GB721520A - Improvements in colour photography - Google Patents

Improvements in colour photography

Info

Publication number
GB721520A
GB721520A GB31796/52A GB3179652A GB721520A GB 721520 A GB721520 A GB 721520A GB 31796/52 A GB31796/52 A GB 31796/52A GB 3179652 A GB3179652 A GB 3179652A GB 721520 A GB721520 A GB 721520A
Authority
GB
United Kingdom
Prior art keywords
pyrazolone
phenyl
tert
benzamido
amylphenoxy
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.)
Expired
Application number
GB31796/52A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Kodak Ltd
Original Assignee
Kodak Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Kodak Ltd filed Critical Kodak Ltd
Publication of GB721520A publication Critical patent/GB721520A/en
Expired legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
    • C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
    • C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D231/44—Oxygen and nitrogen or sulfur and nitrogen atoms
    • C07D231/52—Oxygen atom in position 3 and nitrogen atom in position 5, or vice versa
    • 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
    • G03C7/36—Couplers containing compounds with active methylene groups
    • G03C7/38—Couplers containing compounds with active methylene groups in rings
    • G03C7/384—Couplers containing compounds with active methylene groups in rings in pyrazolone rings

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Physics & Mathematics (AREA)
  • General Physics & Mathematics (AREA)
  • Silver Salt Photography Or Processing Solution Therefor (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

a - {41 - {11 - (211 : 411 : 611 - Trichlorophenyl) - 31 - [3111 - (2111 : 4111 - di - tert. - amylphenoxyacetamido) - benzamido] - 51 - pyrazolonyl}} - 1 - phenyl - 3 - methyl - 4 - (p - methoxybenzyl) - 5 - pyrazolone is prepared by refluxing together 1-phenyl-3-methyl-4-(41-methoxybenzylidene) - 5 - pyrazolone and 1-(21 : 41 : 61 - trichlorophenyl) - 3 - [311\h - (2111 : 4111 - di - tert. - amylphenoxyacetamido) - benzamido] - 5 - pyrazolone in acetic acid containing sodium acetate. a -{41 - {(11 - Benzthiazolyl) - 31 - [(311 - tert. - amylphenoxy) - benzamido] - 51-pyrazolonyl}} - 1 - phenyl - 3 - amino - 4 - (p-methoxybenzyl) - 5 - pyrazolone, a - {41 - [11-phenyl - 31 - a - phenylbutyramido - 51 - pyrazolonyl]} - 1 - [411 - (4111 - tert. - butylphenoxy)-phenyl] - 3 - [41111 - (41111 - tert. - butylphenoxy)-phenyl] - carbamyl - 4 - (p - methoxybenzyl) - 5-pyrazolone, and a - {1 - (21 - benzthiazolyl) - 3-d - [41 - (311 - p - tert. - amylphenoxy) - benzamido phenyl] - valeramido - 5 - pyrazolonyl} - 1-phenyl - 3 - a - phenylbutyrylamino - 4 - p-methoxybenzyl - 5 - pyrazolone are similarly prepared. 1 - Phenyl - 3 - methyl - 4 - (41 - methoxybenzylidene) - 5 - pyrazolone is prepared by heating together 1 - phenyl - 3 - methyl - 5-pyrazolone and p-methoxybenzaldehyde in glacial acetic acid. 1-Benzthiazolyl-3-[31-(tert.-amylphenoxy) - benzamido] - 4 - p - methoxybenzylidene - 5 - pyrazolone and 1 - phenyl - 3-a - phenylbutyramido - 4 - anisal - 5 - pyrazolone are similarly prepared. 1 - [41 - [411 - Tert. - Butylphenoxy) - phenyl]-3 - [4111 - (41111 - tert. - butylphenoxy) - phenyl]-carbamyl - 5 - pyrazolone is prepared by acylating 4-tert.-butylphenoxyaniline with 1-(41 - tert. - butylphenoxy) - phenyl - 3 - carboxy-5-pyrazolone. 1 - (21 - Benzthiazolyl) - 3 - d - [41 - (311 - p-tert. - amylphenoxy) - benzamido] - phenylvaleramido) - 5 - pyrazolone is prepared by acylating 1 - (21 - benzthiazolyl) - 3 - (d - 41-aminophenylvaleramido) - 5 - pyrazolone with 4 - (31 - p - tert.-amylphenoxy) - benzoyl chloride. Specifications 524,154, 524,555, 541,589, [all in Group XX], 599,919 and 680,488 are referred to.
GB31796/52A 1951-12-15 1952-12-15 Improvements in colour photography Expired GB721520A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US261909A US2706683A (en) 1951-12-15 1951-12-15 Bis-pyrazolone for color photography

Publications (1)

Publication Number Publication Date
GB721520A true GB721520A (en) 1955-01-05

Family

ID=22995400

Family Applications (1)

Application Number Title Priority Date Filing Date
GB31796/52A Expired GB721520A (en) 1951-12-15 1952-12-15 Improvements in colour photography

Country Status (4)

Country Link
US (1) US2706683A (en)
BE (1) BE516241A (en)
FR (1) FR1067680A (en)
GB (1) GB721520A (en)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2879341A (en) * 1954-05-06 1959-03-24 Ford Motor Co Tape recorder and player
BE544737A (en) * 1955-01-28
US2933391A (en) * 1956-09-06 1960-04-19 Eastman Kodak Co Photographic emulsions containing 5-pyrazolone coupler compounds
GB852922A (en) * 1957-09-04 1960-11-02 Gen Aniline & Film Corp Color formers containing a m-alkylphenoxyacyl group
BE619301A (en) * 1959-04-06
US3148062A (en) * 1959-04-06 1964-09-08 Eastman Kodak Co Photographic elements and processes using splittable couplers
JPS55105248A (en) * 1979-02-06 1980-08-12 Konishiroku Photo Ind Co Ltd Dye image forming method
JPS57111536A (en) 1980-12-27 1982-07-12 Konishiroku Photo Ind Co Ltd Color photographic sensitive silver halide material
US5091291A (en) * 1990-10-25 1992-02-25 Eastman Kodak Company Alkyl substituted photographic couplers and photographic elements and processes employing same

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB513596A (en) * 1938-04-08 1939-10-17 John David Kendall Improvements in and relating to the production of coloured photographic images by colour development
US2294909A (en) * 1939-02-13 1942-09-08 Du Pont Chemical process and composition
US2411951A (en) * 1944-09-28 1946-12-03 Gen Aniline & Film Corp 4,4'-bis (pyrazolone) couplers for color photography
US2435550A (en) * 1945-11-08 1948-02-03 Gen Aniline & Film Corp 4, 4'-bis (pyrazolone-1-carboxamide and thiocarboxamide) couplers for color photography

Also Published As

Publication number Publication date
US2706683A (en) 1955-04-19
BE516241A (en)
FR1067680A (en) 1954-06-17

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