GB454687A - Improvements in the preparation of derivatives of pyridine and quinoline - Google Patents
Improvements in the preparation of derivatives of pyridine and quinolineInfo
- Publication number
- GB454687A GB454687A GB22537/35A GB2253735A GB454687A GB 454687 A GB454687 A GB 454687A GB 22537/35 A GB22537/35 A GB 22537/35A GB 2253735 A GB2253735 A GB 2253735A GB 454687 A GB454687 A GB 454687A
- Authority
- GB
- United Kingdom
- Prior art keywords
- condensed
- substituted
- dichlorphenylmercaptan
- chlorphenylmercaptan
- naphthylmercaptan
- 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
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/62—Oxygen or sulfur atoms
- C07D213/70—Sulfur atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pyridine Compounds (AREA)
Abstract
Quaternary salts of a 2-(substituted mercapto) pyridine or quinoline are made by heating one molecular proportion of a mercaptan with one molecular proportion of a quaternary salt of an iodo derivative of a heterocyclic nitrogen base of the formula <FORM:0454687/IV/1> wherein R is an alkyl or substituted alkyl group, R<11> stands for a vinylene, phenylene, or a substituted vinylene or phenylene group, and X for an acid radicle. Reaction may take place in a diluent and an acid-binding agent such as a tertiary organic base is preferably present. In examples: 2-iodoquinoline ethiodide is condensed with phenylmercaptan, p - tolylmercaptan, b - naphthylmercaptan, p-chlorphenylmercaptan, 2.5 - dichlorphenylmercaptan, n-propylmercaptan, n-butylmercaptan; 2-iodo-6-methylquinoline ethiodide is condensed with b -naphthyl mercaptan; 2-iodopyridine methiodide is condensed with b - naphthylmercaptan, 2.5 - dichlorphenylmercaptan and 2-p-chlorphenylmercaptan; in all cases condensation is effected in alcohol in presence of triethylamine. Reference is also made to the production of 2-mercaptans of pyridinium or quinolinium salts wherein attached to the sulphur atom is a benzyl, benzthiazole or pyrazolone radicle. The products are of use in the production of cyanine dyes.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US454687XA | 1934-08-09 | 1934-08-09 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB454687A true GB454687A (en) | 1936-10-06 |
Family
ID=21938060
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB22537/35A Expired GB454687A (en) | 1934-08-09 | 1935-08-09 | Improvements in the preparation of derivatives of pyridine and quinoline |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB454687A (en) |
-
1935
- 1935-08-09 GB GB22537/35A patent/GB454687A/en not_active Expired
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