ES265401A1 - 5-aryl-2-amino-2-oxazolin-4-ones - Google Patents
5-aryl-2-amino-2-oxazolin-4-onesInfo
- Publication number
- ES265401A1 ES265401A1 ES0265401A ES265401A ES265401A1 ES 265401 A1 ES265401 A1 ES 265401A1 ES 0265401 A ES0265401 A ES 0265401A ES 265401 A ES265401 A ES 265401A ES 265401 A1 ES265401 A1 ES 265401A1
- Authority
- ES
- Spain
- Prior art keywords
- alkyl
- aryl
- phenyl
- general formula
- hydrogen atoms
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
- C07D263/02—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings
- C07D263/30—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D263/34—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members 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
- C07D263/46—Sulfur atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
- C07D263/02—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings
- C07D263/30—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D263/34—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members 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
- C07D263/48—Nitrogen atoms not forming part of a nitro radical
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Epidemiology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
The invention comprises 5-aryl-2-amino-2-oxazolin-4-ones of the general formula: <FORM:0907848/IV (b)/1> and the non toxic acid addition salts and tautomers thereof, wherein X is a halogen atom and R1 and R2 are the same or different and are hydrogen atoms or C1-6 alkyl groups or X is a hydrogen atom and R1 and R2 are the same or different C1-6 alkyl groups and the preparation thereof (a) by condensing a 2-oxazolid-4-one of the formula <FORM:0907848/IV (b)/2> with an alkylating or aminating agent, wherein (i) when Y is NHR1, in which R1 is a hydrogen atom or a C1-6 alkyl group and X is aydrogen or halogen atom the alkylating agent is a C1-6 alkyl sulphate or sulphonate, the alkylation being carried out in the presence of a base (ii) when Y is -NR3R4 or SR3 in which R3 and/or R4 are hydrogen atoms or alkyl or aryl groups then the aminating agent is R1R2NH X, R1 and R2 being defined as in I or (b) by cyclizing a phenylacetic acid derivative of the general formula <FORM:0907848/IV (b)/3> wherein (i) K is -NH-C:Z-NR1R2 in which Z is O when Y is halogen or sulphonyloxy and Z is NH or S when Y is OH or (ii) K is NHCN and Y is OH, or (iii) K is NR3R4 or OR5 in which R3 and R4 are hydrogen atoms, alkyl or aryl groups and R5 is an alkyl or aryl group and Y is -O-C:NH-NR1R2. The starting materials for process (b) are prepared in situ from an appropriate reactive phenylacetic acid derivative and a urea, thiourea, guanidine, or cyanamide. Acyl ureas derived from urea or dialkylurea and 2-phenyl-2-haloacetyl halides, alkyl 2-phenyl-2-haloacetates, 2-phenyl-2-(p-toluenesulphonyloxy)-acetyl halides or their o-halophenyl analogues may be isolated. Ethyl o-fluoromandelate is prepared by esterification of the acid with ethanol in the presence of p-toluenesulphonic acid. Pharmaceutical compositions useful as central nervous system stimulants comprise the compounds of general formula I together with a pharmaceutical excipient and may be in the form of tablets, dragees, capsules, suppositories, liquids to be administered in drops, emulsions, suspensions, syrups, chocolate, candy and chewing gum. U.S.A. Specification 2,892,753 is referred to.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US3511560A | 1960-06-10 | 1960-06-10 | |
US3511660A | 1960-06-10 | 1960-06-10 |
Publications (1)
Publication Number | Publication Date |
---|---|
ES265401A1 true ES265401A1 (en) | 1961-09-01 |
Family
ID=26711766
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ES0265401A Expired ES265401A1 (en) | 1960-06-10 | 1961-03-04 | 5-aryl-2-amino-2-oxazolin-4-ones |
Country Status (6)
Country | Link |
---|---|
AT (1) | AT256101B (en) |
CH (4) | CH437293A (en) |
DK (2) | DK102861C (en) |
ES (1) | ES265401A1 (en) |
FR (1) | FR1555453A (en) |
GB (1) | GB907848A (en) |
-
1961
- 1961-02-23 GB GB662561A patent/GB907848A/en not_active Expired
- 1961-03-03 FR FR1555453D patent/FR1555453A/fr not_active Expired
- 1961-03-04 ES ES0265401A patent/ES265401A1/en not_active Expired
- 1961-03-06 DK DK97861A patent/DK102861C/en active
- 1961-03-06 CH CH1536765A patent/CH437293A/en unknown
- 1961-03-06 CH CH264561A patent/CH413840A/en unknown
- 1961-03-06 CH CH1314365A patent/CH421965A/en unknown
- 1961-03-06 CH CH264661A patent/CH401057A/en unknown
- 1961-03-06 AT AT656464A patent/AT256101B/en active
- 1961-03-06 DK DK168762A patent/DK105405C/en active
Also Published As
Publication number | Publication date |
---|---|
CH401057A (en) | 1965-10-31 |
FR1555453A (en) | 1969-01-31 |
DK105405C (en) | 1966-09-26 |
CH413840A (en) | 1966-05-31 |
CH421965A (en) | 1966-10-15 |
CH437293A (en) | 1967-06-15 |
GB907848A (en) | 1962-10-10 |
DK102861C (en) | 1965-10-18 |
AT256101B (en) | 1967-08-10 |
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