GB2006192A - Sulphamphthalein and sulphamnaphthalein derivatives - Google Patents

Sulphamphthalein and sulphamnaphthalein derivatives

Info

Publication number
GB2006192A
GB2006192A GB7837753A GB7837753A GB2006192A GB 2006192 A GB2006192 A GB 2006192A GB 7837753 A GB7837753 A GB 7837753A GB 7837753 A GB7837753 A GB 7837753A GB 2006192 A GB2006192 A GB 2006192A
Authority
GB
United Kingdom
Prior art keywords
sulfam
sulphamphthalein
sulphamnaphthalein
derivatives
hydroxy
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.)
Granted
Application number
GB7837753A
Other versions
GB2006192B (en
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.)
Polaroid Corp
Original Assignee
Polaroid Corp
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
Priority claimed from US05/836,009 external-priority patent/US4228075A/en
Priority claimed from US05/836,021 external-priority patent/US4204061A/en
Priority claimed from US05/835,998 external-priority patent/US4178446A/en
Priority claimed from US05/836,005 external-priority patent/US4231929A/en
Application filed by Polaroid Corp filed Critical Polaroid Corp
Publication of GB2006192A publication Critical patent/GB2006192A/en
Application granted granted Critical
Publication of GB2006192B publication Critical patent/GB2006192B/en
Expired legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D275/00—Heterocyclic compounds containing 1,2-thiazole or hydrogenated 1,2-thiazole rings
    • C07D275/04—Heterocyclic compounds containing 1,2-thiazole or hydrogenated 1,2-thiazole rings condensed with carbocyclic rings or ring systems
    • C07D275/06—Heterocyclic compounds containing 1,2-thiazole or hydrogenated 1,2-thiazole rings condensed with carbocyclic rings or ring systems with hetero atoms directly attached to the ring sulfur atom
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D455/00—Heterocyclic compounds containing quinolizine ring systems, e.g. emetine alkaloids, protoberberine; Alkylenedioxy derivatives of dibenzo [a, g] quinolizines, e.g. berberine
    • C07D455/03—Heterocyclic compounds containing quinolizine ring systems, e.g. emetine alkaloids, protoberberine; Alkylenedioxy derivatives of dibenzo [a, g] quinolizines, e.g. berberine containing quinolizine ring systems directly condensed with at least one six-membered carbocyclic ring, e.g. protoberberine; Alkylenedioxy derivatives of dibenzo [a, g] quinolizines, e.g. berberine
    • C07D455/04—Heterocyclic compounds containing quinolizine ring systems, e.g. emetine alkaloids, protoberberine; Alkylenedioxy derivatives of dibenzo [a, g] quinolizines, e.g. berberine containing quinolizine ring systems directly condensed with at least one six-membered carbocyclic ring, e.g. protoberberine; Alkylenedioxy derivatives of dibenzo [a, g] quinolizines, e.g. berberine containing a quinolizine ring system condensed with only one six-membered carbocyclic ring, e.g. julolidine
    • 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
    • G03C1/00—Photosensitive materials
    • G03C1/76—Photosensitive materials characterised by the base or auxiliary layers
    • G03C1/825—Photosensitive materials characterised by the base or auxiliary layers characterised by antireflection means or visible-light filtering means, e.g. antihalation
    • G03C1/83—Organic dyestuffs therefor
    • 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
    • G03C8/00—Diffusion transfer processes or agents therefor; Photosensitive materials for such processes
    • G03C8/42—Structural details
    • G03C8/44—Integral units, i.e. the image-forming section not being separated from the image-receiving section
    • G03C8/48—Integral units, i.e. the image-forming section not being separated from the image-receiving section characterised by substances used for masking the image-forming section

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Physics & Mathematics (AREA)
  • General Physics & Mathematics (AREA)
  • Materials Engineering (AREA)
  • Architecture (AREA)
  • Structural Engineering (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Nitrogen- Or Sulfur-Containing Heterocyclic Ring Compounds With Rings Of Six Or More Members (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)

