GB935381A - 2, 4-diaminoquinazolines and their preparation - Google Patents
2, 4-diaminoquinazolines and their preparationInfo
- Publication number
- GB935381A GB935381A GB39469/59A GB3946959A GB935381A GB 935381 A GB935381 A GB 935381A GB 39469/59 A GB39469/59 A GB 39469/59A GB 3946959 A GB3946959 A GB 3946959A GB 935381 A GB935381 A GB 935381A
- Authority
- GB
- United Kingdom
- Prior art keywords
- amino
- quinazolines
- diamino
- methyl
- lower alkyl
- 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
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/70—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings condensed with carbocyclic rings or ring systems
- C07D239/72—Quinazolines; Hydrogenated quinazolines
- C07D239/95—Quinazolines; Hydrogenated quinazolines with hetero atoms directly attached in positions 2 and 4
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
The invention comprises the following 2,4-diamino-R-quinazolines where R is 5,6-trimethylene, 5-methyl, 6-n-propyl, 6-n-butyl, 5,6-tetramethyl and 5-ethyl; and the preparation of 2,4-diaminoquinazolines of the general formula <FORM:0935381/IV(a)/1> wherein R1 is a lower alkyl group and R2 is a hydrogen atom or a lower alkyl group and R1 may be a hydrogen atom when R2 is a lower alkyl group, R1 and R2 together having not more than 10 carbon atoms, or R1 and R2 together form an alkylene chain having 3 or 4 carbon atoms, by reacting an anthranilonitrile of the formula <FORM:0935381/IV(a)/2> with dicyandiamide, and pharmaceutical compositions containing the specified 2,4-diamino-R-quinazolines (see Group VI). 2-Amino-5-ethylebenzonitrile is prepared by decomposition of 5-ethylisatin b -oxime. Similarly are prepared 2-amino-6-methyl-benzonitrile, 2-amino-5-n-propylbenzonitrile, 2-amino-5-n-butylbenzonitrile, 2-amino-5,6,7, 8-tetrahydro-1-naphthonitrile and 2-amino-6-ethylbenzonitrile. 5-Amino-4-cyanoindane is prepared by reacting 5-acetylamino-4-bromoindane with cuprous cyanide to give 5-acetylamino-4-cyano-indane and removing the acetyl group by hydrolysis.ALSO:Antibacterial compositions contain 2,4-diamino-R-quinazolines, wherein R is 5,6-trimethylene, 5-methyl, 6-n-propyl, 6-n-butyl, 5,6-tetramethyl and 5-ethyl, together with a pharmaceutically acceptable carrier. The compositions may also contain antibiotics and/or antibacterials. The compositions may be presented as capsules or cachets containing fine powders or granules of the compounds in the dry state or in a non-aqueous suspension, in tablets, dragees, as solutions, suspensions or emulsions for oral administration; as aqueous solutions for injection; as suppositories or pessaries; as ointments, creams or solutions for topical use.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US78022058A | 1958-12-15 | 1958-12-15 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB935381A true GB935381A (en) | 1963-08-28 |
Family
ID=25118979
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB39469/59A Expired GB935381A (en) | 1958-12-15 | 1959-11-20 | 2, 4-diaminoquinazolines and their preparation |
Country Status (5)
Country | Link |
---|---|
CH (1) | CH389628A (en) |
DE (1) | DE1125939B (en) |
ES (1) | ES253914A1 (en) |
FR (1) | FR605M (en) |
GB (1) | GB935381A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3485842A (en) * | 1963-09-20 | 1969-12-23 | John Davoll | Heterocyclic compounds and means for producing the same |
WO2005011758A2 (en) * | 2003-07-25 | 2005-02-10 | Ciba Specialty Chemicals Holding Inc. | Use of substituted 2,4-bis (alkylamino) pyrimidines or -quinazolines as antimicrobials |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE737931C (en) * | 1940-07-10 | 1943-07-29 | Ig Farbenindustrie Ag | Process for the preparation of 2,4-diaminochinazoline |
-
1959
- 1959-11-20 GB GB39469/59A patent/GB935381A/en not_active Expired
- 1959-11-27 CH CH8118059A patent/CH389628A/en unknown
- 1959-12-03 ES ES0253914A patent/ES253914A1/en not_active Expired
- 1959-12-12 DE DEW26879A patent/DE1125939B/en active Pending
-
1960
- 1960-08-31 FR FR837354A patent/FR605M/fr active Active
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3485842A (en) * | 1963-09-20 | 1969-12-23 | John Davoll | Heterocyclic compounds and means for producing the same |
US3505330A (en) * | 1963-09-20 | 1970-04-07 | Parke Davis & Co | 2,4-diaminoquinazoline compounds |
WO2005011758A2 (en) * | 2003-07-25 | 2005-02-10 | Ciba Specialty Chemicals Holding Inc. | Use of substituted 2,4-bis (alkylamino) pyrimidines or -quinazolines as antimicrobials |
WO2005011758A3 (en) * | 2003-07-25 | 2005-04-28 | Ciba Sc Holding Ag | Use of substituted 2,4-bis (alkylamino) pyrimidines or -quinazolines as antimicrobials |
US7722893B2 (en) | 2003-07-25 | 2010-05-25 | Ciba Specialty Chemicals Corporation | Use of substitute 2,4-bis (alkylamino) pyrimidines or quinzolines as antimicrobials |
Also Published As
Publication number | Publication date |
---|---|
FR605M (en) | 1961-06-19 |
ES253914A1 (en) | 1960-05-01 |
DE1125939B (en) | 1962-03-22 |
CH389628A (en) | 1965-03-31 |
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