ES8201166A1 - Un procedimiento para preparar un solvato solido del acido sin-7-(2-(2-amino-4-tiazolil)-2-metoximino)-acetamido-3-acetoximetil-3-cefem-4-carboxilico - Google Patents

Un procedimiento para preparar un solvato solido del acido sin-7-(2-(2-amino-4-tiazolil)-2-metoximino)-acetamido-3-acetoximetil-3-cefem-4-carboxilico

Info

Publication number
ES8201166A1
ES8201166A1 ES495753A ES495753A ES8201166A1 ES 8201166 A1 ES8201166 A1 ES 8201166A1 ES 495753 A ES495753 A ES 495753A ES 495753 A ES495753 A ES 495753A ES 8201166 A1 ES8201166 A1 ES 8201166A1
Authority
ES
Spain
Prior art keywords
solvate
preparation
cefem
acid
ether
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.)
Expired
Application number
ES495753A
Other languages
English (en)
Other versions
ES495753A0 (es
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.)
Eli Lilly and Co
Original Assignee
Eli Lilly and Co
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 Eli Lilly and Co filed Critical Eli Lilly and Co
Publication of ES495753A0 publication Critical patent/ES495753A0/es
Publication of ES8201166A1 publication Critical patent/ES8201166A1/es
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D501/00Heterocyclic 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
    • C07D501/02Preparation
    • C07D501/12Separation; Purification
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/54Heterocyclic 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
    • A61K31/542Heterocyclic 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
    • A61K31/545Compounds 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D501/00Heterocyclic 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
    • C07D501/14Compounds having a nitrogen atom directly attached in position 7
    • C07D501/16Compounds having a nitrogen atom directly attached in position 7 with a double bond between positions 2 and 3
    • C07D501/207-Acylaminocephalosporanic or substituted 7-acylaminocephalosporanic acids in which the acyl radicals are derived from carboxylic acids
    • C07D501/247-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
    • C07D501/26Methylene radicals, substituted by oxygen atoms; Lactones thereof with the 2-carboxyl group
    • C07D501/34Methylene 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)

Abstract

PROCEDIMIENTO PARA LA OBTENCION DE UN SOLVATO SOLIDO DEL ACIDO SIN-7-(2-AMINO-4/TIAZOLIL)-2-METAXIIMINO)-ACETAMIDO-3-ACETOXIMETIL-3-CEFEM-4-CARBOXILICO. CONSISTE EN COMBINAR, EN UN MEDIO ACUOSO, ACIDO CEFEM CON UN ETER ALICICLICO, COMO TERRAHIDROFURANO; 1,4-DIOXANO, 1,3-DIOXOLANO O TERRAHIDROPIRANO. SE AJUSTA EL PH DE LA MEZCLA A UN VALOR COMPRENDIDO ENTRE 2,2 Y 3,5, Y SE DEJA QUE LA MISMA REPOSE, A TEMPERATURA AMBIENTE, HASTA QUE SE FORME UN PRECIPITADO DE SOLVATO, QUE SE AISLA. A PARTIR DE ESTE MOMENTO PUEDE VIEN SEPARARSE EL ETER DEL SOLVATO,PARA PRODUCIR EL ACIDO LIBRE, O BIEN HACERLO REACCIONAR CON UNA BASE PARA OBTENER UNA SAL DE ACIDO. DE APLICACION COMO COMPUESTOS INTERMEDIO EN LA ELABORACION DE SALES PARA PRODUCIR ANTIBIOTICOS.
ES495753A 1979-10-09 1980-10-08 Un procedimiento para preparar un solvato solido del acido sin-7-(2-(2-amino-4-tiazolil)-2-metoximino)-acetamido-3-acetoximetil-3-cefem-4-carboxilico Expired ES8201166A1 (es)

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 (2)

Publication Number Publication Date
ES495753A0 ES495753A0 (es) 1981-12-01
ES8201166A1 true ES8201166A1 (es) 1981-12-01

