Patent US2313747A successfully refreshed from Google Patents.
Patent US3956339A successfully refreshed from Google Patents.
← Back to Patent Explorer
US3956339A Expired / Lapsed US ⏱️ 0.0 years remaining

4-Pyridinio-5-pyrazolone salts, process for their preparation and their use

Assignee: Fujifilm Holdings Corp
•
Filing: 1974-09-17
•
Granted: 1976-05-11
•
Expires: 1994-09-17
📄 Original PDF 🌐 Google Patents 🔄 Sync Now

Abstract

Abstract 4-Pyridinio-5-pyrazolone salts useful as dyes and particularly useful as intermediates for photographic couplers and processes for the preparation thereof.

Inventors

  • 👤 Nobuo Furutachi
  • 👤 Atsuaki Arai

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-04 16:21
CPC Classifications
G; G03; G03C; G03C7/00; G03C7/30; G03C7/32; G03C7/36; G03C7/38; G03C7/384

Claims Analysis

Total Claims: 15
Claim 1
Independent Claim 619 words
A 4-pyridinio-5-pyrazolone salt represented by the following formula (IVa) ##SPC15## the formula (IVb) ##SPC16## the formula (VI) ##SPC17## or a mixture thereof, wherein R 1 represents a hydrogen atom; sulfamoyl; alkyl having 1 to 40 carbon atoms, alkoxycarbonyl having 1 to 40 carbon atoms, carboxy having 1 to 40 carbon atoms, aryl having 1 to 40 carbon atoms, aryl comprising phenyl substituted with alkyl having 1 to 30 carbon atoms, alkoxy having 1 to 30 carbon atoms, aryloxy comprising phenoxy or naphthoxy, or phenoxy or naphthoxy having a substituent group having 1 to 10 carbon atoms, acylamino having 1 to 30 carbon atoms, carbamoyl having 1 to 30 carbon atoms, alkylsulfonamido having 1 to 30 carbon atims, arylsulfonamido comprising phenylsulfonamido or naphthylsulfonamido, and arylsulfonamido comprising phenylsulfonamido or naphthylsulfonamido having a substituent group having 1 to 20 carbon atoms; R 2 represents a hydrogen atom, hydroxy, amino, sulfo, alkyl having 1 to 45 carbon atoms, aryl comprising phenyl or naphthyl, or phenyl or naphthyl having a substituent group having 1 to 30 carbon atoms, alkoxy having 1 to 45 carbon atoms, aryloxy having 1 to 45 carbon atoms, alkoxycarbonyl having 1 to 40 carbons atoms, alkylamino having 1 to 45 atoms, cycloalkylamino having 3 to 8 carbon atoms and comprising cyclopentylamino, cyclohexylamino, and cycloheptylamino, cycloakylamino having 3 to 8 carbon atoms having a substituent group having 1 to 30 carbon atoms, dialkylamino wherein the alkyl 1 to 20 carbon atoms, diarylamino comprising diphenylamino or dinaphthylamino, or diphenylamino or dinaphthylamino having a substituent group having 1 to 15 carbon atoms, arylamino wherein the aryl has 6 to 45 carbon atoms, acylamino wherein the acyl has 1 to 45 carbon atoms, N-alkylacylamino wherein the acyl has 1 to 30 carbon atoms and the alkyl has 1 to 10 carbon atoms, carbamoyl having 1 to 45 carbon atoms, N-arylacylamino comprising phenyl-acylamino or naphthylacylamino, or phenylacylamino having a substituent group containing phenyl having 1 to 10 carbon atoms and wherein the acyl has 1 to 20 carbon atoms, ureido comprising ureido, N-alkylureido, N-phenylureido, N-naphthyl ureido having 1 to 45 carbon atoms and N-substituted phenyl ureido, N-substituted naphthyl ureido having 1 to 20 carbon atoms in the substituent group and and N-cycloalkyl ureido having 5 to 30 carbon atoms, diacyl amino wherein the acyl has 1 to 20 carbon atoms, and carboxy; R 3 , R 4 and R 5 each represents a hydrogen atom, hydroxy, a halogen atom, amino, sulfonamido, sulfo, alkyl having 1 to 20 carbon atoms, alkoxy having 1 to 20 carbon atoms, alkoxycarbonyl having 1 to 20 carbon atoms, aralkyl having 1 to 20 carbon atoms, aryloxy comprising phenoxy or naphthoxy, or phenoxy having a substituent group having 1 to 14 carbon atoms or napthoxy having a substituent group having 1 to 10 carbon atoms, carboxy, carbamoyl having 1 to 20 carbon atoms, carbamido having 1 to 20 carbon atoms, acylamino wherein the acyl has 1 to 20 carbon atoms, alkylsulfonamido having 1 to 20 carbon