KR890004347B1 - 카르바페넴 중간생성물 및 그 제조방법 - Google Patents

카르바페넴 중간생성물 및 그 제조방법 Download PDF

Info

Publication number
KR890004347B1
KR890004347B1 KR1019860003078A KR860003078A KR890004347B1 KR 890004347 B1 KR890004347 B1 KR 890004347B1 KR 1019860003078 A KR1019860003078 A KR 1019860003078A KR 860003078 A KR860003078 A KR 860003078A KR 890004347 B1 KR890004347 B1 KR 890004347B1
Authority
KR
South Korea
Prior art keywords
compound
alkyl
hydrogen
nitrobenzyl
general formula
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
KR1019860003078A
Other languages
English (en)
Korean (ko)
Other versions
KR860008191A (ko
Inventor
우에다 야수쓰가
로버즈 가이
Original Assignee
브리스톨-마이어즈 컴페니
아이삭 자아코브스키
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 브리스톨-마이어즈 컴페니, 아이삭 자아코브스키 filed Critical 브리스톨-마이어즈 컴페니
Publication of KR860008191A publication Critical patent/KR860008191A/ko
Application granted granted Critical
Publication of KR890004347B1 publication Critical patent/KR890004347B1/ko
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F7/00Compounds containing elements of Groups 4 or 14 of the Periodic Table
    • C07F7/02Silicon compounds
    • C07F7/08Compounds having one or more C—Si linkages
    • C07F7/18Compounds having one or more C—Si linkages as well as one or more C—O—Si linkages
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C205/00Compounds containing nitro groups bound to a carbon skeleton
    • C07C205/39Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by esterified hydroxy groups
    • C07C205/42Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by esterified hydroxy groups having nitro groups or esterified hydroxy groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C245/00Compounds containing chains of at least two nitrogen atoms with at least one nitrogen-to-nitrogen multiple bond
    • C07C245/12Diazo compounds, i.e. compounds having the free valencies of >N2 groups attached to the same carbon atom
    • C07C245/14Diazo compounds, i.e. compounds having the free valencies of >N2 groups attached to the same carbon atom having diazo groups bound to acyclic carbon atoms of a carbon skeleton
    • C07C245/18Diazo compounds, i.e. compounds having the free valencies of >N2 groups attached to the same carbon atom having diazo groups bound to acyclic carbon atoms of a carbon skeleton the carbon skeleton being further substituted by carboxyl groups
    • 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
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F7/00Compounds containing elements of Groups 4 or 14 of the Periodic Table
    • C07F7/02Silicon compounds
    • C07F7/08Compounds having one or more C—Si linkages
    • C07F7/12Organo silicon halides
    • C07F7/16Preparation thereof from silicon and halogenated hydrocarbons direct synthesis
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F7/00Compounds containing elements of Groups 4 or 14 of the Periodic Table
    • C07F7/02Silicon compounds
    • C07F7/08Compounds having one or more C—Si linkages
    • C07F7/18Compounds having one or more C—Si linkages as well as one or more C—O—Si linkages
    • C07F7/1804Compounds having Si-O-C linkages
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F7/00Compounds containing elements of Groups 4 or 14 of the Periodic Table
    • C07F7/02Silicon compounds
    • C07F7/08Compounds having one or more C—Si linkages
    • C07F7/18Compounds having one or more C—Si linkages as well as one or more C—O—Si linkages
    • C07F7/1896Compounds having one or more Si-O-acyl linkages
    • 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)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
KR1019860003078A 1985-04-22 1986-04-21 카르바페넴 중간생성물 및 그 제조방법 Expired KR890004347B1 (ko)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US725,594 1985-04-22
US06/725,594 US4683296A (en) 1983-03-07 1985-04-22 Carbapenem intermediates

Publications (2)

Publication Number Publication Date
KR860008191A KR860008191A (ko) 1986-11-12
KR890004347B1 true KR890004347B1 (ko) 1989-10-31

Family

ID=24915191

Family Applications (1)

Application Number Title Priority Date Filing Date
KR1019860003078A Expired KR890004347B1 (ko) 1985-04-22 1986-04-21 카르바페넴 중간생성물 및 그 제조방법

Country Status (35)

