KR830007670A - 페니실란오일옥시메틸 페니실라네이트 1, 1, 1', 1'-테트라옥사이드의 제조방법 - Google Patents
페니실란오일옥시메틸 페니실라네이트 1, 1, 1', 1'-테트라옥사이드의 제조방법 Download PDFInfo
- Publication number
- KR830007670A KR830007670A KR1019810003366A KR810003366A KR830007670A KR 830007670 A KR830007670 A KR 830007670A KR 1019810003366 A KR1019810003366 A KR 1019810003366A KR 810003366 A KR810003366 A KR 810003366A KR 830007670 A KR830007670 A KR 830007670A
- Authority
- KR
- South Korea
- Prior art keywords
- penicillate
- tetraoxide
- general formula
- compound represented
- following general
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims 4
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical group CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 claims 3
- SJRJJKPEHAURKC-UHFFFAOYSA-N N-Methylmorpholine Chemical group CN1CCOCC1 SJRJJKPEHAURKC-UHFFFAOYSA-N 0.000 claims 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical group CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 claims 3
- RXYPXQSKLGGKOL-UHFFFAOYSA-N 1,4-dimethylpiperazine Chemical group CN1CCN(C)CC1 RXYPXQSKLGGKOL-UHFFFAOYSA-N 0.000 claims 2
- PAMIQIKDUOTOBW-UHFFFAOYSA-N 1-methylpiperidine Chemical group CN1CCCCC1 PAMIQIKDUOTOBW-UHFFFAOYSA-N 0.000 claims 2
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 claims 2
- JGFZNNIVVJXRND-UHFFFAOYSA-N N,N-Diisopropylethylamine (DIPEA) Chemical group CCN(C(C)C)C(C)C JGFZNNIVVJXRND-UHFFFAOYSA-N 0.000 claims 2
- -1 chloro, bromo, iodo Chemical group 0.000 claims 2
- 150000001875 compounds Chemical class 0.000 claims 2
- GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical group CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 claims 2
- AVFZOVWCLRSYKC-UHFFFAOYSA-N 1-methylpyrrolidine Chemical group CN1CCCC1 AVFZOVWCLRSYKC-UHFFFAOYSA-N 0.000 claims 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical group [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical group C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims 1
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 claims 1
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 claims 1
- YVBSECQAHGIWNF-UHFFFAOYSA-N N-methyl-1,2,3,4-tetrahydroquinoline Chemical group C1=CC=C2N(C)CCCC2=C1 YVBSECQAHGIWNF-UHFFFAOYSA-N 0.000 claims 1
- AHVYPIQETPWLSZ-UHFFFAOYSA-N N-methyl-pyrrolidine Chemical group CN1CC=CC1 AHVYPIQETPWLSZ-UHFFFAOYSA-N 0.000 claims 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical group [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims 1
- 125000005278 alkyl sulfonyloxy group Chemical group 0.000 claims 1
- 229910052788 barium Inorganic materials 0.000 claims 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical group [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 claims 1
- 239000011575 calcium Chemical group 0.000 claims 1
- 229910052791 calcium Inorganic materials 0.000 claims 1
- 125000004432 carbon atom Chemical group C* 0.000 claims 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims 1
- 150000001768 cations Chemical class 0.000 claims 1
- 239000003495 polar organic solvent Substances 0.000 claims 1
- 239000002798 polar solvent Substances 0.000 claims 1
- 239000011591 potassium Chemical group 0.000 claims 1
- 229910052700 potassium Inorganic materials 0.000 claims 1
- 239000011734 sodium Substances 0.000 claims 1
- 229910052708 sodium Inorganic materials 0.000 claims 1
- IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical group CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 claims 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D499/00—Heterocyclic compounds containing 4-thia-1-azabicyclo [3.2.0] heptane ring systems, i.e. compounds containing a ring system of the formula:, e.g. penicillins, penems; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulfur-containing hetero ring
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/04—Antibacterial agents
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Communicable Diseases (AREA)
- Pharmacology & Pharmacy (AREA)
- Oncology (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
내용 없음
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (5)
- 하기 일반식(VII)로 표시되는 화합물을 하기 일반식(III)으로 표시되는 화합물과 반응시킴을 특징으로 하는 페니실란 오일옥시메틸 페니실라네이트 1,1,1',1'-테트라옥사이드의 제조방법.(식중, M는 카르복실산업 생성 양이온이고, X는 탈리가 용이한 이탈기임).
