KR830007596A - 3,4-비스-치환된 1,2,5-옥스디아졸 2-옥사이드의 제조방법 - Google Patents

3,4-비스-치환된 1,2,5-옥스디아졸 2-옥사이드의 제조방법 Download PDF

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KR830007596A
KR830007596A KR1019810004968A KR810004968A KR830007596A KR 830007596 A KR830007596 A KR 830007596A KR 1019810004968 A KR1019810004968 A KR 1019810004968A KR 810004968 A KR810004968 A KR 810004968A KR 830007596 A KR830007596 A KR 830007596A
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쉐나핀게르 칼
바이에를르 루디
모길레프 안톤
본 헬무트
주스트 멜리타
아 마르토라나 피에로
니츠 롤프-에베르하르트
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쿠르트 발세르, 한스-게오르그 우르바하
카셀라 아크티엔 게젤샤프트
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    • AHUMAN NECESSITIES
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    • A61K31/47Quinolines; Isoquinolines
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Abstract

내용 없음

Description

3,4-비스-치환된 1,2,5-옥스디아졸 2-옥사이드의 제조방법
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음

Claims (10)

  1. 일반식(Ⅱ)의 히드록사모일클로라이드를 0° 내지 50℃에서 용매 또는 분산제에 도입시켜, HCl을 탈이시키고 이합체화시킴을 특징으로 하여 일반식(Ⅰ)의 3, 4-비스-치환된 1, 2, 5-옥스디아졸 2-옥사이드 및 그의 약물학적으로 무독한 산부가염을 제조하는 방법.
    상기식에서, R은 -NHR1, -NR2R3, -NHR4OR2, -NHR5COR6또는이고, R1은 탄소원자 1 내지 6의 알킬 또는 탄소원자 4 내지 7의 시클로알킬이며, R2및 R3는 탄소원자 1 내지 4의 알킬이고, R4는 -CnH2n- 인 알킬렌라디칼이며, n은 2,3 또는 4의 정수이고 R5는 일반식 -CmH2m-인 알킬렌 라디칼이며 m은 1,2 또는 3의 정수이고 R6는 -OR2, -NHR1, -NR2R3또는-NH2이고, X는 (CH2)p-, -(CH2)2- O-(CH2)2-또는이며 p는 4,5 또는 6의 정수이다.
  2. 제 1항에 있어서, 일반식(Ⅱ)의 히드록사모일클로라이드를 10 내지 25℃에서 용매 또는 분산제에 도입시킴을 특징으로 하는 방법.
  3. 제 1항 또는 제 2항에 있어서, 염기를 바람직하게는 동몰량 가함을 특징으로하는 방법.
  4. 제 1항 내지 제3항중의 어느 하나에 있어서, 라디칼 R이 -NH 그룹을 함유함을 특징으로하는 방법.
  5. 제 1항 내지 제4항중의 어느 하나에 있어서, R4가 -(CH2)2- 또는 -(CH2)3를 나타냄을 특징으로하는 방법.
  6. 제 1항 내지 제4항중의 어느 하나에 있어서, R5가 -CH2-또는 (CH2)2를 나타냄을 특징으로하는 방법.
  7. 제 1항 내지 제4항중의 어느 하나에 있어서, R2가 메틸 또는 에틸을 나타냄을 특징으로 하는 방법.
  8. 제 1항 내지 제7항중의 어느 하나에 있어서, 사용한 용매가 디메틸포름아미드, 디메틸설폭사이드, N-메틸피롤리돈, 저급알콜, 디에틸에테르, 물 또는 이들 용매의 혼합물인 것을 특징으로 하는 방법.
  9. 제 1항 내지 제9항중의 어느 하나에 있어서, 부가한 염기가 2금 또는 3급아민, 알칼리금속 히이드록사이드, 알칼리금속탄산염, 알칼리금속중탄산염 또는 알칼리금속 아세테이트인 것을 특징으로 하는 방법.
  10. 제 1항 내지 제9항중의 어느 하나에 있어서, 염기를 서서히 또는 소량씩 부가함을 특징으로 하는 방법.
    ※참고사항:최초출원 내용에 의하여 공개하는 것임.
KR1019810004968A 1980-12-18 1981-12-17 3,4-비스-치환된 1,2,5-옥스디아졸 2-옥사이드의 제조방법 KR880000543B1 (ko)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
DE19803047730 DE3047730A1 (de) 1980-12-18 1980-12-18 3,4-bis-substituierte 1,2,5-oxdiazol-2-oxide, verfahren zu ihrer herstellung, ihre verwendung und sie enthaltende pharmazeutische zubereitungen
DE3047730.6 1980-12-18
DEP304773006 1980-12-18

