GB881340A - Novel hydrazine derivatives and a process for the manufacture thereof - Google Patents
Novel hydrazine derivatives and a process for the manufacture thereofInfo
- Publication number
- GB881340A GB881340A GB18648/60A GB1864860A GB881340A GB 881340 A GB881340 A GB 881340A GB 18648/60 A GB18648/60 A GB 18648/60A GB 1864860 A GB1864860 A GB 1864860A GB 881340 A GB881340 A GB 881340A
- Authority
- GB
- United Kingdom
- Prior art keywords
- formula
- group
- represents hydrogen
- carboxy
- hydroxy
- 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
- C07D253/00—Heterocyclic compounds containing six-membered rings having three nitrogen atoms as the only ring hetero atoms, not provided for by group C07D251/00
- C07D253/02—Heterocyclic compounds containing six-membered rings having three nitrogen atoms as the only ring hetero atoms, not provided for by group C07D251/00 not condensed with other rings
- C07D253/06—1,2,4-Triazines
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
The invention comprises triazine-hydrazine derivatives of the formula <FORM:0881340/IV (b)/1> wherein R1 represents a hydrazino, hydroxy, carboxy, alkyl or aralkyl group and R2 represents hydrogen or a hydroxy, carboxy, aryl or aralkyl group and also an alkyl group when R1 represents hydrazino, and acid addition salts thereof, e.g. with hydrohalic, nitric, sulphuric, phosphoric, arylsulphonic, malic, salicylic, tartaric, citric, ascorbic and mandelic acids. The compounds of the above formula are prepared by reacting a compound of the formula <FORM:0881340/IV (b)/2> wherein R1 represents hydrogen or a methyl group, R4 represents a mercapto, methylmercapto, hydroxy, carboxy, alkyl or aralkyl group, and R2 represents hydrogen or a hydroxy, carboxy, aryl or aralkyl group and also an alkyl group when R4 represents mercapto or methylmercapto, with hydrazine or hydrazine hydrate. Monomercapto-triazines of the formula <FORM:0881340/IV (b)/3> are prepared by refluxing thiosemicarbazones of the formula <FORM:0881340/IV (b)/4> with sodium hydroxide. The mercapto group may be subsequently converted to a methylmercapto group by treatment with methyl iodide. Dimercapto-triazines of the formula <FORM:0881340/IV (b)/5> where R3 represents hydrogen, are prepared by reacting monomercapto hydrazines of the formula <FORM:0881340/IV (b)/6> with phosphorus pentasulphide. The mercapto groups may be subsequently converted to methylmercapto groups (R3=methyl) by treatment with methyl iodide. Thiosemicarbazones of the formula <FORM:0881340/IV (b)/7> wherein R represents hydrogen, a monovalent metal atom or C1-4 alkyl group, are prepared by reacting an acid-aldehyde or an acid ketone of the formula: R2-CO-COOR with thiosemicarbazide.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR881340X | 1959-05-28 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB881340A true GB881340A (en) | 1961-11-01 |
Family
ID=9370933
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB18648/60A Expired GB881340A (en) | 1959-05-28 | 1960-05-26 | Novel hydrazine derivatives and a process for the manufacture thereof |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB881340A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4157392A (en) * | 1977-05-17 | 1979-06-05 | Diamond Shamrock Corporation | Pharmacologically active substituted 1,2,4-triazines |
WO2002009715A2 (en) * | 2000-07-28 | 2002-02-07 | The Procter & Gamble Company | Use of an arylaldehyde 5-oxo-1, 2, 4-triazine hydrazide for the treatment of cancer |
WO2002009716A2 (en) * | 2000-07-28 | 2002-02-07 | The Procter & Gamble Company | Use of an aldehyde 5-oxo-1,2,4-triazine hydrazide for the treatment of cancer |
-
1960
- 1960-05-26 GB GB18648/60A patent/GB881340A/en not_active Expired
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4157392A (en) * | 1977-05-17 | 1979-06-05 | Diamond Shamrock Corporation | Pharmacologically active substituted 1,2,4-triazines |
WO2002009715A2 (en) * | 2000-07-28 | 2002-02-07 | The Procter & Gamble Company | Use of an arylaldehyde 5-oxo-1, 2, 4-triazine hydrazide for the treatment of cancer |
WO2002009716A2 (en) * | 2000-07-28 | 2002-02-07 | The Procter & Gamble Company | Use of an aldehyde 5-oxo-1,2,4-triazine hydrazide for the treatment of cancer |
WO2002009715A3 (en) * | 2000-07-28 | 2003-01-03 | Procter & Gamble | Use of an arylaldehyde 5-oxo-1, 2, 4-triazine hydrazide for the treatment of cancer |
WO2002009716A3 (en) * | 2000-07-28 | 2003-01-09 | Procter & Gamble | Use of an aldehyde 5-oxo-1,2,4-triazine hydrazide for the treatment of cancer |
US6518269B1 (en) | 2000-07-28 | 2003-02-11 | University Of Arizona Foundation | Cancer treatment |
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