IE35897B1 - Azapurinones - Google Patents
AzapurinonesInfo
- Publication number
- IE35897B1 IE35897B1 IE1583/71A IE158371A IE35897B1 IE 35897 B1 IE35897 B1 IE 35897B1 IE 1583/71 A IE1583/71 A IE 1583/71A IE 158371 A IE158371 A IE 158371A IE 35897 B1 IE35897 B1 IE 35897B1
- Authority
- IE
- Ireland
- Prior art keywords
- compounds
- prepared
- reaction
- reacting
- triazole
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 abstract 52
- 238000006243 chemical reaction Methods 0.000 abstract 24
- 125000000217 alkyl group Chemical group 0.000 abstract 7
- 125000003545 alkoxy group Chemical group 0.000 abstract 5
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 abstract 4
- -1 aralkoxy Chemical group 0.000 abstract 4
- 125000001475 halogen functional group Chemical group 0.000 abstract 4
- MNKBSXULTGYFFR-UHFFFAOYSA-N 5-amino-2h-triazole-4-carboxamide Chemical compound NC(=O)C1=NNN=C1N MNKBSXULTGYFFR-UHFFFAOYSA-N 0.000 abstract 3
- IOVCWXUNBOPUCH-UHFFFAOYSA-N Nitrous acid Chemical compound ON=O IOVCWXUNBOPUCH-UHFFFAOYSA-N 0.000 abstract 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 3
- NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 abstract 2
- SPSJTSUTONSWEX-UHFFFAOYSA-N 5-amino-1-benzyltriazole-4-carboxamide Chemical compound NC1=C(C(=O)N)N=NN1CC1=CC=CC=C1 SPSJTSUTONSWEX-UHFFFAOYSA-N 0.000 abstract 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 2
- SKZKKFZAGNVIMN-UHFFFAOYSA-N Salicilamide Chemical compound NC(=O)C1=CC=CC=C1O SKZKKFZAGNVIMN-UHFFFAOYSA-N 0.000 abstract 2
- 229910021529 ammonia Inorganic materials 0.000 abstract 2
- 150000001450 anions Chemical class 0.000 abstract 2
- 125000001589 carboacyl group Chemical group 0.000 abstract 2
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 2
- VAYGXNSJCAHWJZ-UHFFFAOYSA-N dimethyl sulfate Chemical compound COS(=O)(=O)OC VAYGXNSJCAHWJZ-UHFFFAOYSA-N 0.000 abstract 2
- DNJIEGIFACGWOD-UHFFFAOYSA-N ethanethiol Chemical compound CCS DNJIEGIFACGWOD-UHFFFAOYSA-N 0.000 abstract 2
- ZIUSEGSNTOUIPT-UHFFFAOYSA-N ethyl 2-cyanoacetate Chemical compound CCOC(=O)CC#N ZIUSEGSNTOUIPT-UHFFFAOYSA-N 0.000 abstract 2
- 229960000581 salicylamide Drugs 0.000 abstract 2
- UHJCPTUYASMZRC-UHFFFAOYSA-N 1,3-benzodioxole-4-carboxamide Chemical compound NC(=O)C1=CC=CC2=C1OCO2 UHJCPTUYASMZRC-UHFFFAOYSA-N 0.000 abstract 1
- RXQVZWBAGZJXSY-UHFFFAOYSA-N 1-benzyl-5-formamidotriazole-4-carboxamide Chemical compound O=CNC1=C(C(=O)N)N=NN1CC1=CC=CC=C1 RXQVZWBAGZJXSY-UHFFFAOYSA-N 0.000 abstract 1
- BGISLJFFULMEBF-UHFFFAOYSA-N 1-benzyl-n-(3-methylbutanoyl)-5-(3-methylbutanoylamino)triazole-4-carboxamide Chemical compound CC(C)CC(=O)NC1=C(C(=O)NC(=O)CC(C)C)N=NN1CC1=CC=CC=C1 BGISLJFFULMEBF-UHFFFAOYSA-N 0.000 abstract 1
- HLVFKOKELQSXIQ-UHFFFAOYSA-N 1-bromo-2-methylpropane Chemical compound CC(C)CBr HLVFKOKELQSXIQ-UHFFFAOYSA-N 0.000 abstract 1
- MYMSJFSOOQERIO-UHFFFAOYSA-N 1-bromodecane Chemical compound CCCCCCCCCCBr MYMSJFSOOQERIO-UHFFFAOYSA-N 0.000 abstract 1
