AU2002219049A1 - Monoazoquinolone pigments, process for their preparation and their use - Google Patents
Monoazoquinolone pigments, process for their preparation and their useInfo
- Publication number
- AU2002219049A1 AU2002219049A1 AU2002219049A AU1904902A AU2002219049A1 AU 2002219049 A1 AU2002219049 A1 AU 2002219049A1 AU 2002219049 A AU2002219049 A AU 2002219049A AU 1904902 A AU1904902 A AU 1904902A AU 2002219049 A1 AU2002219049 A1 AU 2002219049A1
- Authority
- AU
- Australia
- Prior art keywords
- c4alkyl
- custom
- halogen
- character
- unsubstituted
- Prior art date
- Legal status (The legal status 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 status listed.)
- Abandoned
Links
- 239000000049 pigment Substances 0.000 title abstract 2
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 7
- 229910052736 halogen Inorganic materials 0.000 abstract 6
- 150000002367 halogens Chemical class 0.000 abstract 6
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 4
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 abstract 3
- 125000003118 aryl group Chemical group 0.000 abstract 2
- 125000000043 benzamido group Chemical group [H]N([*])C(=O)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 abstract 2
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 abstract 2
- -1 carboxy, sulfo Chemical group 0.000 abstract 2
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 2
- 150000002431 hydrogen Chemical class 0.000 abstract 2
- 229910052739 hydrogen Inorganic materials 0.000 abstract 2
- 239000001257 hydrogen Substances 0.000 abstract 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 2
- 125000004769 (C1-C4) alkylsulfonyl group Chemical group 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- 125000005236 alkanoylamino group Chemical group 0.000 abstract 1
- 125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 abstract 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 1
- 150000003839 salts Chemical group 0.000 abstract 1
- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B29/00—Monoazo dyes prepared by diazotising and coupling
- C09B29/0025—Monoazo dyes prepared by diazotising and coupling from diazotized amino heterocyclic compounds
- C09B29/0029—Monoazo dyes prepared by diazotising and coupling from diazotized amino heterocyclic compounds the heterocyclic ring containing only nitrogen as heteroatom
- C09B29/0048—Monoazo dyes prepared by diazotising and coupling from diazotized amino heterocyclic compounds the heterocyclic ring containing only nitrogen as heteroatom containing a six-membered heterocyclic ring with one nitrogen atom
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B29/00—Monoazo dyes prepared by diazotising and coupling
- C09B29/32—Monoazo dyes prepared by diazotising and coupling from coupling components containing a reactive methylene group
- C09B29/33—Aceto- or benzoylacetylarylides
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B29/00—Monoazo dyes prepared by diazotising and coupling
- C09B29/32—Monoazo dyes prepared by diazotising and coupling from coupling components containing a reactive methylene group
- C09B29/33—Aceto- or benzoylacetylarylides
- C09B29/331—Aceto- or benzoylacetylarylides containing acid groups, e.g. COOH, SO3H, PO3H2, OSO3H2, OPO2H2; salts thereof
- C09B29/332—Carbocyclic arylides
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B29/00—Monoazo dyes prepared by diazotising and coupling
- C09B29/32—Monoazo dyes prepared by diazotising and coupling from coupling components containing a reactive methylene group
- C09B29/33—Aceto- or benzoylacetylarylides
- C09B29/335—Aceto- or benzoylacetylarylides free of acid groups
- C09B29/337—Carbocyclic arylides
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Inks, Pencil-Leads, Or Crayons (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Heat Sensitive Colour Forming Recording (AREA)
- Paints Or Removers (AREA)
- Coloring (AREA)
- Cosmetics (AREA)
Abstract
Monoazoquilolone pigments which, in one of the tautomeric forms thereof, correspond to formula (1), wherein Ar is a radical of formula (2a), (2b), (2c), (2d), 2(e) or (2f) wherein R1 is C1-C4alkyl, R2 and R3 are each independently of other hydrogen, halogen. C1-C4alkyl, carboxy, sulfo, cyano, C1-C4alkoxycarbonal, C1-C4alkylcarbonyl, C1-C4alkanoylamino, benzoylamino that is unsubstituted or substituted in the phenyl ring by halogen, nitro, C1-C4alkyl or by C1-C<custom-character file="US20040034204A1-20040219-P00900.TIF" wi="20" he="20" id="custom-character-00001"/>4alkoxy; carbamoyl, N-C1-C4alkylaminocarbonyl, N-arylaminocarbonyl that is unsubstituted or substituted in the aryl moiety by halogen, nitro, C1-C4alkyl or by C1-C4alkoxy; N,N-di-C1-C4alkylaminocarbonyl, C1-C4alkoxysulfonyl, C1-C4alkylsulfonyl, sulfamoyl, N-C1-C4alkylaminosulfonyl, N-alkylaminosulfonyl that is