GB1522173A – Indoline derivatives and methods of preparing them
– Google Patents
GB1522173A – Indoline derivatives and methods of preparing them
– Google Patents
Indoline derivatives and methods of preparing them
Info
Publication number
GB1522173A
GB1522173A
GB38266/75A
GB3826675A
GB1522173A
GB 1522173 A
GB1522173 A
GB 1522173A
GB 38266/75 A
GB38266/75 A
GB 38266/75A
GB 3826675 A
GB3826675 A
GB 3826675A
GB 1522173 A
GB1522173 A
GB 1522173A
Authority
GB
United Kingdom
Prior art keywords
compounds
sept
reversible
alkoxy
atoms
Prior art date
1974-09-18
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
GB38266/75A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Panasonic Holdings Corp
Original Assignee
Matsushita Electric Industrial Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
1974-09-18
Filing date
1975-09-17
Publication date
1978-08-23
1975-09-17
Application filed by Matsushita Electric Industrial Co Ltd
filed
Critical
Matsushita Electric Industrial Co Ltd
1978-08-23
Publication of GB1522173A
publication
Critical
patent/GB1522173A/en
Status
Expired
legal-status
Critical
Current
Links
Espacenet
Global Dossier
Discuss
125000003387
indolinyl group
Chemical class
N1(CCC2=CC=CC=C12)*
0.000
title
1
150000001875
compounds
Chemical class
0.000
abstract
3
125000003545
alkoxy group
Chemical group
0.000
abstract
2
125000000217
alkyl group
Chemical group
0.000
abstract
2
125000003118
aryl group
Chemical group
0.000
abstract
2
150000002832
nitroso derivatives
Chemical class
0.000
abstract
2
230000002441
reversible effect
Effects
0.000
abstract
2
125000002947
alkylene group
Chemical group
0.000
abstract
1
125000004104
aryloxy group
Chemical group
0.000
abstract
1
125000004429
atom
Chemical group
0.000
abstract
1
125000004432
carbon atom
Chemical group
C*
0.000
abstract
1
238000006243
chemical reaction
Methods
0.000
abstract
1
239000003593
chromogenic compound
Substances
0.000
abstract
1
230000005494
condensation
Effects
0.000
abstract
1
238000009833
condensation
Methods
0.000
abstract
1
125000004122
cyclic group
Chemical group
0.000
abstract
1
238000010894
electron beam technology
Methods
0.000
abstract
1
125000002485
formyl group
Chemical class
[H]C(*)=O
0.000
abstract
1
229910052736
halogen
Inorganic materials
0.000
abstract
1
150000002367
halogens
Chemical class
0.000
abstract
1
-1
heterocyclic aldehyde
Chemical class
0.000
abstract
1
229910052760
oxygen
Inorganic materials
0.000
abstract
1
125000001997
phenyl group
Chemical group
[H]C1=C([H])C([H])=C(*)C([H])=C1[H]
0.000
abstract
1
238000007142
ring opening reaction
Methods
0.000
abstract
1
230000000638
stimulation
Effects
0.000
abstract
1
229910052717
sulfur
Inorganic materials
0.000
abstract
1
Classifications
B—PERFORMING OPERATIONS; TRANSPORTING
B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
B41M5/00—Duplicating or marking methods; Sheet materials for use therein
B41M5/26—Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used
B41M5/28—Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used using thermochromic compounds or layers containing liquid crystals, microcapsules, bleachable dyes or heat- decomposable compounds, e.g. gas- liberating
B41M5/286—Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used using thermochromic compounds or layers containing liquid crystals, microcapsules, bleachable dyes or heat- decomposable compounds, e.g. gas- liberating using compounds undergoing unimolecular fragmentation to obtain colour shift, e.g. bleachable dyes
C—CHEMISTRY; METALLURGY
C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
C09B23/00—Methine or polymethine dyes, e.g. cyanine dyes
C09B23/10—The polymethine chain containing an even number of >CH- groups
C09B23/105—The polymethine chain containing an even number of >CH- groups two >CH- groups
C—CHEMISTRY; METALLURGY
C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
C09B23/00—Methine or polymethine dyes, e.g. cyanine dyes
C09B23/14—Styryl dyes
