KR900007851A - How to prepare sodium amoxicillin - Google Patents

How to prepare sodium amoxicillin Download PDF

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Publication number
KR900007851A
KR900007851A KR1019880015164A KR880015164A KR900007851A KR 900007851 A KR900007851 A KR 900007851A KR 1019880015164 A KR1019880015164 A KR 1019880015164A KR 880015164 A KR880015164 A KR 880015164A KR 900007851 A KR900007851 A KR 900007851A
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KR
South Korea
Prior art keywords
prepare sodium
sodium amoxicillin
amoxicillin
prepare
spray
Prior art date
Application number
KR1019880015164A
Other languages
Korean (ko)
Other versions
KR910000418B1 (en
Inventor
정순간
표진격
엄창선
Original Assignee
최승주·조의환
삼진제약 주식회사
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.)
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Publication date
Application filed by 최승주·조의환, 삼진제약 주식회사 filed Critical 최승주·조의환
Priority to KR1019880015164A priority Critical patent/KR910000418B1/en
Publication of KR900007851A publication Critical patent/KR900007851A/en
Application granted granted Critical
Publication of KR910000418B1 publication Critical patent/KR910000418B1/en

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    • 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
    • C07D499/04—Preparation
    • C07D499/14—Preparation of salts
    • 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

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicinal Preparation (AREA)

Abstract

내용 없음No content

Description

소디움아목시실린을 제조하는 방법How to prepare sodium amoxicillin

내용없음No content

Claims (1)

아목시실린삼수화물을 n-프로필알코올과 물의 혼합용매에 용해시키고 10℃-20℃로 냉각하고, 입구온도 200℃-250℃ 및 출구온도 110℃-120℃로 하여 분무건조 시켜서 고형의 고디움아목시실린을 제조하는 방법Amoxicillin trihydrate was dissolved in a mixed solvent of n-propyl alcohol and water, cooled to 10 ° C.-20 ° C., spray-dried at an inlet temperature of 200 ° C.-250 ° C. and an outlet temperature of 110 ° C.-120 ° C. How to make ※ 참고사항：최초출원 내용에 의하여 공개하는 것임.※ Note: The disclosure is based on the initial application.
KR1019880015164A 1988-11-17 1988-11-17 Process for preparing sodium amoxacillin KR910000418B1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
KR1019880015164A KR910000418B1 (en) 1988-11-17 1988-11-17 Process for preparing sodium amoxacillin

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
KR1019880015164A KR910000418B1 (en) 1988-11-17 1988-11-17 Process for preparing sodium amoxacillin

Publications (2)

Publication Number Publication Date
KR900007851A true KR900007851A (en) 1990-06-02
KR910000418B1 KR910000418B1 (en) 1991-01-25

Family

ID=19279364

Family Applications (1)

Application Number Title Priority Date Filing Date
KR1019880015164A KR910000418B1 (en) 1988-11-17 1988-11-17 Process for preparing sodium amoxacillin

Country Status (1)

Country Link
KR (1) KR910000418B1 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AT412213B (en) * 2000-05-30 2004-11-25 Sandoz Ag METHOD FOR DRYING AMOXICILLIN OR AMOXICILLIN-CONTAINING, ORAL, SOLID PHARMACEUTICAL COMPOSITIONS USING A GAS WITH A DEFINED GAS HUMIDITY

Also Published As

Publication number Publication date
KR910000418B1 (en) 1991-01-25

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