- WNVCQNAHZHTDQI-UHFFFAOYSA-N 2,5-bis(phenylmethoxy)benzamide Chemical compound C=1C=C(OCC=2C=CC=CC=2)C(C(=O)N)=CC=1OCC1=CC=CC=C1 WNVCQNAHZHTDQI-UHFFFAOYSA-N 0.000 abstract 1
- FVPWCKBAQIZSFS-UHFFFAOYSA-N 2-(2-methylpropoxy)benzamide Chemical compound CC(C)COC1=CC=CC=C1C(N)=O FVPWCKBAQIZSFS-UHFFFAOYSA-N 0.000 abstract 1
- JIJWMCODIIBUSA-UHFFFAOYSA-N 2-(4-methoxyphenoxy)benzamide Chemical compound C1=CC(OC)=CC=C1OC1=CC=CC=C1C(N)=O JIJWMCODIIBUSA-UHFFFAOYSA-N 0.000 abstract 1
- ICEINTPQBJRYDE-UHFFFAOYSA-N 2-bromo-5-(trifluoromethyl)benzonitrile Chemical compound FC(F)(F)C1=CC=C(Br)C(C#N)=C1 ICEINTPQBJRYDE-UHFFFAOYSA-N 0.000 abstract 1
- XBAKLNIZALFPMK-UHFFFAOYSA-N 2-butylsulfanylbenzoic acid Chemical compound CCCCSC1=CC=CC=C1C(O)=O XBAKLNIZALFPMK-UHFFFAOYSA-N 0.000 abstract 1
- LKOWLXLHBFLWJB-UHFFFAOYSA-N 2-butylsulfonylbenzamide Chemical compound CCCCS(=O)(=O)C1=CC=CC=C1C(N)=O LKOWLXLHBFLWJB-UHFFFAOYSA-N 0.000 abstract 1
- RHHIBSFKGKUZBX-UHFFFAOYSA-N 2-butylsulfonylbenzoic acid Chemical compound CCCCS(=O)(=O)C1=CC=CC=C1C(O)=O RHHIBSFKGKUZBX-UHFFFAOYSA-N 0.000 abstract 1
- RHXCIWRRFMVVLI-UHFFFAOYSA-N 2-decoxybenzamide Chemical compound CCCCCCCCCCOC1=CC=CC=C1C(N)=O RHXCIWRRFMVVLI-UHFFFAOYSA-N 0.000 abstract 1
- MCFGYHKPYCQXJH-UHFFFAOYSA-N 2-hydroxy-3,5-dimethylbenzoic acid Chemical compound CC1=CC(C)=C(O)C(C(O)=O)=C1 MCFGYHKPYCQXJH-UHFFFAOYSA-N 0.000 abstract 1
- YNAXKCRTFJQYDT-UHFFFAOYSA-N 2-hydroxy-5-methylbenzamide Chemical compound CC1=CC=C(O)C(C(N)=O)=C1 YNAXKCRTFJQYDT-UHFFFAOYSA-N 0.000 abstract 1
- PNERJPORNFOLIT-UHFFFAOYSA-N 2-hydroxy-5-phenylmethoxybenzoic acid Chemical compound C1=C(O)C(C(=O)O)=CC(OCC=2C=CC=CC=2)=C1 PNERJPORNFOLIT-UHFFFAOYSA-N 0.000 abstract 1
- OEIJFITVPJVPFC-UHFFFAOYSA-N 2-methoxy-3,5-dimethylbenzamide Chemical compound COC1=C(C)C=C(C)C=C1C(N)=O OEIJFITVPJVPFC-UHFFFAOYSA-N 0.000 abstract 1
- WEUQEKDZMFUQFT-UHFFFAOYSA-N 2-methoxy-3,5-dimethylbenzoic acid Chemical compound COC1=C(C)C=C(C)C=C1C(O)=O WEUQEKDZMFUQFT-UHFFFAOYSA-N 0.000 abstract 1
- CITXHLJVRBQDKP-UHFFFAOYSA-N 2-methoxy-4-phenylmethoxybenzamide Chemical compound C1=C(C(N)=O)C(OC)=CC(OCC=2C=CC=CC=2)=C1 CITXHLJVRBQDKP-UHFFFAOYSA-N 0.000 abstract 1
- KAJZODLWVHKBSI-UHFFFAOYSA-N 2-methoxy-5-(trifluoromethyl)benzonitrile Chemical compound COC1=CC=C(C(F)(F)F)C=C1C#N KAJZODLWVHKBSI-UHFFFAOYSA-N 0.000 abstract 1
- UNLCCNOMAQCSGD-UHFFFAOYSA-N 2-methoxy-5-phenylmethoxybenzoic acid Chemical compound C1=C(C(O)=O)C(OC)=CC=C1OCC1=CC=CC=C1 UNLCCNOMAQCSGD-UHFFFAOYSA-N 0.000 abstract 1
- RZNHSEZOLFEFGB-UHFFFAOYSA-N 2-methoxybenzoyl chloride Chemical compound COC1=CC=CC=C1C(Cl)=O RZNHSEZOLFEFGB-UHFFFAOYSA-N 0.000 abstract 1
- BNMAPENIBVRJMZ-UHFFFAOYSA-N 2-methylpropanimidamide;sulfuric acid Chemical compound OS(O)(=O)=O.CC(C)C(N)=N BNMAPENIBVRJMZ-UHFFFAOYSA-N 0.000 abstract 1
- CJKJNTJPOYSDQL-UHFFFAOYSA-N 2-methylsulfonylbenzamide Chemical compound CS(=O)(=O)C1=CC=CC=C1C(N)=O CJKJNTJPOYSDQL-UHFFFAOYSA-N 0.000 abstract 1
