JP2003514944A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2003514944A5 JP2003514944A5 JP2001539025A JP2001539025A JP2003514944A5 JP 2003514944 A5 JP2003514944 A5 JP 2003514944A5 JP 2001539025 A JP2001539025 A JP 2001539025A JP 2001539025 A JP2001539025 A JP 2001539025A JP 2003514944 A5 JP2003514944 A5 JP 2003514944A5
- Authority
- JP
- Japan
- Prior art keywords
- compound
- acid
- mixture
- substituted
- reaction step
- 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.)
- Pending
Links
- 150000001875 compounds Chemical class 0.000 description 16
- 239000000203 mixture Substances 0.000 description 14
- 239000000758 substrate Substances 0.000 description 6
- 125000000217 alkyl group Chemical group 0.000 description 5
- 125000004429 atom Chemical group 0.000 description 4
- 229910052757 nitrogen Inorganic materials 0.000 description 4
- 229910052760 oxygen Inorganic materials 0.000 description 4
- 229910052717 sulfur Inorganic materials 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- 125000002947 alkylene group Chemical group 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 238000009472 formulation Methods 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 229920000742 Cotton Polymers 0.000 description 2
- RGHNJXZEOKUKBD-SQOUGZDYSA-N D-gluconic acid Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C(O)=O RGHNJXZEOKUKBD-SQOUGZDYSA-N 0.000 description 2
- AEMRFAOFKBGASW-UHFFFAOYSA-N Glycolic acid Chemical compound OCC(O)=O AEMRFAOFKBGASW-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- -1 Hydroxyl- Chemical group 0.000 description 2
- 102000011782 Keratins Human genes 0.000 description 2
- 108010076876 Keratins Proteins 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 125000003545 alkoxy group Chemical group 0.000 description 2
- 229920002678 cellulose Polymers 0.000 description 2
- 239000001913 cellulose Substances 0.000 description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 2
- 229910052736 halogen Inorganic materials 0.000 description 2
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
- 239000010985 leather Substances 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- 150000007522 mineralic acids Chemical class 0.000 description 2
- 230000000269 nucleophilic effect Effects 0.000 description 2
- 150000007524 organic acids Chemical class 0.000 description 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 2
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 description 1
- 125000006681 (C2-C10) alkylene group Chemical group 0.000 description 1
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
- 125000002853 C1-C4 hydroxyalkyl group Chemical group 0.000 description 1
- RGHNJXZEOKUKBD-UHFFFAOYSA-N D-gluconic acid Natural products OCC(O)C(O)C(O)C(O)C(O)=O RGHNJXZEOKUKBD-UHFFFAOYSA-N 0.000 description 1
- 235000011054 acetic acid Nutrition 0.000 description 1
- 125000003342 alkenyl group Chemical group 0.000 description 1
- 125000004453 alkoxycarbonyl group Chemical group 0.000 description 1
- 230000002152 alkylating effect Effects 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 125000003785 benzimidazolyl group Chemical group N1=C(NC2=C1C=CC=C2)* 0.000 description 1
- 125000004618 benzofuryl group Chemical group O1C(=CC2=C1C=CC=C2)* 0.000 description 1
- 125000001164 benzothiazolyl group Chemical group S1C(=NC2=C1C=CC=C2)* 0.000 description 1
- 125000004196 benzothienyl group Chemical group S1C(=CC2=C1C=CC=C2)* 0.000 description 1
- 125000004541 benzoxazolyl group Chemical group O1C(=NC2=C1C=CC=C2)* 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 description 1
- 125000000609 carbazolyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3NC12)* 0.000 description 1
- 235000015165 citric acid Nutrition 0.000 description 1
- 125000004093 cyano group Chemical group *C#N 0.000 description 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- 150000004985 diamines Chemical class 0.000 description 1
- 238000004043 dyeing Methods 0.000 description 1
- 150000002118 epoxides Chemical class 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- 125000002485 formyl group Chemical class [H]C(*)=O 0.000 description 1
- 125000002541 furyl group Chemical group 0.000 description 1
- 239000000174 gluconic acid Substances 0.000 description 1
- 235000012208 gluconic acid Nutrition 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 150000002391 heterocyclic compounds Chemical class 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 125000002768 hydroxyalkyl group Chemical group 0.000 description 1
- 125000003453 indazolyl group Chemical group N1N=C(C2=C1C=CC=C2)* 0.000 description 1
- 125000001041 indolyl group Chemical group 0.000 description 1
- 239000004310 lactic acid Substances 0.000 description 1
