AR066191A1 - Proceso e intermediarios para la sintesis de compuestos 8- [ ( 1- (3,5- bis- ( trifluorometil) fenil) - etoxi ) - metil]- 8 fenil - 1,7- diaza - espiro (4, 5) decan -2 ona - Google Patents
Proceso e intermediarios para la sintesis de compuestos 8- [ ( 1- (3,5- bis- ( trifluorometil) fenil) - etoxi ) - metil]- 8 fenil - 1,7- diaza - espiro (4, 5) decan -2 onaInfo
- Publication number
- AR066191A1 AR066191A1 ARP080101154A AR066191A1 AR 066191 A1 AR066191 A1 AR 066191A1 AR P080101154 A ARP080101154 A AR P080101154A AR 066191 A1 AR066191 A1 AR 066191A1
- Authority
- AR
- Argentina
- Prior art keywords
- phenyl
- compounds
- espiro
- trifluorometil
- etoxi
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/10—Spiro-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/08—Drugs for disorders of the alimentary tract or the digestive system for nausea, cinetosis or vertigo; Antiemetics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/04—Centrally acting analgesics, e.g. opioids
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/06—Antimigraine agents
-
- 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]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D211/36—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members 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
- C07D211/38—Halogen atoms or nitro radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D211/36—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members 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
- C07D211/56—Nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D498/10—Spiro-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Pain & Pain Management (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Rheumatology (AREA)
- Hospice & Palliative Care (AREA)
- Otolaryngology (AREA)
- Hydrogenated Pyridines (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Abstract
Los compuestos de la presente se pueden utilizar, por ejemplo, como compuestos inhibidores de NK-1 en preparaciones farmacéuticas y son utiles en el tratamiento de náuseas y emesis. Reivindicacion 1: Un proceso para producir un compuesto de lactama de formula 1 el proceso que comprende hacer reaccionar un compuesto de la formula 27a-sulfonato con zinc en presencia de ácido acético, formando de este modo la lactama de formula 1, donde R1 se selecciona de alquilo lineal, ramificado o cíclico que tiene hasta 6 átomos de carbono, fenilo, 2-metoxi-etilo, 2-(dimetilamino)etilo, (L)-mentilo, (D)-mentilo, dimetilamida, (R)-bencil-oxazolidinonamida, (S)-bencil-oxazolidinonamida, isobornilo, cis-pinan-2-ilo, isopinocamfeílo, adamantilmetilo, 2-adamantilo, 1-adamantilo, y (-)-8-fenilmentilo.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US91966607P | 2007-03-22 | 2007-03-22 |
Publications (1)
Publication Number | Publication Date |
---|---|
AR066191A1 true AR066191A1 (es) | 2009-08-05 |
Family
ID=39789180
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP080101154 AR066191A1 (es) | 2007-03-22 | 2008-03-19 | Proceso e intermediarios para la sintesis de compuestos 8- [ ( 1- (3,5- bis- ( trifluorometil) fenil) - etoxi ) - metil]- 8 fenil - 1,7- diaza - espiro (4, 5) decan -2 ona |