- HBMNLIUYGBEWRG-UHFFFAOYSA-N 5-amino-1-benzyl-n-methyltriazole-4-carboxamide Chemical compound NC1=C(C(=O)NC)N=NN1CC1=CC=CC=C1 HBMNLIUYGBEWRG-UHFFFAOYSA-N 0.000 abstract 1
- UIAACPLFXIYDHE-UHFFFAOYSA-N 5-benzamido-1-benzyltriazole-4-carboxamide Chemical compound C=1C=CC=CC=1C(=O)NC1=C(C(=O)N)N=NN1CC1=CC=CC=C1 UIAACPLFXIYDHE-UHFFFAOYSA-N 0.000 abstract 1
- GNVPJDKGTPCPQE-UHFFFAOYSA-N 5-benzamido-n-benzoyl-1-benzyltriazole-4-carboxamide Chemical compound N1=NN(CC=2C=CC=CC=2)C(NC(=O)C=2C=CC=CC=2)=C1C(=O)NC(=O)C1=CC=CC=C1 GNVPJDKGTPCPQE-UHFFFAOYSA-N 0.000 abstract 1
- HLYNVXXFYXVMCD-UHFFFAOYSA-N 5-methyl-2-propoxybenzamide Chemical compound CCCOC1=CC=C(C)C=C1C(N)=O HLYNVXXFYXVMCD-UHFFFAOYSA-N 0.000 abstract 1
- XWWHEVCXDNAOKH-UHFFFAOYSA-N 5-tert-butyl-2-methoxybenzonitrile Chemical compound COC1=CC=C(C(C)(C)C)C=C1C#N XWWHEVCXDNAOKH-UHFFFAOYSA-N 0.000 abstract 1
- XZLIYCQRASOFQM-UHFFFAOYSA-N 5h-imidazo[4,5-d]triazine Chemical group N1=NC=C2NC=NC2=N1 XZLIYCQRASOFQM-UHFFFAOYSA-N 0.000 abstract 1
- OROLSQGHDGQZTH-UHFFFAOYSA-N 6-amino-2-propan-2-yl-1h-pyrimidin-4-one Chemical compound CC(C)C1=NC(N)=CC(=O)N1 OROLSQGHDGQZTH-UHFFFAOYSA-N 0.000 abstract 1
- QXNVGIXVLWOKEQ-UHFFFAOYSA-N Disodium Chemical class [Na][Na] QXNVGIXVLWOKEQ-UHFFFAOYSA-N 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- 150000007513 acids Chemical class 0.000 abstract 1
- 230000001476 alcoholic effect Effects 0.000 abstract 1
- 229910052783 alkali metal Inorganic materials 0.000 abstract 1
- 125000003342 alkenyl group Chemical group 0.000 abstract 1
- 125000003302 alkenyloxy group Chemical group 0.000 abstract 1
- 125000005083 alkoxyalkoxy group Chemical group 0.000 abstract 1
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 1
- 125000004414 alkyl thio group Chemical group 0.000 abstract 1
- 125000000304 alkynyl group Chemical group 0.000 abstract 1
- 125000005133 alkynyloxy group Chemical group 0.000 abstract 1
- 150000001412 amines Chemical class 0.000 abstract 1
- 125000003277 amino group Chemical group 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- UDLLFLQFQMACJB-UHFFFAOYSA-N azidomethylbenzene Chemical compound [N-]=[N+]=NCC1=CC=CC=C1 UDLLFLQFQMACJB-UHFFFAOYSA-N 0.000 abstract 1
- PASDCCFISLVPSO-UHFFFAOYSA-N benzoyl chloride Chemical compound ClC(=O)C1=CC=CC=C1 PASDCCFISLVPSO-UHFFFAOYSA-N 0.000 abstract 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 238000009903 catalytic hydrogenation reaction Methods 0.000 abstract 1
- 125000004663 dialkyl amino group Chemical group 0.000 abstract 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 1
- 150000001261 hydroxy acids Chemical class 0.000 abstract 1
- 125000002768 hydroxyalkyl group Chemical group 0.000 abstract 1
- 239000000543 intermediate Substances 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 230000004048 modification Effects 0.000 abstract 1
- 238000012986 modification Methods 0.000 abstract 1
- PVWOIHVRPOBWPI-UHFFFAOYSA-N n-propyl iodide Chemical compound CCCI PVWOIHVRPOBWPI-UHFFFAOYSA-N 0.000 abstract 1
