GB1360946A - Process of separating optical geometric structural isomers and the compounds used therefor - Google Patents
Process of separating optical geometric structural isomers and the compounds used thereforInfo
- Publication number
- GB1360946A GB1360946A GB1104172A GB1104172A GB1360946A GB 1360946 A GB1360946 A GB 1360946A GB 1104172 A GB1104172 A GB 1104172A GB 1104172 A GB1104172 A GB 1104172A GB 1360946 A GB1360946 A GB 1360946A
- Authority
- GB
- United Kingdom
- Prior art keywords
- prepared
- binaphthalene
- reaction
- diol
- resolving agents
- 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
- 150000001875 compounds Chemical class 0.000 title abstract 8
- 230000003287 optical effect Effects 0.000 title abstract 3
- 238000000034 method Methods 0.000 title abstract 2
- 238000006243 chemical reaction Methods 0.000 abstract 5
- 239000003795 chemical substances by application Substances 0.000 abstract 4
- LOUPRKONTZGTKE-UHFFFAOYSA-N cinchonine Natural products C1C(C(C2)C=C)CCN2C1C(O)C1=CC=NC2=CC=C(OC)C=C21 LOUPRKONTZGTKE-UHFFFAOYSA-N 0.000 abstract 3
- KWGRBVOPPLSCSI-WPRPVWTQSA-N (-)-ephedrine Chemical compound CN[C@@H](C)[C@H](O)C1=CC=CC=C1 KWGRBVOPPLSCSI-WPRPVWTQSA-N 0.000 abstract 2
- -1 Binaphthyl phosphate Chemical compound 0.000 abstract 2
- LOUPRKONTZGTKE-WZBLMQSHSA-N Quinine Chemical compound C([C@H]([C@H](C1)C=C)C2)C[N@@]1[C@@H]2[C@H](O)C1=CC=NC2=CC=C(OC)C=C21 LOUPRKONTZGTKE-WZBLMQSHSA-N 0.000 abstract 2
- 150000001412 amines Chemical class 0.000 abstract 2
- KMPWYEUPVWOPIM-KODHJQJWSA-N cinchonidine Chemical compound C1=CC=C2C([C@H]([C@H]3[N@]4CC[C@H]([C@H](C4)C=C)C3)O)=CC=NC2=C1 KMPWYEUPVWOPIM-KODHJQJWSA-N 0.000 abstract 2
- KMPWYEUPVWOPIM-UHFFFAOYSA-N cinchonidine Natural products C1=CC=C2C(C(C3N4CCC(C(C4)C=C)C3)O)=CC=NC2=C1 KMPWYEUPVWOPIM-UHFFFAOYSA-N 0.000 abstract 2
- BQJCRHHNABKAKU-KBQPJGBKSA-N morphine Chemical compound O([C@H]1[C@H](C=C[C@H]23)O)C4=C5[C@@]12CCN(C)[C@@H]3CC5=CC=C4O BQJCRHHNABKAKU-KBQPJGBKSA-N 0.000 abstract 2
- LOUPRKONTZGTKE-LHHVKLHASA-N quinidine Chemical compound C([C@H]([C@H](C1)C=C)C2)C[N@@]1[C@H]2[C@@H](O)C1=CC=NC2=CC=C(OC)C=C21 LOUPRKONTZGTKE-LHHVKLHASA-N 0.000 abstract 2
- RQEUFEKYXDPUSK-UHFFFAOYSA-N 1-phenylethylamine Chemical compound CC(N)C1=CC=CC=C1 RQEUFEKYXDPUSK-UHFFFAOYSA-N 0.000 abstract 1
- MYRXDLASSYFCAC-UHFFFAOYSA-N 3-methylnaphthalen-2-ol Chemical compound C1=CC=C2C=C(O)C(C)=CC2=C1 MYRXDLASSYFCAC-UHFFFAOYSA-N 0.000 abstract 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 abstract 1
- 235000001258 Cinchona calisaya Nutrition 0.000 abstract 1
- YXHKONLOYHBTNS-UHFFFAOYSA-N Diazomethane Chemical compound C=[N+]=[N-] YXHKONLOYHBTNS-UHFFFAOYSA-N 0.000 abstract 1
- 229910004373 HOAc Inorganic materials 0.000 abstract 1
- 229910004013 NO 2 Inorganic materials 0.000 abstract 1
- QMGVPVSNSZLJIA-UHFFFAOYSA-N Nux Vomica Natural products C1C2C3C4N(C=5C6=CC=CC=5)C(=O)CC3OCC=C2CN2C1C46CC2 QMGVPVSNSZLJIA-UHFFFAOYSA-N 0.000 abstract 1
- 229910019142 PO4 Inorganic materials 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- 150000007513 acids Chemical class 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 229910052794 bromium Inorganic materials 0.000 abstract 1
