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US4766211A Expired / Lapsed US ⏱️ 0.0 years remaining

Chromogenic quinazolines

Assignee: Novartis Corp
•
Filing: 1986-08-27
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Granted: 1988-08-23
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Expires: 2006-08-27
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Abstract

Abstract Chromogenic quinazolines of formula ##STR1## wherein R is an aryl radical or a heterocyclic radical, Z 1 is oxygen or sulfur, Z 2 is oxygen, sulfur or ##STR2## R' is hydrogen, alkyl which is unsubstituted or substituted by halogen, cyano or lower alkoxy, or is cycloalkyl, phenyl, benzyl, phenethyl or acyl, or --NRR' is a 5- or 6-membered heterocyclic radical, Q is an aliphatic radical which may be interrupted by a further member Z 2 , Y is the radical of a couplable compound, and the ring A is unsubstituted or substituted by halogen, cyano, nitro, lower alkyl, lower alkoxy or lower alkoxycarbonyl. These quinazolines are exceedingly fast to sublimation and are particularly suitable color formers in pressure-sensitive or heat-sensitive recording materials and give strong and lightfast yellow and orange colorations.

Inventors

  • 👤 Rudolf Zink
  • 👤 Ian J. Fletcher

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-02 08:41
CPC Classifications
C; C07; C07D; C07D239/00; C07D239/70; C07D239/72; C07D239/86; C07D239/88; C07D239/91; B; B41; B41M; B41M5/00; B41M5/124; B41M5/132; B41M5/136; B41M5/26; B41M5/30; B41M5/323; C07D401/00; C07D401/02; C07D401/04; C07D413/00; C07D413/02; C07D413/04

