DK424680A - Cephalosporinsolvater med alicycliske ethere og fremgangsmaade til fremstilling heraf - Google Patents

Cephalosporinsolvater med alicycliske ethere og fremgangsmaade til fremstilling heraf

Info

Publication number
DK424680A
DK424680A DK424680A DK424680A DK424680A DK 424680 A DK424680 A DK 424680A DK 424680 A DK424680 A DK 424680A DK 424680 A DK424680 A DK 424680A DK 424680 A DK424680 A DK 424680A
Authority
DK
Denmark
Prior art keywords
cephalosporine
solvates
procedures
preparing
alicyclic ethers
Prior art date
Application number
DK424680A
Other languages
Danish (da)
English (en)
Inventor
Jackson B Grinnell
D Nezich
Original Assignee
Lilly Co Eli
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 Lilly Co Eli filed Critical Lilly Co Eli
Publication of DK424680A publication Critical patent/DK424680A/da

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D501/00—Heterocyclic compounds containing 5-thia-1-azabicyclo [4.2.0] octane ring systems, i.e. compounds containing a ring system of the formula:, e.g. cephalosporins; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulfur-containing hetero ring
    • C07D501/02—Preparation
    • C07D501/12—Separation; Purification
    • 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
    • A61K31/54—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one sulfur as the ring hetero atoms, e.g. sulthiame
    • A61K31/542—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one sulfur as the ring hetero atoms, e.g. sulthiame ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/545—Compounds containing 5-thia-1-azabicyclo [4.2.0] octane ring systems, i.e. compounds containing a ring system of the formula:, e.g. cephalosporins, cefaclor, or cephalexine
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D501/00—Heterocyclic compounds containing 5-thia-1-azabicyclo [4.2.0] octane ring systems, i.e. compounds containing a ring system of the formula:, e.g. cephalosporins; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulfur-containing hetero ring
    • C07D501/14—Compounds having a nitrogen atom directly attached in position 7
    • C07D501/16—Compounds having a nitrogen atom directly attached in position 7 with a double bond between positions 2 and 3
    • C07D501/20—7-Acylaminocephalosporanic or substituted 7-acylaminocephalosporanic acids in which the acyl radicals are derived from carboxylic acids
    • C07D501/24—7-Acylaminocephalosporanic or substituted 7-acylaminocephalosporanic acids in which the acyl radicals are derived from carboxylic acids with hydrocarbon radicals, substituted by hetero atoms or hetero rings, attached in position 3
    • C07D501/26—Methylene radicals, substituted by oxygen atoms; Lactones thereof with the 2-carboxyl group
    • C07D501/34—Methylene radicals, substituted by oxygen atoms; Lactones thereof with the 2-carboxyl group with the 7-amino radical acylated by carboxylic acids containing hetero rings

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Epidemiology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Cephalosporin Compounds (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
DK424680A 1979-10-09 1980-10-08 Cephalosporinsolvater med alicycliske ethere og fremgangsmaade til fremstilling heraf DK424680A (da)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US06/082,822 US4252951A (en) 1979-10-09 1979-10-09 Isolation of syn-7-(2-amino-4-thiazolyl)-(methoxyimino)acetamido-3-acetoxymethyl-3-cephem-4-carboxylic acid

Publications (1)

Publication Number Publication Date
DK424680A true DK424680A (da) 1981-04-10

Family

ID=22173679

Family Applications (1)

Application Number Title Priority Date Filing Date
DK424680A DK424680A (da) 1979-10-09 1980-10-08 Cephalosporinsolvater med alicycliske ethere og fremgangsmaade til fremstilling heraf

Country Status (27)

