CA1059988A - Procede pour la fabrication de derives enol - Google Patents

Procede pour la fabrication de derives enol

Info

Publication number
CA1059988A
CA1059988A CA220,745A CA220745A CA1059988A CA 1059988 A CA1059988 A CA 1059988A CA 220745 A CA220745 A CA 220745A CA 1059988 A CA1059988 A CA 1059988A
Authority
CA
Canada
Prior art keywords
lower alkyl
phenoxyacetamido
formula
methoxy
carboxylic acid
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
CA220,745A
Other languages
English (en)
Inventor
Robert B. Woodward
Hans Bickel
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.)
Novartis AG
Original Assignee
Ciba Geigy AG
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
Priority claimed from CH269374A external-priority patent/CH601310A5/de
Priority claimed from CH776674A external-priority patent/CH610584A5/de
Application filed by Ciba Geigy AG filed Critical Ciba Geigy AG
Application granted granted Critical
Publication of CA1059988A publication Critical patent/CA1059988A/fr
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C313/00Sulfinic acids; Sulfenic acids; Halides, esters or anhydrides thereof; Amides of sulfinic or sulfenic acids, i.e. compounds having singly-bound oxygen atoms of sulfinic or sulfenic groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
    • C07C313/02Sulfinic acids; Derivatives thereof
    • C07C313/04Sulfinic acids; Esters thereof
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D205/00Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom
    • C07D205/02Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings
    • C07D205/06Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
    • C07D205/08Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with one oxygen atom directly attached in position 2, e.g. beta-lactams
    • C07D205/09Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with one oxygen atom directly attached in position 2, e.g. beta-lactams with a sulfur atom directly attached in position 4
    • C07D205/095Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with one oxygen atom directly attached in position 2, e.g. beta-lactams with a sulfur atom directly attached in position 4 and with a nitrogen atom directly attached in position 3
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00Technologies relating to chemical industry
    • Y02P20/50Improvements relating to the production of bulk chemicals
    • Y02P20/55Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Cephalosporin Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
CA220,745A 1974-02-26 1975-02-25 Procede pour la fabrication de derives enol Expired CA1059988A (fr)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
CH269374A CH601310A5 (en) 1974-02-26 1974-02-26 7-Amino-3-hydroxy-2(or 3)-cephem-4-carboxylic acid derivs prepn
CH776674A CH610584A5 (en) 1974-02-26 1974-06-05 Process for the preparation of 2-(3-amino-2-oxo-4-sulphonylthio-1- azetidinyl)-3-methylenebutyric acid derivatives
CH1100074 1974-08-12

Publications (1)

Publication Number Publication Date
CA1059988A true CA1059988A (fr) 1979-08-07

Family

ID=27173851

Family Applications (2)

Application Number Title Priority Date Filing Date
CA220,745A Expired CA1059988A (fr) 1974-02-26 1975-02-25 Procede pour la fabrication de derives enol
CA325,019A Expired CA1080713A (fr) 1974-02-26 1979-04-06 Preparation industrielle de derives des acides hydroxycrotonique et hydroxyisocrotonique substitutes en 3

Family Applications After (1)

Application Number Title Priority Date Filing Date
CA325,019A Expired CA1080713A (fr) 1974-02-26 1979-04-06 Preparation industrielle de derives des acides hydroxycrotonique et hydroxyisocrotonique substitutes en 3

Country Status (21)

Country Link
JP (1) JPS625919B2 (fr)
AR (1) AR208538A1 (fr)
AT (2) AT337362B (fr)
AU (1) AU498131B2 (fr)
BE (1) BE825919A (fr)
BG (1) BG26201A3 (fr)
CA (2) CA1059988A (fr)
DD (1) DD117074A5 (fr)
DE (1) DE2506330A1 (fr)
DK (2) DK73475A (fr)
ES (2) ES435110A1 (fr)
FI (1) FI66389C (fr)
FR (1) FR2261761B1 (fr)
GB (1) GB1503581A (fr)
HU (1) HU175212B (fr)
IE (1) IE40695B1 (fr)
IL (1) IL46699A (fr)
NL (1) NL7502292A (fr)
NO (1) NO750625L (fr)
NZ (1) NZ176623A (fr)
SE (3) SE431652B (fr)

