KR840005445A - 크산린 유도체의 제조방법 - Google Patents

크산린 유도체의 제조방법 Download PDF

Info

Publication number
KR840005445A
KR840005445A KR1019830003383A KR830003383A KR840005445A KR 840005445 A KR840005445 A KR 840005445A KR 1019830003383 A KR1019830003383 A KR 1019830003383A KR 830003383 A KR830003383 A KR 830003383A KR 840005445 A KR840005445 A KR 840005445A
Authority
KR
South Korea
Prior art keywords
group
compound
carbon atoms
formula
alkyl
Prior art date
Application number
KR1019830003383A
Other languages
English (en)
Other versions
KR870001268B1 (ko
Inventor
르니에(외 3) 질베르
Original Assignee
마리-샨딸 웬츠
아디르
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 마리-샨딸 웬츠, 아디르 filed Critical 마리-샨딸 웬츠
Publication of KR840005445A publication Critical patent/KR840005445A/ko
Application granted granted Critical
Publication of KR870001268B1 publication Critical patent/KR870001268B1/ko

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D239/00Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
    • C07D239/28Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
    • C07D239/46Two or more oxygen, sulphur or nitrogen atoms
    • C07D239/52Two oxygen atoms
    • C07D239/54Two oxygen atoms as doubly bound oxygen atoms or as unsubstituted hydroxy radicals
    • C07D239/545Two oxygen atoms as doubly bound oxygen atoms or as unsubstituted hydroxy radicals with other hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • A61P11/08Bronchodilators
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • A61P37/08Antiallergic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D473/00Heterocyclic compounds containing purine ring systems
    • C07D473/02Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6
    • C07D473/04Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6 two oxygen atoms
    • C07D473/06Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6 two oxygen atoms with radicals containing only hydrogen and carbon atoms, attached in position 1 or 3
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D473/00Heterocyclic compounds containing purine ring systems
    • C07D473/02Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6
    • C07D473/04Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6 two oxygen atoms
    • C07D473/06Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6 two oxygen atoms with radicals containing only hydrogen and carbon atoms, attached in position 1 or 3
    • C07D473/08Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6 two oxygen atoms with radicals containing only hydrogen and carbon atoms, attached in position 1 or 3 with methyl radicals in positions 1 and 3, e.g. theophylline
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D473/00Heterocyclic compounds containing purine ring systems
    • C07D473/02Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6
    • C07D473/04Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6 two oxygen atoms
    • C07D473/06Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6 two oxygen atoms with radicals containing only hydrogen and carbon atoms, attached in position 1 or 3
    • C07D473/10Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6 two oxygen atoms with radicals containing only hydrogen and carbon atoms, attached in position 1 or 3 with methyl radicals in positions 3 and 7, e.g. theobromine
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D473/00Heterocyclic compounds containing purine ring systems
    • C07D473/02Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6
    • C07D473/04Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6 two oxygen atoms
    • C07D473/06Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6 two oxygen atoms with radicals containing only hydrogen and carbon atoms, attached in position 1 or 3
    • C07D473/12Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6 two oxygen atoms with radicals containing only hydrogen and carbon atoms, attached in position 1 or 3 with methyl radicals in positions 1, 3, and 7, e.g. caffeine

Abstract

내용 없음

Description

크산린 유도체의 제조방법
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음

Claims (9)

