CS235320B2 - Method of sultamiciline's addition salt preparation - Google Patents

Method of sultamiciline's addition salt preparation Download PDF

Info

Publication number
CS235320B2
CS235320B2 CS832817A CS281783A CS235320B2 CS 235320 B2 CS235320 B2 CS 235320B2 CS 832817 A CS832817 A CS 832817A CS 281783 A CS281783 A CS 281783A CS 235320 B2 CS235320 B2 CS 235320B2
Authority
CS
Czechoslovakia
Prior art keywords
formula
compound
salt
salts
aqueous
Prior art date
Application number
CS832817A
Other languages
Czech (cs)
English (en)
Inventor
Wayne E Barth
Vytautas J Jasys
Original Assignee
Pfizer
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 Pfizer filed Critical Pfizer
Publication of CS235320B2 publication Critical patent/CS235320B2/cs

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D499/00Heterocyclic 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
    • C07D499/21Heterocyclic 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
    • C07D499/28Heterocyclic 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
    • C07D499/32Esters
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D499/00Heterocyclic 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/04Antibacterial agents

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Oncology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Communicable Diseases (AREA)
  • Animal Behavior & Ethology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Cephalosporin Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
CS832817A 1982-04-23 1983-04-20 Method of sultamiciline's addition salt preparation CS235320B2 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US06/371,156 US4432987A (en) 1982-04-23 1982-04-23 Crystalline benzenesulfonate salts of sultamicillin

Publications (1)

Publication Number Publication Date
CS235320B2 true CS235320B2 (en) 1985-05-15

Family

ID=23462725

Family Applications (1)

Application Number Title Priority Date Filing Date
CS832817A CS235320B2 (en) 1982-04-23 1983-04-20 Method of sultamiciline's addition salt preparation

Country Status (27)

Country Link
US (1) US4432987A (fi)
EP (1) EP0092968B1 (fi)
JP (1) JPS58201792A (fi)
KR (1) KR860001279B1 (fi)
AU (1) AU536854B2 (fi)
CA (1) CA1187484A (fi)
CS (1) CS235320B2 (fi)
DD (1) DD209632A5 (fi)
DE (1) DE3362502D1 (fi)
DK (1) DK162168C (fi)
EG (1) EG16412A (fi)
ES (1) ES521728A0 (fi)
FI (1) FI76092C (fi)
GR (1) GR78582B (fi)
HK (1) HK20588A (fi)
HU (1) HU187068B (fi)
IE (1) IE54628B1 (fi)
IL (1) IL68453A (fi)
NO (1) NO156202C (fi)
NZ (1) NZ203988A (fi)
PH (1) PH18035A (fi)
PL (1) PL134978B1 (fi)
PT (1) PT76587B (fi)
SG (1) SG104087G (fi)
SU (1) SU1138030A3 (fi)
YU (1) YU43170B (fi)
ZA (1) ZA832845B (fi)

Families Citing this family (24)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5336762A (en) * 1985-11-18 1994-08-09 Access Pharmaceuticals, Inc. Polychelating agents for image and spectral enhancement (and spectral shift)
WO1987002893A1 (en) * 1985-11-18 1987-05-21 Board Of Regents, The University Of Texas System 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
KR100314558B1 (ko) * 1994-05-02 2002-02-28 시오노 호히코 피롤리딜티오카르바페넴유도체의결정과,상기결정을함유한동결건조제제및그제조방법
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
NZ538956A (en) 2002-08-29 2006-08-31 Taisho Pharmaceutical Co Ltd Benzenesulfonate salt of 4-fluoro-2-cyanopyrrolidine derivative used to inhibit dipeptidyl peptidase IV (DPPIV)
AU2004224181B2 (en) * 2003-03-27 2011-06-02 Basilea Pharmaceutica Ag Cephalosporin in crystalline form
JP2007509974A (ja) * 2003-10-31 2007-04-19 アルザ・コーポレーシヨン 3−アミノプロピル−n−ブチルホスフィン酸の増大した吸収のための組成物および薬用量形態
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
KR101588466B1 (ko) 2007-08-22 2016-01-25 아스트라제네카 아베 시클로프로필 아미드 유도체
EP2620432A3 (en) 2007-10-26 2013-12-18 The Regents Of the University of California Diarylhydantoin compounds
US20110288142A1 (en) * 2009-01-30 2011-11-24 Chen Pingyun Y CRYSTALLINE N--5-chloro-4-(4-chloro-1-methyl-1H-pyrazol-5-yl)-2-thiophenecarboxamide hydrochloride
TW201039825A (en) 2009-02-20 2010-11-16 Astrazeneca Ab Cyclopropyl amide derivatives 983
JP2012532886A (ja) * 2009-07-10 2012-12-20 エボルバ アクチェンゲゼルシャフト ジイン組成物
NZ602108A (en) * 2010-02-18 2014-09-26 Astrazeneca Ab Solid forms comprising a cyclopropyl amide derivative
MX2012009473A (es) 2010-02-18 2012-09-12 Astrazeneca Ab Procesos para preparar derivados de ciclopropilamidas e intermedios asociados con estas.
WO2014087972A1 (ja) * 2012-12-03 2014-06-12 株式会社カネカ 還元型補酵素q10誘導体およびその製造方法
TWI637943B (zh) * 2013-09-05 2018-10-11 田邊三菱製藥股份有限公司 新穎結晶性芳烷基胺化合物及其製造方法
CN111888368B (zh) * 2014-10-21 2024-02-02 武田药品工业株式会社 5-氯-n4-[2-(二甲基磷酰基)苯基]-n2-{2-甲氧基-4-[4-(4-甲基哌嗪-1-基)哌啶-1-基]苯基}嘧啶-2,4-二胺的晶形
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
AU2017208574B2 (en) * 2016-01-22 2022-09-22 Sandoz Ag Crystalline eravacycline bis-hydrochloride
US10889577B2 (en) 2016-07-07 2021-01-12 Cyclerion Therapeutics, Inc. Solid forms of an sGC stimulator
EP3703686A4 (en) * 2017-10-30 2021-11-17 Theracaine LLC HYDROPHOBIC ARENE SULFONATE 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)