Country Status (11)
Country | Link |
---|---|
US (3) | US8552191B2 (es) |
EP (2) | EP3138836A1 (es) |
JP (2) | JP5451404B2 (es) |
CN (2) | CN104447510B (es) |
AR (1) | AR066191A1 (es) |
CA (1) | CA2682221C (es) |
ES (1) | ES2579771T3 (es) |
HK (1) | HK1136297A1 (es) |
MX (1) | MX2009010211A (es) |
SG (1) | SG182226A1 (es) |
WO (1) | WO2008118328A2 (es) |
Families Citing this family (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AR060303A1 (es) | 2006-04-05 | 2008-06-04 | Schering Corp | Formulaciones farmaceuticas sales de 8- [1- (3,5 -bis- (trifluorometil) fenil) -etoximetil] -8-fenil-1,7 -diaza-espiro [4.5] decan -2- ona y metodos de tratamiento utilizando las mismas |
HUE028908T2 (en) * | 2006-04-05 | 2017-01-30 | Opko Health Inc | The hydrochloride salt of 8 - [{1- (3,5-bis (trifluoromethyl) phenyl) ethoxy} methyl] -8-phenyl-1,7-diazaspiro [4.5] decan-2-one, and process |
AR066191A1 (es) | 2007-03-22 | 2009-08-05 | Schering Corp | Proceso e intermediarios para la sintesis de compuestos 8- [ ( 1- (3,5- bis- ( trifluorometil) fenil) - etoxi ) - metil]- 8 fenil - 1,7- diaza - espiro (4, 5) decan -2 ona |
AU2009289598B2 (en) * | 2008-09-05 | 2014-09-11 | Opko Health, Inc. | Process and intermediates for the synthesis of 8-[{1-(3,5-Bis-(trifluoromethyl)phenyl) -ethoxy}-methyl]-8-phenyl-1,7-diaza-spiro[4.5]decan-2-one compounds |
CN102573475B (zh) * | 2009-08-14 | 2016-01-20 | 欧科生医股份有限公司 | 神经激肽-1拮抗剂的静脉内制剂 |
GB2504076A (en) | 2012-07-16 | 2014-01-22 | Nicoventures Holdings Ltd | Electronic smoking device |
GB2504075A (en) | 2012-07-16 | 2014-01-22 | Nicoventures Holdings Ltd | Electronic smoking device |
GB201505595D0 (en) | 2015-03-31 | 2015-05-13 | British American Tobacco Co | Cartridge for use with apparatus for heating smokeable material |
GB201505597D0 (en) | 2015-03-31 | 2015-05-13 | British American Tobacco Co | Article for use with apparatus for heating smokable material |
CN105017251B (zh) * | 2015-06-30 | 2018-06-29 | 齐鲁制药有限公司 | 一种nk-1受体拮抗剂的制备方法及其中间体 |
JP6384536B2 (ja) * | 2015-10-23 | 2018-09-05 | 信越化学工業株式会社 | フッ化イットリウム溶射材料及びオキシフッ化イットリウム成膜部品の製造方法 |
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US3094522A (en) * | 1961-07-25 | 1963-06-18 | Merck & Co Inc | Alkanoylthio and pyrazolo androstane derivatives |
AU678409B2 (en) | 1992-10-28 | 1997-05-29 | Merck Sharp & Dohme Limited | 4-arylmethyloxymethyl piperidines as tachykinin antagonists |
AU682838B2 (en) | 1992-12-14 | 1997-10-23 | Merck Sharp & Dohme Limited | 4-aminomethyl/thiomethyl/sulfonylmethyl-4-phenylpiperidines as tachykinin receptor antagonists |
US5760018A (en) | 1994-01-13 | 1998-06-02 | Merck Sharp & Dohme Ltd. | Gem-disubstituted azacyclic tachykinin antagonists |
GB9601680D0 (en) | 1996-01-27 | 1996-03-27 | Pfizer Ltd | Therapeutic agents |
GB9626746D0 (en) | 1996-12-23 | 1997-02-12 | Knoll Ag | Process |
WO1998047514A1 (en) | 1997-04-24 | 1998-10-29 | Merck Sharp & Dohme Limited | Use of an nk-1 receptor antagonist and an ssri for treating obesity |
