JPS51113893A - Production ammoxyline trihydrate - Google Patents

Production ammoxyline trihydrate

Info

Publication number
JPS51113893A
JPS51113893A JP51025667A JP2566776A JPS51113893A JP S51113893 A JPS51113893 A JP S51113893A JP 51025667 A JP51025667 A JP 51025667A JP 2566776 A JP2566776 A JP 2566776A JP S51113893 A JPS51113893 A JP S51113893A
Authority
JP
Japan
Prior art keywords
ammoxyline
trihydrate
production
production ammoxyline
ammoxyline trihydrate
Prior art date
Legal status (The legal status 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 status listed.)
Granted
Application number
JP51025667A
Other languages
English (en)
Other versions
JPS566432B2 (ja
Inventor
Eichi Gurosuman Jiyosefu
Ei Haadokiyatsusuru Jiyu Guren
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Bristol Myers Co
Original Assignee
Bristol Myers 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 Co filed Critical Bristol Myers Co
Publication of JPS51113893A publication Critical patent/JPS51113893A/ja
Publication of JPS566432B2 publication Critical patent/JPS566432B2/ja
Granted legal-status Critical Current

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
    • C07D499/44—Compounds with an amino radical acylated by carboxylic acids, attached in position 6
    • C07D499/48—Compounds with an amino radical acylated by carboxylic acids, attached in position 6 with a carbon chain, substituted by hetero atoms or by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, attached to the carboxamido radical
    • C07D499/58—Compounds with an amino radical acylated by carboxylic acids, attached in position 6 with a carbon chain, substituted by hetero atoms or by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, attached to the carboxamido radical substituted in alpha-position to the carboxamido radical
    • C07D499/64—Compounds with an amino radical acylated by carboxylic acids, attached in position 6 with a carbon chain, substituted by hetero atoms or by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, attached to the carboxamido radical substituted in alpha-position to the carboxamido radical by nitrogen atoms
    • C07D499/68—Compounds with an amino radical acylated by carboxylic acids, attached in position 6 with a carbon chain, substituted by hetero atoms or by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, attached to the carboxamido radical substituted in alpha-position to the carboxamido radical by nitrogen atoms with aromatic rings as additional substituents on the carbon chain

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
JP51025667A 1975-03-17 1976-03-11 Production ammoxyline trihydrate Granted JPS51113893A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US05/558,763 US3980637A (en) 1975-03-17 1975-03-17 Production of amoxicillin

Publications (2)

Publication Number Publication Date
JPS51113893A true JPS51113893A (en) 1976-10-07
JPS566432B2 JPS566432B2 (ja) 1981-02-10

Family

ID=24230895

Family Applications (1)

Application Number Title Priority Date Filing Date
JP51025667A Granted JPS51113893A (en) 1975-03-17 1976-03-11 Production ammoxyline trihydrate

Country Status (8)

Country Link
US (1) US3980637A (ja)
JP (1) JPS51113893A (ja)
BE (1) BE839682A (ja)
DE (1) DE2611286C3 (ja)
DK (1) DK144476C (ja)
GB (1) GB1535291A (ja)
NL (1) NL165748C (ja)
SE (1) SE430336B (ja)

Families Citing this family (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ES459494A1 (es) * 1977-06-04 1978-05-01 Palomo Coll A Luis Procedimiento de preparacion de hidrox-alfa-aminobencilpeni-cilina.
JPS5576886A (en) * 1978-12-07 1980-06-10 Mitsubishi Chem Ind Ltd Synthetic method of penicillin
US4240960A (en) * 1979-03-19 1980-12-23 Bristol-Myers Company Trimethylsilyl substituted penicillins
US4278600A (en) * 1979-03-19 1981-07-14 Bristol-Myers Company Production of penicillins
US4310458A (en) * 1979-03-19 1982-01-12 Bristol-Myers Company Production of penicillins
US4351766A (en) * 1979-07-12 1982-09-28 Bristol-Myers Company Production of penicillins
US4248780A (en) * 1979-08-21 1981-02-03 Canada Packers Limited Process for preparing ampicillin
IT1193836B (it) * 1979-11-02 1988-08-24 Dobfar Spa Procedimento per la produzione di acido 6-d-alfa-amino-p-idrossifenilacetamido enicillanico
BE1009264A3 (nl) * 1995-03-31 1997-01-07 Dsm Nv Werkwijze voor de winning van ampicilline.
US5916762A (en) * 1995-03-31 1999-06-29 Chemferm V.O.F. Process for the recovery of ampicillin
US7829720B2 (en) 2004-05-04 2010-11-09 Bristol-Myers Squibb Company Process for preparing atazanavir bisulfate and novel forms
US8272618B2 (en) * 2004-11-30 2012-09-25 The Boeing Company Minimum bond thickness assembly feature assurance
AU2008268537B2 (en) * 2007-06-22 2012-11-01 Bristol-Myers Squibb Holdings Ireland Tableted compositions containing atazanavir
DE602008005462D1 (de) * 2007-06-22 2011-04-21 Bristol Myers Squibb Co Tablettierte atazanavirhaltige zusammensetzungen
ES2360336T3 (es) * 2007-06-22 2011-06-03 Bristol-Myers Squibb Company Composiciones en comprimidos que contienen atazanavir.
MX2009013504A (es) * 2007-06-22 2010-03-26 Bristol Myers Squibb Co Composiciones comprimidas que tienen atazanavir.
RU2671400C2 (ru) * 2013-02-13 2018-10-31 Редхилл Байофарма Лтд. Фармацевтические композиции для лечения от helicobacter pylori

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ES401263A1 (es) * 1972-03-28 1975-02-16 Beecham Group Ltd Un procedimiento para la produccion de alfa - amino-(p-hi- droxibencil) penicilina.

Also Published As

Publication number Publication date
JPS566432B2 (ja) 1981-02-10
DE2611286A1 (de) 1976-09-23
US3980637A (en) 1976-09-14
BE839682A (fr) 1976-09-17
DK144476C (da) 1982-08-30
GB1535291A (en) 1978-12-13
NL165748C (nl) 1981-05-15
NL165748B (nl) 1980-12-15
NL7602634A (nl) 1976-09-21
DK113476A (da) 1976-09-18
DK144476B (da) 1982-03-15
DE2611286B2 (de) 1980-01-03
SE430336B (sv) 1983-11-07
SE7602825L (sv) 1976-09-18
DE2611286C3 (de) 1980-09-04

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