SK23498A3 - Synthesis of hydroxysulfone and related compounds - Google Patents
Synthesis of hydroxysulfone and related compounds Download PDFInfo
- Publication number
- SK23498A3 SK23498A3 SK234-98A SK23498A SK23498A3 SK 23498 A3 SK23498 A3 SK 23498A3 SK 23498 A SK23498 A SK 23498A SK 23498 A3 SK23498 A3 SK 23498A3
- Authority
- SK
- Slovakia
- Prior art keywords
- formula
- anhydride
- compound
- process according
- temperature
- Prior art date
Links
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 title claims abstract description 11
- 150000001875 compounds Chemical class 0.000 title claims description 22
- 230000015572 biosynthetic process Effects 0.000 title abstract description 4
- 238000003786 synthesis reaction Methods 0.000 title abstract description 4
- 238000000034 method Methods 0.000 claims abstract description 27
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 44
- QAEDZJGFFMLHHQ-UHFFFAOYSA-N trifluoroacetic anhydride Chemical group FC(F)(F)C(=O)OC(=O)C(F)(F)F QAEDZJGFFMLHHQ-UHFFFAOYSA-N 0.000 claims description 16
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 claims description 15
- 239000007800 oxidant agent Substances 0.000 claims description 13
- 150000008064 anhydrides Chemical class 0.000 claims description 10
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 10
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims description 8
- 239000002253 acid Substances 0.000 claims description 7
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims description 6
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 claims description 6
- 238000007254 oxidation reaction Methods 0.000 claims description 6
- 238000002360 preparation method Methods 0.000 claims description 6
- CIHOLLKRGTVIJN-UHFFFAOYSA-N tert‐butyl hydroperoxide Chemical compound CC(C)(C)OO CIHOLLKRGTVIJN-UHFFFAOYSA-N 0.000 claims description 6
- 230000003647 oxidation Effects 0.000 claims description 5
- 125000004183 alkoxy alkyl group Chemical group 0.000 claims description 4
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims description 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 4
- 235000011007 phosphoric acid Nutrition 0.000 claims description 4
- 239000002904 solvent Substances 0.000 claims description 4
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 claims description 3
- 150000007522 mineralic acids Chemical class 0.000 claims description 3
- VLTRZXGMWDSKGL-UHFFFAOYSA-M perchlorate Inorganic materials [O-]Cl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-M 0.000 claims description 3
- VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical compound OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 claims description 3
- KHIWWQKSHDUIBK-UHFFFAOYSA-N periodic acid Chemical compound OI(=O)(=O)=O KHIWWQKSHDUIBK-UHFFFAOYSA-N 0.000 claims description 3
- LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 claims description 3
- MEFKFJOEVLUFAY-UHFFFAOYSA-N (2,2,2-trichloroacetyl) 2,2,2-trichloroacetate Chemical compound ClC(Cl)(Cl)C(=O)OC(=O)C(Cl)(Cl)Cl MEFKFJOEVLUFAY-UHFFFAOYSA-N 0.000 claims description 2
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 2
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 claims description 2
- 229910000147 aluminium phosphate Inorganic materials 0.000 claims description 2
- 238000006056 electrooxidation reaction Methods 0.000 claims description 2
- 239000008096 xylene Substances 0.000 claims description 2
- HINSMVRGSUGPBM-UHFFFAOYSA-N acetyl 2,2,2-trifluoroacetate Chemical compound CC(=O)OC(=O)C(F)(F)F HINSMVRGSUGPBM-UHFFFAOYSA-N 0.000 claims 1
- HZKDMKLENBOQMC-UHFFFAOYSA-N acetyl 2-chloroacetate Chemical compound CC(=O)OC(=O)CCl HZKDMKLENBOQMC-UHFFFAOYSA-N 0.000 claims 1
- YWEUIGNSBFLMFL-UHFFFAOYSA-N diphosphonate Chemical compound O=P(=O)OP(=O)=O YWEUIGNSBFLMFL-UHFFFAOYSA-N 0.000 claims 1
