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US3936564A Expired / Lapsed US ⏱️ 0.0 years remaining

Pressure-sensitive copying paper containing lactone compounds of pyridine-carboxylic acid

Assignee: Fujifilm Holdings Corp
•
Filing: 1974-07-24
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Granted: 1976-02-03
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Expires: 1994-07-24
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Abstract

Abstract A pressure-sensitive copying paper comprising an adsorbent solid acid and a microencapsulated color former capable of forming a distinct color when reacted with the adsorbent acid coated on the same or a different surface of a support or supports, the microencapsulated color former being at least one lactone compound of a pyridine-carboxylic acid represented by the formula OR A MIXTURE THEREOF, WHEREIN R1, R2, R3, R4 and A are as defined hereinafter, is disclosed.

Inventors

  • 👤 Yoshihide Miyazawa
  • 👤 Minoru Ozutsumi
  • 👤 Satoshi Ogawa
  • 👤 Keiso Saeki
  • 👤 Akio Watanabe

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-08 18:11
CPC Classifications
C; C07; C07D; C07D213/00; C07D213/02; C07D213/04; C07D213/60; C07D213/78; C07D213/79; B; B41; B41M; B41M5/00; B41M5/124; B41M5/132; B41M5/136; B41M5/145; C07D455/00; C07D455/03; C07D455/04; Y; Y10; Y10T; Y10T428/00; Y10T428/25; Y10T428/252

