KR840004437A - 설타미실린의 결정형 벤젠설포네이트 염의 제조방법 - Google Patents
설타미실린의 결정형 벤젠설포네이트 염의 제조방법 Download PDFInfo
- Publication number
- KR840004437A KR840004437A KR1019830001708A KR830001708A KR840004437A KR 840004437 A KR840004437 A KR 840004437A KR 1019830001708 A KR1019830001708 A KR 1019830001708A KR 830001708 A KR830001708 A KR 830001708A KR 840004437 A KR840004437 A KR 840004437A
- Authority
- KR
- South Korea
- Prior art keywords
- salt
- sulfamicillin
- formula
- general formula
- chlorine
- Prior art date
Links
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
- C07D499/21—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 with a nitrogen atom directly attached in position 6 and a carbon atom having three bonds to hetero atoms with at the most one bond to halogen, e.g. an ester or nitrile radical, directly attached in position 2
- C07D499/28—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 with a nitrogen atom directly attached in position 6 and a carbon atom having three bonds to hetero atoms with at the most one bond to halogen, e.g. an ester or nitrile radical, directly attached in position 2 with modified 2-carboxyl group
- C07D499/32—Esters
-
- 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
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Cephalosporin Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
Abstract
내용 없음
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (6)
- (a) 다음 구조식(B)의 유리염기 또는 이의 산부 가염을 일반식 4-XC6H4SO3H의 벤젠-설폰산과 적합한 용매 존재하에 접촉 반응시키거나 : (b) Y가 염소, 브롬 또는 요오드인 일반식 B·HY의 산부가염을 M이 알칼리금속 또는 알칼리 토금속 양이온인 일반식 4-XC6H4SO3M의 벤젠설폰산 염과 물존재하에서 접촉 반응시킴을 특징으로 하는 하기의 일반식(Ⅰ)을 갖는 설타미실린의 벤젠설폰산 부가염의 제조방법.4-XC6H4SO3H·Bn(H2O) (Ⅰ)상기식에서 n은 0내지 2이고, X는 수소 또는 염소이며, B는 다음 구조식을 나타낸다.
- 제1항에 있어서, 반응을 실온 또는 그 이하의 온도에서 수행하는 방법.
- 제1항에 있어서, n이 2인 방법.
- 제1(b)항에 있어서, Y가 염소원자이고 M이 나트륨인 방법.
- 제3항에 있어서, X가 수소이고 결정형 2수화 벤젠설폰산 부가염을 수득하는 방법.
- 제3항에 있어서, X가 염소원자이고 결정형 2수화 벤젠설폰산 염을 수득하는 방법.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US371,156 | 1982-04-23 | ||
US06/371,156 US4432987A (en) | 1982-04-23 | 1982-04-23 | Crystalline benzenesulfonate salts of sultamicillin |
Publications (2)
Publication Number | Publication Date |
---|---|
KR840004437A true KR840004437A (ko) | 1984-10-15 |
KR860001279B1 KR860001279B1 (ko) | 1986-09-05 |
Family
ID=23462725
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019830001708A KR860001279B1 (ko) | 1982-04-23 | 1983-04-22 | 설타미실린의 결정형 벤젠설포네이트 염의 제조방법 |
Country Status (27)
Country | Link |
---|---|
US (1) | US4432987A (ko) |
EP (1) | EP0092968B1 (ko) |
JP (1) | JPS58201792A (ko) |
KR (1) | KR860001279B1 (ko) |
AU (1) | AU536854B2 (ko) |
CA (1) | CA1187484A (ko) |
CS (1) | CS235320B2 (ko) |
DD (1) | DD209632A5 (ko) |
DE (1) | DE3362502D1 (ko) |
DK (1) | DK162168C (ko) |
EG (1) | EG16412A (ko) |
ES (1) | ES521728A0 (ko) |
FI (1) | FI76092C (ko) |
GR (1) | GR78582B (ko) |
HK (1) | HK20588A (ko) |
HU (1) | HU187068B (ko) |
IE (1) | IE54628B1 (ko) |
IL (1) | IL68453A (ko) |
NO (1) | NO156202C (ko) |
NZ (1) | NZ203988A (ko) |
PH (1) | PH18035A (ko) |
PL (1) | PL134978B1 (ko) |