- DLYUQMMRRRQYAE-UHFFFAOYSA-N phosphorus pentoxide Inorganic materials O1P(O2)(=O)OP3(=O)OP1(=O)OP2(=O)O3 DLYUQMMRRRQYAE-UHFFFAOYSA-N 0.000 claims 1
- 229920000137 polyphosphoric acid Polymers 0.000 claims 1
- 125000003944 tolyl group Chemical group 0.000 claims 1
- 208000010412 Glaucoma Diseases 0.000 abstract description 5
- 239000003489 carbonate dehydratase inhibitor Substances 0.000 abstract description 5
- 230000004406 elevated intraocular pressure Effects 0.000 abstract description 5
- IAVUPMFITXYVAF-XPUUQOCRSA-N dorzolamide Chemical compound CCN[C@H]1C[C@H](C)S(=O)(=O)C2=C1C=C(S(N)(=O)=O)S2 IAVUPMFITXYVAF-XPUUQOCRSA-N 0.000 abstract description 2
- 229960003933 dorzolamide Drugs 0.000 abstract description 2
- 229940006133 antiglaucoma drug and miotics carbonic anhydrase inhibitors Drugs 0.000 abstract 2
- 239000000243 solution Substances 0.000 description 19
- 238000006243 chemical reaction Methods 0.000 description 12
- 239000011541 reaction mixture Substances 0.000 description 11
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 10
- 239000000047 product Substances 0.000 description 10
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 9
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 8
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 6
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 6
- 229910052757 nitrogen Inorganic materials 0.000 description 5
- 125000004432 carbon atom Chemical group C* 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 229910001385 heavy metal Inorganic materials 0.000 description 4
- 239000000543 intermediate Substances 0.000 description 4
- 239000010410 layer Substances 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical group CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- 229940122072 Carbonic anhydrase inhibitor Drugs 0.000 description 3
- DWAQJAXMDSEUJJ-UHFFFAOYSA-M Sodium bisulfite Chemical compound [Na+].OS([O-])=O DWAQJAXMDSEUJJ-UHFFFAOYSA-M 0.000 description 3
- 229910052739 hydrogen Inorganic materials 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 235000010267 sodium hydrogen sulphite Nutrition 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 150000003462 sulfoxides Chemical class 0.000 description 3
- RGSFGYAAUTVSQA-UHFFFAOYSA-N Cyclopentane Chemical group C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- BZLVMXJERCGZMT-UHFFFAOYSA-N Methyl tert-butyl ether Chemical group COC(C)(C)C BZLVMXJERCGZMT-UHFFFAOYSA-N 0.000 description 2
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical group CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 2
- 241000223252 Rhodotorula Species 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical class C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- 239000008186 active pharmaceutical agent Substances 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 230000002051 biphasic effect Effects 0.000 description 2
- DKPFZGUDAPQIHT-UHFFFAOYSA-N butyl acetate Chemical group CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 239000012043 crude product Substances 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 239000003112 inhibitor Substances 0.000 description 2
- 230000004410 intraocular pressure Effects 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 230000014759 maintenance of location Effects 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 244000005700 microbiome Species 0.000 description 2
- 150000002978 peroxides Chemical class 0.000 description 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
- 238000006798 ring closing metathesis reaction Methods 0.000 description 2
- 238000007363 ring formation reaction Methods 0.000 description 2
- 235000010265 sodium sulphite Nutrition 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 150000003457 sulfones Chemical class 0.000 description 2
