TNSN87101A1 - Compose b - lactamique, son procede de preparation, composition medicinale pour la therapie des maladies infectieuses bacteriennes le contenant, et intermediaires pour la synthese - Google Patents

Compose b - lactamique, son procede de preparation, composition medicinale pour la therapie des maladies infectieuses bacteriennes le contenant, et intermediaires pour la synthese

Info

Publication number
TNSN87101A1
TNSN87101A1 TNTNSN87101A TNSN87101A TNSN87101A1 TN SN87101 A1 TNSN87101 A1 TN SN87101A1 TN TNSN87101 A TNTNSN87101 A TN TNSN87101A TN SN87101 A TNSN87101 A TN SN87101A TN SN87101 A1 TNSN87101 A1 TN SN87101A1
Authority
TN
Tunisia
Prior art keywords
compound
synthesis
lactamique
intermediates
therapy
Prior art date
Application number
TNTNSN87101A
Other languages
English (en)
Inventor
Shimizu Shigeo
Takano Hiroyuki
Original Assignee
Nippon Pharmaceutical Dev Inst Company Ltd
Sankei Yakuhin Kk
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 Nippon Pharmaceutical Dev Inst Company Ltd, Sankei Yakuhin Kk filed Critical Nippon Pharmaceutical Dev Inst Company Ltd
Publication of TNSN87101A1 publication Critical patent/TNSN87101A1/fr

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D501/00—Heterocyclic 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
    • C07D501/14—Compounds having a nitrogen atom directly attached in position 7
    • C07D501/16—Compounds having a nitrogen atom directly attached in position 7 with a double bond between positions 2 and 3
    • C07D501/20—7-Acylaminocephalosporanic or substituted 7-acylaminocephalosporanic acids in which the acyl radicals are derived from carboxylic acids
    • C07D501/24—7-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
    • C07D501/36—Methylene radicals, substituted by sulfur atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D501/00—Heterocyclic 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
    • C07D501/14—Compounds having a nitrogen atom directly attached in position 7
    • C07D501/16—Compounds having a nitrogen atom directly attached in position 7 with a double bond between positions 2 and 3
    • C07D501/20—7-Acylaminocephalosporanic or substituted 7-acylaminocephalosporanic acids in which the acyl radicals are derived from carboxylic acids
    • C07D501/24—7-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
    • C07D501/26—Methylene radicals, substituted by oxygen atoms; Lactones thereof with the 2-carboxyl group
    • C07D501/34—Methylene radicals, substituted by oxygen atoms; Lactones thereof with the 2-carboxyl group with the 7-amino radical acylated by carboxylic acids containing hetero rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
    • Y—GENERAL 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
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00—Technologies relating to chemical industry
    • Y02P20/50—Improvements relating to the production of bulk chemicals
    • Y02P20/55—Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Cephalosporin Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)

Abstract

CETTE INVENTION CONCERNE UN NOUVEAU COMPOSE B - LACTAMIQUE, PLUS PARTICULIEREMENT UN COMPOSE NOUVEAU DE LA SERIE DES CEPHALOSPORINES UTILE EN TANT QU'ANTIBIOTIQUE, UN PROCEDE POUR LE PREPARER, UN INTERMEDIAIRE DE SYNTHESE ET SON EMPLOI
TNTNSN87101A 1986-07-21 1987-08-19 Compose b - lactamique, son procede de preparation, composition medicinale pour la therapie des maladies infectieuses bacteriennes le contenant, et intermediaires pour la synthese TNSN87101A1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP16986086 1986-07-21
JP27318286 1986-11-17

Publications (1)

Publication Number Publication Date
TNSN87101A1 true TNSN87101A1 (fr) 1990-01-01

Family

ID=26493073

Family Applications (1)

Application Number Title Priority Date Filing Date
TNTNSN87101A TNSN87101A1 (fr) 1986-07-21 1987-08-19 Compose b - lactamique, son procede de preparation, composition medicinale pour la therapie des maladies infectieuses bacteriennes le contenant, et intermediaires pour la synthese

Country Status (17)

Country Link
US (1) US4966900A (fr)
EP (1) EP0254495A3 (fr)
KR (1) KR880001677A (fr)
CN (1) CN87104995A (fr)
AU (1) AU597695B2 (fr)
DK (1) DK378187A (fr)
FI (1) FI872879A (fr)
HU (1) HU198944B (fr)
IL (1) IL83194A0 (fr)
MA (1) MA21148A1 (fr)
MC (2) MC1838A1 (fr)
NZ (1) NZ221052A (fr)
OA (1) OA08639A (fr)
PH (1) PH25108A (fr)
PT (1) PT85375B (fr)
TN (1) TNSN87101A1 (fr)
ZW (1) ZW13387A1 (fr)

