FI20011921A - syn isomer of 2- (2-aminothiazol-4-yl) -2-methoxyimonoacetyl chloride hydrochloride and process for its preparation - Google Patents

syn isomer of 2- (2-aminothiazol-4-yl) -2-methoxyimonoacetyl chloride hydrochloride and process for its preparation Download PDF

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Publication number
FI20011921A
FI20011921A FI20011921A FI20011921A FI20011921A FI 20011921 A FI20011921 A FI 20011921A FI 20011921 A FI20011921 A FI 20011921A FI 20011921 A FI20011921 A FI 20011921A FI 20011921 A FI20011921 A FI 20011921A
Authority
FI
Finland
Prior art keywords
aminothiazol
preparation
chloride hydrochloride
methoxyimonoacetyl
isomer
Prior art date
Application number
FI20011921A
Other languages
Finnish (fi)
Swedish (sv)
Other versions
FI119811B (en
Inventor
Gary M F Lim
John M Roubie
Elisabeth Ann Garofalo
Original Assignee
Bristol Myers Squibb Co
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 Bristol Myers Squibb Co filed Critical Bristol Myers Squibb Co
Publication of FI20011921A publication Critical patent/FI20011921A/en
Application granted granted Critical
Publication of FI119811B publication Critical patent/FI119811B/en

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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
    • 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
    • C07D501/38Methylene radicals, substituted by nitrogen atoms; Lactams thereof with the 2-carboxyl group; Methylene radicals substituted by nitrogen-containing hetero rings attached by the ring nitrogen atom; Quaternary compounds thereof
    • C07D501/46Methylene radicals, substituted by nitrogen atoms; Lactams thereof with the 2-carboxyl group; Methylene radicals substituted by nitrogen-containing hetero rings attached by the ring nitrogen atom; Quaternary compounds thereof with the 7-amino radical acylated by carboxylic acids containing hetero rings
    • 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
    • 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)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Communicable Diseases (AREA)
  • Animal Behavior & Ethology (AREA)
  • Oncology (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Cephalosporin Compounds (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Ultra Sonic Daignosis Equipment (AREA)
  • Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
  • Revetment (AREA)
  • Artificial Fish Reefs (AREA)

Abstract

The present invention provides an anhydrous acylation process for the preparation of antibiotic, cefepime dihydrochloride hydrate which is substantially free of the anti-isomer and the DELTA <2> isomer comprising the N-acylation of a silylated derivative of 7-amino-3-[(1-methyl-1-pyrrolidinio)-methyl]ceph-3-em-4-carboxylate with the syn-isomer of 2-(2-aminothiazol-4-yl)-2-methoxyimino acetyl chloride hydrochloride.
FI20011921A 1991-09-10 2001-10-01 syn isomer of 2- (2-aminothiazol-4-yl) -2-methoxyimonoacetyl chloride hydrochloride and process for its preparation FI119811B (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US75710491A 1991-09-10 1991-09-10
US75710491 1991-09-10

Publications (2)

Publication Number Publication Date
FI20011921A true FI20011921A (en) 2001-10-01
FI119811B FI119811B (en) 2009-03-31

Family

ID=25046366

Family Applications (2)

Application Number Title Priority Date Filing Date
FI924031A FI109127B (en) 1991-09-10 1992-09-09 Process for the preparation of cefepime dihydrochloride hydrate antibiotic
FI20011921A FI119811B (en) 1991-09-10 2001-10-01 syn isomer of 2- (2-aminothiazol-4-yl) -2-methoxyimonoacetyl chloride hydrochloride and process for its preparation

Family Applications Before (1)

Application Number Title Priority Date Filing Date
FI924031A FI109127B (en) 1991-09-10 1992-09-09 Process for the preparation of cefepime dihydrochloride hydrate antibiotic

Country Status (29)