  1. 다음 일반식(Ⅱ)의 할로 화합물을 다음 일반식(Ⅲ)의 아미노 화합물과 반응시켜 다음 일반식(I)의 크산틴 화합물을 얻고 필요하다면 그렇게 얻어진 일반식(I)의 화합물을 적당한 산으로 처리하여 상용하는 산 부가염을 얻음을 특징으로 하는 다음 일반식(I)의 크산틴 화합물 및 그것의 생리학적으로 내성을 갖는 산부가염의 제조방법.
  2. 상기식에서, R1은 수소원자 및 직쇄 및 측쇄를 포함하는 1내지 5탄소 원자를 갖는 알킬기로 구성된 그룹에서 선택하는 것이고, R2는 6탄소원자까지 포함하는 직쇄 및 측쇄 탄화수소기로서 이들 탄화수소기는 이중 결합을 가지며 페닐 및 벤질기를 포함하며, R3는 수소원자, 1내지 5탄소원자까지 함유하는 알킬, 히드록시알킬 및 디히드록시알킬로 구성된 그룹에서 선택된 것이고, R4
  3. 일반식의 기로 구성된 그룹에서 선택한 것이고, 여기서 Y는 수소원자, 할로겐원자, 1내지 5탄소원자까지 각각 함유하는 알킬 및 알콕시기와 히드록시기로 구성된 그룹에서 선택한 치환기이며; Z는 메틸렌기, 2내지 5탄소원자를 갖는 직쇄 및 측쇄 탄화수소기로 구성된 그룹에서 선택한 것으로 이들 탄화수소기는 히드록시기로 치환된 것이며, A는로 구성된 그룹에서 선택한 아미노 잔기이며 여기서 p는 2 및 3에서 선택한 정수이고 q는 1 및 2에서 선택한 정수이고 X는 산소원자 및기로서 단일 결합을 구성하는 그룹에서 선택한 것이며 여기서 R5는 수소원자 및 1내지 5 탄소원자를 각각 갖는 알킬 및 알킬렌기로 구성된 그룹에서 선택한 것이며 m는 2내지 6까지 사이의 정수이고, R6는 1내지 5탄소원자까지 갖는 알킬로 구성된 그룹에서 선택한 것이고 은 염소 및 브롬으로 구성된 그룹에서 선택한 것이다.
  4. 다음 일반식(Ⅱ')의 화합물을 다음 일반식(Ⅲ')의 할로 화합물과 축합시켜 다음 구조식(I')의 화합물을 얻고 그렇게 얻어진 일반식(I')의 화합물을 적당한 산으로 처리하여 상용하는 산 부가염을 얻음을 특징으로 하는 다음 일반식(I')의 화합물과 그것의 생리학적으로 내성을 갖는 산 부가염의 제조방법.
  5. 상기식에서, R2R4및 Z 및 A는 상기 1항에서 주어진 의미를 갖고, R'1는 1내지 5탄소원자까지 함유하는 직쇄 및 측쇄 알킬로 구성된 그룹에서 선택한 것이고, R'3는 1내지 5탄소원자까지 함유하는 알킬, 히드록시 알킬 및 디히드록시 알킬로 구성된 그룹에서 선택한 것이고 X는 염소 및 브롬으로 구성된 그룹에서 선택한 것이다.
  6. ※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
KR1019830003383A 1982-07-28 1983-07-22 크산틴 유도체의 제조 방법 KR870001268B1 (ko)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
FR8213155A FR2531085A1 (fr) 1982-07-28 1982-07-28 Nouveaux derives de la xanthine, leur procede de preparation et les compositions pharmaceutiques les renfermant
FR82-13155 1982-07-28
FR8213155 1982-07-28

Publications (2)

Publication Number Publication Date
KR840005445A true KR840005445A (ko) 1984-11-12
KR870001268B1 KR870001268B1 (ko) 1987-06-30

Family

ID=9276395

Family Applications (1)

Application Number Title Priority Date Filing Date
KR1019830003383A KR870001268B1 (ko) 1982-07-28 1983-07-22 크산틴 유도체의 제조 방법

Country Status (24)

Country Link
US (1) US4548820A (ko)
EP (1) EP0103497B1 (ko)
JP (1) JPS5942383A (ko)
KR (1) KR870001268B1 (ko)
AT (1) ATE17728T1 (ko)
AU (1) AU560809B2 (ko)
CA (1) CA1207766A (ko)
DD (1) DD216934A5 (ko)
DE (1) DE3362022D1 (ko)
DK (1) DK157550C (ko)
ES (1) ES524532A0 (ko)
FR (1) FR2531085A1 (ko)
GR (1) GR78891B (ko)
HU (1) HU188353B (ko)
IE (1) IE55773B1 (ko)
IL (1) IL69362A (ko)
MA (1) MA19860A1 (ko)
NO (1) NO159091C (ko)
NZ (1) NZ205035A (ko)
OA (1) OA07508A (ko)
PH (1) PH19275A (ko)
PT (1) PT77110B (ko)
SU (2) SU1240361A3 (ko)
ZA (1) ZA835496B (ko)

