ES421274A1 - Procedimiento para la obtencion de derivados de acidos 12- epi-prostanoicos. - Google Patents
Procedimiento para la obtencion de derivados de acidos 12- epi-prostanoicos.Info
- Publication number
- ES421274A1 ES421274A1 ES421274A ES421274A ES421274A1 ES 421274 A1 ES421274 A1 ES 421274A1 ES 421274 A ES421274 A ES 421274A ES 421274 A ES421274 A ES 421274A ES 421274 A1 ES421274 A1 ES 421274A1
- Authority
- ES
- Spain
- Prior art keywords
- radical
- carbon atoms
- formula
- alkyl
- see formula
- 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
- 125000001511 cyclopentyl group Chemical class [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 title 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 34
- -1 alkanoyloxy radical Chemical group 0.000 abstract 33
- 150000001875 compounds Chemical class 0.000 abstract 17
- 150000003254 radicals Chemical class 0.000 abstract 9
- 125000000217 alkyl group Chemical group 0.000 abstract 6
- 125000001424 substituent group Chemical group 0.000 abstract 6
- 229910052799 carbon Inorganic materials 0.000 abstract 5
- 239000002253 acid Substances 0.000 abstract 4
- 238000006243 chemical reaction Methods 0.000 abstract 4
- ORTFAQDWJHRMNX-UHFFFAOYSA-N hydroxidooxidocarbon(.) Chemical group O[C]=O ORTFAQDWJHRMNX-UHFFFAOYSA-N 0.000 abstract 4
- 150000003839 salts Chemical class 0.000 abstract 4
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 abstract 3
- 125000005843 halogen group Chemical group 0.000 abstract 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 3
- 125000000475 sulfinyl group Chemical group [*:2]S([*:1])=O 0.000 abstract 3
- 229910052717 sulfur Inorganic materials 0.000 abstract 3
- 125000003258 trimethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])[*:1] 0.000 abstract 3
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 abstract 2
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical group C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 abstract 2
- 239000005977 Ethylene Substances 0.000 abstract 2
- 150000001350 alkyl halides Chemical class 0.000 abstract 2
- 150000002148 esters Chemical class 0.000 abstract 2
- 125000001188 haloalkyl group Chemical group 0.000 abstract 2
- CBOIHMRHGLHBPB-UHFFFAOYSA-N hydroxymethyl Chemical group O[CH2] CBOIHMRHGLHBPB-UHFFFAOYSA-N 0.000 abstract 2
- 229910052760 oxygen Inorganic materials 0.000 abstract 2
- 239000001301 oxygen Substances 0.000 abstract 2
- JQWHASGSAFIOCM-UHFFFAOYSA-M sodium periodate Chemical compound [Na+].[O-]I(=O)(=O)=O JQWHASGSAFIOCM-UHFFFAOYSA-M 0.000 abstract 2
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 abstract 2
- 125000004434 sulfur atom Chemical group 0.000 abstract 2
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 abstract 2
- CPVNCBJFUQQXSU-UHFFFAOYSA-N 5-triphenylphosphaniumylpentanoate Chemical class C1(=CC=CC=C1)[P+](CCCCC(=O)[O-])(C1=CC=CC=C1)C1=CC=CC=C1 CPVNCBJFUQQXSU-UHFFFAOYSA-N 0.000 abstract 1
- HSFWRNGVRCDJHI-UHFFFAOYSA-N Acetylene Chemical group C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 abstract 1
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 abstract 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 abstract 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 abstract 1
- KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 abstract 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract 1
- IPEWNTLWCRYSRY-UHFFFAOYSA-N [CH2]C1=CC=CO1 Chemical group [CH2]C1=CC=CO1 IPEWNTLWCRYSRY-UHFFFAOYSA-N 0.000 abstract 1
- 150000007513 acids Chemical class 0.000 abstract 1
- 125000004442 acylamino group Chemical group 0.000 abstract 1
- 125000003302 alkenyloxy group Chemical group 0.000 abstract 1
- 125000003545 alkoxy group Chemical group 0.000 abstract 1
- 150000001351 alkyl iodides Chemical class 0.000 abstract 1
- 150000008064 anhydrides Chemical class 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- 150000005840 aryl radicals Chemical group 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
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 1
- 230000018044 dehydration Effects 0.000 abstract 1
- 238000006297 dehydration reaction Methods 0.000 abstract 1
- 125000004663 dialkyl amino group Chemical group 0.000 abstract 1
- 230000007062 hydrolysis Effects 0.000 abstract 1
- 238000006460 hydrolysis reaction Methods 0.000 abstract 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 1
- 125000001841 imino group Chemical group [H]N=* 0.000 abstract 1
- 239000012280 lithium aluminium hydride Substances 0.000 abstract 1
- 229910052987 metal hydride Inorganic materials 0.000 abstract 1
