WO1995004048A1 - Benzoxazinones and benzothiazinones endowed with therapeutic activity - Google Patents
Benzoxazinones and benzothiazinones endowed with therapeutic activity Download PDFInfo
- Publication number
- WO1995004048A1 WO1995004048A1 PCT/EP1994/002354 EP9402354W WO9504048A1 WO 1995004048 A1 WO1995004048 A1 WO 1995004048A1 EP 9402354 W EP9402354 W EP 9402354W WO 9504048 A1 WO9504048 A1 WO 9504048A1
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- WIPO (PCT)
- Prior art keywords
- mole
- alkyl
- dihydro
- benzoxazin
- compound
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D265/00—Heterocyclic compounds containing six-membered rings having one nitrogen atom and one oxygen atom as the only ring hetero atoms
- C07D265/04—1,3-Oxazines; Hydrogenated 1,3-oxazines
- C07D265/12—1,3-Oxazines; Hydrogenated 1,3-oxazines condensed with carbocyclic rings or ring systems
- C07D265/14—1,3-Oxazines; Hydrogenated 1,3-oxazines condensed with carbocyclic rings or ring systems condensed with one six-membered ring
- C07D265/20—1,3-Oxazines; Hydrogenated 1,3-oxazines condensed with carbocyclic rings or ring systems condensed with one six-membered ring with hetero atoms directly attached in position 4
- C07D265/22—Oxygen atoms
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/08—Vasodilators for multiple indications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D279/00—Heterocyclic compounds containing six-membered rings having one nitrogen atom and one sulfur atom as the only ring hetero atoms
- C07D279/04—1,3-Thiazines; Hydrogenated 1,3-thiazines
- C07D279/08—1,3-Thiazines; Hydrogenated 1,3-thiazines condensed with carbocyclic rings or ring systems
Definitions
- the present invention relates to the therapeutic use of 2,3-dihydro-4H-l,3-benzoxazin- and -benzo- thiazin-4-ones.
- 2,3-Dihydro-4H-l,3-benzoxazin-4-ones unsubstituted on the nitrogen atom were described by B.W. Horrom et al., J. Org. Chem., 72, 721 (1950) as endowed with analgesic activity.
- Other 2,3-dihydro-4H-l,3- benzoxazin-4-ones were disclosed by R.B. Ga mil, J.
- X is an oxygen or a sulphur atom
- Y represents methylene, ethylene, (C 3 _ g )alkylene optionally branched, or cyclopentylene, cyclohexylene or cycloheptylene optionally substituted with
- A is hydroxy; (C,_ g )alkoxy, formyloxy; (C 2 _ g )acyloxy; mercapto; (C, g )alkyl-mercapto; mesyloxy; (C 2 _ g )alkyl- sulfonyloxy; tosyloxy; phenyl-sulfonyloxy optionally substituted
- R 3 is a (C, g )alkyl group, methylene, ethylene or (C 3 _ g )alky ⁇ lene 0- ⁇ -substituted with a 2,3-dihydro-4H-l,3-benzo- xazin-4-one-N-yl residue;
- R represents hydrogen, (C, g )alkyl or phenyl; R.. and R 2 are independently hydrogen, halogen, (C, g )alkoxy, trifluoromethyl, and (C, g )alkyl; and the pharmaceutically acceptable acid or base salts thereof, useful as therapeutically active substances.
- the invention relates to the use of the compounds of formula (I) as agents useful in the cardiovascular field.
- the alkyl groups essentially identify methyl, ethyl, propyl, i-propyl, butyl, 2-methyl-propyl, n-pentyl, 3-methylbutyl, i- pentyl, n-hexyl and the like, while the alkoxy groups are preferably selected from the group consisting of methoxy, ethoxy, propoxy, i-propoxy, butoxy, 2- methylbutoxy and t-butoxy.
- linear or branched (C,_ g )alkylene group it is intended, e.g., 2- methylethylene, 1,3-propylene, 1,4-butylene, 2- ethylethylene, 3-methylpropylene, 1,5-pentylene, 2- ethylpropylene, 2-methylbutylene, 1,6-hexylene, 1- ethyl-1-methylpropylene, 3-methylpentylene and the like.
- (C 2 _ g )acyloxy it is intended, e.g., acetyloxy, propionyloxy, butyryloxy, hexanoyloxy, oxalyloxy, malonyloxy, succinyloxy.