unsubstituted or substituted in the aryl moiety by halogen, nitro, C1-C4alkyl or by C1-C<custom-character file="US20040034204A1-20040219-P00900.TIF" wi="20" he="20" id="custom-character-00002"/>4alkoxy; or N,N-di-C1-C4alkylaminosulfonyl, wherein carboxy and sulfo are in the form of the free acid or in salt form, R8and R9are each independently of the other hydrogen, halogen, C1-C4alkyl, C1-C4alkoxy, carboxy, sulfo, cyano, C1-C4alkoxycarbonyl, C1-C4alkylcarbonyl, C<custom-character file="US20040034204A1-20040219-P00900.TIF" wi="20" he="20" id="custom-character-00003"/>1<-C>4 ?alkanoylamino, benzoylamino that is unsubstituted or substituted in the phenyl ring by halogen, nitro, C1-C4alkyl or by C1-C4alkoxy; carbamoyl, N-C1 -C4al
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH20702000 | 2000-10-23 | ||
| CH2070/00 | 2000-10-23 | ||
| PCT/EP2001/012178 WO2002034839A1 (en) | 2000-10-23 | 2001-10-22 | Monoazoquinolone pigments, process for their preparation and their use |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AU2002219049A1 true AU2002219049A1 (en) | 2002-05-06 |
Family
ID=4567385
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU2002219049A Abandoned AU2002219049A1 (en) | 2000-10-23 | 2001-10-22 | Monoazoquinolone pigments, process for their preparation and their use |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US6756487B2 (en) |
| EP (1) | EP1328587B1 (en) |
| JP (1) | JP4204314B2 (en) |
| KR (1) | KR100812681B1 (en) |
| CN (1) | CN1262606C (en) |
| AT (1) | ATE506416T1 (en) |
| AU (1) | AU2002219049A1 (en) |
| BR (1) | BR0114825A (en) |
| CA (1) | CA2426288A1 (en) |
| DE (1) | DE60144484D1 (en) |
| MX (1) | MXPA03003540A (en) |
| WO (1) | WO2002034839A1 (en) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2003012957A (en) * | 2001-04-27 | 2003-01-15 | Canon Inc | Colored composition for color filter containing microcapsuled pigment comprising polyhydroxyalkanoate |
| RU2316223C2 (en) * | 2001-05-04 | 2008-02-10 | Баркон Ньютрасайнс (Мб) Корп. | Method for producing of protein isolate from oil-bearing crop seeds |
| KR20040047933A (en) * | 2001-10-19 | 2004-06-05 | 시바 스페셜티 케미칼스 홀딩 인크. | Process for making green pigment compositions useful for colour filters and LCDs |
| EP1606352A1 (en) * | 2003-03-25 | 2005-12-21 | Ciba SC Holding AG | Monoazoquinolone pigments, process for their preparation and their use |
| KR20060028412A (en) * | 2003-06-13 | 2006-03-29 | 시바 스페셜티 케미칼스 홀딩 인크. | Bisazoquinolone pigments, processes for their preparation and their use |
| US7105732B1 (en) * | 2005-03-24 | 2006-09-12 | Wu-Hong Hsieh | Musical instrument stand with a self-locking neck lock assembly |
| ZA200800899B (en) | 2005-07-01 | 2009-04-29 | Burcon Nutrascience Mb Corp | Production of canola protein |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2754293A (en) | 1952-12-23 | 1956-07-10 | American Cyanamid Co | Azo dyes from 6-aminocarbostyrils |
| US3137685A (en) * | 1960-11-14 | 1964-06-16 | Ici Ltd | Aceto-acetarylide azo quinoline coloring compounds |
| US3119808A (en) * | 1960-11-14 | 1964-01-28 | Ici Ltd | 7-(monoacetoacet monoarylide)-azo-4-methyl-2-hydroxy-quinoline coloring matters |
| CH611642A5 (en) * | 1976-11-09 | 1979-06-15 | Ciba Geigy Ag |
-
2001
- 2001-10-22 JP JP2002537818A patent/JP4204314B2/en not_active Expired - Fee Related
- 2001-10-22 KR KR1020037005639A patent/KR100812681B1/en not_active IP Right Cessation
- 2001-10-22 MX MXPA03003540A patent/MXPA03003540A/en active IP Right Grant
- 2001-10-22 AT AT01988748T patent/ATE506416T1/en not_active IP Right Cessation
- 2001-10-22 CA CA002426288A patent/CA2426288A1/en not_active Abandoned
- 2001-10-22 WO PCT/EP2001/012178 patent/WO2002034839A1/en active Application Filing
- 2001-10-22 AU AU2002219049A patent/AU2002219049A1/en not_active Abandoned
- 2001-10-22 CN CNB018178464A patent/CN1262606C/en not_active Expired - Fee Related
- 2001-10-22 DE DE60144484T patent/DE60144484D1/en not_active Expired - Lifetime
- 2001-10-22 EP EP01988748A patent/EP1328587B1/en not_active Expired - Lifetime
- 2001-10-22 US US10/399,441 patent/US6756487B2/en not_active Expired - Lifetime
- 2001-10-22 BR BR0114825-7A patent/BR0114825A/en not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| US20040034204A1 (en) | 2004-02-19 |
| JP2004512415A (en) | 2004-04-22 |
| BR0114825A (en) | 2004-02-03 |
| CN1471561A (en) | 2004-01-28 |
| DE60144484D1 (en) | 2011-06-01 |
| CN1262606C (en) | 2006-07-05 |
| CA2426288A1 (en) | 2002-05-02 |
| KR100812681B1 (en) | 2008-03-27 |
| MXPA03003540A (en) | 2003-07-14 |
| ATE506416T1 (en) | 2011-05-15 |
| EP1328587B1 (en) | 2011-04-20 |
| WO2002034839A1 (en) | 2002-05-02 |
| EP1328587A1 (en) | 2003-07-23 |
| JP4204314B2 (en) | 2009-01-07 |
| KR20030048445A (en) | 2003-06-19 |
| US6756487B2 (en) | 2004-06-29 |
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