Abstract

Phenol sulfam(na)phthaleins substituted on the N atom of the sulfam(na)phthalein ring have the formula <IMAGE> wherein A' is a 4-hydroxy-1-phenyl or 4- hydroxy-1-naphthyl moiety and B is a phenyl or naphthyl moiety, A and B not being both naphthyl moieties, X' completes a 2,3-dihydrobenz [d] isothiazole-1,1-dioxide or 2,3- dihydronaphtho [1,8 de]-1,2-thiazine- 1,1-dioxide ring and Z is a group linked via a -CO- radical. The compounds are useful as photographic optical filter agents and filter agent precursors.
GB7837753A 1977-09-23 1978-09-22 Phenol sulpham(na) phthaleins Expired GB2006192B (en)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US05/836,009 US4228075A (en) 1977-09-23 1977-09-23 Novel sulfam(na)phthaleins
US05/836,021 US4204061A (en) 1977-09-23 1977-09-23 Sulfam(na)phthaleins
US05/835,998 US4178446A (en) 1977-09-23 1977-09-23 Sulfam(na)phthaleins
US05/836,005 US4231929A (en) 1977-09-23 1977-09-23 Sulfam(na)phthaleins

Publications (2)

Publication Number Publication Date
GB2006192A true GB2006192A (en) 1979-05-02
GB2006192B GB2006192B (en) 1982-04-21

Family

ID=27505888

Family Applications (1)

Application Number Title Priority Date Filing Date
GB7837753A Expired GB2006192B (en) 1977-09-23 1978-09-22 Phenol sulpham(na) phthaleins

Country Status (7)

Country Link
AU (1) AU523247B2 (en)
CA (1) CA1110238A (en)
DE (1) DE2841322A1 (en)
FR (1) FR2408596B1 (en)
GB (1) GB2006192B (en)
IT (1) IT1099604B (en)
NL (1) NL7809678A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2472594A1 (en) * 1979-12-26 1981-07-03 Polaroid Corp XANTHENE COMPOUNDS, PHOTOGRAPHIC PRODUCTS AND METHODS EMPLOYING THEM
EP0032036A1 (en) * 1979-12-26 1981-07-15 Polaroid Corporation Triarylmethane dyes, photographic recording materials, a process in which they are used, and methods for forming triarylmethane dyes
FR2479496A1 (en) * 1979-12-26 1981-10-02 Polaroid Corp NEW XANTHENE COMPOUNDS, PHOTOGRAPHIC PRODUCTS AND METHODS EMPLOYING THEM

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4139381A (en) * 1977-09-23 1979-02-13 Polaroid Corporation Photographic products and processes employing pH sensitive filter dyes

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3702245A (en) * 1970-06-05 1972-11-07 Polaroid Corp Photographic diffusion-transfer processes and elements utilizing ph-sensitive optical filter agents to prevent fogging by extraneous actinic radiation during development

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2472594A1 (en) * 1979-12-26 1981-07-03 Polaroid Corp XANTHENE COMPOUNDS, PHOTOGRAPHIC PRODUCTS AND METHODS EMPLOYING THEM
EP0032036A1 (en) * 1979-12-26 1981-07-15 Polaroid Corporation Triarylmethane dyes, photographic recording materials, a process in which they are used, and methods for forming triarylmethane dyes
FR2479496A1 (en) * 1979-12-26 1981-10-02 Polaroid Corp NEW XANTHENE COMPOUNDS, PHOTOGRAPHIC PRODUCTS AND METHODS EMPLOYING THEM

Also Published As

Publication number Publication date
FR2408596B1 (en) 1985-10-04
AU4005078A (en) 1980-03-27
FR2408596A1 (en) 1979-06-08
CA1110238A (en) 1981-10-06
IT1099604B (en) 1985-09-18
NL7809678A (en) 1979-03-27
AU523247B2 (en) 1982-07-22
DE2841322C2 (en) 1988-07-28
IT7828047A0 (en) 1978-09-25
GB2006192B (en) 1982-04-21
DE2841322A1 (en) 1979-04-05

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Legal Events

Date Code Title Description
PCNP Patent ceased through non-payment of renewal fee

Effective date: 19960922