KR830006179A - 헤테로알킬렌비스 안트라퀴논 제조방법 - Google Patents
헤테로알킬렌비스 안트라퀴논 제조방법 Download PDFInfo
- Publication number
- KR830006179A KR830006179A KR1019810002337A KR810002337A KR830006179A KR 830006179 A KR830006179 A KR 830006179A KR 1019810002337 A KR1019810002337 A KR 1019810002337A KR 810002337 A KR810002337 A KR 810002337A KR 830006179 A KR830006179 A KR 830006179A
- Authority
- KR
- South Korea
- Prior art keywords
- formula
- iii
- hydrogen
- heteroalkylenebis
- anthraquinone process
- Prior art date
Links
- PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 title 1
- 150000004056 anthraquinones Chemical class 0.000 title 1
- 229910052739 hydrogen Inorganic materials 0.000 claims 3
- 239000001257 hydrogen Substances 0.000 claims 3
- 125000000217 alkyl group Chemical group 0.000 claims 2
- 125000004432 carbon atom Chemical group C* 0.000 claims 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 2
- 239000012442 inert solvent Substances 0.000 claims 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
- 125000005263 alkylenediamine group Chemical group 0.000 claims 1
- BKNBVEKCHVXGPH-UHFFFAOYSA-N anthracene-1,4,9,10-tetrol Chemical compound C1=CC=C2C(O)=C3C(O)=CC=C(O)C3=C(O)C2=C1 BKNBVEKCHVXGPH-UHFFFAOYSA-N 0.000 claims 1
- 229910052799 carbon Inorganic materials 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 claims 1
- 230000005494 condensation Effects 0.000 claims 1
- 238000009833 condensation Methods 0.000 claims 1
- 150000002431 hydrogen Chemical class 0.000 claims 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 1
- 229910052757 nitrogen Inorganic materials 0.000 claims 1
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 1
- 230000001590 oxidative effect Effects 0.000 claims 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C221/00—Preparation of compounds containing amino groups and doubly-bound oxygen atoms bound to the same carbon skeleton
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F5/00—Softening water; Preventing scale; Adding scale preventatives or scale removers to water, e.g. adding sequestering agents
- C02F5/08—Treatment of water with complexing chemicals or other solubilising agents for softening, scale prevention or scale removal, e.g. adding sequestering agents
- C02F5/10—Treatment of water with complexing chemicals or other solubilising agents for softening, scale prevention or scale removal, e.g. adding sequestering agents using organic substances
- C02F5/12—Treatment of water with complexing chemicals or other solubilising agents for softening, scale prevention or scale removal, e.g. adding sequestering agents using organic substances containing nitrogen
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C225/00—Compounds containing amino groups and doubly—bound oxygen atoms bound to the same carbon skeleton, at least one of the doubly—bound oxygen atoms not being part of a —CHO group, e.g. amino ketones
- C07C225/24—Compounds containing amino groups and doubly—bound oxygen atoms bound to the same carbon skeleton, at least one of the doubly—bound oxygen atoms not being part of a —CHO group, e.g. amino ketones the carbon skeleton containing carbon atoms of quinone rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C225/00—Compounds containing amino groups and doubly—bound oxygen atoms bound to the same carbon skeleton, at least one of the doubly—bound oxygen atoms not being part of a —CHO group, e.g. amino ketones
- C07C225/24—Compounds containing amino groups and doubly—bound oxygen atoms bound to the same carbon skeleton, at least one of the doubly—bound oxygen atoms not being part of a —CHO group, e.g. amino ketones the carbon skeleton containing carbon atoms of quinone rings
- C07C225/26—Compounds containing amino groups and doubly—bound oxygen atoms bound to the same carbon skeleton, at least one of the doubly—bound oxygen atoms not being part of a —CHO group, e.g. amino ketones the carbon skeleton containing carbon atoms of quinone rings having amino groups bound to carbon atoms of quinone rings or of condensed ring systems containing quinone rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Hydrology & Water Resources (AREA)
- Health & Medical Sciences (AREA)