Country Link
US (1) US4683296A (enExample)
JP (1) JPS61275284A (enExample)
KR (1) KR890004347B1 (enExample)
CN (1) CN86102077A (enExample)
AR (1) AR244236A1 (enExample)
AT (1) AT386208B (enExample)
AU (1) AU599022B2 (enExample)
BE (1) BE904645A (enExample)
CA (1) CA1302426C (enExample)
CH (1) CH667273A5 (enExample)
CS (1) CS266585B2 (enExample)
DD (1) DD251352A5 (enExample)
DE (1) DE3613366A1 (enExample)
DK (1) DK182386A (enExample)
ES (1) ES8708234A1 (enExample)
FI (1) FI861633A7 (enExample)
FR (1) FR2580653B1 (enExample)
GB (1) GB2173801B (enExample)
GR (1) GR861064B (enExample)
HU (1) HU195824B (enExample)
IE (1) IE59042B1 (enExample)
IL (1) IL78533A (enExample)
IT (1) IT1213061B (enExample)
LU (1) LU86401A1 (enExample)
MY (1) MY102926A (enExample)
NL (1) NL8601010A (enExample)
NO (1) NO861558L (enExample)
NZ (1) NZ215263A (enExample)
OA (1) OA08235A (enExample)
PT (1) PT82435B (enExample)
SE (1) SE8601824L (enExample)
YU (1) YU43696B (enExample)
ZA (1) ZA862987B (enExample)
ZM (1) ZM6286A1 (enExample)
ZW (1) ZW8986A1 (enExample)

Families Citing this family (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4772683A (en) * 1986-02-24 1988-09-20 Bristol-Myers Company High percentage beta-yield synthesis of carbapenem intermediates
JP2675625B2 (ja) * 1989-01-12 1997-11-12 鐘淵化学工業株式会社 エノールシリルエーテル化合物の製造方法
US5340927A (en) * 1989-07-18 1994-08-23 Merck & Co., Inc. Process for the preparation of 2-diazo-3-trisubstituted silyloxy 3-butenoates
NZ234411A (en) * 1989-07-18 1991-05-28 Merck & Co Inc Preparation of 2-diazo-3-silyloxy-3-butenoate esters
DE4014649A1 (de) * 1990-05-08 1991-11-14 Hoechst Ag Neue mehrfunktionelle verbindungen mit (alpha)-diazo-ss-ketoester- und sulfonsaeureester-einheiten, verfahren zu ihrer herstellung und deren verwendung
JP2000166962A (ja) * 1998-12-08 2000-06-20 Tatsu Ifukube 触覚刺激装置及び方法
ES2335889T3 (es) 2003-08-28 2010-04-06 Ranbaxy Laboratories Limited Proceso para la preparacion de esteres de acido 2-diazo-3-trimetilsililoxi-3-butenoico.
US20070037971A1 (en) * 2005-07-29 2007-02-15 Meeran Hashim Nizar P N Process for desilylation of carbapenem intermediates
WO2010013223A1 (en) * 2008-07-30 2010-02-04 Ranbaxy Laboratories Limited Process for the preparation of carbapenem compounds
WO2011048583A1 (en) 2009-10-23 2011-04-28 Ranbaxy Laboratories Limited Process for the preparation of carbapenem compounds
CN102690282A (zh) * 2011-07-07 2012-09-26 深圳市海滨制药有限公司 晶体形式的1β甲基碳青霉烯类抗生素中间体及其制备方法
CN102643211A (zh) * 2012-04-10 2012-08-22 平顶山佳瑞高科实业有限公司 一种2-重氮乙酰乙酸对硝基苄酯的制备方法
US10695322B2 (en) 2016-01-29 2020-06-30 The Johns Hopkins University Inhibitors of bacterial growth
CN106565535B (zh) * 2016-11-15 2018-07-17 山西师范大学 2-重氮-1-芳基酮类化合物的制备方法
CN107556212B (zh) * 2017-09-14 2020-03-24 台州昌霖化工科技有限公司 一种制备2-重氮乙酰乙酸对硝基苄酯的方法
CN114516820A (zh) * 2022-02-25 2022-05-20 山东艾孚特科技有限公司 一种制备2-重氮乙酰乙酸对硝基苄酯的方法

