KR840005450A - 말론산에스테르의 이성화 방법 - Google Patents
말론산에스테르의 이성화 방법 Download PDFInfo
- Publication number
- KR840005450A KR840005450A KR1019830002960A KR830002960A KR840005450A KR 840005450 A KR840005450 A KR 840005450A KR 1019830002960 A KR1019830002960 A KR 1019830002960A KR 830002960 A KR830002960 A KR 830002960A KR 840005450 A KR840005450 A KR 840005450A
- Authority
- KR
- South Korea
- Prior art keywords
- isomerization
- carried out
- acid ester
- formula
- substituted
- Prior art date
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D498/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D505/00—Heterocyclic compounds containing 5-oxa-1-azabicyclo [4.2.0] octane ring systems, i.e. compounds containing a ring system of the formula:, e.g. oxacephalosporins; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulfur-containing hetero ring
-
- 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)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Cephalosporin Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Abstract
내용 없음
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (7)
- 염기로 식(Ⅱ)의 해당하는 이성체를 이성화 시켜 생성물을 침전시킴을 특징으로 하는식(Ⅰ)의 7β-말론아미도-7α-메톡시-3-테트라졸릴티오메틸-1-데티아-1-옥사-3-세펨-4-카르복실산 에스테르의 제조방법.상기식에서, Ar은 적절히 치환된 아릴 또는 헤테로고리기이다 ; Tet는 저급알킬기로 치환된 테트라졸릴기이다 ; B1및 B2는 페닐실린 또는 세팔로스포린 화학의 분야에서 각각 에스테르 형성기이다.
- 제1항에 있어서, Ar이 페닐, 히드록시페닐 또는 티에닐임을 특징으로 하는 방법.
- 제1항에 있어서, B1및 B2는 각각 같거나 또는 다른기로써, C1∼C6알킬 또는 할로겐에 의해 치환 가능한 C7∼C12아랄킬, C1∼C3-알콕시 또는 니트로기 임을 특징으로 하는 방법.
- 제1항에 있어서, 염기가 탄산수소알칼리금속, 3개의 저급알킬아민, 디에탄올아민, 트리에탄올아민,피리딘, 피콜린, 또는 루티딘으로부터 선택됨을 특징으로 하는 방법.
- 제1항에 있어서, 이성화는 벤젠, 디클로로메탄, 클로로포름, 에테르, 초산에틸, 메탄올, 에탄올, 물 및 이들의 혼합물로부터 선택된 용매에서 실행됨을 특징으로 하는 방법.
- 제1항에 있어서, 침전은 난용성 용매를 가하고, 농축 또는 결정화에 의해 실행됨을 특징으로 하는 방법.
- 제1항에 있어서, 이성화는 5분∼10시간동안, 0℃∼50℃의 온도에서 실행됨을 특징으로 하는 방법.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP116048 | 1982-07-02 | ||
JP57116048A JPS597193A (ja) | 1982-07-02 | 1982-07-02 | マロニルメチル基の異性化方法 |
Publications (2)
Publication Number | Publication Date |
---|---|
KR840005450A true KR840005450A (ko) | 1984-11-12 |
KR890000812B1 KR890000812B1 (ko) | 1989-04-08 |
Family
ID=14677411
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019830002960A KR890000812B1 (ko) | 1982-07-02 | 1983-06-30 | 말론산에스테르의 이성화 방법 |
Country Status (30)
Country | Link |
---|---|
US (1) | US4504658A (ko) |
EP (1) | EP0098545B1 (ko) |
JP (1) | JPS597193A (ko) |
KR (1) | KR890000812B1 (ko) |
AR (1) | AR242391A1 (ko) |
AT (1) | ATE19401T1 (ko) |
AU (1) | AU564850B2 (ko) |
BG (1) | BG37526A3 (ko) |
CA (1) | CA1192193A (ko) |
CS (1) | CS244940B2 (ko) |
DD (1) | DD210052A5 (ko) |
DE (2) | DE3363161D1 (ko) |
DK (1) | DK160502C (ko) |
EG (1) | EG16539A (ko) |
ES (1) | ES8500954A1 (ko) |
FI (1) | FI832407L (ko) |
GB (1) | GB2124217B (ko) |
GR (1) | GR78620B (ko) |
HU (1) | HU187944B (ko) |
IE (1) | IE55767B1 (ko) |
IL (1) | IL69146A (ko) |
NO (1) | NO832387L (ko) |
NZ (1) | NZ204627A (ko) |
PH (1) | PH21139A (ko) |
PL (1) | PL141782B1 (ko) |
PT (1) | PT76973B (ko) |
RO (1) | RO86355B (ko) |
SU (1) | SU1225488A3 (ko) |
YU (1) | YU44011B (ko) |
ZA (1) | ZA834495B (ko) |
Families Citing this family (29)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS60123490A (ja) * | 1983-12-07 | 1985-07-02 | Shionogi & Co Ltd | マロニルオキサセフェムカルボン酸誘導体 |
US4998060A (en) * | 1989-07-12 | 1991-03-05 | Pacific Scientific Company | Fault indicator with hot stick clamping mechanism |