* Cited by examiner, † Cited by third party
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
IE49881B1 (en) * 1979-02-13 1986-01-08 Leo Pharm Prod Ltd B-lactam intermediates
ZA80796B (en) * 1979-02-13 1981-02-25 Leo Pharm Prod Ltd Chemical compounds
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

Also Published As

Publication number Publication date
DK162168B (da) 1991-09-23
NO831430L (no) 1983-10-24
NZ203988A (en) 1986-01-24
KR840004437A (ko) 1984-10-15
IE830926L (en) 1983-10-23
FI831392A0 (fi) 1983-04-22
FI76092B (fi) 1988-05-31
DK101783A (da) 1983-10-24
ES8406075A1 (es) 1984-07-01
PT76587A (en) 1983-05-01
FI831392L (fi) 1983-10-24
AU1387183A (en) 1983-11-17
HK20588A (en) 1988-03-25
EG16412A (en) 1989-03-30
DK101783D0 (da) 1983-02-28
KR860001279B1 (ko) 1986-09-05
DD209632A5 (de) 1984-05-16
PL134978B1 (en) 1985-09-30
GR78582B (fi) 1984-09-27
AU536854B2 (en) 1984-05-24
CA1187484A (en) 1985-05-21
SU1138030A3 (ru) 1985-01-30
PH18035A (en) 1985-03-06
YU43170B (en) 1989-04-30
NO156202B (no) 1987-05-04
DE3362502D1 (en) 1986-04-17
FI76092C (fi) 1988-09-09
ZA832845B (en) 1984-11-28
JPS58201792A (ja) 1983-11-24
ES521728A0 (es) 1984-07-01
US4432987A (en) 1984-02-21
IL68453A0 (en) 1983-07-31
YU90483A (en) 1986-04-30
HU187068B (en) 1985-11-28
NO156202C (no) 1987-08-19
DK162168C (da) 1992-03-02
PL241553A1 (en) 1983-11-21
SG104087G (en) 1988-07-15
IL68453A (en) 1986-08-31
JPH0119395B2 (fi) 1989-04-11
EP0092968B1 (en) 1986-03-12
IE54628B1 (en) 1989-12-20
PT76587B (en) 1986-02-27
EP0092968A1 (en) 1983-11-02

Similar Documents

Publication Publication Date Title
CS235320B2 (en) Method of sultamiciline's addition salt preparation
CA1180696A (en) Method for producing chemical compounds
JPH0314811B2 (fi)
CS235502B2 (en) Method of 1-ethyl or vinyl-6-halogen-1-4-dihydro-4-oxo-7- (1-piperazinyl)-1,8-naphtyridin-3-carboxyl acid production
HU182604B (en) Process for preparing penicilline esters
KR830001903B1 (ko) 페니실란산유도체의 제조방법
FI68237B (fi) Foerfarande foer framstaellning av farmakologiskt vaerdefulla 3-(4-hydroxi-5-pyrimidyl)ureido-bensylpenicilliner
KR19990014669A (ko) 항균성 세팔로스포린
SU845789A3 (ru) Способ получени -7- -(4-окси-6-метил-НиКОТиНАМидО)- -(4-ОКСифЕНил)АцЕТАМидО -3- (1-МЕТилТЕТРАзОл-5-ил)ТиОМЕТил-3-цЕфЕМ-4-КАРбО-НОВОй КиСлОТы
KR0178956B1 (ko) 항균성 페넴 에스테르 유도체
JPS60126284A (ja) ピリドンカルボン酸誘導体およびその塩
KR0178957B1 (ko) 페넴 화합물
JPH0516437B2 (fi)
SU1015830A3 (ru) Способ получени сложных эфиров 6-амидинопенициллановых кислот или их аддитивных солей с кислотами и его вариант
KR840002214B1 (ko) 2β-클로로메틸-2α-메틸페남-3α-카르복실산 술폰, 염 또는 그의 에스테르의 제조방법
JPH05508170A (ja) 新規なジフルオロキノロンと、その合成方法と、それを含む医薬
EP0105912B1 (en) Improved melaminylthioarsenites
KR850001066B1 (ko) 2β-클로로메틸-2α-메틸페남-3α-카르복실산술폰, 2염 또는 그의 에스테르의 제조방법
IE47929B1 (en) Substituted imidazolidinyl-3-chloro-3-cephem-4-carboxylic acids
US4086236A (en) 6,7-Methylenedioxy-1-(2,2,2-trifluoroethyl)-4(1H)-quinolone-3-carboxylic acid
CA2328965A1 (en) Novel cephalosporin compounds, processes for preparation thereof and antimicrobial compositions containing the same
HU203869B (en) Process for producing salts ofnew acrylic acid derivatives and pharmaceutical compositions containing them
JPH05117280A (ja) アミノ酸置換チアゼトキノリン−3−カルボン酸誘導体
KR830001902B1 (ko) 폐니실란산유도체의 제조방법
KR970001162B1 (ko) 7-디하이드로피롤로피리미딘 라디칼을 갖는 신규 퀴놀린 카복실산 유도체 및 그의 제조방법