Families Citing this family (23)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CH648559A5 (de) * 1981-07-20 1985-03-29 Siegfried Ag Theophyllinderivate und verfahren zu deren herstellung.
FR2558162B1 (fr) * 1984-01-17 1986-04-25 Adir Nouveaux derives de la xanthine, leurs procedes de preparation et les compositions pharmaceutiques les renfermant
HU197746B (en) * 1985-09-05 1989-05-29 Sandoz Ag Process for producing xantin derivatives and pharmaceutical compositions containing them
US4810706A (en) * 1985-12-20 1989-03-07 Recherche Syntex Piperazine derivatives of theophylline and theobromine
GB8716313D0 (en) * 1987-07-10 1987-08-19 Janssen Pharmaceutica Nv 2-(heterocyclylalkyl)imidazopyridines
US5298508A (en) * 1988-07-19 1994-03-29 The United States Of America As Represented By The Department Of Health And Human Services Irreversible inhibitors of adenosine receptors
US5290782A (en) * 1989-09-01 1994-03-01 Kyowa Hakko Kogyo Co., Ltd. Xanthine derivatives
FR2659656B1 (fr) * 1990-03-15 1994-09-09 Sanofi Sa Derives de pyrimidinedione-2,4 et medicaments les contenant.
DE4019892A1 (de) * 1990-06-22 1992-01-02 Boehringer Ingelheim Kg Neue xanthinderivate
US5484920A (en) * 1992-04-08 1996-01-16 Kyowa Hakko Kogyo Co., Ltd. Therapeutic agent for Parkinson's disease
JP2613355B2 (ja) * 1992-09-28 1997-05-28 協和醗酵工業株式会社 パーキンソン氏病治療剤
WO1994025462A1 (en) * 1993-05-03 1994-11-10 The United States Of America, Represented By The 8-substituted 1,3,7-trialkyl-xanthine derivatives as a2-selective adenosine receptor antagonists
US5661153A (en) * 1994-07-19 1997-08-26 Japan Energy Corporation 1-arylpyrimidine derivatives and pharmaceutical use thereof
DE19702785A1 (de) * 1997-01-27 1998-07-30 Bayer Ag Neue cyclische Harnstoffderivate
JP5038568B2 (ja) 1999-08-21 2012-10-03 ニコメッド ゲゼルシャフト ミット ベシュレンクテル ハフツング 協力剤の組合せ物
BRPI0409229A (pt) 2003-04-01 2006-03-28 Applied Research Systems inibidores das fosfodiesterases na infertilidade
NZ543109A (en) 2003-04-25 2008-06-30 Novacardia Inc Method of improved diuresis in individuals with impaired renal function
BRPI0509753A (pt) * 2004-04-16 2007-10-16 Novacardia Inc composição farmacêutica e método de tratamento de doença cardiovascular
EP1805180A1 (en) * 2004-10-22 2007-07-11 SmithKline Beecham Corporation Xanthine derivatives with hm74a receptor activity
EP2024364A1 (en) * 2006-05-26 2009-02-18 Neuromed Pharmaceuticals, Ltd. Heterocyclic compounds as calcium channel blockers
JP2008025761A (ja) * 2006-07-24 2008-02-07 Kanaflex Corporation 排水管更生用樹脂管
RU2333212C3 (ru) * 2007-03-29 2019-08-26 Общество С Ограниченной Ответственностью "Фармвинг" ПРОИЗВОДНЫЕ 1-И 7-[ω-(БЕНЗГИДРИЛ-4-ПИПЕРАЗИНИЛ-1)АЛКИЛ]-3-АЛКИЛКСАНТИНОВ, ОБЛАДАЮЩИЕ ПРОТИВОГИСТАМИННОЙ И АНТИАЛЛЕРГИЧЕСКОЙ АКТИВНОСТЬЮ
PT2159226T (pt) 2007-03-29 2016-12-16 Joint-Stock Company Obninsk Chemical Pharmaceutical Company Agente anti-histamínico e antialérgico e um método para a produção do mesmo

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CH409974A (de) * 1959-03-25 1966-03-31 Merckle Kg Chem Pharm L Verfahren zur Herstellung neuer therapeutisch wirksamer Coffeino-(8)-alkylendiamine
GB1133989A (en) * 1964-12-08 1968-11-20 Chugai Pharmaceutical Co Ltd Theophylline derivatives, their salts and process for preparing the same
FR7828M (ko) * 1967-11-13 1970-05-25
JPS55118488A (en) * 1979-03-05 1980-09-11 Eisai Co Ltd Theobromine derivative and its preparation
JPS5618983A (en) * 1979-07-25 1981-02-23 Eisai Co Ltd Theophylline derivative and its preapration
US4426383A (en) * 1980-09-04 1984-01-17 Eisai Co., Ltd. Theophylline and theobromine derivatives
DE3046927A1 (de) * 1980-12-11 1982-07-15 Josef Dipl.-Chem.Dr.rer.nat. 1000 Berlin Klosa 8-dialkylaminoalkylaether-coffein-platin-komplexe , verfahren zu ihrer herstellung und sie enthaltende arzneimittel
ES8303412A1 (es) * 1981-10-06 1983-02-01 Invest Tecnica Aplicada Procedimiento de obtencion de nuevas xantinas con actividad farmacologica