- RRKTZKIUPZVBMF-IBTVXLQLSA-N brucine Chemical compound O([C@@H]1[C@H]([C@H]2C3)[C@@H]4N(C(C1)=O)C=1C=C(C(=CC=11)OC)OC)CC=C2CN2[C@@H]3[C@]41CC2 RRKTZKIUPZVBMF-IBTVXLQLSA-N 0.000 abstract 1
- RRKTZKIUPZVBMF-UHFFFAOYSA-N brucine Natural products C1=2C=C(OC)C(OC)=CC=2N(C(C2)=O)C3C(C4C5)C2OCC=C4CN2C5C31CC2 RRKTZKIUPZVBMF-UHFFFAOYSA-N 0.000 abstract 1
- 238000009903 catalytic hydrogenation reaction Methods 0.000 abstract 1
- 229910052801 chlorine Inorganic materials 0.000 abstract 1
- ITVPBBDAZKBMRP-UHFFFAOYSA-N chloro-dioxido-oxo-$l^{5}-phosphane;hydron Chemical compound OP(O)(Cl)=O ITVPBBDAZKBMRP-UHFFFAOYSA-N 0.000 abstract 1
- GKIRPKYJQBWNGO-OCEACIFDSA-N clomifene Chemical compound C1=CC(OCCN(CC)CC)=CC=C1C(\C=1C=CC=CC=1)=C(\Cl)C1=CC=CC=C1 GKIRPKYJQBWNGO-OCEACIFDSA-N 0.000 abstract 1
- 229960003608 clomifene Drugs 0.000 abstract 1
- KWGRBVOPPLSCSI-UHFFFAOYSA-N d-ephedrine Natural products CNC(C)C(O)C1=CC=CC=C1 KWGRBVOPPLSCSI-UHFFFAOYSA-N 0.000 abstract 1
- 229960002179 ephedrine Drugs 0.000 abstract 1
- 229910052731 fluorine Inorganic materials 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 150000002367 halogens Chemical class 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 230000007062 hydrolysis Effects 0.000 abstract 1
- 238000006460 hydrolysis reaction Methods 0.000 abstract 1
- 150000004702 methyl esters Chemical class 0.000 abstract 1
- 229960005181 morphine Drugs 0.000 abstract 1
- 239000010452 phosphate Substances 0.000 abstract 1
- RLOWWWKZYUNIDI-UHFFFAOYSA-N phosphinic chloride Chemical compound ClP=O RLOWWWKZYUNIDI-UHFFFAOYSA-N 0.000 abstract 1
- 238000002360 preparation method Methods 0.000 abstract 1
- 150000003222 pyridines Chemical class 0.000 abstract 1
- 238000000197 pyrolysis Methods 0.000 abstract 1
- 229960001404 quinidine Drugs 0.000 abstract 1
- 229960000948 quinine Drugs 0.000 abstract 1
Classifications
-
- 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
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/6564—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms
- C07F9/6571—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms having phosphorus and oxygen atoms as the only ring hetero atoms
- C07F9/6574—Esters of oxyacids of phosphorus
- C07F9/65744—Esters of oxyacids of phosphorus condensed with carbocyclic or heterocyclic rings or ring systems
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)
- Hydrogenated Pyridines (AREA)
- Pyridine Compounds (AREA)
- Braiding, Manufacturing Of Bobbin-Net Or Lace, And Manufacturing Of Nets By Knotting (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IT49167/71A IT951631B (it) | 1971-03-18 | 1971-03-18 | Composti utili per la separazione di isomeri ottici geometrici e strutturali e relativo procedimen to di sintesi |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1360946A true GB1360946A (en) | 1974-07-24 |
Family
ID=11269830
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB1104172A Expired GB1360946A (en) | 1971-03-18 | 1972-03-09 | Process of separating optical geometric structural isomers and the compounds used therefor |
Country Status (18)
| Country | Link |
|---|---|
| US (1) | US3848030A (enExample) |
| JP (1) | JPS5547013B1 (enExample) |
| AU (1) | AU462431B2 (enExample) |
| BE (1) | BE780887A (enExample) |
| CA (1) | CA961500A (enExample) |