- 229910052717 sulfur Inorganic materials 0.000 description 2
- 238000011200 topical administration Methods 0.000 description 2
- 230000000699 topical effect Effects 0.000 description 2
- SIFFRIHCTBGQTC-LURJTMIESA-N (3s)-3-thiophen-2-ylsulfanylbutanoic acid Chemical compound OC(=O)C[C@H](C)SC1=CC=CS1 SIFFRIHCTBGQTC-LURJTMIESA-N 0.000 description 1
- YBFHILNBYXCJKD-UHFFFAOYSA-N 1-(6-methylpyridin-3-yl)-2-(4-methylsulfonylphenyl)ethanone Chemical compound C1=NC(C)=CC=C1C(=O)CC1=CC=C(S(C)(=O)=O)C=C1 YBFHILNBYXCJKD-UHFFFAOYSA-N 0.000 description 1
- 238000001644 13C nuclear magnetic resonance spectroscopy Methods 0.000 description 1
- 238000005160 1H NMR spectroscopy Methods 0.000 description 1
- ZWPJFUYDBVTBQI-UHFFFAOYSA-N 5h-thieno[3,2-b]thiopyran Chemical group C1=CCSC2=C1SC=C2 ZWPJFUYDBVTBQI-UHFFFAOYSA-N 0.000 description 1
- 241001508809 Ambrosiozyma Species 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
- SNHBGEDHHQFRLN-XPUUQOCRSA-N CCN[C@H]1C[C@H](C)Sc2sc(cc12)S(N)(=O)=O Chemical group CCN[C@H]1C[C@H](C)Sc2sc(cc12)S(N)(=O)=O SNHBGEDHHQFRLN-XPUUQOCRSA-N 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 1
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical group O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 1
- 208000018522 Gastrointestinal disease Diseases 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical group CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 1
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Chemical group CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 1
- 241000235003 Saccharomycopsis Species 0.000 description 1
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 1
- 239000000150 Sympathomimetic Substances 0.000 description 1
- SWEDAZLCYJDAGW-UHFFFAOYSA-N Thiophene-2-thiol Chemical compound SC1=CC=CS1 SWEDAZLCYJDAGW-UHFFFAOYSA-N 0.000 description 1
- JFBZPFYRPYOZCQ-UHFFFAOYSA-N [Li].[Al] Chemical compound [Li].[Al] JFBZPFYRPYOZCQ-UHFFFAOYSA-N 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 239000002671 adjuvant Substances 0.000 description 1
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical compound [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 description 1
- 230000036528 appetite Effects 0.000 description 1
- 235000019789 appetite Nutrition 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000002876 beta blocker Substances 0.000 description 1
- 229940097320 beta blocking agent Drugs 0.000 description 1
- SIPUZPBQZHNSDW-UHFFFAOYSA-N bis(2-methylpropyl)aluminum Chemical compound CC(C)C[Al]CC(C)C SIPUZPBQZHNSDW-UHFFFAOYSA-N 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000001110 calcium chloride Substances 0.000 description 1
- 229910001628 calcium chloride Inorganic materials 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 239000000544 cholinesterase inhibitor Substances 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 238000004817 gas chromatography Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- DMEGYFMYUHOHGS-UHFFFAOYSA-N heptamethylene Chemical group C1CCCCCC1 DMEGYFMYUHOHGS-UHFFFAOYSA-N 0.000 description 1
- 238000004128 high performance liquid chromatography Methods 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 239000012280 lithium aluminium hydride Substances 0.000 description 1
- -1 lithium aluminum hydride Chemical compound 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- SYSQUGFVNFXIIT-UHFFFAOYSA-N n-[4-(1,3-benzoxazol-2-yl)phenyl]-4-nitrobenzenesulfonamide Chemical class C1=CC([N+](=O)[O-])=CC=C1S(=O)(=O)NC1=CC=C(C=2OC3=CC=CC=C3N=2)C=C1 SYSQUGFVNFXIIT-UHFFFAOYSA-N 0.000 description 1
- 239000012038 nucleophile Substances 0.000 description 1
- 210000000056 organ Anatomy 0.000 description 1
- 239000012044 organic layer Substances 0.000 description 1