PT (1) | PT76587B (ko) |
SG (1) | SG104087G (ko) |
SU (1) | SU1138030A3 (ko) |
YU (1) | YU43170B (ko) |
ZA (1) | ZA832845B (ko) |
Families Citing this family (24)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
ATE90879T1 (de) * | 1985-11-18 | 1993-07-15 | Access Pharma Inc | Polychelierende stoffe fuer abbildung- und spektralerhoehung (und spektrale verschiebung). |
US5336762A (en) * | 1985-11-18 | 1994-08-09 | Access Pharmaceuticals, Inc. | Polychelating agents for image and spectral enhancement (and spectral shift) |
KR910009271B1 (ko) * | 1989-06-20 | 1991-11-08 | 김영설 | 1,1-디옥소페닐실라노일 옥시메틸 D-6-[α-(메틸렌아미노)페닐-아세트아미도]-페니실라네이트와 그의 파라-톨루엔술폰산염 |
PT758651E (pt) * | 1994-05-02 | 2002-12-31 | Shionogi & Co | Cristal de derivado de pirrolidiltiocarbapenem formulacao liofilizada contendo o citado cristal e processo para a producao do mesmo |
JP3382159B2 (ja) * | 1998-08-05 | 2003-03-04 | 株式会社東芝 | 情報記録媒体とその再生方法及び記録方法 |
UA78104C2 (en) | 2002-08-29 | 2007-02-15 | Taisho Pharmaceutical Co Ltd | Benzenesulfonate salts of 4-fluoro-2-cyanopyrrolidine derivatives |
US7531650B2 (en) * | 2003-03-27 | 2009-05-12 | Basilea Pharmaceutica Ag | Cephalosporin salts in crystalline form |
KR20060130571A (ko) * | 2003-10-31 | 2006-12-19 | 알자 코포레이션 | 개선된 흡수를 위한 조성물 및 제형 |
FR2877696B1 (fr) | 2004-11-09 | 2009-09-18 | Renault Sas | Dispositif et procede d'estimation en temps reel de l'angle de debut de combustion d'un moteur a combustion interne |
EP2195293B1 (en) | 2007-08-22 | 2013-10-16 | AstraZeneca AB | Cycloptopyl amide derivatives |
EP2220050A2 (en) | 2007-10-26 | 2010-08-25 | The Regents Of The University Of California | Diarylhydantoin compounds as androgen receptor modulators |
UA106740C2 (uk) * | 2009-01-30 | 2014-10-10 | Глаксосмітклайн Ллс | Кристалічний гідрохлорид n-{(1s)-2-аміно-1-[(3-фторфеніл)метил]етил}-5-хлор-4-(4-хлор-1-метил-1h-піразол-5-іл)-2-тіофенкарбоксаміду |
TW201039825A (en) | 2009-02-20 | 2010-11-16 | Astrazeneca Ab | Cyclopropyl amide derivatives 983 |
WO2011006061A1 (en) * | 2009-07-10 | 2011-01-13 | Evolva Sa | Diyne compositions |
BR112012020629A2 (pt) | 2010-02-18 | 2018-06-19 | Astrazeneca Ab | forma cristalina, e, método para a terapia de um distúrbio |
BR112012020780A2 (pt) * | 2010-02-18 | 2016-05-03 | Astrazeneca Ab | forma sólida, composição farmacêutica, e, uso de uma forma sólida. |
US9518004B2 (en) * | 2012-12-03 | 2016-12-13 | Kaneka Corporation | Reduced coenzyme Q10 derivative and method for production thereof |
WO2015034031A1 (ja) * | 2013-09-05 | 2015-03-12 | 田辺三菱製薬株式会社 | 新規な結晶性アリールアルキルアミン化合物およびその製造方法 |
SG11201702980QA (en) * | 2014-10-21 | 2017-05-30 | Ariad Pharma Inc | Crystalline forms of 5-chloro-n4-[-2-(dimethylphosphoryl) phenyl]-n2-{2-methoxy-4-[4-(4-methylpiperazin-1-yl) piperidin-1-yl] pyrimidine-2,4-diamine |
CN104958318A (zh) * | 2015-08-04 | 2015-10-07 | 青岛蓝盛洋医药生物科技有限责任公司 | 一种治疗感染性疾病的药物舒巴坦钠组合物 |
CA3011323A1 (en) * | 2016-01-22 | 2017-07-27 | Sandoz Ag | Crystalline eravacycline bis-hydrochloride |
CN109563087A (zh) * | 2016-07-07 | 2019-04-02 | 铁木医药有限公司 | sGC刺激剂的固体形式 |
