GB926696A - Pyrimidine derivatives - Google Patents
Pyrimidine derivativesInfo
- Publication number
- GB926696A GB926696A GB549161A GB549161A GB926696A GB 926696 A GB926696 A GB 926696A GB 549161 A GB549161 A GB 549161A GB 549161 A GB549161 A GB 549161A GB 926696 A GB926696 A GB 926696A
- Authority
- GB
- United Kingdom
- Prior art keywords
- group
- signifies
- pyrimido
- pyrimidines
- alkoxy
- 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
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
The invention comprises compounds of the general formula: <FORM:0926696/IV(a)/1> wherein R1, R2 and R3, which may be the same or different, each signify a basic group NR4R5 (in which R4 signifies an alkyl, cycloalkyl, hydroxyalkyl, alkoxyalkyl, alkylaminoalkyl, aryl, aralkyl, or amino group and R5 signifies a hydrogen atom or an alkyl or hydroxyalkyl group or together with R4 and the nitrogen atom, a substituted or unsubstituted heterocyclic ring, which, if desired, can be interrupted by further hetero-atoms) or R1 and R2 may have the above meanings and R3 signifies an alkoxy, alkoxyalkoxy, alkylaminoalkoxy, or alkylthio group; their salts with non-toxic inorganic or organic acids; the preparation thereof by reacting a pyrimido-pyrimidine of the formula: <FORM:0926696/IV(a)/2> (in which 1-3 of the groups Z1-Z3, which may be the same or different, represent a halogen atom, a quaternary ammonium mercapto, or alkylmercapto group and the remaining groups Z1-Z3, which may be the same or different, represent the basic group NR4R5, and Z3 may also signify a hydroxy, alkoxy, alkoxyalkoxy, alkylaminoalkoxy or alkylthio group) with one or more molecular proportions of one or more amines HNR4R5 or with an alkali metal derivative of an alkanol, alkoxyalkanol, alkylaminoalkanol or alkylmercaptan, (where Z3 signifies a halogen atom and R3 signifies an unsubstituted or substituted alkoxy or alkylthio group) and, if Z3 signifies a free hydroxyl group and a compound is to be obtained in which R3 signifies an unsubstituted or substituted alkoxy group or an alkylthio group, the free hydroxyl group is then converted into an alkoxy or alkylthio group; and pharamceutical compositions containing them. 2,7-Diamino- 4-hydroxy-pyrimido- [4,5-d]-pyrimidines are prepared from a 2,7-dialkylmercapto-4-hydroxy- [4,5-d]-pyrimidine and morpholine, piperidine, pyrrolidine, methylpiperazine, diethyl- and dibutylamines. 2,7-Diamino-4- mercapto-pyrimido- [4,5-d]-pyrimidines are prepared from 2,7-dimorpholino-, -dipiperidino- and -dipyrrolidino-4-chloro-pyrimidino- [4,5-d]-pyrimidines and thiourea. 2,7-Diamino- 4-chloro-pyrimido- [4,5-d]-pyrimidines are prepared by chlorination of the 4-hydroxy analogues. Pharmaceutical compositions comprise the pyrimido-[4,5-d] pyrimidines in association with a pharmaceutical carrier or diluent and may be formulated as powders, tablets, dragees, capsules, granules, suppositories, emulsions, suspensions, syrups or solutions suitable for oral, parenteral or rectal administration. The compounds are coronary-dilators and sedatives.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DET0017892 | 1960-02-15 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB926696A true GB926696A (en) | 1963-05-22 |
Family
ID=7548755
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB549161A Expired GB926696A (en) | 1960-02-15 | 1961-02-14 | Pyrimidine derivatives |
Country Status (8)
Country | Link |
---|---|
BE (1) | BE600194A (en) |
CH (2) | CH411915A (en) |
DE (1) | DE1445156A1 (en) |
DK (1) | DK103779C (en) |
FR (1) | FR1472006A (en) |
GB (1) | GB926696A (en) |
NL (1) | NL6406735A (en) |
SE (3) | SE301145B (en) |
-
1960
- 1960-02-15 DE DE19601445156 patent/DE1445156A1/en active Pending
-
1961
- 1961-01-30 CH CH108561A patent/CH411915A/en unknown
- 1961-01-30 CH CH490565A patent/CH421126A/en unknown
- 1961-02-10 SE SE138761A patent/SE301145B/en unknown
- 1961-02-14 BE BE600194A patent/BE600194A/en unknown
- 1961-02-14 DK DK60761A patent/DK103779C/en active
- 1961-02-14 GB GB549161A patent/GB926696A/en not_active Expired
- 1961-02-14 FR FR852697A patent/FR1472006A/en not_active Expired
-
1962
- 1962-10-03 SE SE1168862A patent/SE301481B/en unknown
- 1962-10-31 SE SE1168962A patent/SE301147B/en unknown
-
1964
- 1964-06-12 NL NL6406735A patent/NL6406735A/xx unknown
Also Published As
Publication number | Publication date |
---|---|
FR1472006A (en) | 1967-03-10 |
NL6406735A (en) | 1964-08-10 |
SE301145B (en) | 1968-05-27 |
CH411915A (en) | 1966-04-30 |
SE301147B (en) | 1968-05-27 |
DK103779C (en) | 1966-02-21 |
BE600194A (en) | 1961-08-14 |
DE1445156A1 (en) | 1972-04-06 |
CH421126A (en) | 1966-09-30 |
SE301481B (en) | 1968-06-10 |
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