ES2002303A6 - Procedimiento para preparar nuevos antibioticos de carbapenem-2-sustituidos. - Google Patents

Procedimiento para preparar nuevos antibioticos de carbapenem-2-sustituidos.

Info

Publication number
ES2002303A6
ES2002303A6 ES8601760A ES8601760A ES2002303A6 ES 2002303 A6 ES2002303 A6 ES 2002303A6 ES 8601760 A ES8601760 A ES 8601760A ES 8601760 A ES8601760 A ES 8601760A ES 2002303 A6 ES2002303 A6 ES 2002303A6
Authority
ES
Spain
Prior art keywords
alkyl
carbapenem antibiotics
moiety
cyanomethyl
propargyl
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
ES8601760A
Other languages
English (en)
Inventor
Alain Martel
Carol Bachand
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.)
Bristol Myers Co
Original Assignee
Bristol Myers 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 Bristol Myers Co filed Critical Bristol Myers Co
Publication of ES2002303A6 publication Critical patent/ES2002303A6/es
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic 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
    • C07D487/04Ortho-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D477/00Heterocyclic compounds containing 1-azabicyclo [3.2.0] heptane ring systems, i.e. compounds containing a ring system of the formula:, e.g. carbapenicillins, thienamycins; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulphur-containing hetero ring
    • C07D477/10Heterocyclic compounds containing 1-azabicyclo [3.2.0] heptane ring systems, i.e. compounds containing a ring system of the formula:, e.g. carbapenicillins, thienamycins; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulphur-containing hetero ring with hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached in position 4, and 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
    • C07D477/12Heterocyclic compounds containing 1-azabicyclo [3.2.0] heptane ring systems, i.e. compounds containing a ring system of the formula:, e.g. carbapenicillins, thienamycins; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulphur-containing hetero ring with hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached in position 4, and 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 hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, attached in position 6
    • C07D477/16Heterocyclic compounds containing 1-azabicyclo [3.2.0] heptane ring systems, i.e. compounds containing a ring system of the formula:, e.g. carbapenicillins, thienamycins; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulphur-containing hetero ring with hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached in position 4, and 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 hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, attached in position 6 with hetero atoms or carbon atoms 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 3
    • C07D477/20Sulfur atoms
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/04Antibacterial agents

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Communicable Diseases (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Oncology (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)

Abstract

PROCEDIMIENTO PARA PREPARAR NUEVOS ANTIBIOTICOS DE CARBAPENEM-2-SUSTITUIDOS DE FORMULA I, DONDE R2 ES H O UN GRUPO PROTECTOR CONVENCIONAL; B ES H O -CH3; N ES 0, 1, 2 O 3; M ES 1 O 2 Y R ES ALQUILO C1-6, ALILO, PROPARGILO, CARBOXIMETILO, CIANOMETILO O ARALQUILO, DONDE EL RADICAL ARILO ES FENILO O HETEROARILO Y EL RADICAL ALQUILO ES ALQUILO C1-6, ESTANDO EL ANILLO HETERO-CICLICO QUE CONTIENE EL GRUPO SULFONIO OPCIONALMENTE SUSTITUIDO EN UNO O DOS ATOMOS DEL ANILLO CON UNO INTERMEDI IV CON UN TIOL (A) EN UN DISOLVENTE ORGANICO PARA FORMAR UN INTERMEDIO II Y POSTERIOR ALQUILACION DE ESTE INTERMEDIO CON UN AGENTE ALQUILANTE R-XK, DONDE XK ES UN GRUPO SALIENTE CONVENCIONAL. LOS COMPUESTOS I OBTENIDOS SON POTENTES ANTIBIOTICOS FRENTE A BACTERIAS GRAM B Y GRAM C. SON UTILES PARA EL TRATAMIENTO DE INFECCIONES MICROBIANAS EN MAMIFEROS. TAMBIEN SE EMPLEAN COMO ADITIVOS EN EL PIENSO DE ANIMALES, BACTERICIDAS EN APLICACIONES INDUSTRIALES Y COMO DESINFECTANTES.
ES8601760A 1985-09-11 1986-09-10 Procedimiento para preparar nuevos antibioticos de carbapenem-2-sustituidos. Expired ES2002303A6 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US06/774,628 US4665169A (en) 1985-09-11 1985-09-11 Carbapenem antibiotics