Claims Analysis

Total Claims: 5
Claim 1
Independent Claim 258 words
A pressure-sensitive copying paper coated with a microencapsulated using as a color former a lactone compound of a pyridine-carboxylic acid represented by the formula ##SPC7## or a mixture thereof, wherein R 1 and R 2 each represents a hydrogen atom, an acyl group, a lower alkyl group which may be substituted with a halogen atom, a cyano, hydroxyl, lower alkoxy, lower alkylamino, acetyl or phenoxy group, or a benzyl or phenyl group which may be substituted with a lower alkyl group, a halogen atom, a lower alkoxy, nitro, amino or lower alkylamino group, or R 1 and R 2 may, when taken together with a nitrogen atom to which R 1 and R 2 are attached, form a part of a saturated hydrocarbon chain of a heterocyclic ring; R 3 represents a hydrogen or halogen atom, a nitro, amino, lower alkylamino group or a lower alkyl group which may be substituted with a halogen atom or a lower alkoxy group, a lower alkoxy group which may be substituted with a halogen atom, or a benzyl, benzyloxy or phenoxy group which may be substituted with a halogen atom, a lower alkyl, alkoxy or lower alkylamino group; R 4 represents a hydrogen or halogen atom, a lower alkyl group or a phenyl group; and A represents a carbazolyl, acridinyl, phenothiazinyl, thienyl, thianaphthenyl, morpholinophenyl, julolidinyl or tetrahydroquinolyl group which may be substituted with a lower alkyl, lower alkylamino, acyl or nitro group; the alkyl moiety in said lower alkyl, lower alkoxy or lower alkylamino group containing 1 to 5 carbon atoms.
Claim 2
Dependent Claim 258 words
A pressure-sensitive copying paper coated with a microencapsulated using as a color former a lactone compound of a pyridine-carboxylic acid represented by the formula ##SPC7## or a mixture thereof, wherein R 1 and R 2 each represents a hydrogen atom, an acyl group, a lower alkyl group which may be substituted with a halogen atom, a cyano, hydroxyl, lower alkoxy, lower alkylamino, acetyl or phenoxy group, or a benzyl or phenyl group which may be substituted with a lower alkyl group, a halogen atom, a lower alkoxy, nitro, amino or lower alkylamino group, or R 1 and R 2 may, when taken together with a nitrogen atom to which R 1 and R 2 are attached, form a part of a saturated hydrocarbon chain of a heterocyclic ring; R 3 represents a hydrogen or halogen atom, a nitro, amino, lower alkylamino group or a lower alkyl group which may be substituted with a halogen atom or a lower alkoxy group, a lower alkoxy group which may be substituted with a halogen atom, or a benzyl, benzyloxy or phenoxy group which may be substituted with a halogen atom, a lower alkyl, alkoxy or lower alkylamino group; R 4 represents a hydrogen or halogen atom, a lower alkyl group or a phenyl group; and A represents a carbazolyl, acridinyl, phenothiazinyl, thienyl, thianaphthenyl, morpholinophenyl, julolidinyl or tetrahydroquinolyl group which may be substituted with a lower alkyl, lower alkylamino, acyl or nitro group; the alkyl moiety in said lower alkyl, lower alkoxy or lower alkylamino group containing 1 to 5 carbon atoms.
Claim 3
Dependent Claim 248 words
The pressure-sensitive copying paper as claimed in claim 1, wherein said color former is a compound selected from the group consisting of a. 3-[α-{1'-methyl-2', 3', 4'-trihydroquinolin-(6')-yl}-α-{4'-diethylamino-2'-ethoxyphenyl}-.alpha.-oxy]-methylpyridine-carboxylic acid-(2)lactone, b. 2-[α-{1'-methyl-2', 3', 4'-trihydroquinolin-(6')-yl}-α-{4'-diethylamino-2'-ethoxyphenyl}-.alpha.-oxy]-methylpyridine-carboxylic acid-(3) lactone, c. an isomer mixture of (a) and (b) above, d. an isomer mixture of 3-[α-{julolidin-(6')-yl}-α-{4'-dimethylaminophenyl}-α-oxy]-methypyridine-carboxylic acid-(2) lactone and 2-[α-{julolidin-(6')-yl}-α-{4'-dimethylaminophenyl}-α-oxy]-methypyridine-carboxylic acid-(3) lactone, e. an isomer mixture of 3-[α-{1'-methyl-2', 3', 4'-trihydroquinolin-(6')-yl}-α-{4'-(N-β-chloroethyl-N-ethyl)-amino-phenyl}-α-oxy]-methylpyridine-carboxylic acid-(2) lactone and 2-[α-{1'-methyl-2', 3', 4'-trihydroquinolin-(6')-yl}-α-{4'-(N-β-chloroethyl-N-ethyl)-aminophenyl}-α-oxy]-methyl-pyridine-carboxylic acid-(3) lactone, f. an isomer mixture of 3-[α-{1'-methyl-2', 3', 4'-trihydroquinolin-(6')-yl}-α-{4'-dibenzylaminophenyl}-α-oxy]-methylpyridine-carboxylic acid-(2) lactone and 2-[α-{1'-methyl2', 3', 4'-trihydroquinolin-(6')-yl}-α-{4'-dibenzylaminophenyl}α-oxy]-methylpyridine-carboxylic acid-(3) lactone, g. an isomer mixture of 3-[α-{4-morpholinophenyl}-α-{1'-methyl-2', 3', 4'-trihydroquinolin-(6')-yl}-α-oxy]-methylpyridine-carboxylic acid-(2) lactone and 2-[α-{4'-morpholinophenyl}-α1{1'-methyl-2', 3', 4'-trihydroquinolin-(6')-yl}-α-oxy]-methypyridine-carboxylic acid-(3) lactone, h. an isomer mixture of 3-[α-}9'-ethylcarbazol-(3')-yl}-α-{4'-dimethylaminophenyl}-.alpha.