Claims Analysis

Total Claims: 17
Claim 1
Independent Claim 383 words
A chromogenic quinazoline of the formula ##STR57## wherein R is a phenyl, biphenylyl or naphthyl radical, each unsubstituted or substituted by halogen, cyano, nitro, lower alkyl, lower alkoxy, lower alkoxycarbonyl or lower alkylcarbonyl, or R is an aromatic heterocyclic radical selected from the group consisting of thienyl, furyl, pyrrolyl, pyrazolyl, imidazolyl and pyridyl, each unsubstituted or substituted by halogen, cyano, lower alkyl, lower alkoxy, lower alkoxycarbonyl or fused benzene, or R is a saturated heterocyclic radical selected from the group consisting of pyrrolidino, piperidino, pipecolino, morpholino, thiomorpholino, piperazino and N-methylpiperazino; Z 1 is oxygen or sulfur; Z 2 is oxygen, sulfur or --NR'; R' is hydrogen, alkyl of not more than 12 carbon atoms, unsubstituted or substituted by halogen, cyano or lower alkoxy, or is C 5 -C 6 cycloalkyl, phenyl, benzyl, phenethyl or C 1 -C 12 -acyl, or --NRR' is a 5- or 6-membered heterocyclic radical selected from the group consisting of pyrrolidino, piperidino, pipecolino, piperazino or morpholino; Q is an aliphatic radical or an aliphatic radical which is interrupted by a further member Z 2 ; Y is the radical of a couplable compound bound to the quinazoline moiety through a phenyl ring and is selected from the group consisting of unsubstituted, N-monosubstituted, or N,N-disubstituted aniline or naphthylamine, N-unsubstituted or N-substituted indole, indoline, carbazole, tetrahydrocarbazole, oxazine, thiazine, dihydroquinoline, tetrahydroquinoline, dibenzylimide or benzomorpholine wherein C-substituents are selected from the group consisting of halogen, hydroxyl, cyano, nitro, lower alkyl, lower alkoxy, lower alkoxycarbonyl, acyl of 1 to 8 carbon atoms, C 1 -C 4 acylamino, alkylene of 3 to 6 carbon atoms, cycloalkyl of 5 or 6 carbon atoms, benzyl and phenyl, and wherein N-substituents are selected from the group consisting of alkyl with 1 to 12 carbon atoms, alkenyl of 2 to 12 carbon atoms, cycloalkyl of 5 or 6 carbon atoms, phenyl, benzyl and phenethyl, each of which is unsubstituted or substituted by cyano, halogen, nitro, hydroxy, lower alkyl, lower alkoxy or lower alkoxycarbonyl, or when N is disubstituted the 2N-substituents and the nitrogen atom to which they are attached are a 5- or 6-membered heterocylic radical selected from the group consisting of pyrrolidino, piperidino, pipecolino, morpholino, thiomorpholino or piperazino; and the ring A is unsubstituted or substituted by halogen, phenyl, cyano, nitro, lower alkyl, lower alkoxy or lower alkoxycarbonyl.
Claim 2
Dependent Claim 383 words
A chromogenic quinazoline of the formula ##STR57## wherein R is a phenyl, biphenylyl or naphthyl radical, each unsubstituted or substituted by halogen, cyano, nitro, lower alkyl, lower alkoxy, lower alkoxycarbonyl or lower alkylcarbonyl, or R is an aromatic heterocyclic radical selected from the group consisting of thienyl, furyl, pyrrolyl, pyrazolyl, imidazolyl and pyridyl, each unsubstituted or substituted by halogen, cyano, lower alkyl, lower alkoxy, lower alkoxycarbonyl or fused benzene, or R is a saturated heterocyclic radical selected from the group consisting of pyrrolidino, piperidino, pipecolino, morpholino, thiomorpholino, piperazino and N-methylpiperazino; Z 1 is oxygen or sulfur; Z 2 is oxygen, sulfur or --NR'; R' is hydrogen, alkyl of not more than 12 carbon atoms, unsubstituted or substituted by halogen, cyano or lower alkoxy, or is C 5 -C 6 cycloalkyl, phenyl, benzyl, phenethyl or C 1 -C 12 -acyl, or --NRR' is a 5- or 6-membered heterocyclic radical selected from the group consisting of pyrrolidino, piperidino, pipecolino, piperazino or morpholino; Q is an aliphatic radical or an aliphatic radical which is interrupted by a further member Z 2 ; Y is the radical of a couplable compound bound to the quinazoline moiety through a phenyl ring and is selected from the group consisting of unsubstituted, N-monosubstituted, or N,N-disubstituted aniline or naphthylamine, N-unsubstituted or N-substituted indole, indoline, carbazole, tetrahydrocarbazole, oxazine, thiazine, dihydroquinoline, tetrahydroquinoline, dibenzylimide or benzomorpholine wherein C-substituents are selected from the group consisting of halogen, hydroxyl, cyano, nitro, lower alkyl, lower alkoxy, lower alkoxycarbonyl, acyl of 1 to 8 carbon atoms, C 1 -C 4 acylamino, alkylene of 3 to 6 carbon atoms, cycloalkyl of 5 or 6 carbon atoms, benzyl and phenyl, and wherein N-substituents are selected from the group consisting of alkyl with 1 to 12 carbon atoms, alkenyl of 2 to 12 carbon atoms, cycloalkyl of 5 or 6 carbon atoms, phenyl, benzyl and phenethyl, each of which is unsubstituted or substituted by cyano, halogen, nitro, hydroxy, lower alkyl, lower alkoxy or lower alkoxycarbonyl, or when N is disubstituted the 2N-substituents and the nitrogen atom to which they are attached are a 5- or 6-membered heterocylic radical selected from the group consisting of pyrrolidino, piperidino, pipecolino, morpholino, thiomorpholino or piperazino; and the ring A is unsubstituted or substituted by halogen, phenyl, cyano, nitro, lower alkyl, lower alkoxy or lower alkoxycarbonyl.
Claim 3
Dependent Claim 30 words
A quinazoline according to claim 1, wherein R is phenyl, biphenylyl or naphthyl, each unsubstituted or substituted by halogen, cyano, nitro, lower alkyl, lower alkoxy, lower alkoxycarbonyl or lower alkylcarbonyl.