- 125000001624 naphthyl group Chemical group 0.000 abstract 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 abstract 1
- 230000009935 nitrosation Effects 0.000 abstract 1
- 238000007034 nitrosation reaction Methods 0.000 abstract 1
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 abstract 1
- 125000003884 phenylalkyl group Chemical group 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more 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, directly attached to ring carbon atoms
- C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
- C07D239/47—One nitrogen atom and one oxygen or sulfur atom, e.g. cytosine
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more 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, directly attached to ring carbon atoms
- C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
- C07D239/48—Two nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D317/00—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms
- C07D317/08—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3
- C07D317/44—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D317/46—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 ortho- or peri-condensed with carbocyclic rings or ring systems condensed with one six-membered ring
- C07D317/48—Methylenedioxybenzenes or hydrogenated methylenedioxybenzenes, unsubstituted on the hetero ring
- C07D317/62—Methylenedioxybenzenes or hydrogenated methylenedioxybenzenes, unsubstituted on the hetero ring 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 atoms of the carbocyclic ring
- C07D317/68—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/55—Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB5955270 | 1970-12-15 | ||
| GB5955670 | 1970-12-15 | ||
| GB4975671A GB1338235A (en) | 1970-12-15 | 1971-10-26 | Azapurinones |
| GB5345771 | 1971-11-17 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| IE35897L IE35897L (en) | 1972-06-15 |
| IE35897B1 true IE35897B1 (en) | 1976-06-23 |
Family
ID=27449009
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| IE1583/71A IE35897B1 (en) | 1970-12-15 | 1971-12-14 | Azapurinones |
Country Status (25)
| Country | Link |
|---|---|
| US (1) | US3987160A (enExample) |
| JP (1) | JPS5310599B1 (enExample) |
| AR (4) | AR192602A1 (enExample) |
| AT (4) | AT317211B (enExample) |
| AU (1) | AU458277B2 (enExample) |
| BE (1) | BE776683A (enExample) |
| BG (3) | BG20805A3 (enExample) |
| CH (5) | CH550814A (enExample) |
| DD (1) | DD95007A5 (enExample) |
| DE (1) | DE2162096A1 (enExample) |
| DK (1) | DK141249B (enExample) |
| FI (1) | FI53457C (enExample) |
| FR (1) | FR2118078B1 (enExample) |
| GB (1) | GB1338235A (enExample) |
| HK (1) | HK42177A (enExample) |
| HU (1) | HU165079B (enExample) |
| IE (1) | IE35897B1 (enExample) |
| IL (1) | IL38364A (enExample) |
| IS (1) | IS1099B6 (enExample) |
| LU (1) | LU64457A1 (enExample) |
| NL (1) | NL174943C (enExample) |
| NO (1) | NO134257C (enExample) |
| OA (1) | OA03930A (enExample) |
| SE (1) | SE393381B (enExample) |