JP2006028154A (ja) * | 2004-06-14 | 2006-02-02 | Sumitomo Chemical Co Ltd | 光学活性化合物の製造方法 |
CN102260280A (zh) * | 2010-05-28 | 2011-11-30 | 上海医药工业研究院 | 拉氧头孢钠的制备方法 |
US9279022B1 (en) | 2014-09-08 | 2016-03-08 | Sirrus, Inc. | Solution polymers including one or more 1,1-disubstituted alkene compounds, solution polymerization methods, and polymer compositions |
US9828324B2 (en) | 2010-10-20 | 2017-11-28 | Sirrus, Inc. | Methylene beta-diketone monomers, methods for making methylene beta-diketone monomers, polymerizable compositions and products formed therefrom |
AU2011317067A1 (en) | 2010-10-20 | 2013-05-23 | Bioformix, Inc. | Synthesis of methylene malonates using rapid recovery in the presence of a heat transfer agent |
US10414839B2 (en) | 2010-10-20 | 2019-09-17 | Sirrus, Inc. | Polymers including a methylene beta-ketoester and products formed therefrom |
US9249265B1 (en) | 2014-09-08 | 2016-02-02 | Sirrus, Inc. | Emulsion polymers including one or more 1,1-disubstituted alkene compounds, emulsion methods, and polymer compositions |
JP2014532625A (ja) | 2011-10-19 | 2014-12-08 | シラス・インコーポレイテッド | メチレンβ−ジケトンモノマー、メチレンβ−ジケトンモノマーを製造するための方法、これらから作られる重合可能な組成物および製品 |
US9234107B2 (en) | 2012-03-30 | 2016-01-12 | Sirrus, Inc. | Ink coating formulations and polymerizable systems for producing the same |
US10913875B2 (en) | 2012-03-30 | 2021-02-09 | Sirrus, Inc. | Composite and laminate articles and polymerizable systems for producing the same |
JP6188252B2 (ja) | 2012-03-30 | 2017-08-30 | シラス・インコーポレイテッド | 重合性組成物の活性化方法、重合系およびこれにより形成される製品 |
US10047192B2 (en) | 2012-06-01 | 2018-08-14 | Sirrus, Inc. | Optical material and articles formed therefrom |
CN105008438B (zh) | 2012-11-16 | 2019-10-22 | 拜奥福米克斯公司 | 塑料粘结体系及方法 |
CN105164797B (zh) | 2012-11-30 | 2019-04-19 | 瑟拉斯公司 | 用于电子应用的复合组合物 |
WO2014110388A1 (en) | 2013-01-11 | 2014-07-17 | Bioformix Inc. | Method to obtain methylene malonate via bis(hydroxymethyl) malonate pathway |
US9416091B1 (en) | 2015-02-04 | 2016-08-16 | Sirrus, Inc. | Catalytic transesterification of ester compounds with groups reactive under transesterification conditions |
US9315597B2 (en) | 2014-09-08 | 2016-04-19 | Sirrus, Inc. | Compositions containing 1,1-disubstituted alkene compounds for preparing polymers having enhanced glass transition temperatures |
US10501400B2 (en) | 2015-02-04 | 2019-12-10 | Sirrus, Inc. | Heterogeneous catalytic transesterification of ester compounds with groups reactive under transesterification conditions |
US9334430B1 (en) | 2015-05-29 | 2016-05-10 | Sirrus, Inc. | Encapsulated polymerization initiators, polymerization systems and methods using the same |
US9217098B1 (en) | 2015-06-01 | 2015-12-22 | Sirrus, Inc. | Electroinitiated polymerization of compositions having a 1,1-disubstituted alkene compound |
US9518001B1 (en) | 2016-05-13 | 2016-12-13 | Sirrus, Inc. | High purity 1,1-dicarbonyl substituted-1-alkenes and methods for their preparation |
US10428177B2 (en) | 2016-06-03 | 2019-10-01 | Sirrus, Inc. | Water absorbing or water soluble polymers, intermediate compounds, and methods thereof |
US9567475B1 (en) | 2016-06-03 | 2017-02-14 | Sirrus, Inc. | Coatings containing polyester macromers containing 1,1-dicarbonyl-substituted 1 alkenes |
US10196481B2 (en) | 2016-06-03 | 2019-02-05 | Sirrus, Inc. | Polymer and other compounds functionalized with terminal 1,1-disubstituted alkene monomer(s) and methods thereof |
