IE39273B1 - Cyclopentane derivatives - Google Patents
Cyclopentane derivativesInfo
- Publication number
- IE39273B1 IE39273B1 IE1070/74A IE107074A IE39273B1 IE 39273 B1 IE39273 B1 IE 39273B1 IE 1070/74 A IE1070/74 A IE 1070/74A IE 107074 A IE107074 A IE 107074A IE 39273 B1 IE39273 B1 IE 39273B1
- Authority
- IE
- Ireland
- Prior art keywords
- formula
- chloro
- compounds
- alkyl
- groups
- Prior art date
Links
- 125000001511 cyclopentyl group Chemical class [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 6
- 125000000217 alkyl group Chemical group 0.000 abstract 5
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical class OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 abstract 2
- 238000006243 chemical reaction Methods 0.000 abstract 2
- 229940094443 oxytocics prostaglandins Drugs 0.000 abstract 2
- 150000003180 prostaglandins Chemical class 0.000 abstract 2
- RIOQSEWOXXDEQQ-UHFFFAOYSA-N triphenylphosphine Chemical compound C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 RIOQSEWOXXDEQQ-UHFFFAOYSA-N 0.000 abstract 2
- 125000006705 (C5-C7) cycloalkyl group Chemical group 0.000 abstract 1
- LQEIHJCPWVRMDQ-UHFFFAOYSA-N 1-butan-2-yloxy-3-chloropropan-2-one Chemical compound CCC(C)OCC(=O)CCl LQEIHJCPWVRMDQ-UHFFFAOYSA-N 0.000 abstract 1
- MBAAZSBVJHIYFR-UHFFFAOYSA-N 1-chloro-3,3-dimethylheptan-2-one Chemical compound CCCCC(C)(C)C(=O)CCl MBAAZSBVJHIYFR-UHFFFAOYSA-N 0.000 abstract 1
- KZHXZSDWLIUHIP-UHFFFAOYSA-N 1-chloro-3-propan-2-yloxypropan-2-one Chemical compound CC(C)OCC(=O)CCl KZHXZSDWLIUHIP-UHFFFAOYSA-N 0.000 abstract 1
- DASDXHZRVCSYEA-UHFFFAOYSA-N 1-chloro-3-propoxypropan-2-one Chemical compound CCCOCC(=O)CCl DASDXHZRVCSYEA-UHFFFAOYSA-N 0.000 abstract 1
- NZMRJUYBKVFDFI-UHFFFAOYSA-N 1-chloro-3-propylhexan-2-one Chemical compound CCCC(CCC)C(=O)CCl NZMRJUYBKVFDFI-UHFFFAOYSA-N 0.000 abstract 1
- BKHLXOAPZZVLIM-UHFFFAOYSA-N 1-chloro-4-ethoxybutan-2-one Chemical compound CCOCCC(=O)CCl BKHLXOAPZZVLIM-UHFFFAOYSA-N 0.000 abstract 1
- RVLHTMZQVHPUPP-UHFFFAOYSA-N 4-(2-chloroethylidene)octane Chemical compound ClCC=C(CCCC)CCC RVLHTMZQVHPUPP-UHFFFAOYSA-N 0.000 abstract 1
- 101100440696 Caenorhabditis elegans cor-1 gene Proteins 0.000 abstract 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 abstract 1
- 239000005977 Ethylene Substances 0.000 abstract 1
- DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 abstract 1
- 125000002777 acetyl group Chemical class [H]C([H])([H])C(*)=O 0.000 abstract 1
- 125000003545 alkoxy group Chemical group 0.000 abstract 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 abstract 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 1
- 238000000576 coating method Methods 0.000 abstract 1
- JBDSSBMEKXHSJF-UHFFFAOYSA-N cyclopentanecarboxylic acid Chemical class OC(=O)C1CCCC1 JBDSSBMEKXHSJF-UHFFFAOYSA-N 0.000 abstract 1
- VONWDASPFIQPDY-UHFFFAOYSA-N dimethyl methylphosphonate Chemical compound COP(C)(=O)OC VONWDASPFIQPDY-UHFFFAOYSA-N 0.000 abstract 1
- 239000003937 drug carrier Substances 0.000 abstract 1
- 150000002148 esters Chemical class 0.000 abstract 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 1
- 125000002485 formyl group Chemical class [H]C(*)=O 0.000 abstract 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 1
- 125000005020 hydroxyalkenyl group Chemical group 0.000 abstract 1
- 125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 abstract 1
- 150000007529 inorganic bases Chemical class 0.000 abstract 1
- 239000000543 intermediate Substances 0.000 abstract 1
- 238000004519 manufacturing process Methods 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 231100000252 nontoxic Toxicity 0.000 abstract 1
- 230000003000 nontoxic effect Effects 0.000 abstract 1
- 230000001590 oxidative effect Effects 0.000 abstract 1
