CN87107149A - 7-[(间位取代的)苯基甘氨酸]1-碳代-1-去硫头孢菌素 - Google Patents

7-[(间位取代的)苯基甘氨酸]1-碳代-1-去硫头孢菌素 Download PDF

Info

Publication number
CN87107149A
CN87107149A CN198787107149A CN87107149A CN87107149A CN 87107149 A CN87107149 A CN 87107149A CN 198787107149 A CN198787107149 A CN 198787107149A CN 87107149 A CN87107149 A CN 87107149A CN 87107149 A CN87107149 A CN 87107149A
Authority
CN
China
Prior art keywords
carba
formula
amino
chloro
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
Application number
CN198787107149A
Other languages
English (en)
Chinese (zh)
Inventor
罗宾·戴维·格雷·床珀
约翰·阿伦·韦伯
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 CN87107149A publication Critical patent/CN87107149A/zh
Pending legal-status Critical Current

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
    • C07D471/04—Ortho-condensed systems
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D463/00—Heterocyclic compounds containing 1-azabicyclo [4.2.0] octane ring systems, i.e. compounds containing a ring system of the formula:, e.g. carbacephalosporins; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulfur-containing hetero ring
    • C07D463/10—Heterocyclic compounds containing 1-azabicyclo [4.2.0] octane ring systems, i.e. compounds containing a ring system of the formula:, e.g. carbacephalosporins; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulfur-containing hetero ring with a carbon atom having three bonds to hetero atoms with at the most one bond to halogen, e.g. an ester or nitrile radical, directly attached in position 2
    • C07D463/14—Heterocyclic compounds containing 1-azabicyclo [4.2.0] octane ring systems, i.e. compounds containing a ring system of the formula:, e.g. carbacephalosporins; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulfur-containing hetero ring with a carbon atom having three bonds to hetero atoms with at the most one bond to halogen, e.g. an ester or nitrile radical, directly attached in position 2 with hetero atoms directly attached in position 7
    • C07D463/16—Nitrogen atoms
    • C07D463/18—Nitrogen atoms further acylated by radicals derived from carboxylic acids or by nitrogen or sulfur analogues thereof
    • C07D463/20—Nitrogen atoms further acylated by radicals derived from carboxylic acids or by nitrogen or sulfur analogues thereof with the acylating radicals further substituted by hetero atoms or by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
    • C07D463/22—Nitrogen atoms further acylated by radicals derived from carboxylic acids or by nitrogen or sulfur analogues thereof with the acylating radicals further substituted by hetero atoms or by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen further substituted by nitrogen atoms
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04—Ortho-condensed systems

Landscapes

  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • Cephalosporin Compounds (AREA)
  • Peptides Or Proteins (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
CN198787107149A 1986-10-03 1987-10-01 7-[(间位取代的)苯基甘氨酸]1-碳代-1-去硫头孢菌素 Pending CN87107149A (zh)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US91517386A 1986-10-03 1986-10-03
US06/915,173 1986-10-03

Publications (1)

Publication Number Publication Date
CN87107149A true CN87107149A (zh) 1988-05-18

Family

ID=25435354

Family Applications (1)

Application Number Title Priority Date Filing Date
CN198787107149A Pending CN87107149A (zh) 1986-10-03 1987-10-01 7-[(间位取代的)苯基甘氨酸]1-碳代-1-去硫头孢菌素

Country Status (17)

Country Link
EP (1) EP0266896B1 (enExample)
JP (1) JPS6396186A (enExample)
KR (1) KR880005125A (enExample)
CN (1) CN87107149A (enExample)
AT (2) ATE79119T1 (enExample)
BG (1) BG47034A3 (enExample)
DE (1) DE3780909T2 (enExample)
DK (1) DK518487A (enExample)
FI (1) FI874311L (enExample)
GR (1) GR3005920T3 (enExample)
HU (1) HU200179B (enExample)
IE (1) IE872646L (enExample)
IL (1) IL84051A0 (enExample)
NZ (1) NZ222015A (enExample)
PL (1) PL151703B1 (enExample)
PT (1) PT85850B (enExample)
ZA (1) ZA877398B (enExample)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102144992A (zh) * 2011-03-10 2011-08-10 浙江大学 苯基甘氨酸衍生物对金黄色葡萄球菌有抑菌和杀菌活性

