Patent US4451475A successfully refreshed from Google Patents.
US4451475A
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Cyclic sulphenamide compounds, their production and their medicinal use
Assignee: Bayer AG
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Filing: 1982-04-14
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Granted: 1984-05-29
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Expires: 2002-04-14
Abstract
Abstract The invention relates to cyclic sulphenamides of Formula I and methods for their manufacture. Also included in the invention are compositions containing said cyclic sulphenamides and methods for the use of said compounds and compositions as lipoxygenase inhibitors.
Inventors
- 👤 Wolf-Dieter Busse
- 👤 Edmund Krauthausen
- 👤 Mithat Mardin
Bibliographic Details
Application Number
—
Jurisdiction
US
Data Source
google_patents
Last Synchronized
2026-10-29 21:59
CPC Classifications
C; C07; C07D; C07D263/00; C07D263/52; C07D263/54; C07D263/58; A; A61; A61P; A61P29/00; A61P37/00; A61P37/08; A61P43/00; C07D263/02; C07D263/08; C07D263/16; C07D263/18; C07D263/20; C07D263/26; C07D277/00; C07D277/02; C07D277/08; C07D277/12; C07D277/14; C07D277/20; C07D277/32; C07D277/34
Claims Analysis
Total Claims: 19
Claim 1
Independent Claim
469 words
A compound which is a sulphenamides of the formula ##STR4## wherein Z denotes oxygen or sulphur, R 1 represents a radical of the general formula ##STR5## wherein Z has the abovementioned meaning and R 1 to R 5 have the meanings given below, and Q represents an alkylene radical with 1 to 12 carbon atoms, in which the alkylene radical is optionally interrupted by one or more oxygen, sulphur or nitrogen atoms, or represents a cycloalkylene radical with 5 to 12 carbon atoms, arylene with 6 to 10 carbon atoms or an alkylene-cyclo-alkylene-alkylene or alkylene-arylene-alkylene radical, or R 1 represents an alkenyl or alkynyl group with 2 to 12 carbon atoms, an aralkyl group with 7 to 11 carbon atoms, a cycloalkyl group with 5 to 8 carbon atoms or an aryl group with 6 to 14 carbon atoms; each of the abovementioned groups optionally being substituted by up to 5 identical or different substituents selected from alkoxy, alkyl, aralkyl, cycloalkyl, aryl, aryloxy, arylthio, alkylthio, carboxyl, carbalkoxy, cyano, carbamoyl, sulphonyl, halogenoalkyl, halogenoalkoxy, halogen, amino and amino by C 1 -C 4 -alkyl or benzyl, and each R 2 and R 5 represent, independently of each other, a hydrogen atom, an alkyl group with 1 to 8 carbon atoms, a cycloalkyl group, with 5 to 8 carbon atoms, an aralkyl group with 7 to 10 carbon atoms, an aryl group with 6 or 10 carbon atoms, an alkoxy group with 1 to 12 carbon atoms, an aralkoxy group with 7 to 10 carbon atoms, an aryloxy group with 6 or 10 carbon atoms, an alkylthio group with 1 to 12 carbon atoms, a benzylthio group, an arylthio group with 6 or 10 carbon atoms, or an amino group which is substituted by alkyl, benzyl and/or aryl, or R 2 together with R 4 forms a direct bond or an alkylene radical with 3 to 6 carbon atoms, or R 2 and R 3 together represent an alkylidene radical with 1 to 4 carbon atoms, an aralkylidene radical with 7 to 10 carbon atoms, or an oxo, thiono or imino radical, or the radicals R 2 and R 3 , together with the carbon atoms to which they are bonded, form a cycloalkyl radical with 5 to 8 ring members, or R 4 and R 5 together represent an alkylidene radical with 1 to 4 carbon atoms, an aralkylidene radical with 7 to 10 carbon atoms, or an oxo or imino radical, or the radicals R 4 and R 5 or R 2 and R 3 , together with the carbon atom to which they are bonded, form a cycloalkyl radical with 5 to 8 ring members, or the radicals R 2 to R 5 , together with the carbon atoms to which they are bonded, form an, fused-on benzene ring.