Families Citing this family (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
IT1044247B (it) * 1974-08-02 1980-03-20 Farmaceutici Italia Intermedi per la sintesi di derivati b lattamici e procedimento per la loro preparazone
CA1136132A (fr) * 1975-02-17 1982-11-23 Teruji Tsuji Cyclisation pour fermer des noyaux cephem et intermediaires ainsi obtenus
JPS5198265A (fr) * 1975-02-17 1976-08-30
AT342197B (de) * 1975-02-20 1978-03-28 Ciba Geigy Ag Neues verfahren zur herstellung von 3-cephemverbindungen
US4029645A (en) * 1975-11-17 1977-06-14 E. R. Squibb & Sons, Inc. Mercury intermediates useful in the preparation of 2-alkoxy cephalosporins
JPH0639474B2 (ja) * 1983-03-04 1994-05-25 大塚化学株式会社 セファロスポリン化合物の製造法
JPS59228854A (ja) * 1983-06-08 1984-12-22 真井 康博 薬液収納兼即効注出器
JPS60115562A (ja) * 1983-11-28 1985-06-22 Otsuka Chem Co Ltd アゼチジノン誘導体の製造法
JPS60237061A (ja) * 1984-05-08 1985-11-25 Otsuka Chem Co Ltd アゼチジノン誘導体の製造法
JPS60126263A (ja) * 1983-12-12 1985-07-05 Otsuka Chem Co Ltd アゼチジノン誘導体の製造法
GB2152497B (en) * 1983-11-28 1987-08-05 Otsuka Kagaku Kk Process for the preparation of azetidinone derivatives
JPS61178961A (ja) * 1985-02-01 1986-08-11 Otsuka Chem Co Ltd アゼチジノン誘導体の製造法
DE3725375A1 (de) * 1987-07-31 1989-02-09 Bayer Ag Stabile oxapenem-3-carbonsaeuren
JP3195959B2 (ja) * 1991-03-13 2001-08-06 大塚化学株式会社 3−ヒドロキシセフェム誘導体の製造法
JP2006507289A (ja) * 2002-11-01 2006-03-02 オーキッド ケミカルズ アンド ファーマシューティカルズ リミテッド 改良されたクロロメチルセフェム誘導体調製方法
MX350810B (es) 2011-12-20 2017-09-20 Riboscience Llc Derivados de los nucleosidos sustituidos en 4 '-azido, 3 '-fluoro como inhibidores de la replicacion del rna del vhc.
CN104011061B (zh) 2011-12-20 2017-06-13 里博科学有限责任公司 作为hcv rna复制抑制剂的2‘,4’‑二氟‑2‘‑甲基取代的核苷衍生物
US20180200280A1 (en) 2013-05-16 2018-07-19 Riboscience Llc 4'-Fluoro-2'-Methyl Substituted Nucleoside Derivatives as Inhibitors of HCV RNA Replication
CN105307661A (zh) 2013-05-16 2016-02-03 里博科学有限责任公司 4’-叠氮基,3’-脱氧基-3’-氟取代的核苷衍生物
KR102241198B1 (ko) 2013-05-16 2021-04-15 리보사이언스 엘엘씨 4'-플루오로-2'-메틸 치환된 뉴클레오시드 유도체
US10682369B2 (en) 2017-09-21 2020-06-16 Riboscience Llc 4′-fluoro-2′-methyl substituted nucleoside derivatives as inhibitors of HCV RNA replication

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2230372A1 (de) * 1972-06-21 1973-01-11 Fujisawa Pharmaceutical Co Verfahren zur herstellung von oxidierten penam-derivaten
AR206201A1 (es) * 1972-06-29 1976-07-07 Ciba Geigy Ag Procedimiento para la obtencion de compuestos de acido 7beta-amino-3-cefem-3-01-4-carboxilico0-substituidos
SE428022B (sv) * 1972-06-29 1983-05-30 Ciba Geigy Ag 7beta-amino-cefam-3-on-4-karboxylsyraforeningar till anvendning for framstellning av cefalosporinderivat