Families Citing this family (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0327364A1 (en) * 1988-02-05 1989-08-09 Eli Lilly And Company Crystalline beta-lactam solvate
US6982251B2 (en) 2000-12-20 2006-01-03 Schering Corporation Substituted 2-azetidinones useful as hypocholesterolemic agents
US7071181B2 (en) 2001-01-26 2006-07-04 Schering Corporation Methods and therapeutic combinations for the treatment of diabetes using sterol absorption inhibitors
HU230253B1 (hu) 2001-01-26 2015-11-30 Merck Sharp & Dohme Corp Peroxiszóma proliferátor-aktivált receptor (PPAR) aktivátor(ok) és szterin-abszorpció inhibitor(ok) kombinációi és alkalmazásuk vaszkuláris indikációk kezelésére
ATE331512T1 (de) 2001-01-26 2006-07-15 Schering Corp Verwendung azetidinone-substituierter verbindungen zur behandlung der sitosterolhämie
JP4145663B2 (ja) 2001-03-28 2008-09-03 シェーリング コーポレイション アゼチジノン中間体化合物のエナンチオ選択性合成
EP1429756B1 (en) 2001-09-21 2006-11-22 Schering Corporation Treatment of xanthoma with azetidinone derivatives as sterol absorption inhibitors
US7056906B2 (en) 2001-09-21 2006-06-06 Schering Corporation Combinations of hormone replacement therapy composition(s) and sterol absorption inhibitor(s) and treatments for vascular conditions in post-menopausal women
US7053080B2 (en) 2001-09-21 2006-05-30 Schering Corporation Methods and therapeutic combinations for the treatment of obesity using sterol absorption inhibitors
WO2004037163A2 (en) * 2002-05-14 2004-05-06 Northwestern University STERICALLY-AWKWARD β-LACTAMASE INHIBITORS
JP2006508189A (ja) 2002-11-06 2006-03-09 シェーリング　コーポレイション 自己免疫障害の処置のためのコレステロール吸収インヒビター
US7192944B2 (en) 2003-03-07 2007-03-20 Schering Corp. Substituted azetidinone compounds, processes for preparing the same, formulations and uses thereof
US7459442B2 (en) 2003-03-07 2008-12-02 Schering Corporation Substituted azetidinone compounds, processes for preparing the same, formulations and uses thereof
JP4589919B2 (ja) 2003-03-07 2010-12-01 シェーリング コーポレイション 高コレステロール血症の処置のための、置換アゼチジノン化合物、これらの処方物および使用
DE602004016123D1 (de) 2003-03-07 2008-10-09 Schering Corp Substituierte azetidinon-derivate, deren pharmazeutische formulierungen und deren verwendung zur behandlung von hypercholesterolemia

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3697515A (en) * 1963-02-18 1972-10-10 Ciba Geigy Corp Process for splitting the 7-n-acyl group from cephalosporin compounds
JPS5672698A (en) * 1979-11-14 1981-06-16 Kyowa Hakko Kogyo Co Ltd Preparation of optically active cephalosporin analogue
NO155548C (no) * 1979-02-10 1987-04-15 Kyowa Hakko Kogyo Kk Fremgangsmaate til fremstilling av optisk aktive cefalosporin-analoger.
NO155547C (no) * 1979-02-10 1987-04-15 Kyowa Hakko Kogyo Kk Optisk aktive cefalosporin-analoge og salter derav samt fremgangsmaate for deres fremstilling.
JPS60174787A (ja) * 1984-02-21 1985-09-09 Kyowa Hakko Kogyo Co Ltd ３位置換カルバセフエム化合物
US4673737A (en) * 1985-08-02 1987-06-16 Harvard University 7-acylamino-(or 7-amino)-3-trifluoromethylsulfonyloxy-1-carba(1-dethia)-3-cephem-4-carboxylic acids and esters thereof

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102144992A (zh) * 2011-03-10 2011-08-10 浙江大学 苯基甘氨酸衍生物对金黄色葡萄球菌有抑菌和杀菌活性
CN102144992B (zh) * 2011-03-10 2013-04-10 浙江大学 苯基甘氨酸衍生物制备对金黄色葡萄球菌有抑菌和杀菌活性的抗菌剂的用途