atoms, arylsulfonamido comprising phenylsulfonamido or naphthylsulfonamido, or phenylsulfonamido having a substituent group having 2 to 14 carbon atoms or naphthylsulfonamido having a substituent group having 1 to 10 carbon atoms, alkylamino having 1 to 20 caron atoms, arylamino comprising phenylamino or naphthylamino, or phenylamino having a substituent group having 1 to 14 carbon atoms or naphthylamino having a substituent group having 1 to 10 carbon atoms, or R 3 and R 4 can combine to form cyclopentane, cyclohexane, cycloheptane, benzene, benzene substituted with a halogen atom, amino, hydroxy, sulfo, carboxy, sulfonamido or alkyl, alkoxy, acylamino, alkylamino or arylamino as defined for R 2 , pyridine ring, dihydrofuran ring, dihydrothiophene ring or a thiophene ring; and Y represents chlorine, bromine, iodine, perchlorate, periodate or p-toluene sulfonate.
Claim 2
Dependent Claim 619 words
A 4-pyridinio-5-pyrazolone salt represented by the following formula (IVa) ##SPC15## the formula (IVb) ##SPC16## the formula (VI) ##SPC17## or a mixture thereof, wherein R 1 represents a hydrogen atom; sulfamoyl; alkyl having 1 to 40 carbon atoms, alkoxycarbonyl having 1 to 40 carbon atoms, carboxy having 1 to 40 carbon atoms, aryl having 1 to 40 carbon atoms, aryl comprising phenyl substituted with alkyl having 1 to 30 carbon atoms, alkoxy having 1 to 30 carbon atoms, aryloxy comprising phenoxy or naphthoxy, or phenoxy or naphthoxy having a substituent group having 1 to 10 carbon atoms, acylamino having 1 to 30 carbon atoms, carbamoyl having 1 to 30 carbon atoms, alkylsulfonamido having 1 to 30 carbon atims, arylsulfonamido comprising phenylsulfonamido or naphthylsulfonamido, and arylsulfonamido comprising phenylsulfonamido or naphthylsulfonamido having a substituent group having 1 to 20 carbon atoms; R 2 represents a hydrogen atom, hydroxy, amino, sulfo, alkyl having 1 to 45 carbon atoms, aryl comprising phenyl or naphthyl, or phenyl or naphthyl having a substituent group having 1 to 30 carbon atoms, alkoxy having 1 to 45 carbon atoms, aryloxy having 1 to 45 carbon atoms, alkoxycarbonyl having 1 to 40 carbons atoms, alkylamino having 1 to 45 atoms, cycloalkylamino having 3 to 8 carbon atoms and comprising cyclopentylamino, cyclohexylamino, and cycloheptylamino, cycloakylamino having 3 to 8 carbon atoms having a substituent group having 1 to 30 carbon atoms, dialkylamino wherein the alkyl 1 to 20 carbon atoms, diarylamino comprising diphenylamino or dinaphthylamino, or diphenylamino or dinaphthylamino having a substituent group having 1 to 15 carbon atoms, arylamino wherein the aryl has 6 to 45 carbon atoms, acylamino wherein the acyl has 1 to 45 carbon atoms, N-alkylacylamino wherein the acyl has 1 to 30 carbon atoms and the alkyl has 1 to 10 carbon atoms, carbamoyl having 1 to 45 carbon atoms, N-arylacylamino comprising phenyl-acylamino or naphthylacylamino, or phenylacylamino having a substituent group containing phenyl having 1 to 10 carbon atoms and wherein the acyl has 1 to 20 carbon atoms, ureido comprising ureido, N-alkylureido, N-phenylureido, N-naphthyl ureido having 1 to 45 carbon atoms and N-substituted phenyl ureido, N-substituted naphthyl ureido having 1 to 20 carbon atoms in the substituent group and and N-cycloalkyl ureido having 5 to 30 carbon atoms, diacyl amino wherein the acyl has 1 to 20 carbon atoms, and carboxy; R 3 , R 4 and R 5 each represents a hydrogen atom, hydroxy, a halogen atom, amino, sulfonamido, sulfo, alkyl having 1 to 20 carbon atoms, alkoxy having 1 to 20 carbon atoms, alkoxycarbonyl having 1 to 20 carbon atoms, aralkyl having 1 to 20 carbon atoms, aryloxy comprising phenoxy or naphthoxy, or phenoxy having a substituent group having 1 to 14 carbon atoms or napthoxy having a substituent group having 1 to 10 carbon atoms, carboxy, carbamoyl having 1 to 20 carbon atoms, carbamido having 1 to 20 carbon atoms, acylamino wherein the acyl has 1 to 20 carbon atoms, alkylsulfonamido