- 제1항에 있어서 M이 나트륨, 칼륨, 칼슘, 바륨, 트리메틸아민, 트리에틸아민, 트리부틸아민, 디이소프로필에틸아민, N-메틸모르폴린, N-메틸피페미딘, N-메틸피롤리딘, N,N'-디메틸피페라진 또는 N-메틸-1,2,3,4-테트라히드로퀴놀린 염임을 특징으로 하는 방법.
- 제1항 또는 제2항에 있어서 X가 클로로, 브로모, 요오도, 탄소원자 1 내지 4의 알킬술포닐옥시, 페닐술포닐옥시 또는 톨릴술포닐옥시임을 특징으로 하는 방법.
- 제1항 내지 제3항에 있어서 반응을 0°내지 80℃온도하의 극성 유기 용매중에서 수행함을 특징으로 하는 방법.
- 제4항에 있어서 유기 극성 용매가 N,N-디메틸포름아미드, N,N-디메틸아세트아미드, N-메틸피롤리돈, 디메틸술폭시드 또는 핵사메틸포스포르아미드임을 특징으로 하는 방법.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US06/185,849 US4309347A (en) | 1979-05-16 | 1980-09-10 | Penicillanoyloxymethyl penicillanate 1,1,1',1'-tetraoxide |
US185849 | 1980-09-10 |
Publications (2)
Publication Number | Publication Date |
---|---|
KR830007670A true KR830007670A (ko) | 1983-11-04 |
KR850001936B1 KR850001936B1 (ko) | 1985-12-31 |
Family
ID=22682685
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019810003366A KR850001936B1 (ko) | 1980-09-10 | 1981-09-09 | 페니실란오일옥시메틸 페니실라네이트 1, 1, 1', 1'-테트라옥사이드의 제조 방법 |
Country Status (18)
Country | Link |
---|---|
US (1) | US4309347A (ko) |
EP (1) | EP0047671B1 (ko) |
JP (1) | JPS5780387A (ko) |
KR (1) | KR850001936B1 (ko) |
AR (1) | AR226744A1 (ko) |
AT (1) | ATE8631T1 (ko) |
AU (1) | AU526672B2 (ko) |
CA (1) | CA1171849A (ko) |
DE (1) | DE3165077D1 (ko) |
DK (1) | DK159158C (ko) |
ES (1) | ES8206530A1 (ko) |
FI (1) | FI72120C (ko) |
GR (1) | GR75029B (ko) |
IE (1) | IE51550B1 (ko) |
IL (1) | IL63773A (ko) |
PH (1) | PH16982A (ko) |
PT (1) | PT73639B (ko) |
YU (1) | YU42698B (ko) |
Families Citing this family (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4376076A (en) * | 1981-03-23 | 1983-03-08 | Pfizer Inc. | Bis-esters of 1,1-alkanediols with 6-beta-hydroxymethylpenicillanic acid 1,1-dioxide |
US4444687A (en) * | 1981-06-08 | 1984-04-24 | Bristol-Myers Company | 2β-Chloromethyl-2α-methylpenam-3α-carboxylic acid sulfone methylene diol mixed esters |
US4540687A (en) * | 1981-09-09 | 1985-09-10 | Pfizer Inc. | Antibacterial 6'-(2-amino-2-[4-acyloxyphenyl]acetamido)penicillanoyloxymethyl penicillanate 1,1-dioxide compounds |
US4582829A (en) * | 1981-09-09 | 1986-04-15 | Pfizer Inc. | Antibacterial 6'-(2-amino-2-[4-acyloxyphenyl]acetamido)penicillanoyloxymethyl penicillanate 1,1-dioxide compounds |
US4457924A (en) * | 1981-12-22 | 1984-07-03 | Pfizer, Inc. | 1,1-Alkanediol dicarboxylate linked antibacterial agents |
US4452796A (en) * | 1982-06-14 | 1984-06-05 | Pfizer Inc. | 6-Aminoalkylpenicillanic acid 1,1-dioxides as beta-lactamase inhibitors |
US4536393A (en) * | 1983-06-06 | 1985-08-20 | Pfizer Inc. | 6-(Aminomethyl)penicillanic acid 1,1-dioxide esters and intermediates therefor |