Claim 2
Dependent Claim
469 words
A compound which is a sulphenamides of the formula ##STR4## wherein Z denotes oxygen or sulphur, R 1 represents a radical of the general formula ##STR5## wherein Z has the abovementioned meaning and R 1 to R 5 have the meanings given below, and Q represents an alkylene radical with 1 to 12 carbon atoms, in which the alkylene radical is optionally interrupted by one or more oxygen, sulphur or nitrogen atoms, or represents a cycloalkylene radical with 5 to 12 carbon atoms, arylene with 6 to 10 carbon atoms or an alkylene-cyclo-alkylene-alkylene or alkylene-arylene-alkylene radical, or R 1 represents an alkenyl or alkynyl group with 2 to 12 carbon atoms, an aralkyl group with 7 to 11 carbon atoms, a cycloalkyl group with 5 to 8 carbon atoms or an aryl group with 6 to 14 carbon atoms; each of the abovementioned groups optionally being substituted by up to 5 identical or different substituents selected from alkoxy, alkyl, aralkyl, cycloalkyl, aryl, aryloxy, arylthio, alkylthio, carboxyl, carbalkoxy, cyano, carbamoyl, sulphonyl, halogenoalkyl, halogenoalkoxy, halogen, amino and amino by C 1 -C 4 -alkyl or benzyl, and each R 2 and R 5 represent, independently of each other, a hydrogen atom, an alkyl group with 1 to 8 carbon atoms, a cycloalkyl group, with 5 to 8 carbon atoms, an aralkyl group with 7 to 10 carbon atoms, an aryl group with 6 or 10 carbon atoms, an alkoxy group with 1 to 12 carbon atoms, an aralkoxy group with 7 to 10 carbon atoms, an aryloxy group with 6 or 10 carbon atoms, an alkylthio group with 1 to 12 carbon atoms, a benzylthio group, an arylthio group with 6 or 10 carbon atoms, or an amino group which is substituted by alkyl, benzyl and/or aryl, or R 2 together with R 4 forms a direct bond or an alkylene radical with 3 to 6 carbon atoms, or R 2 and R 3 together represent an alkylidene radical with 1 to 4 carbon atoms, an aralkylidene radical with 7 to 10 carbon atoms, or an oxo, thiono or imino radical, or the radicals R 2 and R 3 , together with the carbon atoms to which they are bonded, form a cycloalkyl radical with 5 to 8 ring members, or R 4 and R 5 together represent an alkylidene radical with 1 to 4 carbon atoms, an aralkylidene radical with 7 to 10 carbon atoms, or an oxo or imino radical, or the radicals R 4 and R 5 or R 2 and R 3 , together with the carbon atom to which they are bonded, form a cycloalkyl radical with 5 to 8 ring members, or the radicals R 2 to R 5 , together with the carbon atoms to which they are bonded, form an, fused-on benzene ring.
Claim 3
Dependent Claim
46 words
A compound according to claim 1, in which R 2 to R 5 have the same meaning as in claim 1, except that R 2 to R 5 , together with the carbon atoms to which they are bonded do not form the, fused-on benzene ring.
Claim 4
Dependent Claim
180 words
A compound according to claim 1, in which Z has the same meaning as in claim 1, R 1 represents a cycloalkyl group with 5 to 8 carbon atoms or an aryl group with 6 to 14 carbon atoms; each of the abovementioned groups optionally being substituted by up to 5 identical or different substituents selected from alkyl and alkoxy with in each case 1 to 4 carbon atoms, aralkyl with 7 to 10 carbon atoms, cycloalkyl with 5 to 7 carbon atoms, phenyl, phenoxy, phenylthio, alkylthio with 1 to 4 carbon atoms, carboxyl, carbalkoxy with 1 to 4 carbon atoms, cyano, trifluoromethyl, trifluoromethoxy, fluorine, chlorine, bromine, amino, alkyl-substituted amino and benzyl-substituted amino, the alkyl substituent(s) of amino carrying 1 to 4 carbon atoms, and R 2 to R 5 represents, independently of one another, a hydrogen atom, an alkyl group with 1 to 4 carbon atoms or a phenyl group, or R 2 forms a direct bond with R 4 , or R 2 and R 3 , or R 4 and R 5 together represent an oxo group.