- 125000005646 oximino group Chemical group 0.000 abstract 1
- 125000004043 oxo group Chemical group O=* 0.000 abstract 1
- 239000008016 pharmaceutical coating Substances 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 230000000144 pharmacologic effect Effects 0.000 abstract 1
- -1 phosphonium halides Chemical class 0.000 abstract 1
- VBQCHPIMZGQLAZ-UHFFFAOYSA-N phosphorane Chemical class [PH5] VBQCHPIMZGQLAZ-UHFFFAOYSA-N 0.000 abstract 1
- 230000002997 prostaglandinlike Effects 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
Classifications
-
- 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
- C07D317/72—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 spiro-condensed with carbocyclic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/38—Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)]
- C07F9/40—Esters thereof
- C07F9/4003—Esters thereof the acid moiety containing a substituent or a structure which is considered as characteristic
- C07F9/4006—Esters of acyclic acids which can have further substituents on alkyl
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB2447373A GB1467813A (en) | 1973-05-22 | 1973-05-22 | Cyclopentane derivatives |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| IE39273L IE39273L (en) | 1974-11-22 |
| IE39273B1 true IE39273B1 (en) | 1978-09-13 |
Family
ID=10212252
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| IE1070/74A IE39273B1 (en) | 1973-05-22 | 1974-05-20 | Cyclopentane derivatives |
Country Status (10)
| Country | Link |
|---|---|
| BE (1) | BE815372R (enrdf_load_stackoverflow) |
| CA (1) | CA1039278A (enrdf_load_stackoverflow) |
| CH (4) | CH599150A5 (enrdf_load_stackoverflow) |
| DE (1) | DE2424862A1 (enrdf_load_stackoverflow) |
| FR (1) | FR2230360B2 (enrdf_load_stackoverflow) |
| GB (1) | GB1467813A (enrdf_load_stackoverflow) |
| HU (1) | HU175493B (enrdf_load_stackoverflow) |
| IE (1) | IE39273B1 (enrdf_load_stackoverflow) |
| NL (1) | NL7406842A (enrdf_load_stackoverflow) |
| ZA (1) | ZA743195B (enrdf_load_stackoverflow) |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1398072A (en) * | 1971-06-14 | 1975-06-18 | May & Baker Ltd | Cyclopentane derivatives |
-
1973
- 1973-05-22 GB GB2447373A patent/GB1467813A/en not_active Expired
-
1974
- 1974-05-20 IE IE1070/74A patent/IE39273B1/xx unknown
- 1974-05-20 HU HU74MA2574A patent/HU175493B/hu unknown
- 1974-05-20 ZA ZA00743195A patent/ZA743195B/xx unknown
- 1974-05-21 BE BE144604A patent/BE815372R/xx active
- 1974-05-21 CH CH5776A patent/CH599150A5/fr not_active IP Right Cessation
- 1974-05-21 FR FR7417641A patent/FR2230360B2/fr not_active Expired
- 1974-05-21 CH CH695674A patent/CH570956A5/xx not_active IP Right Cessation
- 1974-05-21 CH CH416375A patent/CH592621A5/xx not_active IP Right Cessation
- 1974-05-21 CH CH416475A patent/CH584674A5/xx not_active IP Right Cessation
- 1974-05-21 NL NL7406842A patent/NL7406842A/xx not_active Application Discontinuation
- 1974-05-22 DE DE19742424862 patent/DE2424862A1/de not_active Withdrawn
- 1974-05-22 CA CA200,518A patent/CA1039278A/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| AU6916174A (en) | 1975-11-20 |
| FR2230360A2 (enrdf_load_stackoverflow) | 1974-12-20 |
| GB1467813A (en) | 1977-03-23 |
| CA1039278A (en) | 1978-09-26 |
| FR2230360B2 (enrdf_load_stackoverflow) | 1979-07-20 |
| CH592621A5 (enrdf_load_stackoverflow) | 1977-10-31 |
| BE815372R (fr) | 1974-11-21 |
| IE39273L (en) | 1974-11-22 |
| NL7406842A (enrdf_load_stackoverflow) | 1974-11-26 |
| CH599150A5 (fr) | 1978-05-12 |
| HU175493B (hu) | 1980-08-28 |
| CH584674A5 (enrdf_load_stackoverflow) | 1977-02-15 |
| ZA743195B (en) | 1975-05-28 |
| CH570956A5 (enrdf_load_stackoverflow) | 1975-12-31 |
| DE2424862A1 (de) | 1974-12-12 |
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