DE19815275B4 (de) | 1998-04-06 | 2009-06-25 | Evonik Degussa Gmbh | Alkylidenkomplexe des Rutheniums mit N-heterozyklischen Carbenliganden und deren Verwendung als hochaktive, selektive Katalysatoren für die Olefin-Metathese |
US6215019B1 (en) | 1998-09-01 | 2001-04-10 | Tilliechem, Inc. | Synthesis of 5-decenyl acetate and other pheromone components |
AU779073B2 (en) | 1998-12-23 | 2005-01-06 | Nps Allelix Corp. | Indole and indolizidine derivatives for the treatment of migraine |
CA2372746C (en) | 1999-05-24 | 2012-10-02 | California Institute Of Technology | Imidazolidine-based metal carbene metathesis catalysts |
US6858414B2 (en) * | 1999-12-01 | 2005-02-22 | BIOGAL Gyógyszergyár Rt. | Multistage process for the preparation of highly pure deferoxamine mesylate salt |
US6436928B1 (en) | 1999-12-17 | 2002-08-20 | Schering Corporation | Selective neurokinin antagonists |
CO5261559A1 (es) | 1999-12-17 | 2003-03-31 | Schering Corp | Antagonistas de neurokinina selectivos |
GB0004699D0 (en) | 2000-02-28 | 2000-04-19 | Merck Sharp & Dohme | Chemical synthesis |
WO2002014376A2 (en) | 2000-08-10 | 2002-02-21 | Trustees Of Boston College | Recyclable metathesis catalysts |
MXPA04004477A (es) | 2001-11-13 | 2004-08-11 | Schering Corp | Antagonistas del neuropeptido neuroquinina-1(nk1). |
PE20030762A1 (es) | 2001-12-18 | 2003-09-05 | Schering Corp | Compuestos heterociclicos como antagonistas nk1 |
WO2004004722A1 (en) | 2002-07-03 | 2004-01-15 | Schering Corporation | 1-amido-4-phenyl-4-benzyloxymethyl-piperidine derivatives and related compounds as neurokinin-1(nk-1) antagonists for the treatment of emesis, depression, anxiety and cough |
PL199412B1 (pl) | 2002-10-15 | 2008-09-30 | Boehringer Ingelheim Int | Nowe kompleksy rutenu jako (pre)katalizatory reakcji metatezy, pochodne 2-alkoksy-5-nitrostyrenu jako związki pośrednie i sposób ich wytwarzania |
CA2522946A1 (en) * | 2003-04-23 | 2004-11-04 | Merck & Co., Inc. | Selective spirocyclic glucocorticoid receptor modulators |
JP2007515425A (ja) * | 2003-12-22 | 2007-06-14 | シェーリング コーポレイション | 医薬組成物 |
US7498438B2 (en) | 2004-04-07 | 2009-03-03 | Schering Corporation | Fused ring NK1 antagonists |
CN101006074B (zh) | 2004-07-01 | 2012-02-15 | 欧科生医股份有限公司 | 作为nk1拮抗剂的哌啶衍生物 |
JP4444745B2 (ja) | 2004-07-08 | 2010-03-31 | キヤノン株式会社 | 偏光分離素子および画像投射装置 |
US7354922B2 (en) * | 2004-12-14 | 2008-04-08 | Schering Corporation | Bridged ring NK1 antagonists |
TW200630380A (en) | 2005-02-18 | 2006-09-01 | Nat Univ Chung Hsing | N-acylamino acid racemase of Deinococcus radiodurans and producing method thereof, and L-amino acid production method therefrom |
CN102643175B (zh) | 2005-07-04 | 2014-12-10 | 赞南科技(上海)有限公司 | 钌络合物配体、钌络合物、固载钌络合物催化剂及其制备方法和用途 |
HUE028908T2 (en) * | 2006-04-05 | 2017-01-30 | Opko Health Inc | The hydrochloride salt of 8 - [{1- (3,5-bis (trifluoromethyl) phenyl) ethoxy} methyl] -8-phenyl-1,7-diazaspiro [4.5] decan-2-one, and process |
AR060303A1 (es) | 2006-04-05 | 2008-06-04 | Schering Corp | Formulaciones farmaceuticas sales de 8- [1- (3,5 -bis- (trifluorometil) fenil) -etoximetil] -8-fenil-1,7 -diaza-espiro [4.5] decan -2- ona y metodos de tratamiento utilizando las mismas |