Country Link
US (1) US4252951A (fr)
EP (1) EP0027050B1 (fr)
JP (1) JPS5661388A (fr)
KR (1) KR840000866B1 (fr)
AT (1) AT369008B (fr)
AU (1) AU6306180A (fr)
BE (1) BE885569A (fr)
CA (1) CA1146539A (fr)
CH (1) CH647523A5 (fr)
CS (1) CS215142B2 (fr)
DD (1) DD153375A5 (fr)
DE (1) DE3065181D1 (fr)
DK (1) DK424680A (fr)
ES (1) ES8201166A1 (fr)
FI (1) FI803200A7 (fr)
FR (1) FR2467211A1 (fr)
GB (1) GB2059966B (fr)
GR (1) GR70219B (fr)
HU (1) HU183230B (fr)
IE (1) IE50390B1 (fr)
IL (1) IL61227A (fr)
IT (1) IT1132926B (fr)
PH (1) PH15023A (fr)
PT (1) PT71886B (fr)
RO (1) RO80664B (fr)
YU (1) YU256480A (fr)
ZA (1) ZA806192B (fr)

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JPS588086A (ja) * 1981-07-07 1983-01-18 Takeda Chem Ind Ltd セフアロスポリン溶媒和物およびその製造法
US4426528A (en) 1982-04-01 1984-01-17 Eli Lilly And Company Purification of syn-(2-aminothiazol-4-yl)methoxyimino)acetic acid
JPH07116200B2 (ja) * 1985-09-20 1995-12-13 富山化学工業株式会社 セファロスポリンの製造方法
JPH08831B2 (ja) * 1985-09-20 1996-01-10 富山化学工業株式会社 セファロスポリンの精製法
USD404431S (en) 1997-06-30 1999-01-19 Hilco Corporation Gumball dispenser
CA2368083A1 (fr) * 1999-04-06 2000-10-12 Sepracor Inc. Derives de la venlafaxine et leurs procedes de preparation et utilisation
AU6731100A (en) * 1999-09-02 2001-04-10 Shionogi & Co., Ltd. Integrase inhibitors containing aromatic heterocycle derivatives
CA2284459C (fr) 1999-10-04 2012-12-11 Neokimia Inc. Synthese combinatoire de bibliotheques de composes macrocycliques utiles pour la decouverte de medicaments
JP4879433B2 (ja) * 2000-01-13 2012-02-22 エミスフェアー・テクノロジーズ・インク 活性剤を送達するための化合物および組成物
AU2002326375B2 (en) * 2001-03-08 2006-12-21 The Trustees Of The University Of Pennsylvania Facially amphiphilic polymers as anti-infective agents
JP2005527467A (ja) * 2001-08-29 2005-09-15 ネオーズ テクノロジーズ， インコーポレイテッド 新規な合成ガングリオシド誘導体およびその組成物
JP4571497B2 (ja) * 2002-09-19 2010-10-27 杏林製薬株式会社 アミノアルコール誘導体とその付加塩及び免疫抑制剤
US7056916B2 (en) * 2002-11-15 2006-06-06 Boehringer Ingelheim Pharma Gmbh & Co. Kg Medicaments for the treatment of chronic obstructive pulmonary disease
US9241917B2 (en) * 2003-03-17 2016-01-26 The Trustees Of The University Of Pennsylvania Facially amphiphilic polymers and oligomers and uses thereof
US7321065B2 (en) * 2003-04-18 2008-01-22 The Regents Of The University Of California Thyronamine derivatives and analogs and methods of use thereof
US20050203184A1 (en) 2003-09-10 2005-09-15 Petasis Nicos A. Benzo lipoxin analogues
WO2005072246A2 (fr) * 2004-01-23 2005-08-11 The Trustees Of The University Of Pennsylvania Polymeres et oligomeres de polyaryle et de polyarylalkynyle amphiphiles au niveau facial
US7825278B2 (en) * 2004-05-06 2010-11-02 The Regents Of The University Of California Substituted enaminones, their derivatives and uses thereof
US20050255050A1 (en) * 2004-05-14 2005-11-17 Boehringer Ingelheim International Gmbh Powder formulations for inhalation, comprising enantiomerically pure beta agonists
US7220742B2 (en) * 2004-05-14 2007-05-22 Boehringer Ingelheim International Gmbh Enantiomerically pure beta agonists, process for the manufacture thereof and use thereof as medicaments
TWI403334B (zh) * 2004-12-23 2013-08-01 Merck Sharp & Dohme 包含生物素殘基之抗血栓雙重抑制劑
KR20080004475A (ko) * 2005-02-25 2008-01-09 유니버시티 오브 매사추세츠 표면적으로 양친매성인 중합체 및 올리고머, 그 조성물 및암치료방법으로서의 그 용도
JP5150807B2 (ja) * 2005-02-28 2013-02-27 株式会社明治 ハイドロキノン長鎖誘導体及び／又はフェノキシ長鎖誘導体及びこれらを含有する医薬
EP1940773B1 (fr) * 2005-08-10 2015-03-18 Johns Hopkins University Polyamines utiles en tant q'agents therapeutiques antiparasites et anticancereux et en tant qu'inhibiteurs de demethylase specifiques a la lysine
