GB965160A - - Google Patents
Info
- Publication number
- GB965160A GB965160A GB965160DA GB965160A GB 965160 A GB965160 A GB 965160A GB 965160D A GB965160D A GB 965160DA GB 965160 A GB965160 A GB 965160A
- Authority
- GB
- United Kingdom
- Prior art keywords
- pyrazolyl
- methyl
- naphthol
- reacted
- give
- 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.)
- Active
Links
- 150000001875 compounds Chemical class 0.000 abstract 4
- NWZSZGALRFJKBT-KNIFDHDWSA-N (2s)-2,6-diaminohexanoic acid;(2s)-2-hydroxybutanedioic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O.NCCCC[C@H](N)C(O)=O NWZSZGALRFJKBT-KNIFDHDWSA-N 0.000 abstract 2
- GGIGKLZFGBGGGJ-UHFFFAOYSA-N 2-(5-methyl-1H-pyrazol-3-yl)naphthalen-1-ol Chemical compound CC1=CC(=NN1)C1=C(C2=CC=CC=C2C=C1)O GGIGKLZFGBGGGJ-UHFFFAOYSA-N 0.000 abstract 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 abstract 2
- IKDUDTNKRLTJSI-UHFFFAOYSA-N hydrazine monohydrate Substances O.NN IKDUDTNKRLTJSI-UHFFFAOYSA-N 0.000 abstract 2
- 229940067157 phenylhydrazine Drugs 0.000 abstract 2
- 125000003226 pyrazolyl group Chemical group 0.000 abstract 2
- FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 abstract 2
- JYSUYJCLUODSLN-UHFFFAOYSA-N 1,3-benzothiazol-2-ylhydrazine Chemical compound C1=CC=C2SC(NN)=NC2=C1 JYSUYJCLUODSLN-UHFFFAOYSA-N 0.000 abstract 1
- GZNTVFDLXWUBQY-UHFFFAOYSA-N 2-(5-methyl-2-phenylpyrazol-3-yl)naphthalen-1-ol Chemical class C1(=CC=CC=C1)N1N=C(C=C1C1=C(C2=CC=CC=C2C=C1)O)C GZNTVFDLXWUBQY-UHFFFAOYSA-N 0.000 abstract 1
- NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 abstract 1
- VKJGZHQYRQGMRH-UHFFFAOYSA-N 3-amino-5-(octadecanoylamino)benzoic acid Chemical compound CCCCCCCCCCCCCCCCCC(=O)NC1=CC(N)=CC(C(O)=O)=C1 VKJGZHQYRQGMRH-UHFFFAOYSA-N 0.000 abstract 1
- HVAABJQILHVHFQ-UHFFFAOYSA-N 3-amino-5-(octadecylamino)benzoic acid Chemical compound NC=1C=C(C(=O)O)C=C(C1)NCCCCCCCCCCCCCCCCCC HVAABJQILHVHFQ-UHFFFAOYSA-N 0.000 abstract 1
- WBABHXJTUIHTCZ-UHFFFAOYSA-N 4-[5-(1-hydroxynaphthalen-2-yl)-3-methylpyrazol-1-yl]benzoic acid Chemical compound C(=O)(O)C1=CC=C(C=C1)N1N=C(C=C1C1=C(C2=CC=CC=C2C=C1)O)C WBABHXJTUIHTCZ-UHFFFAOYSA-N 0.000 abstract 1
- AQPKUVRMQWPICF-UHFFFAOYSA-N 5-chloro-2-isocyanatobenzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC(Cl)=CC=C1N=C=O AQPKUVRMQWPICF-UHFFFAOYSA-N 0.000 abstract 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 abstract 1
- 150000001412 amines Chemical class 0.000 abstract 1
- OTAFHZMPRISVEM-UHFFFAOYSA-N chromone Chemical compound C1=CC=C2C(=O)C=COC2=C1 OTAFHZMPRISVEM-UHFFFAOYSA-N 0.000 abstract 1
- 235000019441 ethanol Nutrition 0.000 abstract 1
- WSQSEIGPFZCRFE-UHFFFAOYSA-N naphthalen-1-ol 1H-pyrazole Chemical class C=1C=NNC=1.C1=CC=C2C(O)=CC=CC2=C1 WSQSEIGPFZCRFE-UHFFFAOYSA-N 0.000 abstract 1
- 125000000636 p-nitrophenyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)[N+]([O-])=O 0.000 abstract 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
- HKOOXMFOFWEVGF-UHFFFAOYSA-N phenylhydrazine Chemical compound NNC1=CC=CC=C1 HKOOXMFOFWEVGF-UHFFFAOYSA-N 0.000 abstract 1
- 150000004031 phenylhydrazines Chemical class 0.000 abstract 1
- 238000010992 reflux Methods 0.000 abstract 1
- 125000001424 substituent group Chemical group 0.000 abstract 1
Classifications
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
- G03C7/00—Multicolour photographic processes or agents therefor; Regeneration of such processing agents; Photosensitive materials for multicolour processes
- G03C7/30—Colour processes using colour-coupling substances; Materials therefor; Preparing or processing such materials
- G03C7/32—Colour coupling substances
- G03C7/34—Couplers containing phenols
Landscapes
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB4479062 | 1962-11-27 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB965160A true GB965160A (enExample) |
Family
ID=10434755
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB965160D Active GB965160A (enExample) | 1962-11-27 |
Country Status (1)
| Country | Link |
|---|---|
| GB (1) | GB965160A (enExample) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2642856A4 (en) * | 2010-11-24 | 2015-05-06 | Univ Ohio State Res Found | INTEGRIN-COUPLED KINASE-HEMMER |
-
0
- GB GB965160D patent/GB965160A/en active Active
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2642856A4 (en) * | 2010-11-24 | 2015-05-06 | Univ Ohio State Res Found | INTEGRIN-COUPLED KINASE-HEMMER |
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