KR950032083A - N-아실옥시알킬-카복스아미드 및 그의 제조방법 - Google Patents

N-아실옥시알킬-카복스아미드 및 그의 제조방법 Download PDF

Info

Publication number
KR950032083A
KR950032083A KR1019950004090A KR19950004090A KR950032083A KR 950032083 A KR950032083 A KR 950032083A KR 1019950004090 A KR1019950004090 A KR 1019950004090A KR 19950004090 A KR19950004090 A KR 19950004090A KR 950032083 A KR950032083 A KR 950032083A
Authority
KR
South Korea
Prior art keywords
optionally substituted
substituted alkyl
formula
acyloxyalkyl
alkyl
Prior art date
Application number
KR1019950004090A
Other languages
English (en)
Other versions
KR100350517B1 (ko
Inventor
란츠쉬 라인하르트
린드너 베르너
Original Assignee
권터 슈마허, 크누트 샤우에르테
바이엘 악티엔게젤샤프트
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 권터 슈마허, 크누트 샤우에르테, 바이엘 악티엔게젤샤프트 filed Critical 권터 슈마허, 크누트 샤우에르테
Publication of KR950032083A publication Critical patent/KR950032083A/ko
Application granted granted Critical
Publication of KR100350517B1 publication Critical patent/KR100350517B1/ko

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C233/00Carboxylic acid amides
    • C07C233/01Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms
    • C07C233/16Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by singly-bound oxygen atoms
    • C07C233/17Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by singly-bound oxygen atoms with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by an acyclic carbon atom
    • C07C233/18Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by singly-bound oxygen atoms with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by an acyclic carbon atom having the carbon atom of the carboxamide group bound to a hydrogen atom or to a carbon atom of an acyclic saturated carbon skeleton

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Cephalosporin Compounds (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)

Abstract

본 발명은 분리된 순수한 형태의 하기 일반식(I)의 신규한 N-아실옥시알킬-카복스아미드, 및 그의 제조방법에 관한 것이다:
상기 식에서, R1은 각각 임의로 치환된 알킬, 알케닐, 알키닐, 사이클로알킬, 사이클로알킬알킬, 아르알킬 또는 헤테로아릴알킬이고, R2는 임의로 치환된 알킬이며, R3는 수소, 할로겐 또는 임의로 치환된 알킬이다.

Description

N-아실옥시알킬-카복스아미드 및 그의 제조방법
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음

Claims (2)

  1. 분리된 순수한 일반식(I)의 N-아실옥시알킬-카복스아미드.
    상기 식에서, R1은 각각 임의로 치환된 알킬, 알케닐, 알키닐, 사이클로알킬, 사이클로알킬알킬, 아르알킬 또는 헤테로아릴알킬이고, R2는 임의로 치환된 알킬이며, R3는 수소, 할로겐 또는 임의로 치환된 알킬이다.
  2. 일반식(Ⅱ)의 이민을 염기의 존재하 및 임의로 희석제의 존재하에 -3O℃ 내지 +50℃에서 일반식(Ⅲ)의 무수물과 반응시켜 일반식(I)의 화합물을 분리함을 특징으로 하여, 일반식(I)의 N-아실옥시알킬-카복스아미드를 제조하는 방법.
    상기 식에서, R1은 각각 임의로 치환된 알킬, 알케닐, 알키닐, 사이클로알킬, 사이클로알킬알킬, 아르알킬 또는 헤테로아릴알킬이고, R2는 임의로 치환된 알킬이며. R3는 수소, 할로겐 또는 임의로 치환된 알킬이다.
    ※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
KR1019950004090A 1994-03-04 1995-02-28 N-아실옥시알킬-카복스아미드및그의제조방법 KR100350517B1 (ko)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DEP4407182.5 1994-03-04
DE4407182A DE4407182A1 (de) 1994-03-04 1994-03-04 N-Acyloxyalkyl-carbonsäureamide und Verfahren zu ihrer Herstellung

Publications (2)

Publication Number Publication Date
KR950032083A true KR950032083A (ko) 1995-12-20
KR100350517B1 KR100350517B1 (ko) 2002-10-31

Family

ID=6511835

Family Applications (1)

Application Number Title Priority Date Filing Date
KR1019950004090A KR100350517B1 (ko) 1994-03-04 1995-02-28 N-아실옥시알킬-카복스아미드및그의제조방법

Country Status (10)