| ZM (1) | ZM18971A1 (enExample) |
Families Citing this family (43)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1493685A (en) * | 1970-12-15 | 1977-11-30 | May & Baker Ltd | 8-azapurinones |
| BE792648A (fr) * | 1971-12-13 | 1973-06-12 | May & Baker Ltd | Derives de l'isoquinoleine |
| FR2406638A1 (fr) * | 1977-10-21 | 1979-05-18 | May & Baker Ltd | Nouvelles aza-8 purinones-6, leur preparation et les compositions pharmaceutiques les contenant |
| DE2966444D1 (en) * | 1978-07-24 | 1984-01-05 | Beecham Group Plc | Benzopyranotriazoles, preparation of these compounds and pharmaceutical composition containing them |
| JPS60226887A (ja) * | 1984-04-25 | 1985-11-12 | Dai Ichi Seiyaku Co Ltd | トリアゾロピリミジン誘導体 |
| CA1303037C (en) * | 1987-02-02 | 1992-06-09 | Smith Kline & French Laboratories Limited | Purinone derivatives as bronchodilators vasodilators and anti-allergic agents |
| ATE79624T1 (de) * | 1987-04-07 | 1992-09-15 | Ciba Geigy Ag | 3h-1,2,3-triazolo(4,5-d>pyrimidine. |
| US5204353A (en) * | 1987-04-07 | 1993-04-20 | Ciba-Geigy Corporation | 3-benzyl-3H-1,2,3-triazolo[4,5-d]pyrimidines, compositions thereof, and method of treating epilepsy therewith |
| FR2618073B1 (fr) * | 1987-07-16 | 1990-09-07 | Pf Medicament | Comprimes de type a matrice hydrophile a base de salbutamol et leur procede de preparation |
| GB8817651D0 (en) * | 1988-07-25 | 1988-09-01 | Smith Kline French Lab | Chemical compounds |
| DE4211239C2 (de) * | 1992-04-03 | 1995-11-16 | Max Planck Gesellschaft | Arzneimittel gegen Herz-Kreislauf-Erkrankungen |
| GB9213623D0 (en) * | 1992-06-26 | 1992-08-12 | Pfizer Ltd | Therapeutic agents |
| US5734053A (en) * | 1992-06-26 | 1998-03-31 | Pfizer Inc | Purinone antianginal agents |
| GB9301192D0 (en) | 1993-06-09 | 1993-06-09 | Trott Francis W | Flower shaped mechanised table |
| US6129930A (en) * | 1993-09-20 | 2000-10-10 | Bova; David J. | Methods and sustained release nicotinic acid compositions for treating hyperlipidemia at night |
| US20080045573A1 (en) * | 1993-09-20 | 2008-02-21 | Bova David J | Methods and Sustained Release Nicotinic Acid Compositions for Treating Hyperlipidemia |
| US6746691B2 (en) | 1993-09-20 | 2004-06-08 | Kos Pharmaceuticals, Inc. | Intermediate release nicotinic acid compositions for treating hyperlipidemia having unique biopharmaceutical characteristics |
| US6818229B1 (en) | 1993-09-20 | 2004-11-16 | Kos Pharmaceuticals, Inc. | Intermediate release nicotinic acid compositions for treating hyperlipidemia |
| US6080428A (en) * | 1993-09-20 | 2000-06-27 | Bova; David J. | Nicotinic acid compositions for treating hyperlipidemia and related methods therefor |
| US6676967B1 (en) | 1993-09-20 | 2004-01-13 | Kos Pharmaceuticals, Inc. | Methods for reducing flushing in individuals being treated with nicotinic acid for hyperlipidemia |
| GB9404485D0 (en) * | 1994-03-09 | 1994-04-20 | Cancer Res Campaign Tech | Benzamide analogues |