- the compounds of the present invention are prepared according to procedures known to the skilled in the art.
- the compounds of formula (I) wherein X, Y, R, R, and R 2 are as defined above, A is hydroxy, (C 1 _ g )alkoxy, formyloxy or (C 2 _ g )acyloxy may be obtained according to what taught by the publication of the Patent application EP-A-0 490 183, by reacting a salicylamide or thiosalicylamide of formula (II)
- R ⁇ , 2 , x and Y are as defined above, and R ⁇ is hydrogen, (C- L _ g )alkyl or (C 1 _ g )acyl, with an aldehyde of formula (III) R-CHO (III) wherein R is as above, or a derivative or a precursor thereof.
- the condensation generally occurs in an acidic environment, for example in a system constituted by a strong mineral acid and acetic acid, thereby obtaining compounds of formula (I) wherein R.
- sulfonic acids such as p-toluenesulfonic acid, methanesulfonic acid, Q and ⁇ -naphthalenesulfonic acids, phosphoric acids, esters and analogues thereof.
- the condensation is carried out in the presence of an organic solvent, preferably an inert organic solvent such as ethyl acetate, acetonitrile, benzene, nitrobenzene or chlorobenzene, halogenated aliphatic hydrocarbons such as methylene chloride, chloroform, 1,2-dichloroethane or 1,1,2- trichloroethylene, cyclohexane, tetrahydrofuran, tetrahydropyran, dimethylformamide, dimethylacetamide.
- the reaction temperature may vary within quite wide limits without prejudice for the course of the reaction. The preferred range of temperature is comprised between about -10°C and the reflux temperature of the reaction mixture, and the reaction is completed in a period of time ranging between about 2 and about 30 hours.
- the molar quantities of the reagents of formula (II) and (III) are not critical for the good course of the cyclization, and such reagents may be used in the widest stoichiometric ratios.
- precursors of the compound of formula (III) such as paraformal ehyde and the paraldehyde are preferably employed.
- R 3 is a (C, g)alkyl group, methylene, ethylene or (C 3 _ g )alkylene -substituted by a 2,3-dihydro-4H-l,3-benzoxazin-4-one-N-yl residue are desired, a compound of formula (I) wherein A is hydroxy is treated with a suitable carboxylic or sulfonic acid activated in form of anhydride, halide or imidazolide, used in excess, preferably in the presence of an organic base such as pyridine.
- Suitable solvents for such synthesis are, e.g., chloroform or methylene chloride, while the reaction temperature ranges between about -10°C and the room temperature, and the reaction time is of about 1-20 hours.
- the reaction temperature ranges between about -10°C and the room temperature, and the reaction time is of about 1-20 hours.
- a sui ⁇ table amount of the R 3 OH desired alcohol is added at the end of the reaction.
- the compounds of formula (I) wherein A is hydroxy may yield compounds of formula (I) wherein A is mercapto or (C, g )alkyl-mercapto, by an intermediate of formula (IV)
- Halo is an halogen atom, preferably chlorine.
- halogenating agents such as, e.g., thionyl chloride, sulfuryl chloride, phosphorous trichloride, phosphorous pentachloride, phosphorous oxytrichloride, phosphorous tribromide, sulfuryl bromide and the like.
- Said halogenation reaction occurs in an organic solvent, preferably in an inert organic solvent selected from the ones employed for the synthesis of the compound of formula (I) described above, at a temperature ranging between the room temperature and the reflux temperature of the reaction mixture.
- the compound of formula (IV) is converted into a compound of formula (I) wherein A is mercapto, by reaction with thiourea in alcoholic solution, at the reflux temperature of the reaction mixture, for about 5-12 hours, and subsequent hydrolysis with strong organic bases such as an alkali metal hydroxide, at the reflux temperature for about 2- 10 hours.
- the compound of formula (I) wherein A is mercapto may be converted into a compound of formula (I) wherein A is (C. gjalkyl-mercapto, by treatment with the suitable acyl halide in the presence of an organic base such as diazabicycloundecene, according to what taught by Patai, 2nd part, pages 721- 735.
- the compounds of formula (I) wherein A is hydroxy may also provide compounds of formula (I) wherein A is (C,_g)alkoxy, according to the so-called Williamson's reaction carried out with the suitable acyl halide.