- 239000000734 parasympathomimetic agent Substances 0.000 description 1
- 208000035824 paresthesia Diseases 0.000 description 1
- 150000004965 peroxy acids Chemical class 0.000 description 1
- 239000003208 petroleum Chemical group 0.000 description 1
- 239000004810 polytetrafluoroethylene Substances 0.000 description 1
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 239000004289 sodium hydrogen sulphite Substances 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 229940127230 sympathomimetic drug Drugs 0.000 description 1
- 229940066528 trichloroacetate Drugs 0.000 description 1
- YNJBWRMUSHSURL-UHFFFAOYSA-N trichloroacetic acid Chemical compound OC(=O)C(Cl)(Cl)Cl YNJBWRMUSHSURL-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
- C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D495/04—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Plural Heterocyclic Compounds (AREA)
- Casings For Electric Apparatus (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US289095P | 1995-08-29 | 1995-08-29 | |
| GBGB9602852.7A GB9602852D0 (en) | 1996-02-13 | 1996-02-13 | Synthesis of hydroxysulfone and related compounds |
| PCT/US1996/013634 WO1997008173A1 (en) | 1995-08-29 | 1996-08-26 | Synthesis of hydroxysulfone and related compounds |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SK23498A3 true SK23498A3 (en) | 1998-08-05 |
Family
ID=26308662
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SK234-98A SK23498A3 (en) | 1995-08-29 | 1996-08-26 | Synthesis of hydroxysulfone and related compounds |
Country Status (22)
| Country | Link |
|---|---|
| EP (1) | EP0853625B1 (de) |
| JP (1) | JP3396484B2 (de) |
| KR (1) | KR100297188B1 (de) |
| CN (1) | CN1200125A (de) |
| AT (1) | ATE208394T1 (de) |
| AU (1) | AU705740B2 (de) |
| BR (1) | BR9610282A (de) |
| CA (1) | CA2229233C (de) |
| CZ (1) | CZ59698A3 (de) |
| DE (1) | DE69616811T2 (de) |
| DK (1) | DK0853625T3 (de) |
| EA (1) | EA001246B1 (de) |
| ES (1) | ES2163650T3 (de) |
| HU (1) | HUP9901543A3 (de) |
| NZ (1) | NZ315966A (de) |
| PL (1) | PL325120A1 (de) |
| PT (1) | PT853625E (de) |
| RO (1) | RO119148B1 (de) |
| SK (1) | SK23498A3 (de) |
| TW (1) | TW432067B (de) |
| UA (1) | UA52619C2 (de) |
| WO (1) | WO1997008173A1 (de) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2128161A1 (de) * | 2008-05-30 | 2009-12-02 | Ragactives, S.L. | Verfahren zur Gewinnung von 4-Hydroxy-6-Methyl-5,6-Dihydro-4H-Thieno[2,3-b]Thiopyran-7,7-Dioxid und seinen Enantiomeren sowie Verwendung dafür |
| CN108822127B (zh) * | 2018-05-30 | 2020-05-15 | 沈阳药科大学 | 4-羟亚胺基噻吩并[2,3-b]噻喃-2-甲酰胺类化合物及其用途 |
| CN108822125B (zh) * | 2018-05-30 | 2020-01-31 | 沈阳药科大学 | 1-(噻吩并[2,3-b]噻喃甲酰基)-4-脂肪烃基哌嗪类化合物及其医药用途 |
-
1996
- 1996-08-23 TW TW085110312A patent/TW432067B/zh active
- 1996-08-26 CN CN96197718A patent/CN1200125A/zh active Pending
- 1996-08-26 JP JP51045497A patent/JP3396484B2/ja not_active Expired - Fee Related
- 1996-08-26 BR BR9610282A patent/BR9610282A/pt not_active Application Discontinuation
- 1996-08-26 NZ NZ315966A patent/NZ315966A/xx unknown
- 1996-08-26 WO PCT/US1996/013634 patent/WO1997008173A1/en not_active Application Discontinuation
- 1996-08-26 CZ CZ98596A patent/CZ59698A3/cs unknown
- 1996-08-26 SK SK234-98A patent/SK23498A3/sk unknown
- 1996-08-26 UA UA98031547A patent/UA52619C2/uk unknown
- 1996-08-26 AU AU67803/96A patent/AU705740B2/en not_active Ceased
- 1996-08-26 DE DE69616811T patent/DE69616811T2/de not_active Expired - Lifetime
- 1996-08-26 PT PT96928260T patent/PT853625E/pt unknown
- 1996-08-26 PL PL96325120A patent/PL325120A1/xx unknown
- 1996-08-26 KR KR1019980701448A patent/KR100297188B1/ko not_active IP Right Cessation
- 1996-08-26 AT AT96928260T patent/ATE208394T1/de active
- 1996-08-26 HU HU9901543A patent/HUP9901543A3/hu unknown
- 1996-08-26 DK DK96928260T patent/DK0853625T3/da active