- Water Supply & Treatment (AREA)
- Environmental & Geological Engineering (AREA)
- Engineering & Computer Science (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
내용 없음
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (1)
- 일반식(가)의 류코 퀴니자린 약 2몰과 일반식(나)(NH2-A-NA2)의 헤테로알킬렌디아민을 비활성 용매중에서 약 5-50℃에서 축합시켜 일반식(다)의 1,1'-비스류코 중간체를 제조한 후 비활성 용매중에서 일반식(라)의 알킬렌디아민과 약 40-60℃에서 비활성분위기하에서 축합시켜 얻은 류코염기를 산화시키므로서 일반식(마)의 화합물을 제조하는 방법.(U와 V는 같거나 상이한 것으로서 각각 2-5의 정수)이고, R은 수소 및 히드록시, R1과 R2는 각각 질소원자에 대한 알파탄소가 히드록시기를 가지지 않는 탄소원자를 2-4개 가진 모노히드록시알킬, 탄소원자수가 1-4인 알킬 및 수소로 된 기이며, R3는 수소 또는 저급 알킬(C1-C3)임.(ⅱ) 일반식 (가)에서 R는 (ⅰ)에서 정의된 바와 같음.(ⅲ) 일반식 (나)에서 A는 (ⅰ)에서 정의된 바와 같음.(ⅳ) 일반식 (다)에서 R과 A는 (ⅰ)에서 정의된 바와 같음.(ⅴ) 일반식 (라)에서 R1과 R2및 Q는 (ⅰ)에서 정의된 바와 같음.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US06/164,615 US4278605A (en) | 1980-06-30 | 1980-06-30 | Heteroalkylenebisanthraquinones |
US164,615 | 1980-06-30 | ||
US164615 | 1998-10-01 |
Publications (2)
Publication Number | Publication Date |
---|---|
KR830006179A true KR830006179A (ko) | 1983-09-20 |
KR840001309B1 KR840001309B1 (ko) | 1984-09-11 |
Family
ID=22595305
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019810002337A KR840001309B1 (ko) | 1980-06-30 | 1981-06-29 | 헤테로알킬렌비스 안트라퀴논 제조방법 |
Country Status (7)
Country | Link |
---|---|
US (1) | US4278605A (ko) |
EP (1) | EP0042940B1 (ko) |
JP (1) | JPS5785345A (ko) |
KR (1) | KR840001309B1 (ko) |
CA (1) | CA1169057A (ko) |
DE (1) | DE3163961D1 (ko) |
NZ (1) | NZ197556A (ko) |
Families Citing this family (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0083683A1 (en) * | 1981-10-26 | 1983-07-20 | American Cyanamid Company | Method of preparing 1,4-bis(substituted-amino)-5,8-dihydroxyanthraquinones and pharmaceutical compositions containing them |
DE3574932D1 (de) * | 1984-02-27 | 1990-02-01 | American Cyanamid Co | Verwendung von 1,4 bisubstituierten anthrachinonen zur herstellung von immunsuppressiva. |
GB8923075D0 (en) * | 1989-10-13 | 1989-11-29 | Patterson Laurence H | Anti-cancer compounds |
IT1237506B (it) * | 1989-10-27 | 1993-06-08 | Boehringer Biochemia Srl | Derivati amminici di 2,3-diaza-antracene-9,10-dioni come farmaci antitumorali |
ATE169614T1 (de) * | 1993-12-27 | 1998-08-15 | Ciba Geigy Ag | Ungesättigte aminoverbindungen zur verwendung als antikrebsmittel und als mittelgegen protozoen |
GB2318349A (en) * | 1996-10-15 | 1998-04-22 | Gyre Ltd | Biocidal composition for wet environment |
US7851172B2 (en) * | 2006-07-25 | 2010-12-14 | University Of Kentucky Research Foundation | Biomarkers of mild cognitive impairment and alzheimer's disease |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1028717B (de) * | 1955-01-22 | 1958-04-24 | Basf Ag | Verfahren zur Herstellung von Anthrachinonfarbstoffen |
FR1529724A (fr) * | 1967-04-21 | 1968-06-21 | Ugine Kuhlmann | Nouveaux colorants anthraquinoniques et intermédiaires pour leur préparation |
US4027021A (en) * | 1974-08-23 | 1977-05-31 | The Upjohn Company | Interferon induction |
DE2722507A1 (de) * | 1977-05-18 | 1978-11-23 | Allied Chem | Anthrachinonderivate |
US4197249A (en) * | 1977-08-15 | 1980-04-08 | American Cyanamid Company | 1,4-Bis(substituted-amino)-5,8-dihydroxyanthraquinones and leuco bases thereof |
SE445996B (sv) * | 1977-08-15 | 1986-08-04 | American Cyanamid Co | Nya atrakinonderivat |
-
1980
- 1980-06-30 US US06/164,615 patent/US4278605A/en not_active Expired - Lifetime
-
1981
- 1981-05-08 DE DE8181103505T patent/DE3163961D1/de not_active Expired
- 1981-05-08 CA CA000377135A patent/CA1169057A/en not_active Expired
- 1981-05-08 EP EP81103505A patent/EP0042940B1/en not_active Expired
- 1981-06-29 KR KR1019810002337A patent/KR840001309B1/ko active
- 1981-06-29 JP JP56099783A patent/JPS5785345A/ja active Granted
- 1981-06-29 NZ NZ197556A patent/NZ197556A/xx unknown
Also Published As
Publication number | Publication date |
---|---|
JPH0243728B2 (ko) | 1990-10-01 |
JPS5785345A (en) | 1982-05-28 |
EP0042940A1 (en) | 1982-01-06 |
KR840001309B1 (ko) | 1984-09-11 |
NZ197556A (en) | 1983-09-30 |
DE3163961D1 (de) | 1984-07-12 |
EP0042940B1 (en) | 1984-06-06 |
CA1169057A (en) | 1984-06-12 |
US4278605A (en) | 1981-07-14 |
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