| CH (1) | CH576921A5 (enExample) |
| DE (1) | DE2212660C3 (enExample) |
| DK (1) | DK139944B (enExample) |
| ES (1) | ES400862A1 (enExample) |
| FR (1) | FR2129741A5 (enExample) |
| GB (1) | GB1360946A (enExample) |
| IL (1) | IL38860A (enExample) |
| IT (1) | IT951631B (enExample) |
| NL (1) | NL7203574A (enExample) |
| NO (1) | NO136357C (enExample) |
| PH (1) | PH10768A (enExample) |
| SE (1) | SE409323B (enExample) |
| ZA (1) | ZA721297B (enExample) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0180276A1 (en) * | 1984-10-24 | 1986-05-07 | Stamicarbon B.V. | Dioxaphosphorinanes, their preparation and use for resolving optically active compounds |
| WO2001030763A1 (en) * | 1999-10-22 | 2001-05-03 | Takeda Chemical Industries, Ltd. | Process for producing optically active naphthalene derivative and optical resolver therefor |
Families Citing this family (28)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4143028A (en) * | 1977-12-05 | 1979-03-06 | Ciba-Geigy Corporation | Alkylated 1,1'-biphenyl-2,2'-diyl phosphonites and stabilized compositions |
| US5288914A (en) * | 1984-08-27 | 1994-02-22 | The Dow Chemical Company | Poly(arylcyclobutenes) |
| DE3940765A1 (de) * | 1989-12-09 | 1991-06-13 | Hoechst Ag | Verfahren zur herstellung reiner cyclischer phosphorsaeurediarylester |
| CN1229346C (zh) * | 1994-05-16 | 2005-11-30 | 默里尔药物公司 | 丁苯哌丁醇的非对映体盐 |
| JP4725757B2 (ja) * | 1999-03-24 | 2011-07-13 | 東ソー株式会社 | ビナフトールリン酸誘導体及びその利用 |
| DE60008807T2 (de) | 1999-03-24 | 2005-01-13 | Tosoh Corp., Shinnanyo | Binaphtol-monophosphorsäurederivate und deren Verwendung |
| WO2001034557A1 (en) * | 1999-11-10 | 2001-05-17 | Takeda Chemical Industries, Ltd. | Process for the production of optically active cyclic enaminone derivatives |
| US6391926B2 (en) * | 2000-03-13 | 2002-05-21 | Tosoh Corporation | Optically active phosphate derivative |
| DK1411916T3 (da) | 2001-07-09 | 2008-12-15 | Repros Therapeutics Inc | Fremgangsmåder og materialer til behandling af testosteronmangel hos mænd |
| WO2004096753A1 (ja) * | 2003-04-25 | 2004-11-11 | Toagosei Co., Ltd. | キラルなブレンステッド酸による不斉合成用触媒および当該触媒を用いた不斉合成方法 |
| US7229557B2 (en) * | 2004-02-04 | 2007-06-12 | Konec, Inc. | Method to separate stereoisomers |
| WO2011042910A2 (en) * | 2009-10-09 | 2011-04-14 | Hetero Research Foundation | Optical resolution of substituted 2-(2- pyridinylmethylsulphinyl)-1h-benzimidazoles |
| UA113291C2 (xx) | 2011-08-04 | 2017-01-10 | Метаболіти транскломіфену і їх застосування | |
| CA2880388A1 (en) | 2012-08-21 | 2014-02-27 | Repros Therapeutics Inc. | Trans-clomiphene formulations and uses thereof |
| HK1216502A1 (zh) | 2012-11-02 | 2016-11-18 | Repros Therapeutics Inc. | 用於癌症治療的反式-克羅米芬 |
| CN106068121A (zh) * | 2014-03-11 | 2016-11-02 | 利普生物药剂公司 | 使用单一溶剂进行克罗米芬合成 |
| RU2020120156A (ru) | 2014-07-24 | 2020-07-03 | Эспен Парк Фармасьютикалз, Инк. | Лечение приливов и потери костной ткани, вызванных андрогенной депривационной терапией с применением цис-кломифена |
| EP3015454A1 (en) * | 2014-10-28 | 2016-05-04 | F.I.S.- Fabbrica Italiana Sintetici S.p.A. | Stable solid form of trans-Clomiphene citrate |
| EP3015453B1 (en) | 2014-10-28 | 2016-10-12 | F.I.S.- Fabbrica Italiana Sintetici S.p.A. | Process for the preparation of Clomiphene |