US4502990A (en) * | 1983-06-06 | 1985-03-05 | Pfizer Inc. | Process for 6-(aminomethyl)penicillanic acid 1,1-dioxide and derivatives thereof |
US4521533A (en) * | 1984-07-12 | 1985-06-04 | Pfizer Inc. | Salts of 6-alpha-(aminomethyl)penicillanic acid 1,1-dioxide esters and beta-lactam antibiotics |
US4958212A (en) * | 1988-12-30 | 1990-09-18 | Texas Instruments Incorporated | Trench memory cell |
CN100384857C (zh) * | 2003-11-28 | 2008-04-30 | 浙江永宁制药厂 | 耐β-内酰胺酶的头孢菌素酯化合物及其盐 |
JP4782489B2 (ja) * | 2005-06-27 | 2011-09-28 | トヨタ紡織株式会社 | フィルタ用濾材 |
Family Cites Families (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
IE34948B1 (en) * | 1970-03-12 | 1975-10-01 | Leo Pharm Prod Ltd | New penicillin esters |
GB1303491A (ko) | 1970-03-24 | 1973-01-17 | ||
GB1335718A (en) * | 1971-05-05 | 1973-10-31 | Leo Pharm Prod Ltd | Penicillin esters salts thereof and methods for their preparation |
GB1578128A (en) | 1976-03-30 | 1980-11-05 | Leo Pharm Prod Ltd | Amidinopenicillanoyloxyalkyl amoxycillinates |
IN149747B (ko) | 1977-06-07 | 1982-04-03 | Pfizer | |
IE49880B1 (en) * | 1979-02-13 | 1986-01-08 | Leo Pharm Prod Ltd | Penicillin derivatives |
BE881675A (fr) | 1979-02-13 | 1980-08-12 | Leo Pharm Prod Ltd | B-lactames derives de l'acide penicillanique leur preparation et leurs utilisations therapeutiques |
US4244951A (en) * | 1979-05-16 | 1981-01-13 | Pfizer Inc. | Bis-esters of methanediol with penicillins and penicillanic acid 1,1-dioxide |
-
1980
- 1980-09-10 US US06/185,849 patent/US4309347A/en not_active Expired - Lifetime
-
1981
- 1981-09-04 AR AR286649A patent/AR226744A1/es active
- 1981-09-08 IE IE2076/81A patent/IE51550B1/en not_active IP Right Cessation
- 1981-09-08 YU YU2145/81A patent/YU42698B/xx unknown
- 1981-09-08 GR GR65986A patent/GR75029B/el unknown
- 1981-09-08 EP EP81304113A patent/EP0047671B1/en not_active Expired
- 1981-09-08 IL IL63773A patent/IL63773A/xx not_active IP Right Cessation
- 1981-09-08 DE DE8181304113T patent/DE3165077D1/de not_active Expired
- 1981-09-08 AT AT81304113T patent/ATE8631T1/de not_active IP Right Cessation
- 1981-09-09 CA CA000385423A patent/CA1171849A/en not_active Expired
- 1981-09-09 DK DK400381A patent/DK159158C/da not_active IP Right Cessation
- 1981-09-09 JP JP56142196A patent/JPS5780387A/ja active Granted
- 1981-09-09 AU AU75082/81A patent/AU526672B2/en not_active Expired
- 1981-09-09 ES ES505345A patent/ES8206530A1/es not_active Expired
- 1981-09-09 PT PT73639A patent/PT73639B/pt unknown
- 1981-09-09 KR KR1019810003366A patent/KR850001936B1/ko active
- 1981-09-09 FI FI812803A patent/FI72120C/fi not_active IP Right Cessation
- 1981-09-09 PH PH26170A patent/PH16982A/en unknown
Also Published As
Publication number | Publication date |