- compounds of formula (I) may be converted into other compounds of formula (I) by means of suitable procedures for modifying the substituents R 1 and R 2 , wholly familiar to the skilled in the art.
- the conversion of an R. or ? group into another R. ⁇ or R 2 group having a meaning comprised by formula (I) may occur following conventional procedures familiar to the skilled in the art. These procedures are in the scope of the invention together with the obvious modifications of the just disclosed methods for preparing the compounds of the invention.
- N-(2 '-hydroxyethyl)-4-methylsalicylamide was prepared according to the procedure of Example 3,A) starting from 20 g of methyl 4- methylsalicylate (Chem. Abs. 64, 6568d) and 9 ml of 2-aminoethanol. Yield: 16.7 g m.p. 78-80°C (hexane) .
- N-(5'-hydroxypentyDsalicylamide was prepared following the procedure of Example 3,A) starting from 17.6 g of methyl salicylate and 8.5 ml of 5- aminopentanol. Yield: 11 g.
- the compound was an oil used as such in the subsequent step.
- N-(2'-hydroxyethyl)-4-methoxy-salicylamide was prepared following the procedure described in
- Example 3A starting from 16.9 g of methyl 4- methoxysalicylate (J. Org. Chem., 23, 756, 1958) and 7 ml of 2-aminoethanol. Yield: 9.5 g. m.p. 92-94°C (hexane).
- N-(1'-methyl-2'-hydroxyethyl)salicylamide was prepared following the procedure of Example 3,A) starting from 18 g (0.118 mole) of salicylic acid methyl ester and 18.8 ml of 2-amino-l-propanol. Yield: 19 g.
- the compound was an oil which was used as such in the subsequent step.
- N-(2 '-hydroxyethyl)-5-methoxysalicylamide was prepared following the procedure of Example 3,A) starting from 25 g (0.137 mole) of 5-methoxy- salicylic acid methyl ester and 9.94 ml of 2- aminoethanol. Yield: 25 g. The compound was used as such in the subsequent step.
- N-(2'-hydroxyethyl)-4-trifluoromethyl-salicylamide was prepared following the procedure of Example 3,A) starting from 26 g (0.118 mole) of 4- trifluoromethyl-salicylic acid methyl ester [J. Am. Chem. Soc, 76, 1051-4 (1954)] and 100 ml of 2-aminoethanol. Yield: 24 g. The compound obtained was used as such in the subsequent step.
- N-(2'-hydroxyethyl)-3-methyl-salicylamide was prepared following the procedure of Example 3,A) starting from 24.2 g (0.145 mole) of 3-methyl- salicylic acid methyl ester and 100 ml of 2- aminoethanol. Yield: 28.9 g. The compound was used as such in the subsequent step.
- N-(2'-hydroxyethyl)-6-methyl-salicylamide was prepared following the procedure of Example 3,A) starting from 18.8 g (0.113 mole) of 6-methyl- salicylic acid methyl ester and 78 ml of 2- aminoethanol. Yield: 19.3 g. m.p.: 134-135 ⁇ C (hexane).
- N-(3'-hydroxypropyl)salicylamide was prepared following the procedure of Example 3,A) starting from 20 g (0.131 mole) of salicylic acid methyl ester and 13.2 ml of 3-aminopropanol. Yield: 24 g as an oil which was used as such in the subsequent step.
- N-(2'-hydroxy-1'-propyl)salicylamide was prepared following the procedure of Example 3,A) starting from 18 g (0.118 mole) of salicylic acid methyl ester and 18.3 ml of l-amino-2-propanol. Yield: 24 g as an oil which was used as such in the subsequent step.
- Example 1,B starting from 20 g (0.102 mole) of the compound under A) . There were obtained 18 g as an oil.
- N-(2 '-hydroxyethyl)-4-isopropoxy-salicylamide was prepared following the procedure of Example 3,A) starting from 25.3 g (0.166 mole) of 4-isopropoxy- salicylic acid methyl ester [obtained by treating 4-isopropoxy-salicylic acid prepared according to Synthesis 758-760 (1984), with methanol and sulfuric acid] and 100 ml of 2-aminoethanol. Yield: 22 g. The compound was used as such in the subsequent step.