Publications (1)

Publication Number Publication Date
ES2002303A6 true ES2002303A6 (es) 1988-08-01

Family

ID=25101800

Family Applications (1)

Application Number Title Priority Date Filing Date
ES8601760A Expired ES2002303A6 (es) 1985-09-11 1986-09-10 Procedimiento para preparar nuevos antibioticos de carbapenem-2-sustituidos.

Country Status (31)

Country Link
US (1) US4665169A (es)
JP (1) JPS6261980A (es)
KR (1) KR910006807B1 (es)
CN (1) CN1015261B (es)
AR (1) AR242577A1 (es)
AT (1) AT396472B (es)
AU (1) AU596990B2 (es)
BE (1) BE905415A (es)
CH (1) CH669381A5 (es)
CS (1) CS259892B2 (es)
DD (1) DD252605A1 (es)
DE (1) DE3630857C2 (es)
DK (1) DK433586A (es)
ES (1) ES2002303A6 (es)
FI (1) FI81803C (es)
FR (1) FR2587704B1 (es)
GB (1) GB2180238B (es)
GR (1) GR862313B (es)
HU (1) HU198491B (es)
IL (1) IL79969A0 (es)
IT (1) IT1207578B (es)
LU (1) LU86575A1 (es)
MY (1) MY102957A (es)
NL (1) NL8602282A (es)
NZ (1) NZ217519A (es)
PT (1) PT83361B (es)
SE (1) SE469630B (es)
SU (1) SU1480764A3 (es)
YU (1) YU45800B (es)
ZA (1) ZA866638B (es)
ZW (1) ZW16186A1 (es)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
HU209817B (en) * 1989-03-28 1994-11-28 Pfizer Process for the production of antibacterial 2-carbapenem derivatives
US5321020A (en) * 1989-03-28 1994-06-14 Pfizer Inc. Antibacterial 2-carbapenem derivatives
US5602118A (en) * 1993-03-16 1997-02-11 American Cyanamid Company 2-thiosubstituted carbapenems
RU2714730C1 (ru) 2019-04-11 2020-02-19 Общество с ограниченной ответственностью "КС-ТЕХНОЛОГИИ" Конусная инерционная дробилка с опорным подшипником скольжения