US9617377B1 (en) | 2016-06-03 | 2017-04-11 | Sirrus, Inc. | Polyester macromers containing 1,1-dicarbonyl-substituted 1 alkenes |
KR102115644B1 (ko) * | 2017-09-13 | 2020-05-27 | 주식회사 동도물산 | 7α-알콕시옥사세펨 중간체의 제조방법 |
CN112480147A (zh) * | 2019-09-12 | 2021-03-12 | 杭州森泽医药科技有限公司 | 一种拉氧头孢中间体溶剂化物及其制备方法和表征 |
Family Cites Families (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3719667A (en) * | 1970-08-24 | 1973-03-06 | Lilly Co Eli | Epimerization of 6-acylamido and 6-imido penicillin sulfoxide esters |
US4167630A (en) * | 1975-12-24 | 1979-09-11 | Merck & Co., Inc. | Process for epimerizing beta-lactam antibiotic compounds, and related products |
CA1085392A (en) * | 1976-03-25 | 1980-09-09 | Masayuki Narisada | Arylmalonamido-1-oxadethiacephalosporins |
US4234596A (en) * | 1976-11-19 | 1980-11-18 | Merck & Co., Inc. | 3-(2-Aminoethylthio)-6-(1-hydroxyethyl)-7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylic acid |
US4259485A (en) * | 1979-04-24 | 1981-03-31 | Eli Lilly And Company | Crystallization process |
US4252953A (en) * | 1979-05-01 | 1981-02-24 | Eli Lilly And Company | Antibiotic crystalline epimer |
US4320055A (en) * | 1980-04-07 | 1982-03-16 | Eli Lilly And Company | Process for penicillin epimerization |
JPS5711909A (en) * | 1980-06-23 | 1982-01-21 | Shionogi & Co Ltd | Stable freeze-dried preparation of beta-lactam |
-
1982
- 1982-07-02 JP JP57116048A patent/JPS597193A/ja active Granted
-
1983
- 1983-06-14 US US06/504,287 patent/US4504658A/en not_active Expired - Lifetime
- 1983-06-17 NZ NZ204627A patent/NZ204627A/en unknown
- 1983-06-20 ZA ZA834495A patent/ZA834495B/xx unknown
- 1983-06-20 GR GR71721A patent/GR78620B/el unknown
- 1983-06-28 CA CA000431350A patent/CA1192193A/en not_active Expired
- 1983-06-29 GB GB08317634A patent/GB2124217B/en not_active Expired
- 1983-06-29 RO RO111456A patent/RO86355B/ro unknown
- 1983-06-29 IE IE1527/83A patent/IE55767B1/en not_active IP Right Cessation
- 1983-06-30 HU HU832380A patent/HU187944B/hu not_active IP Right Cessation
- 1983-06-30 FI FI832407A patent/FI832407L/fi not_active Application Discontinuation
- 1983-06-30 NO NO832387A patent/NO832387L/no unknown
- 1983-06-30 AR AR83293493A patent/AR242391A1/es active
- 1983-06-30 KR KR1019830002960A patent/KR890000812B1/ko not_active IP Right Cessation
- 1983-06-30 BG BG8361551A patent/BG37526A3/xx unknown
- 1983-06-30 PH PH29144A patent/PH21139A/en unknown
- 1983-07-01 AT AT83106437T patent/ATE19401T1/de not_active IP Right Cessation
- 1983-07-01 AU AU16496/83A patent/AU564850B2/en not_active Ceased
- 1983-07-01 EP EP83106437A patent/EP0098545B1/en not_active Expired
- 1983-07-01 DD DD83252667A patent/DD210052A5/de unknown
- 1983-07-01 ES ES523774A patent/ES8500954A1/es not_active Expired
- 1983-07-01 DE DE8383106437T patent/DE3363161D1/de not_active Expired
- 1983-07-01 PT PT76973A patent/PT76973B/pt unknown
- 1983-07-01 DE DE198383106437T patent/DE98545T1/de active Pending
- 1983-07-01 SU SU833613971A patent/SU1225488A3/ru active
- 1983-07-01 PL PL1983242776A patent/PL141782B1/pl unknown
- 1983-07-01 YU YU1445/83A patent/YU44011B/xx unknown
- 1983-07-01 DK DK304983A patent/DK160502C/da not_active IP Right Cessation
- 1983-07-02 EG EG406/83A patent/EG16539A/xx active
- 1983-07-03 IL IL69146A patent/IL69146A/xx not_active IP Right Cessation
- 1983-07-04 CS CS835036A patent/CS244940B2/cs unknown
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