- Example 34 starting from 10 g (0.051 mole) of the compound of Example 1, 3.78 ml (0.051 mole) of thionyl chloride and 398 ml (5.17 moles) of isopropyl alcohol.
- 4,5-Dimethoxy-N-(2'-hydroxyethyl)-salicylamide was prepared by reacting 23 g (0.108 mole) of 4,5- dimethoxy-salicylic acid methyl ester (obtained as described in Synthesis, 758, 1984) with 100 ml of 2-aminoethanol at 170 ⁇ C for 3 hours. After cooling to room temperature, the mixture was taken up in ethyl acetate, washed with 5% aqueous hydrochloric acid and dried over sodium sulfate. Yield: 18 g. The compound was used as such in the subsequent step.
- 5-Ethyl-N-(2'-hydroxyethyl)-salicylamide was prepared as described in Example 3 A) , starting from 26.8 g (0.148 mole) of 5-ethyl-salicylic acid methyl ester (prepared as described in Synthesis, 758, 1984) and 10.7 ml (0.178 mole) of 2- aminoethanol. Yield: 29.8 g.
- the compounds of the invention can be considered as potential drugs with a specific antianginal activity.
- the ill vivo antianginal activity was determined on anaesthetized Sprague Dawley rats (average weight - 350-400 g) , according to the method described by M. Leitold et al., Arzneim. Forsch. 3>, 1454, 1986.
- the test was carried out by intravenously administering the animals with 1 U.I/kg, equal to 3 mg/kg of Arg- vasopressin which induce a coronary spasm reproducible and electrocardiographically detectable by an increase of the T-wave.
- the animals were then intravenously treated with four increasing doses of compounds representative of the invention to measure their ED 5Q , i.e. the dose yielding a 50% of inhibition of the increasing of the T-wave.
- the compounds of the invention showed to have ED 5Q ranging between about 1 and about 300 ⁇ g/Kg. Specifically, the compounds of Examples 1, 2 and 34 showed an ED 5Q of, respectively, 87, 215 and 10.5 ⁇ g/Kg. Also, some compounds were tested as above, but orally administered. For example, the compound of Example 1 showed an ED,. Q of 0.23 mg/Kg.
- the antianginal activity of the claimed compounds was also tested by the metacholine-induced angina test described by Sakai K. et al., Pharmacol. Met., 5_, 325- 336, 1981, The percentage of inhibition of the ST-wave increase induced by metacholine (0.8 ⁇ g/kg i.v.) was measured after intravenous administration of the compounds of the invention. The results are set forth in the following Table 1.
- Example % of Inhibition at 3 ⁇ g/kg 1 min. 10 min. 30 min.
- the ED_ Q of the compound of Example 1 was determined to be 73.5 ⁇ g/kg.
- the compounds of the invention have an ED 5Q per os ranging between about 100 and about 0.01 mg/kg.
- the favourable biological properties above are also accompanied by a low toxicity.
- the D 50 values calculated according to the method of Lichtfield and Wilcoxon, J. Pharm. Expt. Ther. 9 , 99, 1949, are in fact higher than 500 mg/kg i.p. in mouse and 800 mg/kg p.o. in rat.
- Object of the present invention is also the use of the claimed compounds as antianginal agents and agents useful in the treatment of ischemic cardiopathies, in connection with all the industrial aspects and applications of said use, comprising their incorporation into pharmaceutical compositions. Examples of these compositions are tablets, sugar- coated and film-coated tablets, syrups and phials, these latter being suitable for both the oral and the intramuscular or intravenous administration. They contain the active principle alone or in combination with common pharmaceutically acceptable carriers and excipients.
- the dosages of active principle used in the antianginal therapy or to treat ischemic cardiopathies may vary within wide limits depending on the specific compound employed, and are chosen to provide the patient with an effective therapeutic protection for.
- unit doses of from about 0.01 to about 1 mg may be administered from 1 to 4 times a day depending on the patient's necessity (prophylaxis, therapy, emergency).