EP1917253B1 (fr) * 2005-08-15 2015-01-07 Boehringer Ingelheim International Gmbh Procede de production de betamimetiques
JP5102771B2 (ja) * 2005-10-28 2012-12-19 アイアールエム・リミテッド・ライアビリティ・カンパニー タンパク質キナーゼとしての化合物および組成物
US7799947B2 (en) * 2005-11-29 2010-09-21 Hammersmith Imanet Limited In vivo imaging compounds
ES2288107B1 (es) * 2006-01-27 2008-11-01 Fundacion Imabis Instituto Mediterraneo Para El Avance De La Biotecnologia Y La Investigacion Sanita Derivados aciclicos saturados e insaturados de cadena larga de sulfamidas como activadores especificos de receptores ppar-alfa.
FR2903004B1 (fr) * 2006-07-03 2009-07-10 Oreal Utilisation en cosmetique d'un derive c-glycoside en association avec de l'acide ascorbique
FR2902996B1 (fr) * 2006-07-03 2008-09-26 Oreal Compositions cosmetiques associant un derive c-glycoside et un derive n-acylaminoamide
US20090075935A1 (en) * 2006-07-03 2009-03-19 L'oreal Composition comprising at least one c-glycoside derivative and at least one hyaluronic acid and its cosmetic use
FR2902999B1 (fr) * 2006-07-03 2012-09-28 Oreal Utilisation de derives c-glycoside a titre d'actif prodesquamant
AU2007334428B2 (en) * 2006-12-14 2014-05-29 Teva Pharmaceutical Industries, Ltd. Crystalline solid rasagiline base
WO2008138200A1 (fr) * 2007-05-11 2008-11-20 Hong Kong University Of Science & Technology Antagonistes des récepteurs de nmda et de mc présentant une activité de neuroprotection et d'amélioration de la mémoire
US7696383B2 (en) * 2007-06-26 2010-04-13 Solvay Pharmaceuticals B.V. N-oxides of venlafaxine and o-desmethylvenlafaxine as prodrugs
FR2920000B1 (fr) * 2007-08-13 2010-01-29 Oreal Composition cosmetique ou pharmaceutique contenant de l'acide hyaluronique, et procede cosmetique pour diminuer les signes du vieilissement
ATE543799T1 (de) * 2007-10-19 2012-02-15 Janssen Pharmaceutica Nv Piperidinyl- und piperazinylmodulatoren von g- sekretase
US8692017B2 (en) * 2007-10-19 2014-04-08 Janssen Pharmaceutica, N.V. Carbon linked modulators of gamma-secretase
EP2212277B1 (fr) * 2007-10-19 2016-08-31 Janssen Pharmaceutica, N.V. Modulateurs de la g-secrétase liés à une amine
EP2093207A1 (fr) * 2008-02-06 2009-08-26 Julius-Maximilians-Universität Würzburg Composés anti-infectieux et anti-tumoraux isolés de lianes tropicales
US8063249B1 (en) * 2008-04-25 2011-11-22 Olema Pharmaceuticals, Inc. Substituted triphenyl butenes
WO2010017328A2 (fr) * 2008-08-06 2010-02-11 Rgo Biosciences Llc Conjugués de cyclodextrine
BRPI0919920A2 (pt) 2008-10-22 2016-02-16 Acucela Inc compostos para tratamento de doenças e desordens oftálmicas
FR2940610B1 (fr) * 2008-12-30 2011-05-06 Oreal Association de monosaccharides avec des derives c-glycosides et son utilisation en cosmetique
WO2010111530A1 (fr) 2009-03-25 2010-09-30 Seneb Biosciences, Inc. Glycolipides en tant que traitement de maladies
EP2430026A1 (fr) 2009-05-14 2012-03-21 Millennium Pharmaceuticals, Inc. Sel de chlorhydrate de ((1s,2s,4r)-4-{4-[(1s)-2,3-dihydro-1h-indèn-1-ylamino]-7h-pyrrolo [2,3-d]pyrimidin-7-yle}-2-hydroxycyclopentyle) méthylsulfamate
US8962639B2 (en) * 2009-05-29 2015-02-24 Abbvie Inc. Potassium channel modulators
US8288592B2 (en) 2009-09-22 2012-10-16 Actavis Group Ptc Ehf Solid state forms of tapentadol salts
WO2012067824A1 (fr) 2010-11-16 2012-05-24 Abbott Laboratories Modulateurs des canaux potassiques
KR101991980B1 (ko) * 2011-09-06 2019-06-21 큐알엔에이, 인크. 소형 분자로 전압-개폐된 나트륨 채널 (SCNxA)의 알파 아단위에 관련된 질환의 치료
US8377946B1 (en) 2011-12-30 2013-02-19 Pharmacyclics, Inc. Pyrazolo[3,4-d]pyrimidine and pyrrolo[2,3-d]pyrimidine compounds as kinase inhibitors

