KR870003057A - Method for preparing acetyldicarnitine dichloride - Google Patents

Method for preparing acetyldicarnitine dichloride Download PDF

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Publication number
KR870003057A
KR870003057A KR1019850007149A KR850007149A KR870003057A KR 870003057 A KR870003057 A KR 870003057A KR 1019850007149 A KR1019850007149 A KR 1019850007149A KR 850007149 A KR850007149 A KR 850007149A KR 870003057 A KR870003057 A KR 870003057A
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KR
South Korea
Prior art keywords
chloride
preparing
dissolved
hours
acetyldicarnitine
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Application number
KR1019850007149A
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Korean (ko)
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KR930009822B1 (en
Inventor
프랑키아 기오르기오
Original Assignee
쥬세프 프랑키아
케미오 신텍스 에스. 알. 엘.
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Priority to KR1019850007149A priority Critical patent/KR930009822B1/en
Publication of KR870003057A publication Critical patent/KR870003057A/en
Application granted granted Critical
Publication of KR930009822B1 publication Critical patent/KR930009822B1/en

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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C227/00Preparation of compounds containing amino and carboxyl groups bound to the same carbon skeleton
    • C07C227/14Preparation of compounds containing amino and carboxyl groups bound to the same carbon skeleton from compounds containing already amino and carboxyl groups or derivatives thereof

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

내용 없음No content

Description

아세틸디카르니틴 디클로라이드의 제조 방법Method for preparing acetyldicarnitine dichloride

본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음Since this is an open matter, no full text was included.

Claims (1)

아세틸 카르니틴 클로라이드 및 즉시 증류한 티오닐 클로라이드, 1:1.5 몰비의 혼합물을 실온에서 0.5 내지 2시간 동안 교반시키고, 과잉 티오닐 클로-라이드를 제거한 후, 생성되는 아실클로라이드를 메틸렌클로라이드에 용해시키고, 여기에 동량의 카르니틴 클로라이드를 가하여 생성되는 혼합물38°내지 42℃의 온도로 18 내지 36시간 동안 유지시켜 조생성물을 수득한 다음, 이 조생성물을 뜨거운 이소프로필 알코올에 용해시킨 후 결정화시킴을 특징으로 하는, 하기 구조식(Ⅰ)의 아세틸디카르니틴 디클로라이드의 제조 방법.A mixture of acetyl carnitine chloride and immediately distilled thionyl chloride, 1: 1.5 molar ratio, was stirred at room temperature for 0.5 to 2 hours, excess thionyl chloride was removed, and the resulting acylchloride was dissolved in methylene chloride, To a mixture obtained by adding an equal amount of carnitine chloride to a temperature of 38 ° to 42 ° C. for 18 to 36 hours to obtain a crude product, which is then dissolved in hot isopropyl alcohol and crystallized. , Method for producing acetyldicarnitine dichloride of formula (I). ※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.※ Note: The disclosure is based on the initial application.
KR1019850007149A 1985-09-27 1985-09-27 Method of producing acetyldicarnitine dichloride KR930009822B1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
KR1019850007149A KR930009822B1 (en) 1985-09-27 1985-09-27 Method of producing acetyldicarnitine dichloride

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
KR1019850007149A KR930009822B1 (en) 1985-09-27 1985-09-27 Method of producing acetyldicarnitine dichloride

Publications (2)

Publication Number Publication Date
KR870003057A true KR870003057A (en) 1987-04-14
KR930009822B1 KR930009822B1 (en) 1993-10-11

Family

ID=19242953

Family Applications (1)

Application Number Title Priority Date Filing Date
KR1019850007149A KR930009822B1 (en) 1985-09-27 1985-09-27 Method of producing acetyldicarnitine dichloride

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Publication number Publication date
KR930009822B1 (en) 1993-10-11

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