SK145999A3 - Production of enantiomer-free biarylketocarboxylic acids - Google Patents
Production of enantiomer-free biarylketocarboxylic acids Download PDFInfo
- Publication number
- SK145999A3 SK145999A3 SK1459-99A SK145999A SK145999A3 SK 145999 A3 SK145999 A3 SK 145999A3 SK 145999 A SK145999 A SK 145999A SK 145999 A3 SK145999 A3 SK 145999A3
- Authority
- SK
- Slovakia
- Prior art keywords
- enantiomer
- acetone
- acid
- acids
- biarylketocarboxylic
- Prior art date
Links
- 239000002253 acid Substances 0.000 title claims abstract description 20
- 150000007513 acids Chemical class 0.000 title claims abstract description 9
- 238000004519 manufacturing process Methods 0.000 title abstract description 7
- 238000000034 method Methods 0.000 claims description 3
- 238000002360 preparation method Methods 0.000 claims description 2
- 102000004190 Enzymes Human genes 0.000 abstract description 4
- 108090000790 Enzymes Proteins 0.000 abstract description 4
- 206010027476 Metastases Diseases 0.000 abstract description 2
- 239000003112 inhibitor Substances 0.000 abstract description 2
- 230000002401 inhibitory effect Effects 0.000 abstract description 2
- 201000008482 osteoarthritis Diseases 0.000 abstract description 2
- 206010039073 rheumatoid arthritis Diseases 0.000 abstract description 2
- 102000002274 Matrix Metalloproteinases Human genes 0.000 abstract 1
- 108010000684 Matrix Metalloproteinases Proteins 0.000 abstract 1
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 44
- 150000003839 salts Chemical class 0.000 description 21
- RMVRSNDYEFQCLF-UHFFFAOYSA-N thiophenol Chemical compound SC1=CC=CC=C1 RMVRSNDYEFQCLF-UHFFFAOYSA-N 0.000 description 18
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 17
- 238000006243 chemical reaction Methods 0.000 description 12
- QSDPWSMTQJZXIT-UHFFFAOYSA-N 1-chloro-4-phenylbenzene 5-oxo-3-(phenylsulfanylmethylidene)pentanoic acid Chemical compound C1=CC(Cl)=CC=C1C1=CC=CC=C1.OC(=O)CC(CC=O)=CSC1=CC=CC=C1 QSDPWSMTQJZXIT-UHFFFAOYSA-N 0.000 description 9
- 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 description 9
- 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 description 8
- 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 description 8
- 239000002904 solvent Substances 0.000 description 8
- 239000000203 mixture Substances 0.000 description 6
- 238000001953 recrystallisation Methods 0.000 description 6
- VEPTXBCIDSFGBF-UHFFFAOYSA-M tetrabutylazanium;fluoride;trihydrate Chemical compound O.O.O.[F-].CCCC[N+](CCCC)(CCCC)CCCC VEPTXBCIDSFGBF-UHFFFAOYSA-M 0.000 description 6
- HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 description 5
- 239000000047 product Substances 0.000 description 5
- 238000000746 purification Methods 0.000 description 5
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 4
- 239000011541 reaction mixture Substances 0.000 description 4
- 238000010992 reflux Methods 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- RQEUFEKYXDPUSK-ZETCQYMHSA-N (1S)-1-phenylethanamine Chemical compound C[C@H](N)C1=CC=CC=C1 RQEUFEKYXDPUSK-ZETCQYMHSA-N 0.000 description 3
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- SEFDLRRKWPJXIR-UHFFFAOYSA-N 3-(2-phenylphenyl)prop-2-enoic acid Chemical compound OC(=O)C=CC1=CC=CC=C1C1=CC=CC=C1 SEFDLRRKWPJXIR-UHFFFAOYSA-N 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- IVNGPTYJANYJIT-UHFFFAOYSA-N OC(=O)CC(=C)CC=O.C1=CC(Cl)=CC=C1C1=CC=CC=C1 Chemical compound OC(=O)CC(=C)CC=O.C1=CC(Cl)=CC=C1C1=CC=CC=C1 IVNGPTYJANYJIT-UHFFFAOYSA-N 0.000 description 3
- 239000013078 crystal Substances 0.000 description 3
- 125000004494 ethyl ester group Chemical group 0.000 description 3
