US4133958A
Expired / Lapsed
US
⏱️ 0.0 years remaining
2-Equivalent yellow couplers
Assignee: Agfa Gevaert AG
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Filing: 1977-05-06
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Granted: 1979-01-09
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Expires: 1997-05-06
Abstract
Abstract Desirable 2-equivalent yellow-forming couplers in which a 1,3-diazolone-2-ring as splittable group is attached by the nitrogen in its 1-position to the coupling position of the 2-equivalent yellow-forming coupler and in which the diazolone ring has a C═C double bond adjacent to the nitrogen atom in its 1-position, have improved photographic properties in particular with respect to improved reactivity on chromogenic development and improved stability of the couplers as well as the dyes produced from them on chromogenic development in a photographic material which has been subjected to storage under moist and/or warm conditions.
Inventors
- 👤 Immo Boie
- 👤 Karl Kuffner
- 👤 Gertrud Kirchhoff
- 👤 Karl-Wilhelm Schranz
Bibliographic Details
Application Number
—
Jurisdiction
US
Data Source
google_patents
Last Synchronized
2026-10-26 23:14
CPC Classifications
G; G03; G03C; G03C7/00; G03C7/30; G03C7/305; G03C7/30511; G03C7/30517; G03C7/30535; C; C07; C07D; C07D233/00; C07D233/54; C07D233/66; C07D233/90; C07D235/00; C07D235/02; C07D235/04; C07D235/24; C07D235/26
Claims Analysis
Total Claims: 6
Claim 1
Independent Claim
175 words
A 2-equivalent yellow-forming coupler having the formula ##STR91## in which R 1 represents hydrogen; an alkyl group containing 1 to 4 carbon atoms; or an alkoxy carbonyl group in which the alkoxy group contains from 1 to 5 carbon atoms; R 2 and R 3 represent either the same or different substituents selected from the group consisting of hydrogen, alkyl, and alkoxycarbonyl in which the alkoxy group contains from 1 to 5 carbon atoms, but at least one of R 2 and R 3 represents an alkoxy carbonyl group; or R 2 and R 3 together represent the atoms required to complete a condensed benzene ring, which ring is further substituted with two chlorine atoms to form the 5, 6-dichlorobenzimidazolone group; and A represents a radical of a yellow-forming coupler having an open-chain keto-methylene structure in which the methylene group is activated by two attached carbonyl groups or by one carbonyl and one cyano group, and the radical being obtained by removing a hydrogen atom from the activated methylene group of a 4-equivalent yellow-forming coupler.
Claim 2
Dependent Claim
175 words
A 2-equivalent yellow-forming coupler having the formula ##STR91## in which R 1 represents hydrogen; an alkyl group containing 1 to 4 carbon atoms; or an alkoxy carbonyl group in which the alkoxy group contains from 1 to 5 carbon atoms; R 2 and R 3 represent either the same or different substituents selected from the group consisting of hydrogen, alkyl, and alkoxycarbonyl in which the alkoxy group contains from 1 to 5 carbon atoms, but at least one of R 2 and R 3 represents an alkoxy carbonyl group; or R 2 and R 3 together represent the atoms required to complete a condensed benzene ring, which ring is further substituted with two chlorine atoms to form the 5, 6-dichlorobenzimidazolone group; and A represents a radical of a yellow-forming coupler having an open-chain keto-methylene structure in which the methylene group is activated by two attached carbonyl groups or by one carbonyl and one cyano group, and the radical being obtained by removing a hydrogen atom from the activated methylene group of a 4-equivalent yellow-forming coupler.
Claim 3
Dependent Claim
20 words
A coupler as claimed in claim 1 in which the R 2 and/or R 3 substituent is a methoxy-carbonyl group.
Claim 4
Dependent Claim
20 words
A coupler as claimed in claim 1 in which the R 2 and/or R 3 substituent is a butoxy-carbonyl group.
Claim 5
Dependent Claim
18 words
A coupler as claimed in claim 1 in which the yellow-forming coupler is a pivaloyl acetanilide or benzoylacetanilide.
Claim 6
Dependent Claim
17 words
A coupler as claimed in claim 1 in which the formula is that of the 3-ethyl-5,6-dichlorobenzimidazolone group.
References Cited (Backward Citations)
USPTO Annuity & Maintenance Windows
| Annuity Stage | Window Opens | Payment Deadline | Surcharge Period Until | Estimated Fee | Status |
|---|---|---|---|---|---|
| 3.5 Years (Year 4) | 1982-01-08 | 1982-07-10 | 1983-01-09 | $2000.00 | Window Closed / Lapsed |
| 7.5 Years (Year 8) | 1986-01-08 | 1986-07-10 | 1987-01-09 | $3760.00 | Window Closed / Lapsed |
| 11.5 Years (Year 12) | 1990-01-08 | 1990-07-10 | 1991-01-09 | $7700.00 | Window Closed / Lapsed |