GB461668A - Improvements in or relating to dyestuffs - Google Patents
Improvements in or relating to dyestuffsInfo
- Publication number
- GB461668A GB461668A GB2307535A GB2307535A GB461668A GB 461668 A GB461668 A GB 461668A GB 2307535 A GB2307535 A GB 2307535A GB 2307535 A GB2307535 A GB 2307535A GB 461668 A GB461668 A GB 461668A
- Authority
- GB
- United Kingdom
- Prior art keywords
- hydrochloride
- condensed
- methyl
- iodide
- toluenesulphonate
- Prior art date
- 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
Links
Classifications
-
- 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
- C09B55/00—Azomethine dyes
- C09B55/009—Azomethine dyes, the C-atom of the group -C=N- being part of a ring (Image)
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
Compounds containing two heterocyclic nitrogen nuclei linked by a single nitrogen atom or by a chain of atoms including two nitrogen atoms, are prepared by condensing a quaternary salt of a heterocyclic nitrogen compound containing a reactive thioether or selenoether group with ammonia or an amidine having at least three replaceable hydrogen atoms attached to the nitrogen atoms or one of their salts. Starting materials comprise on the one hand quaternary salts derived from thioether, selenoether, thione or selenone derivatives of thiazolines, oxazoles, oxazolines, selenazoles, selenazolines, pyridines, quinolines, indolenines, pyrimidines, thiodiazoles, quinazolines, benz-, naphtha- and anthrathiazoles; and on the other hand ammonia and amidines of the general formula NH2--CZ=NH wherein Z stands for hydrogen, an alkyl, aryl or aralkyl group or an oxy, alkoxy, thiol, thioether, amino or substituted amino group, specific mention being made of formamidine, acetamidine, benzamidine, guanidine, urea, thiourea, O-alkyl pseudo ureas, S-alkyl pseudo-thio-ureas. In examples: (a) 1-methylthiolbenzthiazole methyl-p-toluenesulphonate is condensed with thiourea methyl sulphate, acetamidine hydrochloride, formamidine hydrochloride, propionamidine hydrochloride, benzamidine hydrochloride, ammonium nitrate and guanidine carbonate, the reaction being carried out in pyridine and the dye in each case being precipitated as the iodide by pouring into potassium iodide; (b) 1-ethylmercaptobenzthiazole ethyl-p-toluenesulphonate is condensed with acetamidine hydrochloride in pyridine and the dye precipitated as the iodide by means of potassium iodide; (c) 2-ethylthiolquinoline methyl-p-toluenesulphonate is condensed with acetamidine hydrochloride and the dye precipitated as the perchlorate, or with ammonia in presence of sodium alcoholate followed by precipitation as the perchlorate; (d) 1-methylthiobenzoxazole methyl-p-toluenesulphonate is condensed with acetamidine hydrochloride, or propionamidine hydrochloride, in pyridine and the dye precipitated as the iodide in each case; (e) 1-methylthio-5.6-benzobenzthiazole methyl-p-toluenesulphonate is condensed with acetamidine hydrochloride, propionamidine hydrochloride or benzamidine hydrochloride in pyridine and the dye precipitated as the iodide in each case; (f) 1-methylthio-3.4-benzobenzthiazole methyl-p-toluenesulphonate is condensed with acetamidine hydrochloride or propionamidine hydrochloride or benzamidine hydrochloride in pyridine and the dyes precipitated either as the iodide or bromide; (g) 1-methylthio-4.5-methylenedioxybenzthiazole-methyl-p -toluenesulphonate is condensed with acetamidine hydrochloride; (h) 1-methylthio-4.5 - dimethoxybenzthiazole methyl-p-toluene-sulphonate is condensed in pyridine with acetamidine hydrochloride or propionamidine hydrochloride in the latter ease the dye being precipitated as the iodide; (i) 4-methylthioquinazoline methyl-p-toluenesulphonate is condensed with acetamidine hydrochloride in pyridine and the dye precipitated as the iodide; (j) dimethylthio-a .b - and b .b <1>-diazole are respectively condensed with methyl-p-toluene-sulphonate and the products with ammonium nitrate in pyridine, the dyes being precipitated as the iodides. Many of the products are sensitizers for photographic silver halide emulsions (cf. Specification 447,109).
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2307535A GB461668A (en) | 1935-08-16 | 1935-08-16 | Improvements in or relating to dyestuffs |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2307535A GB461668A (en) | 1935-08-16 | 1935-08-16 | Improvements in or relating to dyestuffs |
Publications (1)
Publication Number | Publication Date |
---|---|
GB461668A true GB461668A (en) | 1937-02-16 |
Family
ID=10189721
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB2307535A Expired GB461668A (en) | 1935-08-16 | 1935-08-16 | Improvements in or relating to dyestuffs |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB461668A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1144280B (en) * | 1961-07-14 | 1963-02-28 | Basf Ag | Process for the preparation of azamonomethine cyanines of the benzothiazole series |
-
1935
- 1935-08-16 GB GB2307535A patent/GB461668A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1144280B (en) * | 1961-07-14 | 1963-02-28 | Basf Ag | Process for the preparation of azamonomethine cyanines of the benzothiazole series |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US2340882A (en) | Sensitized photographic material | |
GB489335A (en) | Improvements in or relating to the manufacture and use of dyestuffs suitable for sensitising photographic emulsions | |
US2304981A (en) | Sensitizing of photographic silver chloride, chloro-bromide, and chloro-bromo-iodideemulsions | |
GB461668A (en) | Improvements in or relating to dyestuffs | |
GB1131191A (en) | New imidazole derivatives, their preparation and use | |
CA1111695A (en) | Imidazole derivatives as corrosion preventatives for stabilizer baths used in photography | |
DE69325605T2 (en) | Silver halide photographic light-sensitive material | |
GB424559A (en) | Improvements in or relating to the production of compounds of the cyanine type | |
US3622340A (en) | 4-thiouracil compounds as fog inhibitors | |
US2307049A (en) | Process of producing aza-methine dyes | |
GB1072413A (en) | New dihydrothieno[3,2-d]pyrimidines | |
GB694744A (en) | Improvements in or relating to dyestuffs and photographic emulsions containing the same | |
US2496899A (en) | Azamerocyanine dyes and a process for the preparation thereof | |
US2394068A (en) | Dyestuffs and dyestuff intermediates | |
US3615621A (en) | 4-pyrimidinethione compounds as fog inhibitors | |
GB1309621A (en) | Disulphonylimides | |
GB546566A (en) | Improvements in or relating to dyestuffs | |
US2610121A (en) | Photographic silver halide emulsions | |
GB1102891A (en) | Process for the preparation of heterocyclammonium betaines | |
GB624027A (en) | Improvements in or relating to dyestuffs and to the sensitising of photographic emulsions therewith | |
Glauert et al. | mero Cyanines derived from thio-oxindole. Part III. Trinuclear mero cyanines | |
GB613458A (en) | Improvements in and relating to the manufacture of meso-alkylmercapto substituted carbocyanine dyes and to photographic emulsions sensitized therewith | |
US2293025A (en) | Guanidine ammonium ferricyanide | |
GB426718A (en) | Improvements in or relating to the production of dyestuffs | |
GB967469A (en) | Heterocyclic thiocyanates and their use as plant fungicides |