GB461668A - Improvements in or relating to dyestuffs - Google Patents

Improvements in or relating to dyestuffs

Info

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
Application number
GB2307535A
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.)
Individual
Original Assignee
Individual
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.)
Filing date
Publication date
Application filed by Individual filed Critical Individual
Priority to GB2307535A priority Critical patent/GB461668A/en
Publication of GB461668A publication Critical patent/GB461668A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09BORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B55/00Azomethine dyes
    • C09B55/009Azomethine 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).
GB2307535A 1935-08-16 1935-08-16 Improvements in or relating to dyestuffs Expired GB461668A (en)

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)

* Cited by examiner, † Cited by third party
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

Cited By (1)

* Cited by examiner, † Cited by third party
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

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