ES2038124T3 - Procedimiento para preparar derivados piranicos. - Google Patents

Procedimiento para preparar derivados piranicos.

Info

Publication number
ES2038124T3
ES2038124T3 ES198686310018T ES86310018T ES2038124T3 ES 2038124 T3 ES2038124 T3 ES 2038124T3 ES 198686310018 T ES198686310018 T ES 198686310018T ES 86310018 T ES86310018 T ES 86310018T ES 2038124 T3 ES2038124 T3 ES 2038124T3
Authority
ES
Spain
Prior art keywords
alkyl
formula
group
aryl
cycloalkyl
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 - Lifetime
Application number
ES198686310018T
Other languages
English (en)
Inventor
Richard William Bayles
Anthony Patrick Flynn
Ralph William Turner
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.)
Imperial Chemical Industries Ltd
Original Assignee
Imperial Chemical Industries Ltd
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 Imperial Chemical Industries Ltd filed Critical Imperial Chemical Industries Ltd
Application granted granted Critical
Publication of ES2038124T3 publication Critical patent/ES2038124T3/es
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • 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
    • C07D477/02Preparation
    • C07D477/04Preparation by forming the ring or condensed ring systems
    • 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D309/00Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings
    • C07D309/16Heterocyclic compounds containing six-membered rings having one oxygen 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
    • C07D309/28Heterocyclic compounds containing six-membered rings having one oxygen 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 hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D309/30Oxygen atoms, e.g. delta-lactones

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Molecular Biology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Saccharide Compounds (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Liquid Crystal Substances (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)

Abstract

LA INVENCION SE REFIERE A COMPUESTOS DE FORMULA (I) EN LA QUE R1 ES HIDROGENO O ALQUILO; R2 ES UN ALQUILO QUE PUEDE ESTAR SUSTITUIDO POR UNO O MAS GRUPOS ALCOXI O ATOMOS DE HALOGENO; X ES UN GRUPO DE FORMULA OR3 EN EL QUE R3 ES ALQUILO, CICLOALQUILO O ARILALQUILO, O BIEN X ES UN GRUPO -NHCVR4 SIENDO V OXIGENO O AZUFRE, R4 HIDROGENO, ALQUILO O CICLOALQUILO, ALQUENILO, ARILO, ARILALQUILO, O UN GRUPO SULFONAMINICO; Y ES ALCOXI-, CICLOALCOXI O ARILALCOXI OPCIONALMENTE SUSTITUIDOS O EL GRUPO -NR6R7 SIENDO R6 Y R7 HIDROGENO O DIVERSOS GRUPOS ALQUILO. ESTOS COMPUESTOS SON UTILES COMO PRODUCTOS INTERMEDIOS EN LA SINTESIS DE ANTIBIOTICOS DE BETA-LACTAMA.
ES198686310018T 1985-12-23 1986-12-22 Procedimiento para preparar derivados piranicos. Expired - Lifetime ES2038124T3 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB858531638A GB8531638D0 (en) 1985-12-23 1985-12-23 Chemical compounds

Publications (1)

Publication Number Publication Date
ES2038124T3 true ES2038124T3 (es) 1993-07-16

Family

ID=10590193

Family Applications (1)

Application Number Title Priority Date Filing Date
ES198686310018T Expired - Lifetime ES2038124T3 (es) 1985-12-23 1986-12-22 Procedimiento para preparar derivados piranicos.

Country Status (18)

Country Link
US (2) US5155236A (es)
EP (1) EP0230771B1 (es)
KR (1) KR940009532B1 (es)
AT (1) ATE64734T1 (es)
AU (1) AU601912B2 (es)
DE (1) DE3679977D1 (es)
DK (1) DK628486A (es)
ES (1) ES2038124T3 (es)
FI (1) FI865229A (es)
GB (2) GB8531638D0 (es)
GR (1) GR3002192T3 (es)
HU (2) HU199136B (es)
IE (1) IE59446B1 (es)
IL (1) IL80986A0 (es)
NO (1) NO865228L (es)
NZ (1) NZ218743A (es)
PT (1) PT84006B (es)
ZA (1) ZA869302B (es)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ES2061439T3 (es) * 1985-12-28 1994-12-16 Sumitomo Pharma Compuesto beta-lactama y su produccion.
US4837343A (en) * 1986-09-08 1989-06-06 Kanegafuchi Kagaku Kogyo Kabushiki Kaisha Optically active β-amino acid derivatives and their salts, and processes for producing the same
WO2021193786A1 (ja) * 2020-03-27 2021-09-30 北興化学工業株式会社 6-(フルオロアルキル)-3,4-ジヒドロ-2h-ピラン-5-カルボン酸エステル誘導体、および当該誘導体の製造方法、並びに2-(フルオロアルキル)ニコチン酸エステル誘導体の製造方法、および2-(フルオロアルキル)ニコチン酸誘導体の製造方法