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0075026B1 (en) * 1981-04-03 1986-12-17 Matsushita Electric Industrial Co., Ltd. Method of cooking
US4444685A (en) * 1981-04-27 1984-04-24 Merck & Co., Inc. Stereospecific synthesis of thienamycin from penicillin
CA1190236A (en) * 1981-10-23 1985-07-09 Edward J.J. Grabowski Antibiotic synthesis
US4525582A (en) * 1982-06-22 1985-06-25 Merck & Co., Inc. Silyl, benzyl, p-nitrobenyl, or methyl esters of diazoacetate, a synthon used in the conversion of penicillin to thienamycin
CA1269978A (en) * 1982-09-28 1990-06-05 Choung U. Kim Carbapenem antibiotics
CA1220215A (en) * 1983-03-07 1987-04-07 Yasutsugu Ueda Carbapenem intermediates

Also Published As

Publication number Publication date
JPS61275284A (ja) 1986-12-05
ZA862987B (en) 1987-12-30
GB8609662D0 (en) 1986-05-29
IL78533A0 (en) 1986-08-31
YU43696B (en) 1989-10-31
CN86102077A (zh) 1987-01-28
IL78533A (en) 1992-05-25
FI861633A7 (fi) 1986-10-23
ZW8986A1 (en) 1986-12-03
FI861633A0 (fi) 1986-04-17
IE861047L (en) 1986-10-22
AT386208B (de) 1988-07-25
AR244236A1 (es) 1993-10-29
ES554217A0 (es) 1987-10-01
GR861064B (en) 1986-09-01
KR860008191A (ko) 1986-11-12
US4683296A (en) 1987-07-28
HU195824B (en) 1988-07-28
MY102926A (en) 1993-03-31
JPS6358836B2 (enExample) 1988-11-17
NO861558L (no) 1986-10-23
OA08235A (fr) 1987-10-30
DD251352A5 (de) 1987-11-11
IE59042B1 (en) 1993-12-15
ES8708234A1 (es) 1987-10-01
HUT41040A (en) 1987-03-30
CA1302426C (en) 1992-06-02
YU65886A (en) 1988-04-30
GB2173801B (en) 1989-08-23
BE904645A (fr) 1986-10-21
CH667273A5 (de) 1988-09-30
DK182386D0 (da) 1986-04-21
DK182386A (da) 1986-10-23
IT8620164A0 (it) 1986-04-21
IT1213061B (it) 1989-12-07
AU599022B2 (en) 1990-07-12
CS266585B2 (en) 1990-01-12
LU86401A1 (fr) 1986-11-05
AU5616786A (en) 1986-11-06
NZ215263A (en) 1989-03-29
CS287386A2 (en) 1989-04-14
NL8601010A (nl) 1986-11-17
DE3613366A1 (de) 1986-11-20
SE8601824D0 (sv) 1986-04-21
PT82435A (en) 1986-05-01
FR2580653B1 (fr) 1989-06-16
SE8601824L (sv) 1986-10-23
PT82435B (pt) 1988-08-17
GB2173801A (en) 1986-10-22
FR2580653A1 (fr) 1986-10-24
ZM6286A1 (en) 1987-04-30
ATA106886A (de) 1987-12-15

Similar Documents

Publication Publication Date Title
KR890004347B1 (ko) 카르바페넴 중간생성물 및 그 제조방법
EP0785205B1 (en) 2-silyloxytetrahydrothienopyridine, salt thereof, and process for producing the same
EP0752984B1 (en) Process for the preparation of cyclohexyl-azetidinones
EP0167155B1 (en) Beta-lactam compound and preparing thereof
JP4659309B2 (ja) 5−ヒドロキシ−3−オキソペンタン酸誘導体の製造法
US4983766A (en) Optically active B hydroxy acids
US5071966A (en) Process for preparing an enol silyl ether compound
EP0018594B1 (en) Process for the preparation of 3-(1-hydroxyethyl)-azetidinones
US5136066A (en) Process for preparing optically active cyclopentenone derivative
US5340927A (en) Process for the preparation of 2-diazo-3-trisubstituted silyloxy 3-butenoates
KR0154534B1 (ko) 2-디아조-3-삼치환된 실릴옥시-3-부테노에이트의 제조방법
JP3565587B2 (ja) 15−ヒドロキシミルベマイシン誘導体の新規合成法
JPH09176113A (ja) カルバペネム中間体の製法
KR100201564B1 (ko) 아제티디논 화합물 및 그 제조방법
US20020198389A1 (en) Process for preparing discodermolide and analogues thereof
US5360904A (en) Process for preparing penem esters
HU197290B (en) Process for preparing intermediate products for the production of 16-phenoxy- and 16-(substituted phenoxy)-prostatriene acid-derivatives
SK1562003A3 (en) Process for preparing discodermolide and analogues thereof
US5216187A (en) Optically active 2-methylenepentane derivative and process for preparing same
SU1682358A1 (ru) Способ получени фосфорилированных полуацеталей полуаминалей кетена
US5250715A (en) Optically active 2-methylenepentane derivative and process for preparing same
US5200538A (en) Optically active 2-methylenecyclopentanone derivative and process for preparing same
JPH0660155B2 (ja) イソカルバサイクリン類
JPH083177A (ja) ルイス酸を用いるエン―イン化合物の製造方法
GB2287709A (en) Silylated azetidinone intermediates