- 1996-08-26 EP EP96928260A patent/EP0853625B1/de not_active Expired - Lifetime
- 1996-08-26 EA EA199800236A patent/EA001246B1/ru not_active IP Right Cessation
- 1996-08-26 RO RO98-00294A patent/RO119148B1/ro unknown
- 1996-08-26 ES ES96928260T patent/ES2163650T3/es not_active Expired - Lifetime
- 1996-08-26 CA CA002229233A patent/CA2229233C/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| ATE208394T1 (de) | 2001-11-15 |
| JP3396484B2 (ja) | 2003-04-14 |
| HUP9901543A3 (en) | 2000-03-28 |
| EP0853625A1 (de) | 1998-07-22 |
| UA52619C2 (uk) | 2003-01-15 |
| DE69616811D1 (de) | 2001-12-13 |
| WO1997008173A1 (en) | 1997-03-06 |
| HUP9901543A1 (hu) | 1999-09-28 |
| AU705740B2 (en) | 1999-06-03 |
| CN1200125A (zh) | 1998-11-25 |
| ES2163650T3 (es) | 2002-02-01 |
| EP0853625B1 (de) | 2001-11-07 |
| CA2229233A1 (en) | 1997-03-06 |
| EA001246B1 (ru) | 2000-12-25 |
| PL325120A1 (en) | 1998-07-06 |
| CZ59698A3 (cs) | 1998-07-15 |
| DE69616811T2 (de) | 2002-05-29 |
| KR100297188B1 (ko) | 2001-10-26 |
| TW432067B (en) | 2001-05-01 |
| RO119148B1 (ro) | 2004-04-30 |
| EA199800236A1 (ru) | 1998-10-29 |
| KR19990044212A (ko) | 1999-06-25 |
| CA2229233C (en) | 2003-10-07 |
| DK0853625T3 (da) | 2001-12-27 |
| PT853625E (pt) | 2002-03-28 |
| JPH11510190A (ja) | 1999-09-07 |
| BR9610282A (pt) | 1999-03-16 |
| NZ315966A (en) | 1999-11-29 |
| AU6780396A (en) | 1997-03-19 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| NO20151341A1 (no) | Prostaglandinnitrooksyderivater | |
| CA2264045A1 (en) | Heterocyclic metalloprotease inhibitors | |
| EP0391799B1 (de) | Von benzocyclischen oder benzoheterocyclischen Säuren abgeleitete Sulfonamide, ihre Herstellung und ihre Anwendung in der Heilkunde | |
| KR100225927B1 (ko) | 콜린에스테라제 저해제로서의 제네세린 유도체 | |
| SK281184B6 (sk) | Substituovaný sulfónamid, farmaceutická kompozícia na jeho báze a spôsob jeho prípravy | |
| US5859036A (en) | 3,4-diarylthiazolin-2-one or -2-thione derivatives, their methods of preparation and their uses in their methods of preparation and their uses in therapeutics | |
| FR2566404A1 (fr) | Nouveaux derives de la 1,4-dihydropyridine, leurs sels, procede pour les preparer, et compositions pharmaceutiques les contenant | |
| US5760249A (en) | Synthesis of hydroxysulfone and related compounds | |
| US4968815A (en) | Synthesis of (S)-3-(thien-2-ylthio)butyric acid analogs | |
| SK23498A3 (en) | Synthesis of hydroxysulfone and related compounds | |
| EP0348257A2 (de) | (Hetero)Aryl-diazol-Derivate, Verfahren zu deren Herstellung und deren Verwendung in der Therapie | |
| CA2112871A1 (fr) | Procede de preparation de derives soufres de l'imidazole et les nouveaux intermediaires obtenus | |
| US4157340A (en) | N,N'-[Bis(N-cyanoguanyl)]cystamine derivatives | |
| AU704210B2 (en) | Synthesis of (S)-3-(2-thienylthio) butyric acid and analogs | |
| LU82290A1 (fr) | Procede de preparation de sulfoxydes de penicilline | |
| JPH0641068A (ja) | インドリン誘導体およびアレルギー性または炎症性疾患治療用組成物 | |
| JPH0320264A (ja) | ジェム置換チア複素環式カルボン酸およびその誘導体 | |
| HUT55372A (en) | Process for producing substituted isoxazole and isothiazole derivatives | |
| AU637938B2 (en) | Phenoxyacetic acid compounds, method for production thereof, and pharmaceutical preparations containing same | |
| EP0412898A1 (de) | Oxazolopyridinderivate, Verfahren zu ihrer Herstellung und diese enthaltende pharmazeutische Zubereitungen | |
| KR100449793B1 (ko) | 하이드라진 유도체 | |
| CA2022460A1 (fr) | Derives benzothiaziniques, leur preparation et leurs applications comme medicaments ou comme intermediaires de synthese de medicaments | |
| SU367601A1 (de) | ||
| EP0113600B1 (de) | Gamma-Butyrolactonderivate mit herzmuskelschonender und antiarrhythmischer Wirkung, Verfahren zu ihrer Herstellung und sie enthaltende Arzneimittel | |
| JPS649980B2 (de) |