- 239000000546 pharmaceutical excipient Substances 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- XTHFKEDIFFGKHM-UHFFFAOYSA-N Dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 description 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 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 230000003287 optical effect Effects 0.000 description 2
- FDPIMTJIUBPUKL-UHFFFAOYSA-N pentan-3-one Chemical compound CCC(=O)CC FDPIMTJIUBPUKL-UHFFFAOYSA-N 0.000 description 2
- 239000002244 precipitate Substances 0.000 description 2
- FPGGTKZVZWFYPV-UHFFFAOYSA-M tetrabutylammonium fluoride Chemical compound [F-].CCCC[N+](CCCC)(CCCC)CCCC FPGGTKZVZWFYPV-UHFFFAOYSA-M 0.000 description 2
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 2
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 1
- -1 4-chloro-biphenyl-4-oxo-2-phenyl-thiomethylene-butanecarboxylic acid Chemical class 0.000 description 1
- 235000001258 Cinchona calisaya Nutrition 0.000 description 1
- WFJNHVWTKZUUTR-QAMTZSDWSA-N Hydrocinchonine Chemical compound C1=CC=C2C([C@H](O)[C@H]3C[C@@H]4CCN3C[C@@H]4CC)=CC=NC2=C1 WFJNHVWTKZUUTR-QAMTZSDWSA-N 0.000 description 1
- 102000005741 Metalloproteases Human genes 0.000 description 1
- 108010006035 Metalloproteases Proteins 0.000 description 1
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 1
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 1
- QMGVPVSNSZLJIA-UHFFFAOYSA-N Nux Vomica Natural products C1C2C3C4N(C=5C6=CC=CC=5)C(=O)CC3OCC=C2CN2C1C46CC2 QMGVPVSNSZLJIA-UHFFFAOYSA-N 0.000 description 1
- JVVXZOOGOGPDRZ-SLFFLAALSA-N [(1R,4aS,10aR)-1,4a-dimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthren-1-yl]methanamine Chemical compound NC[C@]1(C)CCC[C@]2(C)C3=CC=C(C(C)C)C=C3CC[C@H]21 JVVXZOOGOGPDRZ-SLFFLAALSA-N 0.000 description 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 description 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 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 238000003776 cleavage reaction Methods 0.000 description 1
- SBZXBUIDTXKZTM-UHFFFAOYSA-N diglyme Chemical compound COCCOCCOC SBZXBUIDTXKZTM-UHFFFAOYSA-N 0.000 description 1
- WFJNHVWTKZUUTR-UHFFFAOYSA-N dihydrocinchonidine Natural products C1=CC=C2C(C(O)C3CC4CCN3CC4CC)=CC=NC2=C1 WFJNHVWTKZUUTR-UHFFFAOYSA-N 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 230000009401 metastasis Effects 0.000 description 1
- 239000005445 natural material Substances 0.000 description 1
- 229960000948 quinine Drugs 0.000 description 1
- 239000011833 salt mixture Substances 0.000 description 1
- 230000007017 scission Effects 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C319/00—Preparation of thiols, sulfides, hydropolysulfides or polysulfides
- C07C319/26—Separation; Purification; Stabilisation; Use of additives
- C07C319/28—Separation; Purification
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B57/00—Separation of optically-active compounds
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19717429A DE19717429A1 (de) | 1997-04-25 | 1997-04-25 | Herstellung enantiomerenreiner Biarylketocarbonsäuren |
| PCT/EP1998/002176 WO1998049124A1 (de) | 1997-04-25 | 1998-04-14 | Herstellung enantiomerenreiner biarylketocarbonsäuren |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SK145999A3 true SK145999A3 (en) | 2000-05-16 |
Family
ID=7827688
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SK1459-99A SK145999A3 (en) | 1997-04-25 | 1998-04-14 | Production of enantiomer-free biarylketocarboxylic acids |
Country Status (22)
| Country | Link |
|---|---|
| US (1) | US6172259B1 (id) |
| EP (1) | EP0977717A1 (id) |
| JP (1) | JP2001524102A (id) |
| KR (1) | KR20010020236A (id) |
| CN (1) | CN1253539A (id) |
| AR (1) | AR012440A1 (id) |
| AU (1) | AU730250B2 (id) |
| BG (1) | BG103776A (id) |
| BR (1) | BR9809418A (id) |
| CA (1) | CA2288107A1 (id) |