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3925372A (en) * 1973-02-23 1975-12-09 Lilly Co Eli Alpha-aminoacyl-3-halo cephalosporins
DK154939C (da) * 1974-12-19 1989-06-12 Takeda Chemical Industries Ltd Analogifremgangsmaade til fremstilling af thiazolylacetamido-cephemforbindelser eller farmaceutisk acceptable salte eller estere deraf
DE2760123C2 (de) * 1976-01-23 1986-04-30 Roussel-Uclaf, Paris 7-Aminothiazolyl-syn-oxyiminoacetamidocephalosporansäuren, ihre Herstellung und sie enthaltende pharmazeutische Zusammensetzungen
US4166115A (en) * 1976-04-12 1979-08-28 Fujisawa Pharmaceutical Co., Ltd. Syn 7-oxoimino substituted derivatives of cephalosporanic acid
DE2760484C2 (fr) 1976-04-14 1992-12-03 Takeda Chemical Industries, Ltd., Osaka, Jp

Also Published As

Publication number Publication date
YU256480A (en) 1983-02-28
CS215142B2 (en) 1982-07-30
RO80664B (ro) 1983-02-28
GB2059966A (en) 1981-04-29
KR830004314A (ko) 1983-07-09
IL61227A0 (en) 1980-12-31
RO80664A (fr) 1983-02-15
PH15023A (en) 1982-05-13
IT8025200A0 (it) 1980-10-08
ATA498080A (de) 1982-04-15
EP0027050B1 (fr) 1983-10-05
FR2467211B1 (fr) 1983-06-10
EP0027050A1 (fr) 1981-04-15
IE50390B1 (en) 1986-04-16
FR2467211A1 (fr) 1981-04-17
DE3065181D1 (en) 1983-11-10
PT71886B (en) 1981-08-13
JPS5661388A (en) 1981-05-26
KR840000866B1 (ko) 1984-06-20
FI803200L (fi) 1981-04-10
ZA806192B (en) 1982-05-26
FI803200A7 (fi) 1981-04-10
PT71886A (en) 1980-11-01
ES495753A0 (es) 1981-12-01
CH647523A5 (fr) 1985-01-31
IL61227A (en) 1983-07-31
GR70219B (fr) 1982-08-31
GB2059966B (en) 1983-09-01
ES8201166A1 (es) 1981-12-01
IT1132926B (it) 1986-07-09
AT369008B (de) 1982-11-25
HU183230B (en) 1984-04-28
US4252951A (en) 1981-02-24
AU6306180A (en) 1981-04-16
BE885569A (fr) 1981-04-08
CA1146539A (fr) 1983-05-17
IE802086L (en) 1981-04-09
DD153375A5 (de) 1982-01-06

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Legal Events

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AHS Application shelved for other reasons than non-payment