---|---|
IE812076L (en) | 1982-03-10 |
DK400381A (da) | 1982-03-11 |
GR75029B (ko) | 1984-07-12 |
AU526672B2 (en) | 1983-01-27 |
IL63773A (en) | 1985-02-28 |
DK159158C (da) | 1991-03-11 |
KR850001936B1 (ko) | 1985-12-31 |
ES505345A0 (es) | 1982-08-16 |
PT73639A (en) | 1981-10-01 |
YU214581A (en) | 1983-06-30 |
AR226744A1 (es) | 1982-08-13 |
JPS643196B2 (ko) | 1989-01-19 |
US4309347A (en) | 1982-01-05 |
PH16982A (en) | 1984-05-04 |
EP0047671B1 (en) | 1984-07-25 |
DE3165077D1 (de) | 1984-08-30 |
FI72120C (fi) | 1987-04-13 |
IL63773A0 (en) | 1981-12-31 |
DK159158B (da) | 1990-09-10 |
CA1171849A (en) | 1984-07-31 |
EP0047671A1 (en) | 1982-03-17 |
PT73639B (en) | 1983-04-29 |
AU7508281A (en) | 1982-03-18 |
YU42698B (en) | 1988-10-31 |
JPS5780387A (en) | 1982-05-19 |
ATE8631T1 (de) | 1984-08-15 |
ES8206530A1 (es) | 1982-08-16 |
FI812803L (fi) | 1982-03-11 |
IE51550B1 (en) | 1987-01-07 |
FI72120B (fi) | 1986-12-31 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
KR830007670A (ko) | 페니실란오일옥시메틸 페니실라네이트 1, 1, 1', 1'-테트라옥사이드의 제조방법 | |
FR2368457A1 (fr) | Procede de preparation de cetones contenant du fluor | |
ES511705A0 (es) | Procedimiento para preparar fluormetilpiridinas. | |
KR970042536A (ko) | 아스코르브산의 제조방법 | |
KR910002865A (ko) | 피라노벤즈옥사디아졸 화합물 및 그 광학적 분할방법 | |
KR840006487A (ko) | 세팔로스포린의 제조방법 | |
GB1527807A (en) | Thiazolines | |
KR830001948A (ko) | 페니실린 설폭사이드의 제조방법 | |
KR830009077A (ko) | 푸란 유도체의 제조방법 | |
KR830007639A (ko) | 락탐 화합물의 제조방법 | |
KR890003777A (ko) | 3-(치환된)프로페닐-7-(아미노티아졸릴아세트아미도)세프-3-엠-4-카복실산과 그것의 에스텔 | |
GB1535149A (en) | Process for the preparation of certain nuclear-chlorinated benzotrichlorides | |
KR830006180A (ko) | 뱃트물감제조용 신규중간물 α-벤즈아미도-5'(또는 8')-할로게노-1, 1'-디안트 리미드류 등의 α-벤즈아미도 -α'-할로게노-1, 1'-디안트리미드류의 제조방법 | |
BR8205950A (pt) | Processo para a obtencao de compostos alfa-diciano-trimetil-sililoxi | |
KR870001174A (ko) | 2-시아노아미노-피리미딘 유도체의 제조방법 | |
KR830003458A (ko) | 2-티옥소-3-벤조치아졸린 아세토니트릴의 유도체 | |
ES549357A0 (es) | Procedimiento para la obtencion de esteres del acido 4-aci- loxi-3-oxo-butirico | |
KR870000276A (ko) | (+)6-메톡시-α-메틸-2-나프탈렌 아세트산의 에스테르 제조방법 | |
KR830007675A (ko) | 6-[D-(-)-α-(4-에칠2,3-디옥소-1-피페라지노 카보닐아미노)-페닐(또는 하이드록시 페닐)아세트아미노]페니실란산 및 그 염의 제조방법 | |
SU977457A1 (ru) | Диангидриды мостиковых динафтилтетракарбоновых кислот в качестве исходных дл получени полинафтоиленбисбензимидазолов и способ их получени | |
KR890002217A (ko) | 신규 디오스민 유도체의 제조 | |
JPS55122757A (en) | Production of thio-di-phthalic acid or anhydride | |
KR850007927A (ko) | 세팔로스포린 유도체 결정성염의 제조방법 | |
KR870000344A (ko) | 7-(d-2-포밀옥시-2-페닐아세트아미도)-3-(1-메틸-1h-테트라졸-5-일티오메틸)-3-세펨-4-카복실산 유도체의 신규 제조방법 | |
JPS6257623B2 (ko) |