- 235000014655 lactic acid Nutrition 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 125000001715 oxadiazolyl group Chemical group 0.000 description 1
- 125000002971 oxazolyl group Chemical group 0.000 description 1
- 125000001484 phenothiazinyl group Chemical group C1(=CC=CC=2SC3=CC=CC=C3NC12)* 0.000 description 1
- 125000001644 phenoxazinyl group Chemical group C1(=CC=CC=2OC3=CC=CC=C3NC12)* 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 235000011007 phosphoric acid Nutrition 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- 125000003226 pyrazolyl group Chemical group 0.000 description 1
- 125000004076 pyridyl group Chemical group 0.000 description 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
- 125000005504 styryl group Chemical group 0.000 description 1
- 125000001113 thiadiazolyl group Chemical group 0.000 description 1
- 125000000335 thiazolyl group Chemical group 0.000 description 1
- 125000001544 thienyl group Chemical group 0.000 description 1
- 125000001425 triazolyl group Chemical group 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH19992102/99 | 1999-11-18 | ||
| CH210299 | 1999-11-18 | ||
| PCT/IB2000/001674 WO2001036543A1 (en) | 1999-11-18 | 2000-11-16 | Oligomeric methine dyes |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2003514944A JP2003514944A (ja) | 2003-04-22 |
| JP2003514944A5 true JP2003514944A5 (enExample) | 2007-10-18 |
Family
ID=4225923
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2001539025A Pending JP2003514944A (ja) | 1999-11-18 | 2000-11-16 | オリゴマーメチン染料 |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US20010012899A1 (enExample) |
| EP (1) | EP1234007B1 (enExample) |
| JP (1) | JP2003514944A (enExample) |
| KR (1) | KR100705185B1 (enExample) |
| CN (1) | CN1192065C (enExample) |
| AT (1) | ATE259865T1 (enExample) |
| BR (1) | BR0015673A (enExample) |
| DE (1) | DE60008417T2 (enExample) |
| ES (1) | ES2215742T3 (enExample) |
| TR (1) | TR200201323T2 (enExample) |
| WO (1) | WO2001036543A1 (enExample) |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2018855A1 (de) * | 1968-12-17 | 1971-11-04 | Cassella Farbwerke Mainkur AG, 6000 Frankfurt-Fechenheim | Verfahren zur Herstellung wasserlöslicher, faseraffiner Farbstoffe |
| TW473525B (en) * | 1994-12-16 | 2002-01-21 | Bic Corp | Erasable ink composition and marking instrument containing same |
-
2000
- 2000-11-16 BR BR0015673-6A patent/BR0015673A/pt not_active Application Discontinuation
- 2000-11-16 DE DE60008417T patent/DE60008417T2/de not_active Expired - Fee Related
- 2000-11-16 AT AT00973152T patent/ATE259865T1/de not_active IP Right Cessation
- 2000-11-16 KR KR1020027006267A patent/KR100705185B1/ko not_active Expired - Fee Related
- 2000-11-16 CN CNB00815676XA patent/CN1192065C/zh not_active Expired - Fee Related
- 2000-11-16 EP EP00973152A patent/EP1234007B1/en not_active Expired - Lifetime
- 2000-11-16 JP JP2001539025A patent/JP2003514944A/ja active Pending
- 2000-11-16 WO PCT/IB2000/001674 patent/WO2001036543A1/en not_active Ceased
- 2000-11-16 ES ES00973152T patent/ES2215742T3/es not_active Expired - Lifetime
- 2000-11-16 TR TR2002/01323T patent/TR200201323T2/xx unknown
-
2001
- 2001-04-18 US US09/792,754 patent/US20010012899A1/en not_active Abandoned
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP2003525949A5 (enExample) | ||
| JP4532907B2 (ja) | ランタニド錯体を含有するインク組成物 | |
| JP2004501930A5 (enExample) | ||
| CA2352436A1 (en) | Polymorphs of telmisartan, processes for preparing them and their use in the preparation of a pharmaceutical composition | |
| CO6280530A2 (es) | Derivados de pirimidina 5-fluoro como fungicidas | |
| RU96119964A (ru) | Нафтиламиды в качестве средств воздействия на центральную нервную систему | |
| JP2006509068A5 (enExample) | ||
| JP2000344940A5 (enExample) | ||
| JP2004502056A5 (enExample) | ||
| JP2009544788A5 (enExample) | ||
| JP2023178294A5 (enExample) | ||
| JPS60186566A (ja) | ジシアノメチリデン‐ジヒドロチオフエンジオキシド誘導体 | |
| UY25227A1 (es) | Procedimiento para preparar 5-[4-[2-(n-metil-n-(2-piridil)amino)etoxi]bencil]-2,4-tiazolidindiona | |
| JP2003514944A5 (enExample) | ||
| CN106748879B (zh) | 一种对硝基苯甲醛席夫碱衍生物及其制备方法与应用 | |
| JPH04366177A (ja) | カチオン性１，３，４−チアジアゾール染料 | |
| CN115028612A (zh) | 一类黄酮类化合物及制备和在制备抗糖尿病药物中的应用 | |
| JP2007528928A5 (enExample) | ||
| JP2009532428A5 (enExample) | ||
| Wang et al. | Direct Synthesis of Benzothiazoles and Benzoxazoles from Carboxylic Acids Utilizing (o-CF3PhO) 3P as a Coupling Reagent | |
| KR100705185B1 (ko) | 올리고머성 메틴 염료 | |
| EP4340839B1 (fr) | Nouveaux derives azaindole en tant qu'agents antiviraux | |
| EP4340833B1 (fr) | Nouveaux derives azaindole en tant qu'agents antiviraux | |
| JP2524628B2 (ja) | 塩基性アゾ染料、その製造法および染色法 | |
| CN104016998A (zh) | 苯并双呋喃类化合物及其制备和应用 |