-oxy]-methylpyridine-carboxylic acid-(2) lactone and 2-[α-{9'-ethylcarbazol-(3')-yl}-α-{4'-dimethylaminophenyl}-.alpha.-oxy]-methylpyridine-carboxylic acid-(3) lactone, i. an isomer mixture of 3-[α-{acridin-(2')-yl}-α-{4'-(N-benzyl-N-methyl)-aminophenyl}-α-oxy]-methylpyridine-carboxylic acid-(2) lactone and 2-[α-{acridin-(2')-yl} -α-{4'-(N-benzyl-N-methyl)-aminophenyl}-α-oxy]-methypyridine-carboxylic acid-(3) lactone, j. an isomer mixture of 3-[α-{phenothiazin-(3')-yl}-α-{4'-(N-methyl-N-phenyl)-aminophenyl}-α-oxy]-methylpyridine-carboxylic acid-(2) lactone and 2-[α-{phenothiazin-(3')-yl}-α-{4'-(N-methyl-N-phenyl)-aminophenyl}-α-oxy]-methylpyridine-carboxylic acid-(3) lactone, k. an isomer mixture of 3-[α-{thiophen-(2')-yl}-α-{4'-(N-methyl-N-4"-ethoxyphenyl)-aminophenyl}-α-oxy]-methylpyridine-carboxylic acid-(2) lactone and 2-[α-{thiophen-(2')-yl}-α-{4'-(N-methyl-N-4"-ethoxyphenyl)-aminophenyl}-α-oxy]-methylpyridine-carboxylic acid-(3) lactone, l. an isomer mixture of 3-[α-{thianaphthen-(2')-yl}-α-{4'-acetonylaminophenyl}-α-oxy]-methylpyridine-carboxylic acid-(2) lactone and 2-[α-{thianaphthen-(2')-yl}-α-{4'-acetonylaminophenyl}-α-oxy]-methylpyridine-carboxylic acid-(3) lactone, m. an isomer mixture of 3-[α-{4'-methylaminophenyl}-α-{6'-nitro-9'-ethylcarbazol-(3')-yl}-α-oxy]-methylpyridine-carboxylic acid-(2) lactone and 2-[α-{4'-methyl-aminophenyl}-α-{6'-nitro-9'-ethylcarbazol-(3')-yl}-α-oxy]-methylpyridine-carboxylic acid-(3) lactone, n. an isomer mixture of 3-[α-{1'-methyl-2', 3', 4'-trihydroquinolin-(6')-yl}-α-}4'-diethylamino-2'-nitrophenyl}-.alpha.-oxy]-methyl-4-methylpyridine-carboxylic acid-(2) lactone and 2-[α-{1'-methyl-2', 3', 4'-trihydroquinolin-(6')-yl}-α-{4'-diethylamino-2'-nitrophenyl}-.alpha.-oxy]-methyl-4-methylpyridine-carboxylic acid-(3) lactone, o. an isomer mixture of 3-[α-{1'-methyl-2', 3', 4'-trihydroquinolin-(6')-yl}-α-{4'-benzamidophenyl}-α-oxy]-methyl-pyridine-carboxylic acid-(2) lactone and 2-[α-{1'-methyl-2', 3', 4'-trihydroquinolin-(6')-yl}-α-{4'-benzamiodphenyl}-α-oxy]-methylpyridine-carboxylic acid-(3) lactone, p. an isomer mixture of 3-[α-{julolidin-(6')-yl}-α-{4'-piperidinophenyl}-α-oxy]-methylpyridine-carboxylic acid-(2) lactone and 2-[α-{julolidin-(6')-yl}-α-{4'-piperidinophenyl}-α-oxy]-methylpyridine-carboxylic acid-(3) lactone, q. an isomer mixture of 3-[α-{1'-methyl-2', 3', 4'-trihydroquinolin-(6')-yl}-α-{4'-diethylamino-2'-(4"-methyl)-benzyl-phenyl}-α-oxy]-methylpyridine-carboxylic acid-(2) lactone and 2-[α-{1'-methyl-2', 3', 4'-trihydroquinolin-(6')-yl}-α-{4'-diethylamino-2'-(4"-methyl)-benzylphenyl}-α-oxy]-methylpyridine-carboxylic acid-(3) lactone, r. an isomer mixture of 3-[α-{9'-ethylcarbazol-(3')-yl}-α-{4'-diethylamino-2'-methoxymethylphenyl}-α-oxy]-methylpyridine-carboxylic acid-(2) lactone and 2-[α-{9'-ethylcarbazol-(3')-yl}-α-{4'-diethylamino-2'-methoxymethylphenyl}-α-oxy]-methylpyridine-carboxylic acid-(3) lactone, and
Claim 4
Dependent Claim 15 words
s. an isomer mixture of 3-[α, α-bis (4'-morpholinophenyl)-α-oxy]-methylpyridine-carboxylic acid-(2) lactone and 2-[α, α-bis(4'-morpholinophenyl)-α-oxy]-methylpyridine-carboxylic acid-(3) lactone.
Claim 5
Dependent Claim 15 words
s. an isomer mixture of 3-[α, α-bis (4'-morpholinophenyl)-α-oxy]-methylpyridine-carboxylic acid-(2) lactone and 2-[α, α-bis(4'-morpholinophenyl)-α-oxy]-methylpyridine-carboxylic acid-(3) lactone.

References Cited (Backward Citations)

US3775424A Cited
US3853869A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1979-02-02 1979-08-04 1980-02-03 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1983-02-02 1983-08-04 1984-02-03 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1987-02-02 1987-08-04 1988-02-03 $7700.00 Window Closed / Lapsed

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