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- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Heart & Thoracic Surgery (AREA)
- General Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Cardiology (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Vascular Medicine (AREA)
- Urology & Nephrology (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Nitrogen- Or Sulfur-Containing Heterocyclic Ring Compounds With Rings Of Six Or More Members (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
Description
Claims
Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AU74945/94A AU7494594A (en) | 1993-07-28 | 1994-07-18 | Benzoxazinones and benzothiazinones endowed with therapeutic activity |
EP94924778A EP0711286A1 (en) | 1993-07-28 | 1994-07-18 | Benzoxazinones and benzothiazinones endowed with therapeutic activity |
JP7505529A JPH09500878A (en) | 1993-07-28 | 1994-07-18 | Benzoxazinone and benzothiazinone with therapeutic activity |
NO960308A NO960308L (en) | 1993-07-28 | 1996-01-25 | Therapeutically active benzoxazines and benzothioanones |
FI960342A FI960342A0 (en) | 1993-07-28 | 1996-01-25 | Benzoxazinones and benzothiazinones with therapeutic activity |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
ITMI93A001678 | 1993-07-28 | ||
IT93MI001678A IT1264812B1 (en) | 1993-07-28 | 1993-07-28 | THERAPEUTICALLY ACTIVE BENZOSSAZINONIC AND BENZOTHIAZINONIC DERIVATIVES |
Publications (1)
Publication Number | Publication Date |
---|---|
WO1995004048A1 true WO1995004048A1 (en) | 1995-02-09 |
Family
ID=11366700
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/EP1994/002354 WO1995004048A1 (en) | 1993-07-28 | 1994-07-18 | Benzoxazinones and benzothiazinones endowed with therapeutic activity |
Country Status (13)
Country | Link |
---|---|
EP (1) | EP0711286A1 (en) |
JP (1) | JPH09500878A (en) |
CN (1) | CN1128025A (en) |
AU (1) | AU7494594A (en) |
CA (1) | CA2168099A1 (en) |
FI (1) | FI960342A0 (en) |
HU (1) | HUT74587A (en) |
IL (1) | IL110473A0 (en) |
IT (1) | IT1264812B1 (en) |
NO (1) | NO960308L (en) |
TW (1) | TW277061B (en) |
WO (1) | WO1995004048A1 (en) |
ZA (1) | ZA945555B (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2014036038A1 (en) * | 2012-08-27 | 2014-03-06 | University Of Tennessee Research Foundation | Lpa2 receptor-specific benzoic acid derivatives |
ITMI20122221A1 (en) * | 2012-12-21 | 2014-06-22 | C4T S C A R L | NEW COMPOUNDS OF 2,3-DIIDRO-4H-1,3-BENZOSSAZIN-4-ONE, METHOD FOR PREPARING THEM AND PHARMACEUTICAL FORM THAT INCLUDES THEM |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102367239B (en) * | 2011-07-20 | 2015-10-28 | 沈阳药科大学 | 2-aryl-2,3-dihydro-4H-1,3-benzothiazine-4-ketone derivatives and uses thereof |
CN105829301A (en) * | 2013-12-19 | 2016-08-03 | 吉利德科学公司 | Fused heterocyclic compounds as ion channel modulators |
Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2443M (en) * | 1962-10-30 | 1964-04-06 | Selvi & C Lab Bioterapico | Thio-derivatives of benzo-oxazine having antiphlogistic, antipyretic and analgesic properties. |
US3459748A (en) * | 1967-04-28 | 1969-08-05 | Squibb & Sons Inc | Hydroxyalkylene-substituted benzoxazines and benzothiazines |
GB2096612A (en) * | 1981-04-15 | 1982-10-20 | Coli Farma Lab | Esters of 2-(2-hydroxyethyl)-2,3-dihydro-4h-1,3-benzoxazin-4-one having analgesic activity |
EP0490183A1 (en) * | 1990-12-14 | 1992-06-17 | ITALFARMACO S.p.A. | Benzoxazinone and benzothiazinone derivatives endowed with cardiovascular activity |