Also Published As

Publication number Publication date
JPS6396186A (ja) 1988-04-27
EP0266896A1 (en) 1988-05-11
FI874311A7 (fi) 1988-04-04
PT85850A (en) 1987-11-01
ATA257587A (de) 1988-11-15
AU7926987A (en) 1988-04-14
PT85850B (en) 1990-01-12
HUT45053A (en) 1988-05-30
IE872646L (en) 1988-04-03
DE3780909D1 (en) 1992-09-10
HU200179B (en) 1990-04-28
ATE79119T1 (de) 1992-08-15
AT388377B (de) 1989-06-12
PL268034A1 (en) 1988-09-01
DE3780909T2 (de) 1993-03-04
EP0266896B1 (en) 1992-08-05
IL84051A0 (en) 1988-03-31
GR3005920T3 (enExample) 1993-06-07
FI874311A0 (fi) 1987-10-01
PL151703B1 (en) 1990-09-28
KR880005125A (ko) 1988-06-28
ZA877398B (en) 1989-05-30
DK518487A (da) 1988-04-04
FI874311L (fi) 1988-04-04
BG47034A3 (bg) 1990-04-16
NZ222015A (en) 1989-10-27
AU591811B2 (en) 1989-12-14
DK518487D0 (da) 1987-10-02

Similar Documents

Publication Publication Date Title
CN1189469C (zh) 作为抗菌剂的3－(杂芳基乙酰氨基)－2－氧化－氮杂环丁烷－1－磺酸衍生物
CN87107149A (zh) 7-[(间位取代的)苯基甘氨酸]1-碳代-1-去硫头孢菌素
CN1145629C (zh) 头孢菌素及合成方法
CN1194980C (zh) 膦酰基头孢烯衍生物,其制备和用途
CN1243755C (zh) 用于制备头孢菌素的偶合方法和中间体
CN1043042C (zh) 7－[2－(2－氨基噻唑－4－基)－2－(Z)－羟亚胺基－乙酰胺基]－3－(甲氧甲基)－3－头孢烯－4－羧酸－α－(2,2－二甲基丙酰氧)乙酯拆分的方法
CN1046535C (zh) 红霉素a9－0－肟衍生物和含它们的药物组合物
CN1043941A (zh) 34-脱(n-乙酰葡萄糖胺基)-34-脱氧-太可普劳宁的c63酰胺衍生物
CN1108029A (zh) 克拉维酸的二胺盐
CN1040109C (zh) 新头孢菌素类抗生素及其制备方法
CN1042536C (zh) 用噻唑基中间体顺式异构体制备头孢菌素抗菌素的方法
US5635500A (en) Cephem compound and pharmaceutical composition containing the compound
WO2002068428A1 (en) Method of preparing cephalosporins using 4-hydroxyphenylglycine derivatives
CN1041731C (zh) 吡啶并[1,2,3—d,e][1,3,4]苯并噁二嗪衍生物
CN1227252C (zh) 制备6－甲基－2－(4－甲基－苯基)－咪唑并[1,2－a]吡啶－3－(N,N－二甲基－乙酰胺)和中间体的方法
CN1253458C (zh) 物质gm－95的制备方法
CN1086706C (zh) 吡啶并[3,2,1－i,j][3,1]苯并噁嗪衍生物
US20090221815A1 (en) Processes for the preparation of cephem derivatives
CN1226245C (zh) 卤化剂和羟基的卤化方法
US7622577B2 (en) Processes for the preparation of cephalosporin derivatives
CN1106412A (zh) 1-(2-氟环丙基)喹诺酮甲酸和1-(2-氟环丙基)二氮杂萘酮甲酸的衍生物
GB2137997A (en) Improvements in or relating to indolylglycyl cephalosporin derivatives
KR100404685B1 (ko) 4-히드록시페닐글리신 무수물을 이용한 세팔로스포린화합물의 제조방법
CN1090185C (zh) 有双环氨基取代的吡啶酮羧酸衍生物,其酯及盐,以及可用作其中间体的双环类胺
CN1606558A (zh) 新型头孢菌素化合物及其制备方法

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C01 Deemed withdrawal of patent application (patent law 1993)
WD01 Invention patent application deemed withdrawn after publication