WO2007114922A2 (en) | 2006-04-05 | 2007-10-11 | Schering Corporation | Salts of 8-[{1-(3,5-bis-(trifluoromethyl) phenyl)-ethoxy}-methyl]-8-phenyl-1,7-diaza-spiro[4.5]decan-2-one and preparation process therefor |
AR066191A1 (es) | 2007-03-22 | 2009-08-05 | Schering Corp | Proceso e intermediarios para la sintesis de compuestos 8- [ ( 1- (3,5- bis- ( trifluorometil) fenil) - etoxi ) - metil]- 8 fenil - 1,7- diaza - espiro (4, 5) decan -2 ona |
AR065802A1 (es) * | 2007-03-22 | 2009-07-01 | Schering Corp | Formulaciones de comprimidos que contienen sales de 8- [( 1- ( 3,5- bis- (trifluorometil) fenil) -etoxi ) - metil) -8- fenil -1, 7- diaza- spiro [ 4,5] decan -2- ona y comprimidos elaborados a partir de estas |
AU2009289598B2 (en) | 2008-09-05 | 2014-09-11 | Opko Health, Inc. | Process and intermediates for the synthesis of 8-[{1-(3,5-Bis-(trifluoromethyl)phenyl) -ethoxy}-methyl]-8-phenyl-1,7-diaza-spiro[4.5]decan-2-one compounds |
CN102573475B (zh) | 2009-08-14 | 2016-01-20 | 欧科生医股份有限公司 | 神经激肽-1拮抗剂的静脉内制剂 |
-
2008
- 2008-03-19 AR ARP080101154 patent/AR066191A1/es unknown
- 2008-03-20 CN CN201410738810.7A patent/CN104447510B/zh not_active Expired - Fee Related
- 2008-03-20 EP EP16168286.9A patent/EP3138836A1/en not_active Withdrawn
- 2008-03-20 US US12/531,859 patent/US8552191B2/en active Active
- 2008-03-20 SG SG2012046439A patent/SG182226A1/en unknown
- 2008-03-20 CA CA2682221A patent/CA2682221C/en active Active
- 2008-03-20 WO PCT/US2008/003640 patent/WO2008118328A2/en active Application Filing
- 2008-03-20 CN CN200880017063.0A patent/CN101679257B/zh not_active Expired - Fee Related
- 2008-03-20 ES ES08742144.2T patent/ES2579771T3/es active Active
- 2008-03-20 JP JP2009554566A patent/JP5451404B2/ja not_active Expired - Fee Related
- 2008-03-20 MX MX2009010211A patent/MX2009010211A/es active IP Right Grant
- 2008-03-20 EP EP08742144.2A patent/EP2137151B1/en active Active
-
2010
- 2010-04-15 HK HK10103699.6A patent/HK1136297A1/zh not_active IP Right Cessation
-
2013
- 2013-09-27 US US14/039,367 patent/US9260428B2/en active Active
- 2013-12-26 JP JP2013268922A patent/JP2014144951A/ja not_active Withdrawn
-
2016
- 2016-02-12 US US15/043,129 patent/US10000493B2/en active Active
Also Published As
Publication number | Publication date |
---|---|
ES2579771T3 (es) | 2016-08-16 |
CN104447510A (zh) | 2015-03-25 |
US9260428B2 (en) | 2016-02-16 |
WO2008118328A3 (en) | 2009-03-05 |
JP5451404B2 (ja) | 2014-03-26 |
CA2682221A1 (en) | 2008-10-02 |
CN101679257A (zh) | 2010-03-24 |
WO2008118328A2 (en) | 2008-10-02 |
US20100087426A1 (en) | 2010-04-08 |
CN101679257B (zh) | 2015-01-07 |
JP2014144951A (ja) | 2014-08-14 |
EP3138836A1 (en) | 2017-03-08 |
EP2137151A2 (en) | 2009-12-30 |
MX2009010211A (es) | 2009-10-19 |
EP2137151B1 (en) | 2016-05-11 |
US10000493B2 (en) | 2018-06-19 |
CA2682221C (en) | 2017-04-25 |
CN104447510B (zh) | 2018-03-30 |
SG182226A1 (en) | 2012-07-30 |
JP2010522171A (ja) | 2010-07-01 |
US20140024834A1 (en) | 2014-01-23 |
US8552191B2 (en) | 2013-10-08 |
HK1136297A1 (es) | 2010-06-25 |
US20170008893A1 (en) | 2017-01-12 |
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