SU1250173A3 - Способ получени производных цефалоспорина - Google Patents

Способ получени производных цефалоспорина Download PDF

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Publication number
SU1250173A3
SU1250173A3 SU833560801A SU3560801A SU1250173A3 SU 1250173 A3 SU1250173 A3 SU 1250173A3 SU 833560801 A SU833560801 A SU 833560801A SU 3560801 A SU3560801 A SU 3560801A SU 1250173 A3 SU1250173 A3 SU 1250173A3
Authority
SU
USSR - Soviet Union
Prior art keywords
mmol
compound
mixture
room temperature
butenyl
Prior art date
Application number
SU833560801A
Other languages
English (en)
Russian (ru)
Inventor
Абураки Симпеи
Камати Хадзиме
Нарита Юкио
Окумура Юн
Наито Такаюки
Original Assignee
Бристоль-Мейерз Компани (Фирма)
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 US06/354,851 external-priority patent/US4406899A/en
Application filed by Бристоль-Мейерз Компани (Фирма) filed Critical Бристоль-Мейерз Компани (Фирма)
Application granted granted Critical
Publication of SU1250173A3 publication Critical patent/SU1250173A3/ru

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Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D501/00Heterocyclic 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
    • C07D501/14Compounds having a nitrogen atom directly attached in position 7
    • C07D501/16Compounds having a nitrogen atom directly attached in position 7 with a double bond between positions 2 and 3
    • C07D501/207-Acylaminocephalosporanic or substituted 7-acylaminocephalosporanic acids in which the acyl radicals are derived from carboxylic acids
    • C07D501/247-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
    • C07D501/38Methylene radicals, substituted by nitrogen atoms; Lactams thereof with the 2-carboxyl group; Methylene radicals substituted by nitrogen-containing hetero rings attached by the ring nitrogen atom; Quaternary compounds thereof
    • C07D501/46Methylene radicals, substituted by nitrogen atoms; Lactams thereof with the 2-carboxyl group; Methylene radicals substituted by nitrogen-containing hetero rings attached by the ring nitrogen atom; Quaternary compounds thereof with the 7-amino radical acylated by carboxylic acids containing hetero rings
    • 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
SU833560801A 1982-03-04 1983-03-03 Способ получени производных цефалоспорина SU1250173A3 (ru)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US06/354,851 US4406899A (en) 1982-03-04 1982-03-04 Cephalosporins
US35753482A 1982-03-12 1982-03-12

Publications (1)

Publication Number Publication Date
SU1250173A3 true SU1250173A3 (ru) 1986-08-07

Family

ID=26998584

Family Applications (1)

Application Number Title Priority Date Filing Date
SU833560801A SU1250173A3 (ru) 1982-03-04 1983-03-03 Способ получени производных цефалоспорина

Country Status (29)

Country Link
KR (1) KR870001986B1 (el)
AT (2) AT382155B (el)
AU (1) AU562776B2 (el)
BE (1) BE896086A (el)
CA (1) CA1213882A (el)
CH (1) CH654313A5 (el)
CS (1) CS249512B2 (el)
DD (1) DD210280A5 (el)
DE (1) DE3307550A1 (el)
DK (1) DK156900C (el)
EG (1) EG15934A (el)
ES (2) ES520224A0 (el)
FI (1) FI74973C (el)
FR (1) FR2522659B1 (el)
GB (1) GB2116180B (el)
GR (1) GR77916B (el)
HU (1) HU193158B (el)
IE (1) IE56647B1 (el)
IL (1) IL68011A0 (el)
IT (1) IT1170307B (el)
LU (1) LU84674A1 (el)
MY (1) MY8700943A (el)
NL (2) NL193284C (el)
NZ (1) NZ203312A (el)
PH (1) PH18002A (el)
PT (1) PT76330B (el)
SE (1) SE453091B (el)
SU (1) SU1250173A3 (el)
YU (2) YU43822B (el)

Families Citing this family (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3409431A1 (de) * 1983-10-08 1985-04-18 Hoechst Ag, 6230 Frankfurt Cephalosporinderivate und verfahren zu ihrer herstellung
DE3404906A1 (de) * 1984-02-11 1985-08-14 Bayer Ag, 5090 Leverkusen 1-oxadethiacephalosporinderivate sowie verfahren zu ihrer herstellung
DE3419013A1 (de) * 1984-05-22 1985-11-28 Bayer Ag, 5090 Leverkusen Neue cephalosporine und verfahren zu ihrer herstellung
GB8424692D0 (en) * 1984-10-01 1984-11-07 Glaxo Group Ltd Chemical compounds
US4698336A (en) * 1985-01-30 1987-10-06 Eisai Co., Ltd. 3-(pyrrolidinio)methyl-3-cephem derivatives
FR2585705B1 (fr) * 1985-08-05 1989-01-13 Bristol Myers Co Sels de cephalosporine et compositions injectables
US4910301A (en) * 1985-08-05 1990-03-20 Bristol-Myers Company Cefepime cephalosporin salts
US4808617A (en) * 1985-12-18 1989-02-28 Bristol-Myers Company Lyophilized or precipitated cephalosporin zwitterion and salt combination
DE3789466T2 (de) * 1986-03-17 1994-07-28 Fujisawa Pharmaceutical Co 3,7-Disubstituierte-3-Cephemverbindungen und Verfahren zu ihrer Herstellung.
CA2011116C (en) * 1989-03-06 1999-11-16 Murray A. Kaplan Lyophilized bmy-28142 dihydrochloride for parenteral use
ATE201025T1 (de) 1991-03-08 2001-05-15 Biochemie Gmbh Verfahren zur herstellung von cephalosporinen und zwischenprodukte in diesem verfahren
MY108872A (en) * 1991-09-10 1996-11-30 Bristol Myers Squibb Co Preparation of a cephalosporin antibiotic using the syn-isomer of a thiazolyl intermediate.
YU81692A (sh) * 1991-09-10 1995-03-27 Bristol-Myers Co. Postupak za proizvodnju cefalosporinskog antibiotika
US5523400A (en) * 1993-04-16 1996-06-04 Hoffmann-La Roche Inc. Cephalosporin antibiotics
EP1699804B1 (en) * 2003-12-23 2008-02-06 Sandoz Gmbh Process for production of intermediates for use in cefalosporin synthesis