| CA2989364C (en) | 2016-04-22 | 2021-07-20 | F.I.S. - Fabbrica Italiana Sintetici S.P.A. | Process for the preparation of enclomiphene citrate having needle shaped crystal habit. |
| CN116832020A (zh) | 2017-09-11 | 2023-10-03 | 阿托萨治疗学公司 | 制备和使用内昔芬的方法 |
| FR3082842A1 (fr) * | 2018-06-21 | 2019-12-27 | Veru Inc. | Polymorphe de cis-clomiphene (zuclomiphene) et procedes d'utilisation de celui-ci |
| JP7662204B2 (ja) | 2019-07-03 | 2025-04-15 | アトッサ・セラピューティクス・インコーポレイテッド | エンドキシフェンの徐放性組成物 |
| CA3098552A1 (en) | 2019-11-14 | 2021-05-14 | Apotex Inc. | Processes for the preparation of zuclomiphene and intermediates thereof |
| CA3098725A1 (en) | 2019-11-14 | 2021-05-14 | Apotex Inc. | Zuclpomiphene salts and crystalline forms thereof |
| CA3105944A1 (en) | 2020-01-22 | 2021-07-22 | Apotex Inc. | Crystalline forms of zuclomiphene citrate |
| EP3907213A1 (en) | 2020-05-04 | 2021-11-10 | Pcas | Processes for the production of isomerically pure or enriched cis-clomiphene |
| US11578025B2 (en) | 2020-10-19 | 2023-02-14 | Apotex Inc. | Processes for the preparation of zuclomiphene intermediates |
-
1971
- 1971-03-18 IT IT49167/71A patent/IT951631B/it active
-
1972
- 1972-02-28 ZA ZA721297A patent/ZA721297B/xx unknown
- 1972-02-29 IL IL38860A patent/IL38860A/xx unknown
- 1972-03-03 PH PH13312A patent/PH10768A/en unknown
- 1972-03-03 AU AU39611/72A patent/AU462431B2/en not_active Expired
- 1972-03-09 CA CA136,671A patent/CA961500A/en not_active Expired
- 1972-03-09 GB GB1104172A patent/GB1360946A/en not_active Expired
- 1972-03-10 US US00233793A patent/US3848030A/en not_active Expired - Lifetime
- 1972-03-15 SE SE7203303A patent/SE409323B/xx unknown
- 1972-03-16 DE DE2212660A patent/DE2212660C3/de not_active Expired
- 1972-03-17 NL NL7203574A patent/NL7203574A/xx not_active Application Discontinuation
- 1972-03-17 ES ES400862A patent/ES400862A1/es not_active Expired
- 1972-03-17 FR FR7209350A patent/FR2129741A5/fr not_active Expired
- 1972-03-17 DK DK127372AA patent/DK139944B/da unknown
- 1972-03-17 CH CH395572A patent/CH576921A5/xx not_active IP Right Cessation
- 1972-03-17 BE BE780887A patent/BE780887A/xx unknown
- 1972-03-17 JP JP2661472A patent/JPS5547013B1/ja active Pending
- 1972-03-17 NO NO880/72A patent/NO136357C/no unknown
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0180276A1 (en) * | 1984-10-24 | 1986-05-07 | Stamicarbon B.V. | Dioxaphosphorinanes, their preparation and use for resolving optically active compounds |
| WO2001030763A1 (en) * | 1999-10-22 | 2001-05-03 | Takeda Chemical Industries, Ltd. | Process for producing optically active naphthalene derivative and optical resolver therefor |
| US6800778B1 (en) | 1999-10-22 | 2004-10-05 | Takeda Chemical Industries, Ltd. | Process for producing optically active naphthalene derivative and optical resolver therefor |
Also Published As
| Publication number | Publication date |
|---|---|
| DE2212660C3 (de) | 1981-09-24 |
| AU3961172A (en) | 1973-09-06 |
| DE2212660A1 (de) | 1972-09-28 |
| CA961500A (en) | 1975-01-21 |
| US3848030A (en) | 1974-11-12 |
| AU462431B2 (en) | 1975-06-09 |
| FR2129741A5 (enExample) | 1972-10-27 |
| ZA721297B (en) | 1973-03-28 |
| NO136357B (enExample) | 1977-05-16 |