Also Published As

Publication number Publication date
SE438854B (sv) 1985-05-13
FR2261761A1 (fr) 1975-09-19
IE40695B1 (en) 1979-08-01
SE431652B (sv) 1984-02-20
CA1080713A (fr) 1980-07-01
JPS625919B2 (fr) 1987-02-07
AU498131B2 (en) 1979-02-15
AT337362B (de) 1977-06-27
IL46699A (en) 1977-11-30
FI66389B (fi) 1984-06-29
ATA108275A (de) 1976-10-15
DK73475A (fr) 1975-10-20
FI750503A (fr) 1975-08-27
FI66389C (fi) 1984-10-10
BG26201A3 (fr) 1979-02-15
ATA28178A (de) 1978-10-15
AU7849875A (en) 1976-08-26
IE40695L (en) 1975-08-26
SE7807811L (sv) 1978-07-13
IL46699A0 (en) 1975-04-25
SE7807810L (sv) 1978-07-13
DK348678A (da) 1978-08-07
NZ176623A (en) 1978-04-03
ES452915A1 (es) 1977-11-01
DD117074A5 (fr) 1975-12-20
JPS50129590A (fr) 1975-10-13
ES435110A1 (es) 1977-03-16
BE825919A (fr) 1975-08-25
SE438855B (sv) 1985-05-13
DE2506330A1 (de) 1975-09-04
AT350068B (de) 1979-05-10
FR2261761B1 (fr) 1978-08-18
SE7501317L (fr) 1975-08-27
NO750625L (fr) 1975-08-27
HU175212B (hu) 1980-06-28
AR208538A1 (es) 1977-02-15
NL7502292A (nl) 1975-08-28
GB1503581A (en) 1978-03-15

Similar Documents

Publication Publication Date Title
CA1059988A (fr) Procede pour la fabrication de derives enol
US4256739A (en) 7β-Amino-3-thio-3-cephem-4-carboxylic acid compounds, and antibacterial compositions and methods using them
US4147864A (en) Process for the manufacture of 7β-amino-3-cephem-3-ol-4 carboxylic acid compounds
US4293462A (en) Process for the manufacture of enol derivatives, and intermediates
CA1110230A (fr) ACIDES O-SUBSTITUES 7.beta.-AMINO-3-CEPHEM-3-OL-4- CARBOXYLIQUES
US4070477A (en) 2-Penem compounds
US4670431A (en) Beta-lactam antibacterial agents
IE43845B1 (en) 4-thia-1-azabicyclo/4.2.0/oct-2-ene derivatives
EP0000645B1 (fr) Isopénicillines, procédés pour leur préparation et compositions qui les contiennent
CA1070688A (fr) Analogues des cephalosporines
US4550162A (en) Process for the manufacture of enol derivatives
US4255328A (en) Sulfide intermediates for the manufacture of enol derivatives
US4434287A (en) Cephalosporin derivatives
US4072674A (en) Cis-4-oxoazetidine intermediates and methods of preparing them
US4301278A (en) Process for the manufacture of enol derivatives
US4579684A (en) Process for the manufacture of enol derivatives
CA1084054A (fr) Preparation industrielle de derives de l'acide 3- hydroxy-crotonique
CA1140554A (fr) Procede industriel d'obtention de derives de l'acide 2-(2-oxoazetidin-1-yl)-crotonique
US4364865A (en) Bicyclic unsaturated thia-aza compounds and 4-acylthio azetidinone intermediates
NO833415L (no) Fremgangsmaate for fremstilling av 6-aminoalkylpenicillansyre-1,1-dioksyder
US4444771A (en) Azeto triazolo pyrazine β-lactam antibacterial agents
JPH0246594B2 (fr)
CA1098512A (fr) Procede industriel d'obtention de derives d'enamine
CA1086755A (fr) Preparation industrielle de derives d'acide 3- methylene-butyrique
CH601224A5 (en) 7-Amino-3-hydroxy-2(or 3)-cephem-4-carboxylic acid derivs prepn