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2715385A1 (de) * 1976-04-14 1977-11-10 Takeda Chemical Industries Ltd Cephalosporinderivate, verfahren zu ihrer herstellung und sie enthaltende arzneimittel
GB1591439A (en) * 1976-10-01 1981-06-24 Glaxo Operations Ltd 7-syn (oxyimino -acylamido) cephalosporins
AR229883A1 (es) * 1978-05-26 1983-12-30 Glaxo Group Ltd Procedimiento para la preparacion de antibiotico(6r,7r)-7-((z)-2-(2-aminotiazol-4-il)-2-(2-carboxiprop-2-oxiimino)-acetamido)-3-(1-piridinometil)-cef-3-em-4-carboxilato
IE49099B1 (en) * 1978-10-27 1985-07-24 Glaxo Group Ltd Cephalosporin compounds
US4443444A (en) * 1980-08-11 1984-04-17 Fujisawa Pharmaceutical Co., Ltd. Cephem compounds

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
Выложенна за вка DE 3037102, кл. С 07 D 501/46, опублик. 1981. Европейский патент № 0045937, кл. С 07 D 501/46, опублик.17.02.82. ; (54) (57) СПОСОБ ПОЛУЧЕНИЯ ПРОИЗВОЛ- : НЬК ЦЕФАЛОСПОРИНА общей формулы T4-jr-C-CONH-r-f „ ®/HiNV fi. ов СОО Щ (I); где R - пр мой или разветвленный . С -Сд-алкил, аллил, 2-бутенил, 3-бу- тенил или 2-карбоксипропил, о т л и - чающийс тем, что соединение общей формулы iry-CONH-T-f Л лм., . BiHNVr оЛу VoСООВо ORj. (II) где R - пр мой нпи разветвленный С -Сд-алкил, аллил, 2-буте- .нил, 3-бутенил или 2-карбок- сипропил, в которбм2-кар- бокситруппа защищена в виде сложного эфира, такого, как трет-бутиловый; В - группа, защищающа аминогруппу ,. така , .как третил; В, ,- группа, образующа сложный эфир, такой, как дифенил- метиловый или бензгидрил;о- вый, подвергают взаимодействию с N-метил- пирролидином в среде растворител при комнатной температуре, в обра- зующемс продукте удал ют защитные группы кислотным гидролизом и выдел ют целевой продукт-. Пр.иоритет по при *

Also Published As

Publication number Publication date
IT8347826A0 (it) 1983-03-01
PT76330A (en) 1983-04-01
GR77916B (el) 1984-09-25
PT76330B (en) 1986-02-04
FI830689A0 (fi) 1983-03-01
AU1130483A (en) 1983-09-08
SE8301178D0 (sv) 1983-03-03
ES526397A0 (es) 1985-09-16
ES8507557A1 (es) 1985-09-16
ES8403919A1 (es) 1984-04-01
BE896086A (fr) 1983-09-05
DD210280A5 (de) 1984-06-06
NL193284C (nl) 1999-05-06
AT384612B (de) 1987-12-10
AU562776B2 (en) 1987-06-18
GB2116180A (en) 1983-09-21
DK86283A (da) 1983-09-05
DK86283D0 (da) 1983-02-24
IL68011A0 (en) 1983-06-15
NL8300755A (nl) 1983-10-03
ATA228285A (de) 1987-05-15
FI74973B (fi) 1987-12-31
KR840004118A (ko) 1984-10-06
NL990039I2 (nl) 2000-04-03
FI74973C (fi) 1988-04-11
DK156900B (da) 1989-10-16
AT382155B (de) 1987-01-26
DE3307550A1 (de) 1983-09-15
NL193284B (nl) 1999-01-04
SE8301178L (sv) 1983-09-05
NL990039I1 (nl) 2000-01-03
YU52383A (en) 1986-02-28
EG15934A (en) 1987-10-30
NZ203312A (en) 1985-12-13
IE56647B1 (en) 1991-10-23
ATA76183A (de) 1986-06-15
YU44777B (en) 1991-02-28
CA1213882A (en) 1986-11-12
FR2522659A1 (fr) 1983-09-09
YU43822B (en) 1989-12-31
DE3307550C2 (el) 1988-11-24
KR870001986B1 (ko) 1987-10-24
IE830455L (en) 1983-09-04
GB2116180B (en) 1985-09-18
GB8305940D0 (en) 1983-04-07
FR2522659B1 (fr) 1986-10-24
LU84674A1 (fr) 1983-11-17
YU149685A (en) 1986-02-28
ES520224A0 (es) 1984-04-01
FI830689L (fi) 1983-09-05
HU193158B (en) 1987-08-28
CS249512B2 (en) 1987-03-12
DK156900C (da) 1990-03-12
MY8700943A (en) 1987-12-31
PH18002A (en) 1985-02-28
SE453091B (sv) 1988-01-11
CH654313A5 (de) 1986-02-14
IT1170307B (it) 1987-06-03

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