| CO (1) | CO4940428A1 (id) |
| DE (1) | DE19717429A1 (id) |
| HU (1) | HUP0003633A3 (id) |
| ID (1) | ID22701A (id) |
| IL (1) | IL132065A0 (id) |
| NO (1) | NO994977D0 (id) |
| PL (1) | PL336323A1 (id) |
| SK (1) | SK145999A3 (id) |
| TR (1) | TR199902451T2 (id) |
| TW (1) | TW382622B (id) |
| WO (1) | WO1998049124A1 (id) |
| ZA (1) | ZA983473B (id) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8768754B2 (en) * | 2006-01-09 | 2014-07-01 | Rent-A-Toll, Ltd. | Billing a rented third party transport including an on-board unit |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GR64816B (en) | 1977-03-08 | 1980-06-03 | Boots Co Ltd | Resolution of flurbiprofen ii/iii |
| IT1222013B (it) * | 1987-07-10 | 1990-08-31 | Chimica Profarmaco Spa Ind | Processo di risoluzione ottica di acido 2 (6 metossi 2 naftil) propionico |
| DE3824353A1 (de) | 1988-07-19 | 1990-01-25 | Paz Arzneimittelentwicklung | Verfahren zur trennung von gemischen enantiomerer arylpropionsaeuren |
| CA2023954C (en) | 1989-10-17 | 1999-05-04 | Hiroyuki Nohira | Process for the optical resolution of 2-(3-benzoyl) phenylpropionic acid |
| JP3574954B2 (ja) | 1993-11-26 | 2004-10-06 | ナガセケムテックス株式会社 | ２−アリールプロピオン酸化合物の光学分割方法 |
| US5789434A (en) * | 1994-11-15 | 1998-08-04 | Bayer Corporation | Derivatives of substituted 4-biarylbutyric acid as matrix metalloprotease inhibitors |
-
1997
- 1997-04-25 DE DE19717429A patent/DE19717429A1/de not_active Withdrawn
-
1998
- 1998-04-02 TW TW087104934A patent/TW382622B/zh not_active IP Right Cessation
- 1998-04-14 AU AU75251/98A patent/AU730250B2/en not_active Ceased
- 1998-04-14 BR BR9809418-1A patent/BR9809418A/pt not_active Application Discontinuation
- 1998-04-14 JP JP54653698A patent/JP2001524102A/ja active Pending
- 1998-04-14 WO PCT/EP1998/002176 patent/WO1998049124A1/de not_active Ceased
- 1998-04-14 ID IDW991186A patent/ID22701A/id unknown
- 1998-04-14 EP EP98922707A patent/EP0977717A1/de not_active Withdrawn
- 1998-04-14 KR KR1019997009828A patent/KR20010020236A/ko not_active Withdrawn
- 1998-04-14 TR TR1999/02451T patent/TR199902451T2/xx unknown
- 1998-04-14 IL IL13206598A patent/IL132065A0/xx unknown
- 1998-04-14 US US09/381,597 patent/US6172259B1/en not_active Expired - Fee Related
- 1998-04-14 CN CN98804521A patent/CN1253539A/zh active Pending
- 1998-04-14 PL PL98336323A patent/PL336323A1/xx unknown
- 1998-04-14 SK SK1459-99A patent/SK145999A3/sk unknown
- 1998-04-14 HU HU0003633A patent/HUP0003633A3/hu unknown
- 1998-04-14 CA CA002288107A patent/CA2288107A1/en not_active Abandoned
- 1998-04-15 AR ARP980101737A patent/AR012440A1/es unknown
- 1998-04-24 ZA ZA983473A patent/ZA983473B/xx unknown
- 1998-04-24 CO CO98022781A patent/CO4940428A1/es unknown
-
1999
- 1999-10-04 BG BG103776A patent/BG103776A/xx unknown
- 1999-10-13 NO NO994977A patent/NO994977D0/no not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| PL336323A1 (en) | 2000-06-19 |
| ZA983473B (en) | 1998-10-29 |
| IL132065A0 (en) | 2001-03-19 |
| CA2288107A1 (en) | 1998-11-05 |
| EP0977717A1 (de) | 2000-02-09 |
| NO994977L (no) | 1999-10-13 |
| TR199902451T2 (xx) | 2000-04-21 |
| WO1998049124A1 (de) | 1998-11-05 |
| BR9809418A (pt) | 2000-06-13 |
| JP2001524102A (ja) | 2001-11-27 |
| KR20010020236A (ko) | 2001-03-15 |
| NO994977D0 (no) | 1999-10-13 |
| DE19717429A1 (de) | 1998-12-24 |
| AU730250B2 (en) | 2001-03-01 |
| CO4940428A1 (es) | 2000-07-24 |
| US6172259B1 (en) | 2001-01-09 |
| HUP0003633A2 (en) | 2001-03-28 |
| AR012440A1 (es) | 2000-10-18 |
| AU7525198A (en) | 1998-11-24 |
| TW382622B (en) | 2000-02-21 |
| ID22701A (id) | 1999-12-09 |
| HUP0003633A3 (en) | 2001-04-28 |
| CN1253539A (zh) | 2000-05-17 |
| BG103776A (en) | 2000-05-31 |
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