Family

ID=22173679

Family Applications (1)

Application Number Title Priority Date Filing Date
ES495753A Expired ES8201166A1 (es) 1979-10-09 1980-10-08 Un procedimiento para preparar un solvato solido del acido sin-7-(2-(2-amino-4-tiazolil)-2-metoximino)-acetamido-3-acetoximetil-3-cefem-4-carboxilico

Country Status (27)

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

Families Citing this family (51)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
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
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
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
USD404431S (en) 1997-06-30 1999-01-19 Hilco Corporation Gumball dispenser
CZ20013607A3 (cs) * 1999-04-06 2002-06-12 Sepracor Inc. Farmaceutický prostředek
EP1219607B1 (en) * 1999-09-02 2011-04-06 Shionogi & Co., Ltd. Integrase inhibitors containing aromatic heterocycle derivatives
CA2284459C (en) 1999-10-04 2012-12-11 Neokimia Inc. Combinatorial synthesis of libraries of macrocyclic compounds useful in drug discovery
WO2001051454A1 (en) * 2000-01-13 2001-07-19 Emisphere Technologies, Inc. Compounds and compositions for delivering active agents
CA2452977C (en) * 2001-03-08 2013-07-16 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
BR0314455A (pt) * 2002-09-19 2005-07-26 Kyorin Seiyaku Kk Derivados de aminoálcool, seus sais e agentes imunosupressores
US7056916B2 (en) * 2002-11-15 2006-06-06 Boehringer Ingelheim Pharma Gmbh & Co. Kg Medicaments for the treatment of chronic obstructive pulmonary disease
WO2004082634A2 (en) 2003-03-17 2004-09-30 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
EP1711455A4 (en) 2004-01-23 2007-11-07 Univ Pennsylvania FAZIAL AMPHIPHILE POLYARYL AND POLYARYL ALKINYL POLYMERS AND OLIGOMERS AND ITS APPLICATIONS
BRPI0510715A (pt) * 2004-05-06 2007-11-20 Univ California enaminonas substituìdas, seus derivados e usos destas
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
US20050255050A1 (en) * 2004-05-14 2005-11-17 Boehringer Ingelheim International Gmbh Powder formulations for inhalation, comprising enantiomerically pure beta agonists
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
JP2008531585A (ja) * 2005-02-25 2008-08-14 ザ・トラステイーズ・オブ・ザ・ユニバーシテイ・オブ・ペンシルベニア 表面が両親媒性のポリマーおよびオリゴマー、それらの組成物そして癌治療方法におけるそれらの使用
KR101270841B1 (ko) * 2005-02-28 2013-06-05 가부시키가이샤 메이지 히드로퀴논 장쇄 유도체 및/또는 페녹시 장쇄 유도체 및 이들을 함유하는 의약
JP5484728B2 (ja) * 2005-08-10 2014-05-07 ジョンズ ホプキンス ユニバーシティ 抗寄生虫治療薬および抗癌治療薬ならびにリジン特異的デメチラーゼ阻害物質として有用なポリアミン類
PL1917253T3 (pl) * 2005-08-15 2015-06-30 Boehringer Ingelheim Int Sposób wytwarzania betamimetyków
DE602006009539D1 (de) * 2005-10-28 2009-11-12 Irm Llc Verbindungen und zusammensetzungen als proteinkinaseinhibitoren
WO2007063286A2 (en) * 2005-11-29 2007-06-07 Hammersmith Imanet Limited Amidine derivatives for in vivo imaging
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
FR2902999B1 (fr) * 2006-07-03 2012-09-28 Oreal Utilisation de derives c-glycoside a titre d'actif prodesquamant
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
ATE528989T1 (de) * 2006-12-14 2011-11-15 Teva Pharma Kristalline feste rasagilin-base
CN104844678B (zh) 2007-05-11 2018-02-09 香港科技大学 具有神经保护和增强记忆活性的受体调节剂
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
AU2008312355B2 (en) * 2007-10-19 2013-07-04 Janssen Pharmaceutica, N.V. Carbon linked modulators of y-secretase
EP2212287B1 (en) * 2007-10-19 2012-02-01 Janssen Pharmaceutica, N.V. PIPERIDINYL AND PIPERAZINYL MODULATORS OF y-SECRETASE
CA2703636A1 (en) * 2007-10-19 2009-04-23 Janssen Pharmaceutica N.V. Amine linked modulators of .gamma.-secretase
EP2093207A1 (en) * 2008-02-06 2009-08-26 Julius-Maximilians-Universität Würzburg Antiinfective and antitumoral compounds isolated from tropical lianas
US8063249B1 (en) * 2008-04-25 2011-11-22 Olema Pharmaceuticals, Inc. Substituted triphenyl butenes
WO2010017328A2 (en) * 2008-08-06 2010-02-11 Rgo Biosciences Llc Cyclodextrin conjugates
CA2740952C (en) * 2008-10-22 2015-12-29 Ian L. Scott Compounds for treating ophthalmic diseases and disorders
FR2940610B1 (fr) * 2008-12-30 2011-05-06 Oreal Association de monosaccharides avec des derives c-glycosides et son utilisation en cosmetique
WO2010111530A1 (en) 2009-03-25 2010-09-30 Seneb Biosciences, Inc. Glycolipids as treatment for disease
BRPI1012142A2 (pt) 2009-05-14 2016-03-29 Millennium Pharm Inc sal cloridrato de ((1s,2s,4r)-4-{4-[(1s)-2,3-diidro-1h-inden-1-ilamino]-7h-pirrolo[2,3-d]pirimidin-7-il}-2-hidroxiciclopentil) metil sulfamato
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 (en) 2010-11-16 2012-05-24 Abbott Laboratories Potassium channel modulators
MX365525B (es) * 2011-09-06 2019-06-06 Curna Inc Compuestos que regulan la expresión de subunidades alfa de canales de sodio regulados por voltaje en enfermedades relacionadas con epilepsia mioclónica severa de la infancia.
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
GR63088B (en) 1976-04-14 1979-08-09 Takeda Chemical Industries Ltd Preparation process of novel cephalosporins

