GB683334A - Manufacture of a new quinazoline derivative - Google Patents
Manufacture of a new quinazoline derivativeInfo
- Publication number
- GB683334A GB683334A GB22796/50A GB2279650A GB683334A GB 683334 A GB683334 A GB 683334A GB 22796/50 A GB22796/50 A GB 22796/50A GB 2279650 A GB2279650 A GB 2279650A GB 683334 A GB683334 A GB 683334A
- Authority
- GB
- United Kingdom
- Prior art keywords
- chloro
- manufacture
- cinnamoylamino
- nitrobenzene
- styryl
- 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
- C09B5/00—Dyes with an anthracene nucleus condensed with one or more heterocyclic rings with or without carbocyclic rings
- C09B5/24—Dyes with an anthracene nucleus condensed with one or more heterocyclic rings with or without carbocyclic rings the heterocyclic rings being only condensed with an anthraquinone nucleus in 1-2 or 2-3 position
- C09B5/44—Azines of the anthracene series
- C09B5/46—Para-diazines
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
The invention comprises 2-styryl-4-chloro-6,7-phthaloyl-quinazoline of the formula <FORM:0683334/IV (b)/1> It is made by heating 3-cyan-2-cinnamoylamino-anthraquinone, (see Group IV (c)), with phosphorus pentachloride, preferably in a diluent such as nitrobenzene. Specification 642,129 is referred to.ALSO:2 - Styryl - 4 - chloro - 6,7 - phthaloylquinazoline (see Group IV (b)) is condensed with 4 - aminoanthraquinone - 2,1(N) - benzacridones, e.g. with halogen substitution products such as the 51- or 61-chloro- or 6,7-dichloro bodies, to give green vat dyes. Specification 642,129, [Group IV (b)], is referred to. 2 - Cinnamoylamino - 3 - cyananthraquinone is obtained by heating the corresponding 3-brom body with cuprous cyanide and pyridine in nitrobenzene, or by acylation of the corresponding 2-amino body with cinnamic acid chloride.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH683334X | 1949-09-16 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB683334A true GB683334A (en) | 1952-11-26 |
Family
ID=4528660
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB22796/50A Expired GB683334A (en) | 1949-09-16 | 1950-09-15 | Manufacture of a new quinazoline derivative |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB683334A (en) |
-
1950
- 1950-09-15 GB GB22796/50A patent/GB683334A/en not_active Expired
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