KR830001243A - Spiro-polycyclic imidazolidine dione derivative - Google Patents

Spiro-polycyclic imidazolidine dione derivative Download PDF

Info

Publication number
KR830001243A
KR830001243A KR1019790004297A KR790004297A KR830001243A KR 830001243 A KR830001243 A KR 830001243A KR 1019790004297 A KR1019790004297 A KR 1019790004297A KR 790004297 A KR790004297 A KR 790004297A KR 830001243 A KR830001243 A KR 830001243A
Authority
KR
South Korea
Prior art keywords
structural formula
following structural
spiro
polycyclic
naphth
Prior art date
Application number
KR1019790004297A
Other languages
Korean (ko)
Other versions
KR830001244B1 (en
Inventor
사지스 레인하드
벨레타이어 죤
Original Assignee
윌리암 지. 맥크리리
화이자 인코포레이티드
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 윌리암 지. 맥크리리, 화이자 인코포레이티드 filed Critical 윌리암 지. 맥크리리
Priority to KR1019790004297A priority Critical patent/KR830001244B1/en
Publication of KR830001243A publication Critical patent/KR830001243A/en
Application granted granted Critical
Publication of KR830001244B1 publication Critical patent/KR830001244B1/en

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
    • C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
    • C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D231/12—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
    • C07D233/56—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
    • C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
    • C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles

Abstract

내용 없음No content

Description

스피로-폴리사이클릭 이미다졸리딘 디온 유도체Spiro-polycyclic imidazolidine dione derivative

본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음This content is subject to disclosure, so the full text is not included.

Claims (1)

다음 구조식(II)의 케톤을 불활성, 극성유기용매내에서 50 내지 150℃로 2 내지 96시간동안 알칼리금속시안화물 및 탄산암모늄(최소한 화학양론적인 양으로)과 축합시킴을 특징으로 하여 다음 구조식(I) 의 스피로-폴리사이클릭 이미다졸리딘디온 유도체를 제조하는 방법.The following structural formula (II) is characterized by condensing the ketone of the following structural formula (II) with alkali metal cyanide and ammonium carbonate (at least in a stoichiometric amount) at 50 to 150°C for 2 to 96 hours in an inert, polar organic solvent. A method for producing a spiro-polycyclic imidazolidindione derivative of I). 상기 구조식에서In the above structural formula A는 다음 구조식(III)의 나프트-α, β-0,A is naphth-α, β-0 of the following structural formula (III), 다음 구조식(IV)의 안트라센-α, β-0,Anthracene-α, β-0 of the following structural formula (IV), 또는 메틸, 클로로 또는 브로모중에서 선택된, 하나 또는 둘의 동일한 치환체를 갖는 치환된 나프트-αβ-0이고Or a substituted naphth-αβ-0 having one or two identical substituents selected from methyl, chloro or bromo, and Y는 CH2, S, SO, SO2또는 0이거나Y is CH 2 , S, SO, SO 2 or 0 or A 및 Y는 함께 다음 구조식(V)의 나프트-α, θ-0를 나타낸다.A and Y together represent naphth-α, θ-0 of the following structural formula (V). ※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.※ Note: It is disclosed according to the contents of the initial application.
KR1019790004297A 1979-12-05 1979-12-05 Process for preparing spiro-polycyclic imidazolidine dione derivatives KR830001244B1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
KR1019790004297A KR830001244B1 (en) 1979-12-05 1979-12-05 Process for preparing spiro-polycyclic imidazolidine dione derivatives

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
KR1019790004297A KR830001244B1 (en) 1979-12-05 1979-12-05 Process for preparing spiro-polycyclic imidazolidine dione derivatives

Publications (2)

Publication Number Publication Date
KR830001243A true KR830001243A (en) 1983-04-29
KR830001244B1 KR830001244B1 (en) 1983-06-27

Family

ID=19213762

Family Applications (1)

Application Number Title Priority Date Filing Date
KR1019790004297A KR830001244B1 (en) 1979-12-05 1979-12-05 Process for preparing spiro-polycyclic imidazolidine dione derivatives

Country Status (1)

Country Link
KR (1) KR830001244B1 (en)

Also Published As

Publication number Publication date
KR830001244B1 (en) 1983-06-27

Similar Documents

Publication Publication Date Title
KR830009084A (en) Method for preparing quinoline carboxylic acid derivative
KR830007604A (en) Process for preparing pyroxycam
KR840005101A (en) Method for preparing 2-quinoline derivative
KR830006198A (en) Method for preparing cyclohexane derivative
KR830003417A (en) Method for preparing methylene-cycloamine
KR840000497A (en) Method for preparing pyridinecarbinol and fungicides containing these compounds
KR840004760A (en) Process for preparing selenium organic compound
KR830002749A (en) Manufacturing method of butyrolactone
KR830006302A (en) Method for preparing novel pyrimidine derivatives
KR830001243A (en) Spiro-polycyclic imidazolidine dione derivative
KR830001952A (en) Manufacturing method of cefuloxim
KR910007945A (en) Process for preparing alkyl methyl-3-carbalkoxyethylphosphinate
KR840001162A (en) Method for preparing new compound with excellent anti-ulcer activity
KR850005836A (en) Method for preparing 2 (3H) -benzthiazolone substituted with 3-position
KR830009044A (en) Method for preparing 3,5-di-tert-butyl-4-hydroxyphenyl-substituted heterocyclic compound
JPS5432448A (en) Preparation of cyclopentanone derivative
KR840001547A (en) Method for preparing compound having anti-inflammatory action, bactericidal action and antibacterial action
KR830002856A (en) Method for manufacturing pyridone dispersion dye
KR830001195A (en) Method for producing (2,6-dichlorobenzylidene-amino)-guanidine
KR830003458A (en) Derivatives of 2-Tioxo-3-benzothiazoline acetonitrile
KR830009091A (en) Method for preparing 5-fluoro uracil derivatives
KR830003451A (en) Imideamides derived from 2-oxo-3-benzothiazoline acetic acid useful as plant growth regulators
KR830006301A (en) Method for preparing benzothiophene derivative
KR830004304A (en) Method for preparing mycopranesin derivative
KR830005175A (en) Process for preparing substituted triarylthiazole compound