Families Citing this family (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
MC1921A1 (fr) * 1987-04-10 1989-04-06 Sankei Yakuhin Kk Derives acyles
DK170088A (da) * 1987-04-10 1988-10-11 Hoffmann La Roche Acylderivater
FI883320A (fi) * 1987-08-07 1989-02-08 Sankei Yakuhin Kk --laktam, dess framstaellning och mellanprodukter foer dess framstaellning.
US5073550A (en) * 1987-08-14 1991-12-17 Hoffmann-La Roche Inc. Cephalosphorins with sulfur-containing oxyimino side chain
US5138066A (en) * 1987-08-14 1992-08-11 Hoffmann-La Roche, Inc. Intermediates for cephalosporins with sulfur-containing oxyimino side chain
EP0303172A3 (fr) * 1987-08-14 1991-05-15 F. Hoffmann-La Roche Ag Oxyimino-céphalosporines
US4904775A (en) * 1988-05-16 1990-02-27 E. R. Squibb & Sons, Inc. Heteroaroylhydrazide derivatives of monocyclic beta-lactam antibiotics
CA2024282A1 (fr) * 1989-09-21 1991-03-22 Peter H. Ermann Derives hydrazide heterocycliques de beta-lactam monocyclique antibiotique
US5077432A (en) * 1990-01-22 1991-12-31 E. R. Squibb & Sons, Inc. Monobactam hydrazides containing catechol sulfonic acid groups
US5030724A (en) * 1990-01-22 1991-07-09 E. R. Squibb & Sons, Inc. Monobactam hydrazides containing catechol sulfonic acid groups
ZA918014B (en) * 1990-11-05 1992-07-29 Squibb & Sons Inc Heteroaroyl derivatives of monocyclic beta-lactam antibiotics
IL99898A (en) * 1990-11-09 1996-10-31 Eisai Co Ltd 7-Noble-3- Compounds Transformed Carbamoylloxy
US5250691A (en) * 1991-09-09 1993-10-05 E. R. Squibb & Sons, Inc. Heteroaryl derivatives of monocyclic beta-lactam antibiotics
CN102659713B (zh) * 2012-05-07 2014-03-05 山东金城柯瑞化学有限公司 头孢地尼侧链酸活性酯的制备方法
CN109721618A (zh) * 2017-10-30 2019-05-07 刘力 头孢匹胺新化合物及其组合物和用途

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GR63088B (en) * 1976-04-14 1979-08-09 Takeda Chemical Industries Ltd Preparation process of novel cephalosporins
US4091671A (en) * 1977-01-05 1978-05-30 Mclees Donald J Electronic fluid level sensor
JPS5874680A (ja) * 1981-10-01 1983-05-06 Kyowa Hakko Kogyo Co Ltd β−ラクタム化合物
DE150507T1 (de) * 1983-12-29 1987-02-26 Mochida Pharmaceutical Co., Ltd., Tokio/Tokyo, Jp Cephalosporinverbindungen, verfahren zu ihrer herstellung und pharmazeutishe praeparate.
US4610824A (en) * 1984-10-09 1986-09-09 E. R. Squibb & Sons, Inc. Hydrazide derivatives of monocyclic beta-lactam antibiotics
AU586215B2 (en) * 1985-01-21 1989-07-06 Nippon Pharmaceutical Development Institute Company Limited Novel ```-lactam antibiotics
US4826834A (en) * 1985-09-27 1989-05-02 Takeda Chemical Industries, Ltd. Cephem compounds
JPS63132893A (ja) * 1986-11-25 1988-06-04 Mochida Pharmaceut Co Ltd 新規セフアロスポリン誘導体、その製法およびそれらを有効成分とする抗菌剤
DK170088A (da) * 1987-04-10 1988-10-11 Hoffmann La Roche Acylderivater
MC1921A1 (fr) * 1987-04-10 1989-04-06 Sankei Yakuhin Kk Derives acyles

Also Published As

Publication number Publication date
KR880001677A (ko) 1988-04-26
IL83194A0 (en) 1987-12-31
ZW13387A1 (en) 1988-05-18
NZ221052A (en) 1989-09-27
HUT45540A (en) 1988-07-28
HU198944B (en) 1989-12-28
EP0254495A3 (fr) 1989-11-29
US4966900A (en) 1990-10-30
FI872879A (fi) 1988-01-22
MC1838A1 (fr) 1988-06-03
EP0254495A2 (fr) 1988-01-27
PT85375B (pt) 1990-04-30
OA08639A (en) 1988-11-30
CN87104995A (zh) 1988-03-09
PH25108A (en) 1991-02-19
FI872879A0 (fi) 1987-06-30
DK378187D0 (da) 1987-07-20
MA21148A1 (fr) 1988-10-01
PT85375A (en) 1987-08-01
DK378187A (da) 1988-01-22
AU7591787A (en) 1988-01-28
AU597695B2 (en) 1990-06-07
MC210A7 (fr) 1989-06-30

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