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WO2008010043A3 - Improved process for the preparation of ceforanide in pure form - Google Patents

Improved process for the preparation of ceforanide in pure form Download PDF

Info

Publication number
WO2008010043A3
WO2008010043A3 PCT/IB2007/001920 IB2007001920W WO2008010043A3 WO 2008010043 A3 WO2008010043 A3 WO 2008010043A3 IB 2007001920 W IB2007001920 W IB 2007001920W WO 2008010043 A3 WO2008010043 A3 WO 2008010043A3
Authority
WO
WIPO (PCT)
Prior art keywords
preparation
pure form
improved process
ceforanide
compound
Prior art date
Application number
PCT/IB2007/001920
Other languages
French (fr)
Other versions
WO2008010043A2 (en
Inventor
Palanisamy Senth Udayampalayam
Sivakumaran Sundaravadivelan
Athmaram Ramesh Konda
Mohamed Anish Raja Raja
Prabhat Kumar Sahoo
Original Assignee
Orchid Chemicals & Pharm Ltd
Palanisamy Senth Udayampalayam
Sivakumaran Sundaravadivelan
Athmaram Ramesh Konda
Mohamed Anish Raja Raja
Prabhat Kumar Sahoo
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 Orchid Chemicals & Pharm Ltd, Palanisamy Senth Udayampalayam, Sivakumaran Sundaravadivelan, Athmaram Ramesh Konda, Mohamed Anish Raja Raja, Prabhat Kumar Sahoo filed Critical Orchid Chemicals & Pharm Ltd
Publication of WO2008010043A2 publication Critical patent/WO2008010043A2/en
Publication of WO2008010043A3 publication Critical patent/WO2008010043A3/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D501/00Heterocyclic compounds containing 5-thia-1-azabicyclo [4.2.0] octane ring systems, i.e. compounds containing a ring system of the formula:, e.g. cephalosporins; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulfur-containing hetero ring
    • C07D501/14Compounds having a nitrogen atom directly attached in position 7
    • C07D501/16Compounds having a nitrogen atom directly attached in position 7 with a double bond between positions 2 and 3
    • C07D501/207-Acylaminocephalosporanic or substituted 7-acylaminocephalosporanic acids in which the acyl radicals are derived from carboxylic acids
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D501/00Heterocyclic compounds containing 5-thia-1-azabicyclo [4.2.0] octane ring systems, i.e. compounds containing a ring system of the formula:, e.g. cephalosporins; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulfur-containing hetero ring
    • C07D501/14Compounds having a nitrogen atom directly attached in position 7
    • C07D501/16Compounds having a nitrogen atom directly attached in position 7 with a double bond between positions 2 and 3
    • C07D501/207-Acylaminocephalosporanic or substituted 7-acylaminocephalosporanic acids in which the acyl radicals are derived from carboxylic acids
    • C07D501/247-Acylaminocephalosporanic or substituted 7-acylaminocephalosporanic acids in which the acyl radicals are derived from carboxylic acids with hydrocarbon radicals, substituted by hetero atoms or hetero rings, attached in position 3
    • C07D501/26Methylene radicals, substituted by oxygen atoms; Lactones thereof with the 2-carboxyl group
    • C07D501/32Methylene radicals, substituted by oxygen atoms; Lactones thereof with the 2-carboxyl group with the 7-amino radical acylated by an araliphatic carboxylic acid, which is substituted on the aliphatic radical by hetero atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D501/00Heterocyclic compounds containing 5-thia-1-azabicyclo [4.2.0] octane ring systems, i.e. compounds containing a ring system of the formula:, e.g. cephalosporins; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulfur-containing hetero ring
    • C07D501/14Compounds having a nitrogen atom directly attached in position 7
    • C07D501/16Compounds having a nitrogen atom directly attached in position 7 with a double bond between positions 2 and 3
    • C07D501/207-Acylaminocephalosporanic or substituted 7-acylaminocephalosporanic acids in which the acyl radicals are derived from carboxylic acids
    • C07D501/247-Acylaminocephalosporanic or substituted 7-acylaminocephalosporanic acids in which the acyl radicals are derived from carboxylic acids with hydrocarbon radicals, substituted by hetero atoms or hetero rings, attached in position 3
    • C07D501/36Methylene radicals, substituted by sulfur atoms

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Cephalosporin Compounds (AREA)

Abstract

The present invention provides an improved process for the preparation of the compound of formula (I) in pure form.
PCT/IB2007/001920 2006-07-18 2007-07-10 Improved process for the preparation of ceforanide in pure form WO2008010043A2 (en)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
IN1245/CHE/2006 2006-07-18
IN1245CH2006 2006-07-18
IN908CH2007 2007-04-27
IN908/CHE/2007 2007-04-27

Publications (2)

Publication Number Publication Date
WO2008010043A2 WO2008010043A2 (en) 2008-01-24
WO2008010043A3 true WO2008010043A3 (en) 2008-04-03

Family

ID=38957141

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/IB2007/001920 WO2008010043A2 (en) 2006-07-18 2007-07-10 Improved process for the preparation of ceforanide in pure form

Country Status (1)

Country Link
WO (1) WO2008010043A2 (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101926804A (en) * 2010-08-24 2010-12-29 中国医药集团总公司四川抗菌素工业研究所 Ceforanide C-type crystal composition for injection and preparation method thereof
CN102898442A (en) * 2012-10-25 2013-01-30 河南中帅医药科技发展有限公司 Refinement method of ceforanide
CN107805225B (en) * 2017-12-07 2020-06-26 九江中星医药化工有限公司 Preparation method of 5-mercapto tetrazole acetic acid and sodium salt thereof

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4100346A (en) * 1975-06-27 1978-07-11 Bristol-Myers Company Certain 7(o-amino-methyl- or methylaminomethylphenyl- or cyclohexadienyl- or thienylacetamide)-3[1-carboxymethyl-(or ethyl- or propyl-)-tetrazol-5-ylthiomethyl]-3-cephem-4-carboxylic acids
US4118563A (en) * 1977-11-25 1978-10-03 Bristol-Myers Company Production of 7-(2-aminomethylphenylacetamido-3-(1-carboxymethyltetrazol-5-ylthiomethyl)-3-cephem-4-carboxylic acid

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4100346A (en) * 1975-06-27 1978-07-11 Bristol-Myers Company Certain 7(o-amino-methyl- or methylaminomethylphenyl- or cyclohexadienyl- or thienylacetamide)-3[1-carboxymethyl-(or ethyl- or propyl-)-tetrazol-5-ylthiomethyl]-3-cephem-4-carboxylic acids
US4118563A (en) * 1977-11-25 1978-10-03 Bristol-Myers Company Production of 7-(2-aminomethylphenylacetamido-3-(1-carboxymethyltetrazol-5-ylthiomethyl)-3-cephem-4-carboxylic acid

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
GOTTSTEIN W.J. ET AL.: "7-(2-aminomethylphenylacetamido)-3-(1-carboxymethyltetrazol-5-ylthiomethyl)-3-cephem-4-carboxylic acid", J ANTIBIOT (TOKYO), vol. 29, no. 11, November 1976 (1976-11-01), pages 1226 - 1229 *

Also Published As

Publication number Publication date
WO2008010043A2 (en) 2008-01-24

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