Family Cites Families (20)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3950357A (en) * 1974-11-25 1976-04-13 Merck & Co., Inc. Antibiotics
US4235920A (en) * 1975-11-21 1980-11-25 Merck & Co., Inc. N-Alkylated derivatives of thienamycin
AU4061378A (en) * 1977-10-19 1980-04-17 Merck & Co., Inc. 1-azabicyclo (3.2.0) hept-2-enes
AU531084B2 (en) * 1977-10-19 1983-08-11 Merck & Co., Inc. Azetidine derivatives
EP0010317B1 (en) * 1978-10-24 1983-12-21 Merck & Co. Inc. 6-, 1- and 2-substituted-1-carbapen-2-em-3-carboxylic acids, processes for the preparation of such compounds and pharmaceutical composition comprising such compounds
US4232036A (en) * 1978-10-24 1980-11-04 Merck & Co., Inc. 6-, 1- and 2-Substituted-1-carbadethiapen-2-em-3-carboxylic acids
EP0017992A1 (en) * 1979-04-19 1980-10-29 Merck & Co. Inc. 2-Substituted-6-substituted-1-carbadethiapen-2-em-3-carboxylic acids, processes for preparing them, antibiotic pharmaceutical compositions containing same and process for preparing intermediates
US4376774A (en) * 1979-05-29 1983-03-15 Merck & Co., Inc. Antibiotic N-heterocyclyl thienamycin
IE52147B1 (en) * 1980-03-27 1987-07-08 Merck & Co Inc 4-(3-carboxy-2-oxopropyl)-azetidin-2-ones and process for their preparation
EP0037082B1 (en) * 1980-03-27 1985-03-20 Merck & Co. Inc. Process for the preparation of 1-carbapenems and intermediates via silyl-substituted dithioacetals
US4309346A (en) * 1980-03-27 1982-01-05 Merck & Co., Inc. Process for the preparation of 1-carbapenems and intermediates via trithioorthoacetates
EP0038869A1 (en) * 1980-04-30 1981-11-04 Merck & Co. Inc. Process for the preparation of 1-carbapenems, and intermediates for their preparation
JPS56161393A (en) * 1980-05-16 1981-12-11 Sanraku Inc Beta-lactam compound
CA1198440A (en) * 1982-04-08 1985-12-24 Choung U. Kim Carbapenem antibiotics
US4552696A (en) * 1982-04-09 1985-11-12 Bristol-Myers Company Carbapenem antibiotics
US4536335A (en) * 1982-06-18 1985-08-20 Bristol-Myers Company Carbapenem antibiotics
FI832619A (fi) * 1982-07-26 1984-01-27 Sandoz Ag Fluoralkylerade karbapenemderivat
CA1269978A (en) * 1982-09-28 1990-06-05 Choung U. Kim Carbapenem antibiotics
DK140584A (da) * 1983-03-08 1984-09-09 Bristol Myers Co Fremgangsmaade til fremstilling af carbapenemderivater
JPS60202886A (ja) * 1984-03-27 1985-10-14 Sankyo Co Ltd 1―置換カルバペネム―3―カルボン酸誘導体

Also Published As

Publication number Publication date
FI863609A (fi) 1987-03-12
SE8603798D0 (sv) 1986-09-10
GB8621759D0 (en) 1986-10-15
AR242577A1 (es) 1993-04-30
ZW16186A1 (en) 1988-03-30
FR2587704A1 (fr) 1987-03-27
PT83361B (pt) 1989-05-12
CN1015261B (zh) 1992-01-01
DK433586D0 (da) 1986-09-10
YU158586A (en) 1988-02-29
KR870003110A (ko) 1987-04-15
CS656786A2 (en) 1988-03-15
AT396472B (de) 1993-09-27
ZA866638B (en) 1987-05-27
SE8603798L (sv) 1987-03-12
GB2180238A (en) 1987-03-25
CN86105933A (zh) 1987-05-20
CH669381A5 (es) 1989-03-15
FI81803C (fi) 1990-12-10
IL79969A0 (en) 1986-12-31
DE3630857C2 (de) 1994-04-07
AU6234886A (en) 1987-03-12
FR2587704B1 (fr) 1989-02-24
DE3630857A1 (de) 1987-03-19
ATA245286A (de) 1993-01-15
HUT42487A (en) 1987-07-28
DK433586A (da) 1987-03-12
US4665169A (en) 1987-05-12
GR862313B (en) 1987-01-12
YU45800B (sh) 1992-07-20
FI863609A0 (fi) 1986-09-08
SE469630B (sv) 1993-08-09
BE905415A (fr) 1987-03-10
DD252605A1 (de) 1987-12-23
MY102957A (en) 1993-03-31
KR910006807B1 (ko) 1991-09-02
GB2180238B (en) 1989-09-06
NL8602282A (nl) 1987-04-01
FI81803B (fi) 1990-08-31
AU596990B2 (en) 1990-05-24
LU86575A1 (fr) 1987-04-02
JPS6261980A (ja) 1987-03-18
IT1207578B (it) 1989-05-25
IT8621666A0 (it) 1986-09-10
HU198491B (en) 1989-10-30
SU1480764A3 (ru) 1989-05-15
CS259892B2 (en) 1988-11-15
NZ217519A (en) 1990-07-26
PT83361A (en) 1986-10-01

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Legal Events

Date Code Title Description
SA6 Expiration date (snapshot 920101)

Free format text: 2006-09-10