| HU227841B1 (en) | 1997-11-12 | 2012-05-02 | Bayer Pharma AG | 2-phenyl substituted imidazotriazinones, process for their preparation and pharmaceutical compositions thereof |
| DE19838705A1 (de) * | 1998-08-26 | 2000-03-02 | Bayer Ag | Neue Dihydro-(1,2,3)-triazolo-[4,5-d]pyrimidin-7-one |
| IT1318674B1 (it) * | 2000-08-08 | 2003-08-27 | Nicox Sa | Faramaci per l'incontinenza. |
| DE10232113A1 (de) | 2002-07-16 | 2004-01-29 | Bayer Ag | Vardenafil Hydrochlorid Trihydrat enthaltende Arzneimittel |
| US7772188B2 (en) | 2003-01-28 | 2010-08-10 | Ironwood Pharmaceuticals, Inc. | Methods and compositions for the treatment of gastrointestinal disorders |
| DE102005009240A1 (de) | 2005-03-01 | 2006-09-07 | Bayer Healthcare Ag | Arzneiformen mit verbesserten pharmakokinetischen Eigenschaften |
| US8969514B2 (en) | 2007-06-04 | 2015-03-03 | Synergy Pharmaceuticals, Inc. | Agonists of guanylate cyclase useful for the treatment of hypercholesterolemia, atherosclerosis, coronary heart disease, gallstone, obesity and other cardiovascular diseases |
| WO2008151257A2 (en) | 2007-06-04 | 2008-12-11 | Synergy Pharmaceuticals Inc. | Agonists of guanylate cyclase useful for the treatment of gastrointestinal disorders, inflammation, cancer and other disorders |
| ES2627848T3 (es) | 2008-06-04 | 2017-07-31 | Synergy Pharmaceuticals Inc. | Agonistas de la guanilato ciclasa útiles para el tratamiento de trastornos gastrointestinales, inflamación, cáncer y otros trastornos |
| ES2624828T3 (es) | 2008-07-16 | 2017-07-17 | Synergy Pharmaceuticals Inc. | Agonistas de la guanilato ciclasa útiles para el tratamiento de trastornos gastrointestinales, inflamación, cáncer y otros |
| US9616097B2 (en) | 2010-09-15 | 2017-04-11 | Synergy Pharmaceuticals, Inc. | Formulations of guanylate cyclase C agonists and methods of use |
| MX357121B (es) | 2011-03-01 | 2018-06-27 | Synergy Pharmaceuticals Inc Star | Proceso de preparacion de agonistas c de guanilato ciclasa. |
| EP2958577A2 (en) | 2013-02-25 | 2015-12-30 | Synergy Pharmaceuticals Inc. | Guanylate cyclase receptor agonists for use in colonic cleansing |
| US9708367B2 (en) | 2013-03-15 | 2017-07-18 | Synergy Pharmaceuticals, Inc. | Agonists of guanylate cyclase and their uses |
| EP2968439A2 (en) | 2013-03-15 | 2016-01-20 | Synergy Pharmaceuticals Inc. | Compositions useful for the treatment of gastrointestinal disorders |
| PL3004138T3 (pl) | 2013-06-05 | 2024-07-29 | Bausch Health Ireland Limited | Ultra-oczyszczeni agoniści peptydowi cyklazy guanylanowej C, sposób ich uzyskiwania i ich zastosowanie |
| CA2920856C (en) | 2013-08-09 | 2026-03-03 | Ardelyx, Inc. | Ph modulating compounds for inhibiting gastrointestinal phosphate uptake |
| EP3554507A1 (en) | 2016-12-14 | 2019-10-23 | Respira Therapeutics, Inc. | Methods and compositions for treatment of pulmonary hypertension and other lung disorders |
| TWI845600B (zh) | 2019-01-24 | 2024-06-21 | 美商普羅米修斯生物科學股份有限公司 | Gpr35調節劑 |
| JP2022533251A (ja) | 2019-05-21 | 2022-07-21 | アルデリックス， インコーポレイテッド | 患者において血清リン酸塩を低下させるための組み合わせ |
