PH12012501153A1 (en) 2012-10-22
BR112012013582A2 (pt) 2016-07-05
EA201200820A1 (ru) 2013-01-30
AU2010328480A1 (en) 2012-05-17
US20110137042A1 (en) 2011-06-09

Similar Documents

Publication Publication Date Title
CN102596908A (zh) 用于制备取代的吲唑和氮杂吲唑化合物的中间体的合成方法
EP2300431B1 (en) Process for the manufacture of an intermediate in the synthesis of dabigatran
CN102285891A (zh) 一种由芳香硝基化合物催化加氢制备芳胺的方法
CN103865964A (zh) 转氨酶法合成(r)-3-氨基哌啶的方法
CA3216002A1 (en) Preparation method for pyrrole amide compound
WO2016055015A1 (zh) 一种不对称还原法制备西他列汀中间体的方法
CN104059021B (zh) 一种n‑羟基苯胺的制备方法
KR102319577B1 (ko) １-알킬-３-디플루오로메틸-５-플루오르-１ｈ-피라졸-４-카르브알데히드 및 １-알킬-３-디플루오로메틸-５-플루오르-１ｈ-피라졸-４-카르복실레이트의 제조 방법
CN108148044A (zh) 酰胺类化合物及该化合物制备富马酸沃诺拉赞的方法
CN110028436B (zh) 一种沃诺拉赞关键中间体的制备方法
CN117402083A (zh) 一种亚氨基腙中间体的制备方法
CN110963959B (zh) 一种合成n-保护及非保护的3-羟基-4,4-二甲基哌啶的制备方法
JP2006503884A (ja) （ｒ）−サルブタモールの調製方法
KR20150066777A (ko) 광학활성 인돌린 유도체 및 이의 제조방법
CN101155820B (zh) 6,7,8-三羟基-1-羟甲基-3-氧代-2-氧杂-4-氮杂双环[3.3.1]壬烷的制备方法
TW200403222A (en) Process for the preparation of amino-pyrrolidine derivatives
JPH07138210A (ja) アミノプロパン誘導体の製造方法
CN111362824B (zh) 2-(氨甲基)-n,n-二乙基-1-苯基环丙烷甲酰胺及其盐的制备方法
JPH10101646A (ja) アミノメチルピリジン化合物の製造法
CN102766147B (zh) 一种芬司匹利及其氢卤酸盐的制备方法
JP2005170848A (ja) ２，３−ジアミノピリジン類の製造方法
CA2337544C (en) Methods for making optically active 3-aminopyrrolidine-2,5-dione derivative and optically active 3-aminopyrrolidine derivative
CN1399625A (zh) 卤代伯胺的制备方法
Cho et al. Ruthenium‐catalyzed formal alkyl group transfer: Synthesis of quinolines from nitroarenes and alkylammonium halides
JP4968602B2 (ja) ベンズアミド誘導体の製造方法

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C02 Deemed withdrawal of patent application after publication (patent law 2001)
WD01 Invention patent application deemed withdrawn after publication

Application publication date: 20120718