Country Link
US (2) US5599940A (ko)
EP (1) EP0670302B1 (ko)
JP (1) JP3794729B2 (ko)
KR (1) KR100350517B1 (ko)
AT (1) ATE163177T1 (ko)
BR (1) BR9500801A (ko)
DE (2) DE4407182A1 (ko)
DK (1) DK0670302T3 (ko)
ES (1) ES2111974T3 (ko)
TW (1) TW462959B (ko)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE19521588A1 (de) * 1995-06-14 1996-12-19 Bayer Ag N-substituierte cis-N-Propenyl-acetamide und Verfahren zu ihrer Herstellung
US6562995B1 (en) 2000-12-21 2003-05-13 Beacon Laboratories, Inc. Delta dicarbonyl compounds and methods for using the same
US6720445B2 (en) 2000-12-21 2004-04-13 Beacon Laboratories, Inc. Acetyloxymethyl esters and methods for using the same

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE428700C (de) * 1924-12-19 1926-08-25 Alfons Pelz Vorrichtung zur Herstellung von Papiersaecken
US2980688A (en) * 1958-12-08 1961-04-18 Ortho Pharma Corp Acetylated aldehyde adducts of 2-amino-5-nitrothiazole
BE626980A (ko) * 1962-01-10
US3317603A (en) * 1963-09-27 1967-05-02 Monsanto Co Improvement in the preparation of n-vinyl-n-methylacetamide
DE4217021A1 (de) * 1991-12-13 1993-06-17 Bayer Ag Verfahren zur herstellung von 5-substituierten 2-chlor-pyridinen

Also Published As

Publication number Publication date
TW462959B (en) 2001-11-11
KR100350517B1 (ko) 2002-10-31
JPH07258184A (ja) 1995-10-09
DE4407182A1 (de) 1995-09-07
DK0670302T3 (da) 1998-09-23
EP0670302A1 (de) 1995-09-06
EP0670302B1 (de) 1998-02-11
DE59501424D1 (de) 1998-03-19
JP3794729B2 (ja) 2006-07-12
BR9500801A (pt) 1995-11-21
ATE163177T1 (de) 1998-02-15
ES2111974T3 (es) 1998-03-16
US5599940A (en) 1997-02-04
US5710279A (en) 1998-01-20

Similar Documents

Publication Publication Date Title
KR860002453A (ko) 3-아미노-2-벤조일아크릴산 유도체의 제조방법
KR950032090A (ko) 지방족 이민의 제조방법
KR950032083A (ko) N-아실옥시알킬-카복스아미드 및 그의 제조방법
KR840004750A (ko) 피라졸로피리딘 화합물의 제조방법
KR870004027A (ko) 디하이드로리제르그산의 n-알킬화 방법
PT83858A (de) Verfahren zur herstellung von cefodizim
KR840004065A (ko) 2-시아노-2-프로페노산 및 그 유도체의 제조방법
ATE106397T1 (de) Verfahren zur herstellung von 3,3- diarylacrylsäureamiden.
KR850005830A (ko) 2-알콕시아미노설포닐벤젠-설포닐우레아의 제조방법
ATE186737T1 (de) Ein verbessertes verfahren für die herstellung von seitenketten-derivaten von cyclohexapeptidyl- lipopeptiden
KR840004103A (ko) 디아졸릴 알칸올의 제조방법
DE59009951D1 (de) Verfahren zur Herstellung von Zwischenprodukten und zur Synthese von N-(2-Hydroxyethyl)-2-hydroxymethyl-3,4,5-trihydroxypiperidine.
DE69410073D1 (de) Verfahren zur Herstellung von 2-Perfluoroalkyl-3-oxazolin-5-one
KR860003204A (ko) 디페닐메틸이민 유도체의 제조방법
KR860002486A (ko) 티아진포스폰산 유도체의 제조방법
KR870003093A (ko) 퀴놀론카복실산 유도체의 제조방법
KR960022533A (ko) 리파마이신 유도체의 제조방법
KR870007907A (ko) 디엔 유도체의 제법
DE59306234D1 (de) Verfahren zur Herstellung von 5-Chloroxindol
KR950032043A (ko) 알릴 퀴논 유도체의 제조 방법 및 그 중간체
KR860000252A (ko) 아실화 엔아미드 화합물의 제조방법
KR850008670A (ko) 약학적특성의 신규아실아미노페놀 유도체의 제조방법
KR860002454A (ko) 살리실아미드 유도체의 제조방법
KR970010772A (ko) 7-아미노-3-메톡시메틸-3-세펨-4-카르복실산의 신규 제조방법
KR960000883A (ko) 신규 아민화합물 및 그의 제조방법

Legal Events

Date Code Title Description
A201 Request for examination
E902 Notification of reason for refusal
E701 Decision to grant or registration of patent right
GRNT Written decision to grant
FPAY Annual fee payment

Payment date: 20120802

Year of fee payment: 11

FPAY Annual fee payment

Payment date: 20130801

Year of fee payment: 12