C09B23/143—Styryl dyes the ethylene chain carrying a COOH or a functionally modified derivative, e.g.-CN, -COR, -COOR, -CON=, C6H5-CH=C-CN
G—PHYSICS
G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
G03C1/00—Photosensitive materials
G03C1/005—Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein
G03C1/06—Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein with non-macromolecular additives
G03C1/08—Sensitivity-increasing substances
G03C1/10—Organic substances
G03C1/12—Methine and polymethine dyes
G03C1/24—Styryl dyes
G—PHYSICS
G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
G03C1/00—Photosensitive materials
G03C1/005—Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein
G03C1/06—Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein with non-macromolecular additives
G03C1/08—Sensitivity-increasing substances
G03C1/28—Sensitivity-increasing substances together with supersensitising substances
G03C1/29—Sensitivity-increasing substances together with supersensitising substances the supersensitising mixture being solely composed of dyes ; Combination of dyes, even if the supersensitising effect is not explicitly disclosed
G—PHYSICS
G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
G03C1/00—Photosensitive materials
G03C1/685—Compositions containing spiro-condensed pyran compounds or derivatives thereof, as photosensitive substances
G—PHYSICS
G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
G03C8/00—Diffusion transfer processes or agents therefor; Photosensitive materials for such processes
G03C8/02—Photosensitive materials characterised by the image-forming section
Abstract
1522173 Chromogenic compounds MATSUSHITA ELECTRIC INDUSTRIAL CO Ltd 17 Sept 1975] [18 Sept 1974] 38266/75 Heading C4P [Also in Division C2] A compound which is capable of undergoing a colour change on stimulation by light, heat, an electric current, pressure or irradiation by an electron beam or α- or y-rays and is of formula: (in which Q is a benzene ring which is optionally substituted and/or forms part of a fused ring system; R 1 and R 2 are each 1-4 C alkyl which is optionally substituted by OH or 1-4 C alkoxy; R 3 is H, alkyl, alkoxy, aryl, aryloxy, halogen or CN; Y is O or S; Z is an alkylene group providing a chain of 2-4 C atoms between the N and Y atoms; A is a condensation residue of an aromatic or heterocyclic aldehyde or nitroso compound). The colour change which may be reversible or non-reversible is caused by ring-opening. The compounds are formed from compounds of Formula (2) or (3) by reaction with (a) a base or (b) the aldehyde or nitroso compound respectively.
GB38266/75A
1974-09-18
1975-09-17
Indoline derivatives and methods of preparing them
Expired
GB1522173A
(en)
Applications Claiming Priority (1)
Application Number
Priority Date
Filing Date
Title
JP10809074A
JPS5733307B2
(en)
1974-09-18
1974-09-18
Publications (1)
Publication Number
Publication Date
GB1522173A
true
GB1522173A
(en)
1978-08-23
Family
ID=14475603
Family Applications (1)
Application Number
Title
Priority Date
Filing Date
GB38266/75A
Expired
GB1522173A
(en)
1974-09-18
1975-09-17
Indoline derivatives and methods of preparing them
Country Status (6)
Country
Link
US
(1)
US4314058A
(en)
JP
(1)
JPS5733307B2
(en)
CA
(1)
CA1064951A
(en)
DE
(1)
DE2541666A1
(en)
FR
(1)
FR2285439A1
(en)
GB
(1)
GB1522173A
(en)
Families Citing this family (12)
* Cited by examiner, † Cited by third party
Publication number
Priority date
Publication date
Assignee
Title
JPS5134885A
(en)
*
1974-09-18
1976-03-24
Matsushita Electric Ind Co Ltd
Henshoku mataha shohatsushokuyozairyo
JPS56149489A
(en)
*
1980-04-21
1981-11-19
Matsushita Electric Ind Co Ltd
Color-developing and color-disappearing material
US5852014A
(en)
*
1992-03-12
1998-12-22
Smithkline Beecham P.L.C.
Condensed indole derivatives as 5HT4 -receptor antagonists
US5998409A
(en)
*
1992-03-12
1999-12-07
Smithkline Beecham Plc
Condensed indole derivatives as 5HT4 -receptor antagonists
WO2006047452A2
(en)
*
2004-10-25
2006-05-04
Anaspec, Inc.