having 1 to 20 carbon atoms, arylsulfonamido comprising phenylsulfonamido or naphthylsulfonamido, or phenylsulfonamido having a substituent group having 2 to 14 carbon atoms or naphthylsulfonamido having a substituent group having 1 to 10 carbon atoms, alkylamino having 1 to 20 caron atoms, arylamino comprising phenylamino or naphthylamino, or phenylamino having a substituent group having 1 to 14 carbon atoms or naphthylamino having a substituent group having 1 to 10 carbon atoms, or R 3 and R 4 can combine to form cyclopentane, cyclohexane, cycloheptane, benzene, benzene substituted with a halogen atom, amino, hydroxy, sulfo, carboxy, sulfonamido or alkyl, alkoxy, acylamino, alkylamino or arylamino as defined for R 2 , pyridine ring, dihydrofuran ring, dihydrothiophene ring or a thiophene ring; and Y represents chlorine, bromine, iodine, perchlorate, periodate or p-toluene sulfonate.
Claim 3
Dependent Claim 43 words
The 4-pyridinio-5-pyrazolone salt of claim 1, wherein the salt has the following formula (IVa) ##SPC18## or the formula (IVb) ##SPC19## wherein R 1 , R 2 , R 3 , R 4 and R 5 are the same as defined in claim 1.
Claim 4
Dependent Claim 52 words
The 4-pyridinio-5-pyrazolone salt of claim 1, wherein the salt has the following formula (V) ##SPC20## wherein R 1 , R 2 , R 3 , R 4 , and R 5 are the same as defined in claim 1, and X is a chlorine atom, a bromine atom or an iodine atom.
Claim 5
Dependent Claim 21 words
The 4-pyridinio-5-pyrazolone salt as claimed in claim 1, wherein R 1 is said alkyl, said aryl, said carboxy, or said alkoxy-carbonyl.
Claim 6
Dependent Claim 5 words
The 4-pyridinio-5-pyrazolone salt of 1-(2,4,6-trichlorophenyl)-3-{3-[(2,4-di-tert-amylphenoxy)acetamido]benzamido}-4-(1-pyridinio)-5-oxo-2-pyrazoline-4-ide.
Claim 7
Dependent Claim 5 words
The 4-pyridinio-5-pyrazolone salt of 1-(2,4,6-trichlorophenyl)-3-{3-[(2,4-di-tert-amylphenoxy)acetamido]benzamido}-4-(1-pyridinio)-5-oxo-2-pyrazoline-4-ide.
Claim 8
Dependent Claim 6 words
The 4-pyridinio-5-pyrazolone salt of 1-(2,4,6-trichlorophenyl)-3-{3-[α-(2,4-di-tert-amylphenoxy)butryramido]benzamido}-4-(1-pyridinio)-5-oxo-2-pyrazoline bromide.
Claim 9
Dependent Claim 6 words
The 4-pyridinio-5-pyrazolone salt of 1-(2,4,6-trichlorophenyl)-3-{3-[α-(2,4-di-tert-amylphenoxy)butryramido]benzamido}-4-(1-pyridinio)-5-oxo-2-pyrazoline bromide.
Claim 10
Dependent Claim 5 words
The 4-pyridinio-5-pyrazolone salt of 1-(2,4,6-trichlorophenyl)-3-{-[(2,4-di-tert-amylphenoxy-acetamido]benzamido}-4-(3-ethyl-4-methyl-1-pyridinio)-5-oxo-2-pyrazolin-4-ide.
Claim 11
Dependent Claim 5 words
The 4-pyridinio-5-pyrazolone salt of 1-(2,4,6-trichlorophenyl)-3-{-[(2,4-di-tert-amylphenoxy-acetamido]benzamido}-4-(3-ethyl-4-methyl-1-pyridinio)-5-oxo-2-pyrazolin-4-ide.
Claim 12
Dependent Claim 6 words
The 4-pyridinio-5-pyrazolone salt of 1-(2,4,6-trichlorophenyl)-3-{3-[α-(2,4-di-tert-amylphenoxy)butyramido]benzamido}-4-(2-isoquinolinio)-5-oxo-2-pyrazoline iodide.
Claim 13
Dependent Claim 6 words
The 4-pyridinio-5-pyrazolone salt of 1-(2,4,6-trichlorophenyl)-3-{3-[α-(2,4-di-tert-amylphenoxy)butyramido]benzamido}-4-(2-isoquinolinio)-5-oxo-2-pyrazoline iodide.
Claim 14
Dependent Claim 5 words
The 4-pyridinio-5-pyrazolone salt of 1-(2,4,6-trichloropehnyl)-3-[2-chloro-5-(n-tetradecanamido)anilinio]-4-(1-pyridinio)-5-oxo-2-pyrazoline-4-ide.
Claim 15
Dependent Claim 5 words
The 4-pyridinio-5-pyrazolone salt of 1-(2,4,6-trichloropehnyl)-3-[2-chloro-5-(n-tetradecanamido)anilinio]-4-(1-pyridinio)-5-oxo-2-pyrazoline-4-ide.

References Cited (Backward Citations)

No citation records indexed.

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1979-05-11 1979-11-10 1980-05-11 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1983-05-11 1983-11-10 1984-05-11 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1987-05-11 1987-11-10 1988-05-11 $7700.00 Window Closed / Lapsed

Assigned Categories & Tags

No categories assigned to this patent yet.

Assign Category Tag