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KR830007596A true KR830007596A (ko) 1983-11-04
KR880000543B1 KR880000543B1 (ko) 1988-04-13

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US (1) US4356178A (ko)
EP (1) EP0054872B1 (ko)
JP (1) JPS57123173A (ko)
KR (1) KR880000543B1 (ko)
AR (1) AR227697A1 (ko)
AT (1) ATE10094T1 (ko)
AU (1) AU542529B2 (ko)
CA (1) CA1157019A (ko)
CS (1) CS219863B2 (ko)
DD (1) DD201897A5 (ko)
DE (2) DE3047730A1 (ko)
DK (1) DK150597C (ko)
ES (1) ES508086A0 (ko)
FI (1) FI813666L (ko)
GR (1) GR81375B (ko)
HK (1) HK51385A (ko)
HU (1) HU183751B (ko)
IE (1) IE52034B1 (ko)
IL (1) IL64563A (ko)
NO (1) NO814045L (ko)
NZ (1) NZ199272A (ko)
PH (1) PH18051A (ko)
PL (1) PL128564B1 (ko)
PT (1) PT74129B (ko)
RO (1) RO84099B (ko)
SG (1) SG21285G (ko)
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ZA (1) ZA818726B (ko)

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Publication number Priority date Publication date Assignee Title
US4507485A (en) * 1984-01-23 1985-03-26 Bristol-Myers Company 3,4-Disubstituted-1,2,5-oxadiazoles having histamine H2 -receptor antagonist activity
DE4217794A1 (de) * 1992-05-29 1993-12-02 Cassella Ag Phenylfuroxane
DE4218582A1 (de) * 1992-06-05 1993-12-09 Cassella Ag Pyridyl-1,2,5-oxadiazol-carbonamid-2-oxide
DE4218979A1 (de) * 1992-06-10 1993-12-16 Cassella Ag Pyrimidofuroxane
DE4220264A1 (de) * 1992-06-20 1993-12-23 Cassella Ag Phenyl-1,2,5-oxadiazol-carbonamid-2-oxide
DE4223800A1 (de) * 1992-07-20 1994-01-27 Cassella Farbwerke Mainkur Ag Verwendung von 1.2.5-Oxadiazol-2-oxiden zur Behandlung erektiler Dysfunktionen
DE4307105A1 (de) * 1993-03-06 1994-09-08 Cassella Ag Hydroxymethylfurazancarbonsäurederivate
US5460669A (en) * 1993-06-28 1995-10-24 Thiokol Corporation 3-nitramino-4-nitrofurazan and salts thereof
DE4401150A1 (de) * 1994-01-17 1995-07-20 Cassella Ag Furazancarbonsäurederivate
JP2008543863A (ja) 2005-06-15 2008-12-04 ハイドラ バイオサイエンシズ インコーポレイテッド 精子の運動亢進のモジュレーター及びその利用

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* Cited by examiner, † Cited by third party
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US4089867A (en) * 1976-11-11 1978-05-16 Texaco Inc. Preparation of diacylfurazan oxides

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US4356178A (en) 1982-10-26
SG21285G (en) 1985-09-13
IE52034B1 (en) 1987-05-27
ES8300101A1 (es) 1982-10-01
CA1157019A (en) 1983-11-15
RO84099A (ro) 1984-05-12
DK150597C (da) 1987-10-26
AU7855881A (en) 1982-06-24
DE3167001D1 (en) 1984-12-06
IL64563A0 (en) 1982-03-31
RO84099B (ro) 1984-06-30
AR227697A1 (es) 1982-11-30
FI813666L (fi) 1982-06-19
GR81375B (ko) 1984-12-11
NZ199272A (en) 1984-03-16
DD201897A5 (de) 1983-08-17
AU542529B2 (en) 1985-02-21
JPH0223551B2 (ko) 1990-05-24
DK150597B (da) 1987-04-06
PT74129B (de) 1983-05-16
PT74129A (de) 1982-01-01
EP0054872A1 (de) 1982-06-30
DE3047730A1 (de) 1982-07-15
ES508086A0 (es) 1982-10-01
ATE10094T1 (de) 1984-11-15
HU183751B (en) 1984-05-28
HK51385A (en) 1985-07-12
PH18051A (en) 1985-03-13
ZA818726B (en) 1982-11-24
EP0054872B1 (de) 1984-10-31
DK533881A (da) 1982-06-19
SU1093246A3 (ru) 1984-05-15
IE812976L (en) 1982-06-18
IL64563A (en) 1985-02-28
PL128564B1 (en) 1984-02-29
NO814045L (no) 1982-06-21
CS219863B2 (en) 1983-03-25
KR880000543B1 (ko) 1988-04-13
JPS57123173A (en) 1982-07-31
PL234257A1 (ko) 1982-08-02

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