Reactive 1,3’-crosslinked carbocyanines and their bioconjugates
FR2888747B1
(en)
2005-07-22
2007-08-24
Oreal
USE FOR THE COLORING OF KERATIN FIBERS OF A COMPOSITION COMPRISING A STYRYLIC OR IMINIC COLORANT
FR2907003B1
(en)
2006-10-13
2008-12-05
Oreal
COMPOSITION COMPRISING A STYRYLIC OR IMINIC DYE AND A THIOLE COMPOUND, COLORING PROCESS AND DEVICE
FR2907004B1
(en)
*
2006-10-13
2008-12-05
Oreal
METHOD FOR COLORING USING STYRYL OR IMINIC DYE IN COMBINATION WITH A ZINC SALT AND DEVICE FOR CARRYING OUT SAID PROCESS
FR2907002B1
(en)
2006-10-13
2009-03-06
Oreal
METHOD FOR COLORING USING A STYRYLIC OR IMINIC TYPE DYE IN COMBINATION WITH A LOW ACID AND DEVICE FOR CARRYING OUT SAID PROCESS
US7660070B2
(en)
*
2007-03-08
2010-02-09
Esgw Holdings Limited
Quiet high performance seek procedure for disk drives
FR2921374A1
(en)
*
2007-09-21
2009-03-27
Oreal
INDOLINIUM THIOL / DISULFIDE DERIVATIVE DYE, TINCTORIAL COMPOSITION COMPRISING THE DYE, METHOD FOR LIGHTENING KERATINIC MATERIALS FROM THAT COLORANT
FR2930141B1
(en)
*
2008-04-16
2011-01-21
Oreal
TREATMENT OF COLORED FIBERS BY STYRYL OR IMINIC COMPOUNDS, IN THE PRESENCE OF ORGANIC OR MINERAL ACIDS AND ZINC SALTS.
Family Cites Families (6)
* Cited by examiner, † Cited by third party
Publication number
Priority date
Publication date
Assignee
Title
DE2060614C3
(en)
*
1970-12-09
1980-06-19
Bayer Ag, 5090 Leverkusen
9a-methyl-23,9,9a-tetrahydrooxazolo- [3,2, -a] indoles
US3975379A
(en)
*
1970-12-09
1976-08-17
Bayer Aktiengesellschaft
Dihydroindoles and indolenine dyestuffs
DE2060615A1
(en)
*
1970-12-09
1972-06-15
Bayer Ag
Heterocyclic compounds and their uses
NL7411935A
(en)
*
1973-09-21
1975-03-25
Matsushita Electric Ind Co Ltd
COLOR DISPLAY DEVICE.
JPS5134885A
(en)
*
1974-09-18
1976-03-24
Matsushita Electric Ind Co Ltd
Henshoku mataha shohatsushokuyozairyo
JPS5161795A
(en)
*
1974-11-26
1976-05-28
Matsushita Electric Ind Co Ltd
1974
1974-09-18
JP
JP10809074A
patent/JPS5733307B2/ja
not_active
Expired
1975
1975-09-17
CA
CA235,619A
patent/CA1064951A/en
not_active
Expired
1975-09-17
FR
FR7528513A
patent/FR2285439A1/en
active
Granted
1975-09-17
GB
GB38266/75A
patent/GB1522173A/en
not_active
Expired
1975-09-18
DE
DE19752541666
patent/DE2541666A1/en
active
Granted
1980
1980-02-06
US
US06/119,147
patent/US4314058A/en
not_active
Expired – Lifetime
Also Published As
Publication number
Publication date
FR2285439B1
(en)
1978-05-19
JPS5733307B2
(en)
1982-07-16
CA1064951A
(en)
1979-10-23
DE2541666C2
(en)
1989-06-01
US4314058A
(en)
1982-02-02
JPS5144127A
(en)
1976-04-15
FR2285439A1
(en)
1976-04-16
DE2541666A1
(en)
1976-04-01
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Legal Events
Date
Code
Title
Description
1979-01-17
PS
Patent sealed [section 19, patents act 1949]
1993-05-12
PCNP
Patent ceased through non-payment of renewal fee
Effective date:
19920917