Claim 5
Dependent Claim
121 words
A compound according to claim 1 in which Z represents oxygen R 1 represents an aryl radical which has 6 or 10 carbon atoms and is optionally substituted by 1 or 2 identical or different substituents selected from alkyl and alkoxy with in each case 1 to 4 carbon atoms, aralkyl with 7 to 10 carbon atoms, cycloalkyl with 5 to 7 carbon atoms, phenyl, phenoxy, phenylthio, alkylthio with 1 to 4 carbon atoms, carbalkoxy with 1 to 4 carbon atoms, cyano, trifluoromethyl, trifluoromethoxy, fluorine, chlorine, bromine, alkyl-substituted amino and benzyl-substituted amino, the alkyl substituent(s) of amino carrying 1 to 4 carbon atoms and R 2 to R 5 represent, independently of one another, a methyl group or a hydrogen atom.
Claim 6
Dependent Claim
8 words
A compound of claim 1 which is 3-phenylithooxazolidin-2-one.
Claim 7
Dependent Claim
8 words
A compound of claim 1 which is 3-(4-chlorophenoxythio)-oxazolidin-2-one.
Claim 8
Dependent Claim
8 words
A compound of claim 1 which is 3-(4-tert.-butylphenylthio)-oxazolidin-2-one.
Claim 9
Dependent Claim
8 words
A compound of claim 1 which is 3-(4-fluorophenylthio)-oxazolidin-2-one.
Claim 10
Dependent Claim
8 words
A compound of claim 1 which is 3-(4-chlorophenylthio)-4-phenyl-thiazolin-2-one.
Claim 11
Dependent Claim
8 words
A compound of claim 1 which is 3-(4-fluorophenylthio)-benzoxazolin-2-one.
Claim 12
Dependent Claim
21 words
A pharmaceutical composition containing as an active ingredient a compound according to claim 1 in admixture with an inert pharmaceutical carrier.
Claim 13
Dependent Claim
35 words
A pharmaceutical composition of claim 11 containing as an active ingredient a compound according to claim 1 in admixture with an inert pharmaceutical carrier in the form of a steril or physiologically isotonic aqueous solution.
Claim 14
Dependent Claim
20 words
A composition according to claim 11 or 12 containing from 0.5 to 95% by weight of the said active ingredient.
Claim 15
Dependent Claim
17 words
A medicament in dosage unit form comprising a lipoxygenase-inhibiting amount of a compound according to claim 1.
Claim 16
Dependent Claim
16 words
A medicament of claim 14 in the form of tablets, pills, dragees, capsules, ampoules, or suppositories.
Claim 17
Dependent Claim
39 words
A method of combating inflammatory or allergic processes in warm-blooded animals which comprises administering to the animals a active compound according to claim 1 either alone or in admixture with a diluent or in the form of a medicament.
Claim 18
Dependent Claim
28 words
A method according to claim 16 in which the active compound is administered intravenously in an amount of 0.01 to 10 mg per kg body weight per day.
Claim 19
Dependent Claim
28 words
A method according to claim 16 in which the active compound is administered orally in an amount of 0.05 to 100 mg per kg body weight per day.
References Cited (Backward Citations)
USPTO Annuity & Maintenance Windows
| Annuity Stage | Window Opens | Payment Deadline | Surcharge Period Until | Estimated Fee | Status |
|---|---|---|---|---|---|
| 3.5 Years (Year 4) | 1987-05-29 | 1987-11-28 | 1988-05-29 | $2000.00 | Window Closed / Lapsed |
| 7.5 Years (Year 8) | 1991-05-29 | 1991-11-28 | 1992-05-29 | $3760.00 | Window Closed / Lapsed |
| 11.5 Years (Year 12) | 1995-05-29 | 1995-11-28 | 1996-05-29 | $7700.00 | Window Closed / Lapsed |