| AR123034A1 (es) * | 2020-07-23 | 2022-10-26 | Prometheus Biosciences Inc | Agentes terapéuticos dirigidos a gpr35 |
| JP2025513455A (ja) | 2022-04-22 | 2025-04-24 | バーテックス ファーマシューティカルズ インコーポレイテッド | 疼痛の治療のためのヘテロアリール化合物 |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2407204A (en) * | 1944-07-22 | 1946-09-03 | American Cyanamid Co | Triazolo (d) pyrimidines and methods of preparing the same |
| US2993039A (en) * | 1959-11-06 | 1961-07-18 | Upjohn Co | Preparing nu-glycosides of aldose and ketose sugars |
-
1971
- 1971-10-26 GB GB4975671A patent/GB1338235A/en not_active Expired
- 1971-12-06 DK DK596371AA patent/DK141249B/da not_active IP Right Cessation
- 1971-12-14 CH CH1853672A patent/CH550814A/fr not_active IP Right Cessation
- 1971-12-14 NO NO4614/71A patent/NO134257C/no unknown
- 1971-12-14 FR FR7144869A patent/FR2118078B1/fr not_active Expired
- 1971-12-14 IS IS2047A patent/IS1099B6/is unknown
- 1971-12-14 SE SE7116090A patent/SE393381B/xx unknown
- 1971-12-14 CH CH222574A patent/CH552610A/fr not_active IP Right Cessation
- 1971-12-14 BE BE776683A patent/BE776683A/xx not_active IP Right Cessation
- 1971-12-14 IE IE1583/71A patent/IE35897B1/xx unknown
- 1971-12-14 CH CH1823271A patent/CH555351A/fr not_active IP Right Cessation
- 1971-12-14 JP JP10078571A patent/JPS5310599B1/ja active Pending
- 1971-12-14 ZM ZM189/71A patent/ZM18971A1/xx unknown
- 1971-12-14 CH CH1853772A patent/CH556860A/xx not_active IP Right Cessation
- 1971-12-14 LU LU64457D patent/LU64457A1/xx unknown
- 1971-12-14 HU HUMA2296A patent/HU165079B/hu unknown
- 1971-12-14 DE DE19712162096 patent/DE2162096A1/de active Granted
- 1971-12-14 CH CH1853872A patent/CH546779A/fr not_active IP Right Cessation
- 1971-12-14 DD DD159572A patent/DD95007A5/xx unknown
- 1971-12-14 IL IL38364A patent/IL38364A/xx unknown
- 1971-12-14 AU AU36867/71A patent/AU458277B2/en not_active Expired
- 1971-12-14 OA OA54440A patent/OA03930A/xx unknown
- 1971-12-14 NL NLAANVRAGE7117142,A patent/NL174943C/xx not_active IP Right Cessation
- 1971-12-14 FI FI3560/71A patent/FI53457C/fi active
- 1971-12-15 AR AR239632A patent/AR192602A1/es active
- 1971-12-15 BG BG019250A patent/BG20805A3/xx unknown
- 1971-12-15 AT AT272373A patent/AT317211B/de not_active IP Right Cessation
- 1971-12-15 BG BG020379A patent/BG20806A3/xx unknown
- 1971-12-15 AT AT272273A patent/AT319235B/de not_active IP Right Cessation
- 1971-12-15 AT AT1075671A patent/AT315838B/de not_active IP Right Cessation
- 1971-12-15 AT AT272473A patent/AT315839B/de not_active IP Right Cessation
- 1971-12-15 BG BG020380A patent/BG20807A3/xx unknown
-
1972
- 1972-12-06 AR AR245509A patent/AR199468A1/es active
- 1972-12-06 AR AR245510A patent/AR192689A1/es active
- 1972-12-06 AR AR245508A patent/AR199467A1/es active
-
1973
- 1973-05-29 US US05/364,425 patent/US3987160A/en not_active Expired - Lifetime
-
1977
- 1977-08-11 HK HK421/77A patent/HK42177A/xx unknown
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