EP0527081A1 (en) * | 1991-08-05 | 1993-02-10 | Pierre Fabre Medicament | Substituted 3-piperazinylalkyl-2,3-dihydro-4H-1,3-benzoxazine-4-ones, their preparation and their therapeutical use |
EP0566018A2 (en) * | 1992-04-16 | 1993-10-20 | ITALFARMACO S.p.A. | Benzoxazinone and benzothiazinone derivatives endowed with cardiovascular activity |
-
1993
- 1993-07-28 IT IT93MI001678A patent/IT1264812B1/en active IP Right Grant
-
1994
- 1994-07-18 AU AU74945/94A patent/AU7494594A/en not_active Abandoned
- 1994-07-18 HU HU9600165A patent/HUT74587A/en unknown
- 1994-07-18 CN CN94192889A patent/CN1128025A/en active Pending
- 1994-07-18 EP EP94924778A patent/EP0711286A1/en not_active Withdrawn
- 1994-07-18 WO PCT/EP1994/002354 patent/WO1995004048A1/en not_active Application Discontinuation
- 1994-07-18 JP JP7505529A patent/JPH09500878A/en active Pending
- 1994-07-18 CA CA002168099A patent/CA2168099A1/en not_active Abandoned
- 1994-07-27 IL IL11047394A patent/IL110473A0/en unknown
- 1994-07-27 TW TW083106854A patent/TW277061B/zh active
- 1994-07-27 ZA ZA945555A patent/ZA945555B/en unknown
-
1996
- 1996-01-25 NO NO960308A patent/NO960308L/en unknown
- 1996-01-25 FI FI960342A patent/FI960342A0/en not_active Application Discontinuation
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2443M (en) * | 1962-10-30 | 1964-04-06 | Selvi & C Lab Bioterapico | Thio-derivatives of benzo-oxazine having antiphlogistic, antipyretic and analgesic properties. |
US3459748A (en) * | 1967-04-28 | 1969-08-05 | Squibb & Sons Inc | Hydroxyalkylene-substituted benzoxazines and benzothiazines |
GB2096612A (en) * | 1981-04-15 | 1982-10-20 | Coli Farma Lab | Esters of 2-(2-hydroxyethyl)-2,3-dihydro-4h-1,3-benzoxazin-4-one having analgesic activity |
EP0490183A1 (en) * | 1990-12-14 | 1992-06-17 | ITALFARMACO S.p.A. | Benzoxazinone and benzothiazinone derivatives endowed with cardiovascular activity |
EP0527081A1 (en) * | 1991-08-05 | 1993-02-10 | Pierre Fabre Medicament | Substituted 3-piperazinylalkyl-2,3-dihydro-4H-1,3-benzoxazine-4-ones, their preparation and their therapeutical use |
EP0566018A2 (en) * | 1992-04-16 | 1993-10-20 | ITALFARMACO S.p.A. | Benzoxazinone and benzothiazinone derivatives endowed with cardiovascular activity |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2014036038A1 (en) * | 2012-08-27 | 2014-03-06 | University Of Tennessee Research Foundation | Lpa2 receptor-specific benzoic acid derivatives |
US9056835B2 (en) | 2012-08-27 | 2015-06-16 | The University Of Tennessee Research Foundation | LPA2 receptor-specific benzoic acid derivatives |
ITMI20122221A1 (en) * | 2012-12-21 | 2014-06-22 | C4T S C A R L | NEW COMPOUNDS OF 2,3-DIIDRO-4H-1,3-BENZOSSAZIN-4-ONE, METHOD FOR PREPARING THEM AND PHARMACEUTICAL FORM THAT INCLUDES THEM |
WO2014097188A1 (en) | 2012-12-21 | 2014-06-26 | C4T S.C. A.R.L. | Compounds of 2,3-dihydro-4h-1,3-benzoxazine-4-one, method for preparing them and pharmaceutical form comprising them |
Also Published As
Publication number | Publication date |
---|---|
NO960308L (en) | 1996-03-13 |
NO960308D0 (en) | 1996-01-25 |
FI960342A (en) | 1996-01-25 |
IT1264812B1 (en) | 1996-10-10 |
ITMI931678A0 (en) | 1993-07-28 |
CN1128025A (en) | 1996-07-31 |
HUT74587A (en) | 1997-01-28 |
TW277061B (en) | 1996-06-01 |
AU7494594A (en) | 1995-02-28 |
IL110473A0 (en) | 1994-10-21 |
CA2168099A1 (en) | 1995-02-09 |
JPH09500878A (en) | 1997-01-28 |
ZA945555B (en) | 1995-03-03 |
ITMI931678A1 (en) | 1995-01-28 |
FI960342A0 (en) | 1996-01-25 |
EP0711286A1 (en) | 1996-05-15 |
HU9600165D0 (en) | 1996-03-28 |
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