Also Published As

Publication number Publication date
IL69362A0 (en) 1983-11-30
IE831762L (en) 1984-01-28
US4548820A (en) 1985-10-22
DK157550B (da) 1990-01-22
DK157550C (da) 1990-06-11
NZ205035A (en) 1986-04-11
NO159091B (no) 1988-08-22
AU1736183A (en) 1984-02-02
SU1245261A3 (ru) 1986-07-15
CA1207766A (fr) 1986-07-15
PT77110A (fr) 1983-08-01
GR78891B (ko) 1984-10-02
IL69362A (en) 1986-07-31
EP0103497B1 (fr) 1986-01-29
NO159091C (no) 1988-11-30
DK342883A (da) 1984-01-29
FR2531085A1 (fr) 1984-02-03
OA07508A (fr) 1985-03-31
IE55773B1 (en) 1991-01-16
DK342883D0 (da) 1983-07-27
PH19275A (en) 1986-02-21
EP0103497A1 (fr) 1984-03-21
FR2531085B1 (ko) 1984-11-23
AU560809B2 (en) 1987-04-16
ES8500275A1 (es) 1984-10-01
JPS5942383A (ja) 1984-03-08
SU1240361A3 (ru) 1986-06-23
ES524532A0 (es) 1984-10-01
KR870001268B1 (ko) 1987-06-30
ATE17728T1 (de) 1986-02-15
JPH0359903B2 (ko) 1991-09-12
DD216934A5 (de) 1985-01-02
PT77110B (fr) 1986-01-27
NO832742L (no) 1984-01-30
ZA835496B (en) 1984-03-28
MA19860A1 (fr) 1984-04-01
HU188353B (en) 1986-04-28
DE3362022D1 (en) 1986-03-13

Similar Documents

Publication Publication Date Title
KR840005445A (ko) 크산린 유도체의 제조방법
KR840004712A (ko) 벤조퀴논 유도체의 제조방법
KR830009054A (ko) 아미노피리미딘 유도체의 제조방법
KR870006039A (ko) 신규 티아졸 화합물, 그 제조방법 및 이 화합물을 함유하는 약학적 조성물
KR850001905A (ko) 벤조시클로 알칸 유도체의 제조방법
KR830001214A (ko) 1,2,4,5-테트라-알킬-4-아릴피페리딘
KR840006206A (ko) 이소퀴놀린 유도체의 제조방법
KR860001048A (ko) 플루오로알릴아민 유도체의 제조방법
KR840005444A (ko) 트리사이클릭 화합물의 제조방법
KR840004103A (ko) 디아졸릴 알칸올의 제조방법
KR840003627A (ko) 4-피페라지닐-4-페닐 퀴나졸린 유도체의 제조방법
KR840005107A (ko) 피리미디온 및 그의 산부가염의 제조방법
KR850004491A (ko) 아릴벤조티아졸린 유도체의 제조방법
KR880011093A (ko) 3,6,9-트리옥사운데칸-1,11-비스(3-n-도데실티오 프로피오네이트)를 제조하는 방법
KR830006176A (ko) 치환된 펜옥시-아미노프로판올 유도체의 제조방법
KR840001578A (ko) 9,10-치환된 2-메시틸이미노-3-알킬-3,4,6,7-테트라하이드로-2H-피리미도(6,1-a)이소퀴놀린-4-온의 제조방법
KR840001144A (ko) 5(6)-페닐설포닐옥시-벤즈이미다졸 유도체의 제조방법
KR840004086A (ko) 1,3,5-트리아크릴일헥사하이드로-s-트리아진-유도체의 제조방법
KR840001150A (ko) 치환페닐(티오노)카바메이트의 제조방법
KR850005413A (ko) 아미노니트로피리딘의 제조방법
KR910011846A (ko) 디옥사닐피리딘
KR840002848A (ko) 유기인산염의 제조방법
KR830002798A (ko) 알킬-케토헥소 피라노사이드 유도체의 제조방법
KR830005163A (ko) 살균작용을 가진 아졸릴-실릴-글리콜에테르류와 그의 제법 및 세균에 대한 그의 사용법
KR870007879A (ko) 노르보르난계 술폰아미드 유도체의 제조방법

Legal Events

Date Code Title Description
A201 Request for examination
E902 Notification of reason for refusal
G160 Decision to publish patent application
E701 Decision to grant or registration of patent right
GRNT Written decision to grant
FPAY Annual fee payment

Payment date: 19930503

Year of fee payment: 8

LAPS Lapse due to unpaid annual fee