- 150000004681 metal hydrides Chemical class 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 abstract 1
- 230000003647 oxidation Effects 0.000 abstract 1
- 238000007254 oxidation reaction Methods 0.000 abstract 1
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Substances [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 abstract 1
- 229910000027 potassium carbonate Inorganic materials 0.000 abstract 1
- 238000000926 separation method Methods 0.000 abstract 1
- 229910052709 silver Inorganic materials 0.000 abstract 1
- 239000004332 silver Substances 0.000 abstract 1
- 229910052708 sodium Inorganic materials 0.000 abstract 1
- 239000011734 sodium Substances 0.000 abstract 1
- 239000012312 sodium hydride Substances 0.000 abstract 1
- 229910000104 sodium hydride Inorganic materials 0.000 abstract 1
- 239000011593 sulfur Substances 0.000 abstract 1
- 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 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical group O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/77—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D307/93—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems condensed with a ring other than six-membered
- C07D307/935—Not further condensed cyclopenta [b] furans or hydrogenated cyclopenta [b] furans
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C405/00—Compounds containing a five-membered ring having two side-chains in ortho position to each other, and having oxygen atoms directly attached to the ring in ortho position to one of the side-chains, one side-chain containing, not directly attached to the ring, a carbon atom having three bonds to hetero atoms with at the most one bond to halogen, and the other side-chain having oxygen atoms attached in gamma-position to the ring, e.g. prostaglandins ; Analogues or derivatives thereof
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/51—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by pyrolysis, rearrangement or decomposition
- C07C45/516—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by pyrolysis, rearrangement or decomposition involving transformation of nitrogen-containing compounds to >C = O groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C49/00—Ketones; Ketenes; Dimeric ketenes; Ketonic chelates
- C07C49/587—Unsaturated compounds containing a keto groups being part of a ring
- C07C49/703—Unsaturated compounds containing a keto groups being part of a ring containing hydroxy groups
- C07C49/743—Unsaturated compounds containing a keto groups being part of a ring containing hydroxy groups having unsaturation outside the rings, e.g. humulones, lupulones
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C49/00—Ketones; Ketenes; Dimeric ketenes; Ketonic chelates
- C07C49/587—Unsaturated compounds containing a keto groups being part of a ring
- C07C49/753—Unsaturated compounds containing a keto groups being part of a ring containing ether groups, groups, groups, or groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D309/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings
- C07D309/02—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
- C07D309/08—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having no 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
- C07D309/10—Oxygen atoms
- C07D309/12—Oxygen atoms only hydrogen atoms and one oxygen atom directly attached to ring carbon atoms, e.g. tetrahydropyranyl ethers
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Furan Compounds (AREA)
- Pyrane Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB5650172A GB1402035A (en) | 1972-12-07 | 1972-12-07 | Cyclopentane derivatives |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES421274A1 true ES421274A1 (es) | 1976-04-16 |
Family
ID=10476784
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES421274A Expired ES421274A1 (es) | 1972-12-07 | 1973-12-07 | Procedimiento para la obtencion de derivados de acidos 12- epi-prostanoicos. |
Country Status (13)
| Country | Link |
|---|---|
| JP (1) | JPS5024252A (en:Method) |
| AU (1) | AU473283B2 (en:Method) |
| BE (1) | BE808398A (en:Method) |
| CA (1) | CA1016940A (en:Method) |
| CH (1) | CH605725A5 (en:Method) |
| DE (1) | DE2360893A1 (en:Method) |
| ES (1) | ES421274A1 (en:Method) |
| FR (1) | FR2209569B1 (en:Method) |
| GB (1) | GB1402035A (en:Method) |
| IE (1) | IE38515B1 (en:Method) |
| LU (1) | LU68940A1 (en:Method) |
| NL (1) | NL7316508A (en:Method) |