| JPS5547013B1 (enExample) | 1980-11-27 |
| NO136357C (no) | 1977-08-24 |
| DE2212660B2 (de) | 1980-07-10 |
| CH576921A5 (enExample) | 1976-06-30 |
| PH10768A (en) | 1977-09-05 |
| IL38860A0 (en) | 1972-04-27 |
| DK139944B (da) | 1979-05-21 |
| ES400862A1 (es) | 1976-04-16 |
| SE409323B (sv) | 1979-08-13 |
| IT951631B (it) | 1973-07-10 |
| NL7203574A (enExample) | 1972-09-20 |
| DK139944C (enExample) | 1979-10-22 |
| IL38860A (en) | 1975-06-25 |
| BE780887A (fr) | 1972-07-17 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| GB1360946A (en) | Process of separating optical geometric structural isomers and the compounds used therefor | |
| FR2362820A1 (fr) | Procede de preparation d'esters d'acide cyclopropane-carboxylique a substituant vinylique | |
| OA03052A (fr) | Procédé de dédoublement d'énantiomères de dérivés de l'acide (cis-1,2-époxypropyl) phosphonique. | |
| ES2152024T3 (es) | Procedimiento para desdoblar acidos quirales con 1-aminoindan-2-oles. | |
| GB1261469A (en) | An optical isomer of chrysanthemic acid and processes for preparing it | |
| ATE920T1 (de) | Verfahren zur herstellung von phosphin- und phosphonsaeureanhydriden. | |
| GB1446304A (en) | 3-substituted cyclopropane carboxylic acids and derivatives thereof | |
| FR2322865A1 (fr) | Procede pour preparer des hydantoines ou des thiohydrantoines modifiees par des radicaux esters d'acide carboxylique | |
| EP0002733A3 (de) | Verfahren zur Herstellung von Phosphin- und Phosponsäure-Anhydriden | |
| DE3382618D1 (de) | Verfahren zur herstellung von(d)2-(6-methoxy-2-naphthyl)propionsaeure und pharmazeutisch verwendbaren salzen davon und neue zwischenprodukte. | |
| FR2329651A1 (fr) | Procede de preparation d'acides cyclopropane-carboxyliques | |
| BE784923A (fr) | Procede de preparation de dihalogenures d'acides phosphoniques | |
| FR2299869A1 (fr) | Procede de preparation d'acides ( | |
| FR2381755A1 (fr) | Sels metalliques d'acides hydroxy-benzoiques utilisables comme stabilisants de polymeres | |
| SE7601948L (sv) | Sett att framstella karboxi-alkan-fosfonsyror och karboxi-alkyl-fosfinsyror | |
| FR2367772A1 (fr) | Triazinyl-phosphonates utilisables comme stabilisants de matieres organiques | |
| BE848498A (fr) | Procede de preparation d'esters d'acides alcane-phosphoniques, | |
| GB1502527A (en) | Cyclopropane derivatives | |
| BE834672A (fr) | Derives phosphores d'acides carboxyliques insatures utilisables comme ignifugeant | |
| SU561505A3 (ru) | Способ получени 3-(4-бифенилил) -масл ной кислоты или ее солей | |
| SU135487A1 (ru) | Способ получени диалкил(арил)ацилфосфитов | |
| BE849467A (fr) | Procede de preparation d'esters alkyliques d'acide propionique alpha -arylsubstitues | |
| FR2318874A1 (fr) | Procede de preparation de dihalogenures d'esters d'acide dithiophosphorique | |
| JPS5219625A (en) | Process for preparation of organophosphorus compounds | |
| SE7602119L (sv) | Sett att framstella 0,0-dimetyl-respektive 0,0-dietyl-0-(2,2-diklorvinyl)-tionofosforsyraestrar |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PS | Patent sealed [section 19, patents act 1949] | ||
| PLE | Entries relating assignments, transmissions, licences in the register of patents | ||
| PCNP | Patent ceased through non-payment of renewal fee |