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US4032347A Expired / Lapsed US ⏱️ 0.0 years remaining

2-equivalent acylacetamide yellow forming couplers with 2,6-dioxo-7-purinyl coupling off group

Assignee: Agfa Gevaert NV
•
Filing: 1975-11-25
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Granted: 1977-06-28
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Expires: 1995-11-25
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Abstract

Abstract A photographic material is described comprising novel 2-equivalent yellow forming color couplers the active methylene group of which carries a 2,6-dioxo-7-purinyl group in its oxo- or enol form.

Inventors

  • 👤 Raphael Karel Van Poucke
  • 👤 Marc Willem Ailliet
  • 👤 Leo August Van Wijnsberghe
  • 👤 Gaston Jacob Benoy

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-29 13:25
CPC Classifications
G; G03; G03C; G03C7/00; G03C7/30; G03C7/305; G03C7/30511; G03C7/30517; G03C7/30535; C; C07; C07D; C07D473/00; C07D473/02; C07D473/04; C07D473/06; C07D473/08

Claims Analysis

Total Claims: 17
Claim 1
Independent Claim 115 words
A photographic material comprising at least one silver halide emulsion layer and a 2-equivalent yellow forming ketomethylene colour coupler wherein the active methylene group carries a 2,6-dioxo-7-purinyl group in its oxo- or enol form and has the formula: ##STR7## wherein: Cp represents a yellow forming open-chain acylacetamide coupler residue linked through the active methylene group, each of R 1 and R 2 , which may be the same or different, represents hydrogen, an alkyl group, or an aryl group, and R 3 represents hydrogen, an alkyl group, an aryl group, a hydroxy group, an alkoxy group, an amino group, a mercapto group, an alkylthio group, a carboxy group, an alkoxycarbonyl group or a carbamoyl group.
Claim 2
Dependent Claim 115 words
A photographic material comprising at least one silver halide emulsion layer and a 2-equivalent yellow forming ketomethylene colour coupler wherein the active methylene group carries a 2,6-dioxo-7-purinyl group in its oxo- or enol form and has the formula: ##STR7## wherein: Cp represents a yellow forming open-chain acylacetamide coupler residue linked through the active methylene group, each of R 1 and R 2 , which may be the same or different, represents hydrogen, an alkyl group, or an aryl group, and R 3 represents hydrogen, an alkyl group, an aryl group, a hydroxy group, an alkoxy group, an amino group, a mercapto group, an alkylthio group, a carboxy group, an alkoxycarbonyl group or a carbamoyl group.
Claim 3
Dependent Claim 15 words
A photographic material according to claim 1, wherein R 1 and R 2 are alkyl.
Claim 4
Dependent Claim 15 words
A photographic material according to claim 2, wherein R 1 and R 2 are methyl.
Claim 5
Dependent Claim 61 words
A photographic material according to claim 1, wherein the yellow forming colour coupler residue carrying the heterocyclic substituent at the coupling position corresponds to the formula: ##STR8## wherein: each of Q 1 and Q 3 , which may be the same or different, represents an aliphatic, aromatic or heterocyclic group, and Q 2 represents hydrogen or C 1 -C 5 alkyl.
Claim 6
Dependent Claim 51 words
A photographic material according to claim 4, wherein Q 1 represents an alkyl group, an alkoxyalkyl group, a dicycloalkyl group, a heterocycle or an aryl group, Q 2 represents hydrogen or C 1 -C 5 alkyl, and Q 3 represents C 1 -C 18 alkyl, a heterocycle or an aryl group.
Claim 7
Dependent Claim 24 words
A photographic material according to claim 5, wherein the yellow forming colour coupler is a pivaloyl acetanilide colour coupler or a benzoylacetanilide colour coupler.
Claim 8
Dependent Claim 15 words
A photographic material according to claim 6, wherein R 1 and R 2 are alkyl.
Claim 9
Dependent Claim 15 words
A photographic material according to claim 7, wherein R 1 and R 2 are methyl.
Claim 10
Dependent Claim 121 words
A photographic material according to claim 8, wherein the yellow forming colour coupler residue corresponds to one of the formula: ##STR9## wherein: Z represents a halogen atom or an alkyl, alkoxy, aryloxy or amino group, each of Z 1 , Z 2 and Z 3 , which may be the same or different represents a hydrogen or halogen atom, an alkyl, alkoxy, aryl, aryloxy, alkoxycarbonyl, aryloxycarbonyl, alkylamino, arylamino, alkylsulphonyl, carbamoyl, sulphamoyl, acylamino, ureido, or hydroxy group or a sulpho or carboxy group in acid or salt form, and each of W, W 1 , W 2 and W 3 , which may be the same or different represents a hydrogen or halogen atom or an alkyl, alkoxy, aryloxy or amino group.
Claim 11
Dependent Claim 25 words
A photographic material according to claim 1, wherein the material also comprises a competing coupler in a light-sensitive or in a non-light-sensitive hydrophilic colloid layer.
Claim 12
Dependent Claim 21 words
A photographic material according to claim 1, wherein the yellow forming colour coupler is present in a silver halide emulsion layer.
Claim 13
Dependent Claim 21 words
A photographic material according to claim 1, wherein the yellow forming colour coupler is present in a non-light-sensitive hydrophilic colloid layer.
Claim 14
Dependent Claim 140 words
Method of producing coloured photographic images in a photographic light-sensitive silver halide material which comprises exposing the material and developing it with an aromatic primary amino colour developing agent in the presence of a 2-equivalent yellow forming ketomethylene colour coupler wherein the colour coupler carries at the active methylene group a 2,6-dioxo-7-purinyl group in its oxo- or enol form and has the formula: ##STR10## wherein: Cp represents a yellow forming open-chain acylacetamide coupler residue linked through the active methylene group, each of R 1 and R 2 , which may be the same or different, represents hydrogen, an alkyl group, or an aryl group, and R 3 represents hydrogen, an alkyl group, an aryl group, a hydroxy group, an alkoxy group, an amino group, a mercapto group, an alkylthio group, a carboxy group, an alkoxycarbonyl group or a carbamoyl group.
Claim 15
Dependent Claim 140 words
Method of producing coloured photographic images in a photographic light-sensitive silver halide material which comprises exposing the material and developing it with an aromatic primary amino colour developing agent in the presence of a 2-equivalent yellow forming ketomethylene colour coupler wherein the colour coupler carries at the active methylene group a 2,6-dioxo-7-purinyl group in its oxo- or enol form and has the formula: ##STR10## wherein: Cp represents a yellow forming open-chain acylacetamide coupler residue linked through the active methylene group, each of R 1 and R 2 , which may be the same or different, represents hydrogen, an alkyl group, or an aryl group, and R 3 represents hydrogen, an alkyl group, an aryl group, a hydroxy group, an alkoxy group, an amino group, a mercapto group, an alkylthio group, a carboxy group, an alkoxycarbonyl group or a carbamoyl group.
Claim 16
Dependent Claim 13 words
Method according to claim 13, wherein R 1 and R 2 are alkyl.
Claim 17
Dependent Claim 13 words
Method according to claim 14, wherein R 1 and R 2 are methyl.

References Cited (Backward Citations)

US3960570A Cited
US3933500A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1980-06-27 1980-12-27 1981-06-28 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1984-06-27 1984-12-27 1985-06-28 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1988-06-27 1988-12-27 1989-06-28 $7700.00 Window Closed / Lapsed

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