| ZA (1) | ZA738797B (en:Method) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0144459A1 (de) * | 1983-12-09 | 1985-06-19 | Dr. Willmar Schwabe GmbH & Co. | Prostaglandine, Verfahren zu ihrer Herstellung und diese enthaltende pharmazeutische Zubereitungen |
| JPS6240987A (ja) * | 1985-08-20 | 1987-02-21 | Nippon Steel Corp | レーザビーム溶接法 |
| US5688819A (en) * | 1992-09-21 | 1997-11-18 | Allergan | Cyclopentane heptanoic acid, 2-cycloalkyl or arylalkyl derivatives as therapeutic agents |
| US5352708A (en) * | 1992-09-21 | 1994-10-04 | Allergan, Inc. | Non-acidic cyclopentane heptanoic acid, 2-cycloalkyl or arylalkyl derivatives as therapeutic agents |
| US5972991A (en) | 1992-09-21 | 1999-10-26 | Allergan | Cyclopentane heptan(ene) oic acid, 2-heteroarylalkenyl derivatives as therapeutic agents |
| WO2010102078A1 (en) | 2009-03-04 | 2010-09-10 | Allergan, Inc. | Enhanced bimatoprost ophthalmic solution |
| US7851504B2 (en) | 2005-03-16 | 2010-12-14 | Allergan, Inc. | Enhanced bimatoprost ophthalmic solution |
| US9522153B2 (en) | 2009-12-22 | 2016-12-20 | Allergan, Inc. | Compositions and methods for lowering intraocular pressure |
-
1972
- 1972-12-07 GB GB5650172A patent/GB1402035A/en not_active Expired
-
1973
- 1973-11-15 IE IE2066/73A patent/IE38515B1/xx unknown
- 1973-11-16 ZA ZA738797*A patent/ZA738797B/xx unknown
- 1973-11-19 CA CA186,104A patent/CA1016940A/en not_active Expired
- 1973-11-22 AU AU62797/73A patent/AU473283B2/en not_active Expired
- 1973-12-03 NL NL7316508A patent/NL7316508A/xx not_active Application Discontinuation
- 1973-12-05 LU LU68940A patent/LU68940A1/xx unknown
- 1973-12-05 FR FR7343446A patent/FR2209569B1/fr not_active Expired
- 1973-12-06 DE DE2360893A patent/DE2360893A1/de not_active Withdrawn
- 1973-12-06 CH CH1714573A patent/CH605725A5/xx not_active IP Right Cessation
- 1973-12-07 BE BE138669A patent/BE808398A/xx unknown
- 1973-12-07 JP JP48137248A patent/JPS5024252A/ja active Pending
- 1973-12-07 ES ES421274A patent/ES421274A1/es not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| IE38515B1 (en) | 1978-03-29 |
| FR2209569A1 (en:Method) | 1974-07-05 |
| CA1016940A (en) | 1977-09-06 |
| JPS5024252A (en:Method) | 1975-03-15 |
| BE808398A (fr) | 1974-06-07 |
| ZA738797B (en) | 1974-07-31 |
| DE2360893A1 (de) | 1974-06-12 |
| LU68940A1 (en:Method) | 1974-02-12 |
| NL7316508A (en:Method) | 1974-06-11 |
| AU6279773A (en) | 1975-11-27 |
| AU473283B2 (en) | 1976-06-17 |
| CH605725A5 (en:Method) | 1978-10-13 |
| IE38515L (en) | 1974-06-07 |
| FR2209569B1 (en:Method) | 1978-07-28 |
| GB1402035A (en) | 1975-08-06 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US4152514A (en) | 9α,5-Nitrilo-9-deoxy-PGF1 compounds | |
| ES402627A1 (es) | Procedimiento para la obtencion de derivados del acido prostanoico. | |
| GB1513347A (en) | Thiolcarbonyl derivatives of n-phosphonomethylglycine | |
| GB1432950A (en) | Cyclopentane aldehydes as chemical intermediates | |
| ES421274A1 (es) | Procedimiento para la obtencion de derivados de acidos 12- epi-prostanoicos. | |
| ES394370A1 (es) | Procedimiento para la preparacion de derivados de la inso-indolina. | |
| IE38241L (en) | Prostanoic acid derivatives | |
| ES438314A1 (es) | Un procedimiento para preparar los compuestos de decahi- droisoquinolina. | |
| ES414343A1 (es) | Procedimiento para la obtencion de derivados del acido prostanoico. | |
| ES454181A1 (es) | Procedimiento para preparar un analogo de prostaglandina. | |
| ES457993A1 (es) | Un procedimiento para la preparacion de una isotiazolopiri- dina. | |
| SE7601206L (sv) | Acetylenderivat | |
| GB1508170A (en) | Substituted cyclopentane compounds useful as intermediates in the synthesis of prostaglandin analogues | |
| US3974193A (en) | 16-Fluoro prostaglandin B2 analogs | |
| ES434955A1 (es) | Procedimiento para la obtencion de azatetraciclos. | |
| US3974189A (en) | 16-Fluoro prostaglandin E2 analogs | |
| US3974190A (en) | 16-Fluoro prostaglandin A1 analogs | |
| US3974192A (en) | 16-Fluoro prostaglandin B1 analogs | |
| ES502668A0 (es) | Procedimiento para preparar una solucion hidrocarbonada de un compuesto de alquilsodio | |
| ES442485A1 (es) | Un procedimiento de preparacion de analogos de prostaglandi-na. | |
| SE7702907L (sv) | Forfarande for framstellning av nya sandwicinderivat | |
| ES430417A1 (es) | Procedimiento para preparar bromuro de amidoalquil-trifenil-fosfonio. | |
| SE7710933L (sv) | 5-alkoxi-pikolinsyror | |
| ES454326A1 (es) | Un procedimiento para la preparacion de nuevos derivados de cumarina. | |
| US3981902A (en) | 5-Oxa-17,18-dehydroprostaglandin-F1.sub.α -type analogs |