Legal Events

Date Code Title Description
PA0109 Patent application

St.27 status event code: A-0-1-A10-A12-nap-PA0109

R17-X000 Change to representative recorded

St.27 status event code: A-3-3-R10-R17-oth-X000

P11-X000 Amendment of application requested

St.27 status event code: A-2-2-P10-P11-nap-X000

P13-X000 Application amended

St.27 status event code: A-2-2-P10-P13-nap-X000

PG1501 Laying open of application

St.27 status event code: A-1-1-Q10-Q12-nap-PG1501

A201 Request for examination
P11-X000 Amendment of application requested

St.27 status event code: A-2-2-P10-P11-nap-X000

P13-X000 Application amended

St.27 status event code: A-2-2-P10-P13-nap-X000

PA0201 Request for examination

St.27 status event code: A-1-2-D10-D11-exm-PA0201

P11-X000 Amendment of application requested

St.27 status event code: A-2-2-P10-P11-nap-X000

P13-X000 Application amended

St.27 status event code: A-2-2-P10-P13-nap-X000

G160 Decision to publish patent application
PG1605 Publication of application before grant of patent

St.27 status event code: A-2-2-Q10-Q13-nap-PG1605

E701 Decision to grant or registration of patent right
PE0701 Decision of registration

St.27 status event code: A-1-2-D10-D22-exm-PE0701

GRNT Written decision to grant
PR0701 Registration of establishment

St.27 status event code: A-2-4-F10-F11-exm-PR0701

PR1002 Payment of registration fee

St.27 status event code: A-2-2-U10-U11-oth-PR1002

Fee payment year number: 1

PR1001 Payment of annual fee

St.27 status event code: A-4-4-U10-U11-oth-PR1001

Fee payment year number: 4

PR1001 Payment of annual fee

St.27 status event code: A-4-4-U10-U11-oth-PR1001

Fee payment year number: 5

PR1001 Payment of annual fee

St.27 status event code: A-4-4-U10-U11-oth-PR1001

Fee payment year number: 6

PR1001 Payment of annual fee

St.27 status event code: A-4-4-U10-U11-oth-PR1001

Fee payment year number: 7

FPAY Annual fee payment

Payment date: 19961029

Year of fee payment: 8

PR1001 Payment of annual fee

St.27 status event code: A-4-4-U10-U11-oth-PR1001

Fee payment year number: 8

LAPS Lapse due to unpaid annual fee
PC1903 Unpaid annual fee

St.27 status event code: A-4-4-U10-U13-oth-PC1903

Not in force date: 19971101

Payment event data comment text: Termination Category : DEFAULT_OF_REGISTRATION_FEE

R18-X000 Changes to party contact information recorded

St.27 status event code: A-5-5-R10-R18-oth-X000

R18-X000 Changes to party contact information recorded

St.27 status event code: A-5-5-R10-R18-oth-X000

R18-X000 Changes to party contact information recorded

St.27 status event code: A-5-5-R10-R18-oth-X000

PC1903 Unpaid annual fee

St.27 status event code: N-4-6-H10-H13-oth-PC1903

Ip right cessation event data comment text: Termination Category : DEFAULT_OF_REGISTRATION_FEE

Not in force date: 19971101

R18-X000 Changes to party contact information recorded

St.27 status event code: A-5-5-R10-R18-oth-X000

R18-X000 Changes to party contact information recorded

St.27 status event code: A-5-5-R10-R18-oth-X000

R18-X000 Changes to party contact information recorded

St.27 status event code: A-5-5-R10-R18-oth-X000