WO2019089540A1 (en) * | 2017-10-30 | 2019-05-09 | Theracaine Llc | Hydrophobic arenesulfonate salts |
US11186556B1 (en) * | 2018-10-16 | 2021-11-30 | Celgene Corporation | Salts of a thiazolidinone compound, solid forms, compositions and methods of use thereof |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4234579A (en) * | 1977-06-07 | 1980-11-18 | Pfizer Inc. | Penicillanic acid 1,1-dioxides as β-lactamase inhibitors |
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 |
IE49881B1 (en) * | 1979-02-13 | 1986-01-08 | Leo Pharm Prod Ltd | B-lactam intermediates |
US4244951A (en) * | 1979-05-16 | 1981-01-13 | Pfizer Inc. | Bis-esters of methanediol with penicillins and penicillanic acid 1,1-dioxide |
GB2084572B (en) * | 1980-10-06 | 1984-07-11 | Leo Pharm Prod Ltd | 1,1-dioxopenicillanoyloxymethyl 6-(d-aphenylacetamido)penicillanate napsylate |
IE51516B1 (en) * | 1980-10-06 | 1987-01-07 | Leo Pharm Prod Ltd | 1,1-dioxapenicillanoyloxymethyl 6-(d-alpha-amino-alpha-phenylacetamido)penicillanate napsylate |
IL64009A (en) * | 1980-10-31 | 1984-09-30 | Rech Applications Therap | Crystalline 1,1-dioxopenicillanoyloxymethyl 6-(d-alpha-amino-alpha-phenylacetamido)penicillanate tosylate hydrates,their production and pharmaceutical compositions containing them |
-
1982
- 1982-04-23 US US06/371,156 patent/US4432987A/en not_active Expired - Lifetime
-
1983
- 1983-02-28 DK DK101783A patent/DK162168C/da not_active IP Right Cessation
- 1983-04-19 SU SU833578255A patent/SU1138030A3/ru active
- 1983-04-19 PL PL1983241553A patent/PL134978B1/pl unknown
- 1983-04-20 DE DE8383302238T patent/DE3362502D1/de not_active Expired
- 1983-04-20 CS CS832817A patent/CS235320B2/cs unknown
- 1983-04-20 EG EG249/83A patent/EG16412A/xx active
- 1983-04-20 EP EP83302238A patent/EP0092968B1/en not_active Expired
- 1983-04-21 YU YU904/83A patent/YU43170B/xx unknown
- 1983-04-21 DD DD83250080A patent/DD209632A5/de not_active IP Right Cessation
- 1983-04-21 CA CA000426451A patent/CA1187484A/en not_active Expired
- 1983-04-21 IL IL68453A patent/IL68453A/xx not_active IP Right Cessation
- 1983-04-21 GR GR71155A patent/GR78582B/el unknown
- 1983-04-21 PH PH28804A patent/PH18035A/en unknown
- 1983-04-21 ES ES521728A patent/ES521728A0/es active Granted
- 1983-04-22 NO NO831430A patent/NO156202C/no not_active IP Right Cessation
- 1983-04-22 KR KR1019830001708A patent/KR860001279B1/ko not_active IP Right Cessation
- 1983-04-22 HU HU831409A patent/HU187068B/hu unknown
- 1983-04-22 PT PT76587A patent/PT76587B/pt unknown
- 1983-04-22 AU AU13871/83A patent/AU536854B2/en not_active Expired
- 1983-04-22 FI FI831392A patent/FI76092C/fi not_active IP Right Cessation
- 1983-04-22 ZA ZA832845A patent/ZA832845B/xx unknown
- 1983-04-22 IE IE926/83A patent/IE54628B1/en not_active IP Right Cessation
- 1983-04-22 JP JP58071315A patent/JPS58201792A/ja active Granted
- 1983-04-22 NZ NZ203988A patent/NZ203988A/en unknown
-
1987
- 1987-11-25 SG SG1040/87A patent/SG104087G/en unknown
-
1988
- 1988-03-17 HK HK205/88A patent/HK20588A/xx not_active IP Right Cessation
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