Also Published As

Publication number Publication date
RO80664B (ro) 1983-02-28
PT71886A (en) 1980-11-01
RO80664A (ro) 1983-02-15
KR840000866B1 (ko) 1984-06-20
FR2467211A1 (fr) 1981-04-17
DD153375A5 (de) 1982-01-06
CH647523A5 (fr) 1985-01-31
KR830004314A (ko) 1983-07-09
IE50390B1 (en) 1986-04-16
IT8025200A0 (it) 1980-10-08
GR70219B (es) 1982-08-31
ES495753A0 (es) 1981-12-01
BE885569A (fr) 1981-04-08
ATA498080A (de) 1982-04-15
GB2059966A (en) 1981-04-29
IT1132926B (it) 1986-07-09
DK424680A (da) 1981-04-10
IE802086L (en) 1981-04-09
PH15023A (en) 1982-05-13
PT71886B (en) 1981-08-13
US4252951A (en) 1981-02-24
YU256480A (en) 1983-02-28
AT369008B (de) 1982-11-25
DE3065181D1 (en) 1983-11-10
FI803200L (fi) 1981-04-10
GB2059966B (en) 1983-09-01
IL61227A0 (en) 1980-12-31
FR2467211B1 (es) 1983-06-10
CS215142B2 (en) 1982-07-30
CA1146539A (en) 1983-05-17
HU183230B (en) 1984-04-28
FI803200A7 (fi) 1981-04-10
JPS5661388A (en) 1981-05-26
EP0027050A1 (en) 1981-04-15
AU6306180A (en) 1981-04-16
EP0027050B1 (en) 1983-10-05
ZA806192B (en) 1982-05-26
IL61227A (en) 1983-07-31

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