Country Link
EP (1) EP0531981B1 (en)
JP (1) JP3434840B2 (en)
KR (1) KR0178280B1 (en)
CN (2) CN1036587C (en)
AT (1) ATE209209T1 (en)
AU (1) AU655838B2 (en)
BG (1) BG61189B1 (en)
CA (1) CA2077836A1 (en)
CZ (2) CZ282315B6 (en)
DE (1) DE69232216T2 (en)
DK (1) DK0531981T3 (en)
EG (1) EG20184A (en)
ES (1) ES2165351T3 (en)
FI (2) FI109127B (en)
HU (1) HU212782B (en)
IL (1) IL103109A (en)
MX (1) MX9205147A (en)
NO (1) NO301930B1 (en)
NZ (1) NZ244295A (en)
OA (1) OA09764A (en)
PH (1) PH31206A (en)
PL (1) PL174820B1 (en)
PT (1) PT531981E (en)
RO (1) RO109651B1 (en)
RU (1) RU2042681C1 (en)
SK (2) SK280934B6 (en)
UY (1) UY23475A1 (en)
YU (1) YU81692A (en)
ZA (1) ZA926866B (en)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
IL103110A (en) * 1991-09-10 1997-04-15 Bristol Myers Squibb Co Anhydrous process for preparing cefepime dihydrochloride hydrate
CA2101571A1 (en) * 1992-09-08 1994-03-09 Elizabeth A. Garofalo Crystalline dihydrate of a cephalosporin dihydrate salt and injectable compositions thereof
KR19980019860A (en) * 1996-09-04 1998-06-25 김윤배 New Manufacturing Method of Cephalosporin Intermediates
EP1618114B1 (en) * 2003-04-16 2010-07-14 Sandoz AG Processes for the preparations of cefepime
US7847093B2 (en) 2003-04-16 2010-12-07 Sandoz Ag Processes for the preparations of cefepime
GB0416379D0 (en) * 2004-07-22 2004-08-25 Sandoz Ag Organic compounds
ITMI20051684A1 (en) * 2005-09-13 2007-03-14 Harvest Lodge Ltd PROCEDURE FOR THE PRODUCTION OF AMINO ACID DICHLORIDRATE
RU2469040C1 (en) * 2011-12-07 2012-12-10 Общество с ограниченной ответственностью "КОМПАНИЯ "ДЕКО" Method of producing 7-[2-(2-aminothiazol-4-yl)-2(z)-methoxyimino acetamido]-3-[(1-methyl-1-pyrrolidino)methyl]-cef-3-em-4-carboxylate dihydrochloride monohydrate (cefepime dihydrochloride monohydrate)

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA1213882A (en) * 1982-03-04 1986-11-12 Jun Okumura Cephalosporins
DE3419015A1 (en) * 1984-05-22 1985-11-28 Bayer Ag, 5090 Leverkusen METHOD FOR PRODUCING CEPHALOSPORINES
GB2165245B (en) * 1984-10-01 1988-05-25 Glaxo Group Ltd Chemical compounds
US4910301A (en) * 1985-08-05 1990-03-20 Bristol-Myers Company Cefepime cephalosporin salts
US4714760A (en) * 1985-08-20 1987-12-22 Bristol-Myers Company Cephalosporin intermediates
IL103110A (en) * 1991-09-10 1997-04-15 Bristol Myers Squibb Co Anhydrous process for preparing cefepime dihydrochloride hydrate

Also Published As

Publication number Publication date
HU9202884D0 (en) 1992-11-30
SK278092A3 (en) 2000-09-12
CZ71996A3 (en) 1997-06-11
IL103109A (en) 1997-07-13
UY23475A1 (en) 1992-10-08
CN1059438C (en) 2000-12-13
HU212782B (en) 1996-11-28
NO923495D0 (en) 1992-09-09
FI119811B (en) 2009-03-31
NZ244295A (en) 1995-08-28
NO301930B1 (en) 1997-12-29
HUT62901A (en) 1993-06-28
FI924031A (en) 1993-03-11
BG61189B1 (en) 1997-02-28
SK33698A3 (en) 2000-09-12
CN1070398A (en) 1993-03-31
DE69232216T2 (en) 2002-06-27
RO109651B1 (en) 1995-04-28
SK280933B6 (en) 2000-09-12
BG96859A (en) 1993-12-24
FI924031A0 (en) 1992-09-09
EP0531981A1 (en) 1993-03-17
ATE209209T1 (en) 2001-12-15
AU655838B2 (en) 1995-01-12
NO923495L (en) 1993-03-11
PT531981E (en) 2002-05-31
PL174820B1 (en) 1998-09-30
IL103109A0 (en) 1993-02-21
CN1158333A (en) 1997-09-03
SK280934B6 (en) 2000-09-12
CZ282315B6 (en) 1997-06-11
PH31206A (en) 1998-05-05
KR930006032A (en) 1993-04-20
CA2077836A1 (en) 1993-03-11
DE69232216D1 (en) 2002-01-03
PL295873A1 (en) 1993-05-04
CZ278092A3 (en) 1993-03-17
FI109127B (en) 2002-05-31
CZ282160B6 (en) 1997-05-14
EP0531981B1 (en) 2001-11-21
JPH05194532A (en) 1993-08-03
KR0178280B1 (en) 1999-03-20
YU81692A (en) 1995-03-27
AU2284492A (en) 1993-03-11
RU2042681C1 (en) 1995-08-27
DK0531981T3 (en) 2002-05-21
ZA926866B (en) 1993-03-09
CN1036587C (en) 1997-12-03
MX9205147A (en) 1993-03-01
JP3434840B2 (en) 2003-08-11
ES2165351T3 (en) 2002-03-16
OA09764A (en) 1993-11-30
EG20184A (en) 1997-09-30

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