Family Cites Families (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3248187A (en) * 1961-12-22 1966-04-26 Exxon Research Engineering Co Alkenyl dicarboxylic acid lactones, their method of preparation and utility
US4312871A (en) * 1979-12-03 1982-01-26 Merck & Co., Inc. 6-, 1- And 2-substituted-1-carbadethiapen-2-em-3-carboxylic acids
US4282148A (en) * 1980-01-14 1981-08-04 Merck & Co., Inc. Synthesis of thienamycin via esters of (3SR, 4RS)-3-[(SR)-1-hydroxyethyl]-β,2-dioxo-4-azetidinebutanoic acid
US4344885A (en) * 1980-01-14 1982-08-17 Merck & Co., Inc. Intermediate for the preparation of thienamycin
US4269772A (en) * 1980-01-14 1981-05-26 Merck & Co., Inc. Synthesis of thienamycin via trans-3-carboxymethylene-4-carboxy-5-methyl-Δ2 -isoxazoline
US4349687A (en) * 1980-01-14 1982-09-14 Merck & Co., Inc. Intermediate for synthesis of thienamycin via (3SR, 4RS)-3-[1 (SR)-hydroxyethyl]-2-oxo-4-azetidineacetic acid
US4287123A (en) * 1980-01-14 1981-09-01 Merck & Co., Inc. Synthesis of thienamycin via (3SR, 4RS)-3-((RS)-1-acyloxyethyl)-2-oxo-4-azetidineacetate
US4341791A (en) * 1980-10-10 1982-07-27 Merck & Co., Inc. 6-, 2- and 1,1-Disubstituted-1-carbadethiapen-2-em-3-carboxylic acid S-oxides
US4491659A (en) * 1981-03-30 1985-01-01 Merck & Co., Inc. 2,6-Didioxy-3-amine,4-carboxy methylglycoside and related compounds
HU190404B (en) * 1982-07-30 1986-09-29 Richter Gedeon Vegyeszeti Gyar Rt,Hu Process for preparing amino-lactone-carboxylic acid
HU194203B (en) * 1984-08-15 1988-01-28 Richter Gedeon Rt Process for producing amino-lactone
US4837343A (en) * 1986-09-08 1989-06-06 Kanegafuchi Kagaku Kogyo Kabushiki Kaisha Optically active β-amino acid derivatives and their salts, and processes for producing the same

Also Published As

Publication number Publication date
IE863212L (en) 1987-06-23
FI865229A (fi) 1987-06-24
PT84006A (en) 1987-01-01
KR870006031A (ko) 1987-07-08
US5155236A (en) 1992-10-13
KR940009532B1 (ko) 1994-10-14
DK628486D0 (da) 1986-12-23
EP0230771A2 (en) 1987-08-05
GB8629053D0 (en) 1987-01-14
HU197892B (en) 1989-06-28
ZA869302B (en) 1987-10-28
GR3002192T3 (en) 1992-12-30
NO865228L (no) 1987-06-24
EP0230771A3 (en) 1987-09-30
DK628486A (da) 1987-06-24
ATE64734T1 (de) 1991-07-15
AU6645986A (en) 1987-06-25
FI865229A0 (fi) 1986-12-19
AU601912B2 (en) 1990-09-20
PT84006B (pt) 1989-07-31
NO865228D0 (no) 1986-12-22
IE59446B1 (en) 1994-02-23
IL80986A0 (en) 1987-03-31
DE3679977D1 (de) 1991-08-01
US5296613A (en) 1994-03-22
GB8531638D0 (en) 1986-02-05
EP0230771B1 (en) 1991-06-26
HUT47094A (en) 1989-01-30
HU199136B (en) 1990-01-29
NZ218743A (en) 1990-02-26
HUT47557A (en) 1989-03-28

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