Claim 4
Dependent Claim 15 words
A quinazoline according to claim 1, wherein R is phenyl, chlorophenyl, methoxyphenyl, tolyl or xylyl.
Claim 5
Dependent Claim 14 words
A quinazoline according to claim 1, wherein Q is C 2 -C 4 alkylene.
Claim 6
Dependent Claim 15 words
A quinazoline according to claim 1, wherein Z 1 and Z 2 are each oxygen.
Claim 7
Dependent Claim 19 words
A quinazoline according to claim 1, wherein Y is the radical of an N-monosubstituted or N,N-disubstituted aniline or naphthylamine.
Claim 8
Dependent Claim 15 words
A quinazoline according to claim 1, wherein Y is the radical of an N,N-disubstituted aniline.
Claim 9
Dependent Claim 15 words
A quinazoline according to claim 1, wherein Y is an indolinyl, tetrahydroquinolinyl or benzomorpholino radical.
Claim 10
Dependent Claim 287 words
A quinazoline according to claim 1, of formula ##STR58## wherein R 1 is a phenyl or naphthyl radical, each unsubstituted or substituted by halogen, methyl or methoxy, Z 1 is oxygen or sulfur, Z 3 is oxygen, sulfur, ##STR59## R" is lower alkyl or --NR 1 R" is morpholino, Q 1 is C 2 -C 4 alkylene or the radical --(CH 2 --CH 2 --O) m --CH 2 CH 2 --, Y 2 is an aminophenol radical of formula ##STR60## or a 5-indolinyl radical of formula ##STR61## or a tetrahydroquinolinyl radical of formula ##STR62## or a tetrahydroquinolinyl radical of formula ##STR63## or a benzomorpholino radical of formula ##STR64## wherein m 1 is 1 to 3, X 4 and X 5 are each independently of the other lower alkyl, cyano-lower alkyl, benzyl, phenyl, phenethyl, lower alkylphenyl or lower alkoxyphenyl; or X 4 and X 5 , together with the nitrogen atom to which they are attached, are pyrrolidino, piperidino or morpholino, X 6 is hydrogen, halogen, lower alkyl or lower alkoxy, Z" is hydrogen, C 1 -C 8 alkyl, C 2 -C 6 alkoxyalkyl, β-cyanoethyl, benzyl or phenethyl, T is hydrogen, halogen, lower alkyl, lower alkoxy, C 1 -C 4 acylamino or phenyl, T 1 and T 2 are each hydrogen, halogen, hydroxy, lower alkyl or lower alkoxy, and V 1 , V 2 , V 3 and V 4 are each hydrogen, lower alkyl, C 5 -C 6 cycloalkyl or benzyl; or (V 1 and V 2 ) or (V 3 and V 4 ) are each together C 4 -C 5 -alkylene, and the ring A 1 is unsubstituted or substituted by one or two members selected from cyano, halogen, lower alkyl, phenyl and lower alkoxy.
Claim 11
Dependent Claim 16 words
A quinazoline according to claim 9, wherein Y 2 is an aminophenyl radical of formula (3a).
Claim 12
Dependent Claim 48 words
A quinazoline according to claim 10, wherein X 4 and X 5 are each lower alkyl or benzyl, X 6 is hydrogen, R 1 is phenyl or chlorophenyl, Q 1 is ethylene or propylene, Z 1 and Z 2 are oxygen, and the ring A 1 is unsubstituted.
Claim 13
Dependent Claim 73 words
A quinazoline according to claim 1, of formula ##STR65## wherein Q 2 is straight chain or branched C 2 -C 4 alkylene, R 2 is phenyl, chlorophenyl, tolyl, methoxyphenyl or naphthyl, Z 1 is oxygen or sulfur, Z" is C 1 -C 8 alkyl, β-cyanoethyl or benzyl, T 3 , V 5 and V 6 are each lower alkyl, T 4 is hydrogen or methyl, and W is hydrogen, halogen, methyl or methoxy.
Claim 14
Dependent Claim 71 words
A quinazoline according to claim 1, of formula ##STR66## wherein Q 2 is straight chain or branched C 2 -C 4 alkylene, R 2 is phenyl, chlorophenyl, tolyl, methoxyphenyl or naphthyl, Z 1 is oxygen or sulfur, X 7 and X 8 are each lower alkyl or benzyl, or --NX 7 X 8 is piperidino, X 9 is hydrogen, halogen, methyl or methoxy and W is hydrogen, halogen, methyl or methoxy.
Claim 15
Dependent Claim 36 words
A quinazoline according to claim 13, wherein Q 2 is ethylene or propylene, R 2 is phenyl or chlorophenyl, X 7 and X 8 are each lower alkyl, and X 9 and W are each hydrogen.
Claim 16
Dependent Claim 41 words
A quinazoline according to claim 1 wherein Y is selected from the group consisting of N-unsubstituted or N-substituted indoline, tetrahydrocarbazole, dihydroquinoline, tetrahydroquinoline, dibenzylimide and benzomorpholine, which radical is attached to the quinazoline moiety through a fused benzene ring of said heterocycle.
Claim 17
Dependent Claim 120 words
A quinazoline according to claim 1 wherein Y is of the formula ##STR67## wherein X 1 and X 2 are each independently of the other hydrogen, alkyl of 1 to 12 carbon atoms, unsubstituted or substituted by halogen, hydroxy, cyano or lower alkoxy, or are C 5 -C 6 cycloalkyl, phenyl, benzyl, phenethyl, or phenyl or benzyl, each substituted by halogen, nitro, cyano, lower alkyl, lower alkoxy or lower alkoxycarbonyl, or X 1 and X 2 together with the nitrogen atom to which they are attached are a 5- or 6-membered heterocyclic radical selected from the group consisting of pyrrolidino, piperidino, pipecolino, morpholino, thiomorpholino and piperazino, and X 3 is hydrogen, halogen, nitro, lower alkyl, lower alkoxy or lower alkoxycarbonyl.

References Cited (Backward Citations)

US4435003A Cited
US4480096A Cited
JPS58172379A Cited
US4625027A Cited
US4555569A Cited
US4668966A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1991-08-23 1992-02-22 1992-08-23 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1995-08-23 1996-02-22 1996-08-23 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1999-08-23 2000-02-22 2000-08-23 $7700.00 Window Closed / Lapsed

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