DE2423389A1 - Arzneimittel mit psychotroper wirkung und verfahren zu ihrer herstellung - Google Patents
Arzneimittel mit psychotroper wirkung und verfahren zu ihrer herstellungInfo
- Publication number
- DE2423389A1 DE2423389A1 DE2423389A DE2423389A DE2423389A1 DE 2423389 A1 DE2423389 A1 DE 2423389A1 DE 2423389 A DE2423389 A DE 2423389A DE 2423389 A DE2423389 A DE 2423389A DE 2423389 A1 DE2423389 A1 DE 2423389A1
- Authority
- DE
- Germany
- Prior art keywords
- pyroglutamyl
- acid
- solution
- filtered
- residue
- 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.)
- Withdrawn
Links
- 230000000506 psychotropic effect Effects 0.000 title claims description 4
- 238000004519 manufacturing process Methods 0.000 title description 2
- 229940126601 medicinal product Drugs 0.000 title description 2
- 238000002360 preparation method Methods 0.000 claims description 10
- 150000001875 compounds Chemical class 0.000 claims description 8
- 239000003814 drug Substances 0.000 claims description 6
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 5
- 238000000034 method Methods 0.000 claims description 4
- 125000004432 carbon atom Chemical group C* 0.000 claims description 2
- 125000005518 carboxamido group Chemical group 0.000 claims description 2
- 229940079593 drug Drugs 0.000 claims description 2
- 239000012059 conventional drug carrier Substances 0.000 claims 1
- 239000000546 pharmaceutical excipient Substances 0.000 claims 1
- 230000001225 therapeutic effect Effects 0.000 claims 1
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- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 39
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 38
- 239000000243 solution Substances 0.000 description 30
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 18
- 239000000203 mixture Substances 0.000 description 18
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- -1 L-pyroglutamyl compounds Chemical class 0.000 description 9
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- DTQVDTLACAAQTR-UHFFFAOYSA-N Trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 description 6
- 229960003692 gamma aminobutyric acid Drugs 0.000 description 6
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- HVCNXQOWACZAFN-UHFFFAOYSA-N 4-ethylmorpholine Chemical compound CCN1CCOCC1 HVCNXQOWACZAFN-UHFFFAOYSA-N 0.000 description 5
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- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 4
- FBPFZTCFMRRESA-KVTDHHQDSA-N D-Mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KVTDHHQDSA-N 0.000 description 4
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- 239000011780 sodium chloride Substances 0.000 description 4
- ODHCTXKNWHHXJC-VKHMYHEASA-N 5-oxo-L-proline Chemical compound OC(=O)[C@@H]1CCC(=O)N1 ODHCTXKNWHHXJC-VKHMYHEASA-N 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
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- 239000002253 acid Substances 0.000 description 3
- ODHCTXKNWHHXJC-UHFFFAOYSA-N acide pyroglutamique Natural products OC(=O)C1CCC(=O)N1 ODHCTXKNWHHXJC-UHFFFAOYSA-N 0.000 description 3
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- IZUPBVBPLAPZRR-UHFFFAOYSA-N pentachlorophenol Chemical class OC1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl IZUPBVBPLAPZRR-UHFFFAOYSA-N 0.000 description 3
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- CZVNLCOJFFYZPG-UHFFFAOYSA-N tert-butyl 4-aminobutanoate;hydrochloride Chemical compound Cl.CC(C)(C)OC(=O)CCCN CZVNLCOJFFYZPG-UHFFFAOYSA-N 0.000 description 3
- UFTFJSFQGQCHQW-UHFFFAOYSA-N triformin Chemical compound O=COCC(OC=O)COC=O UFTFJSFQGQCHQW-UHFFFAOYSA-N 0.000 description 3
- CLNSLBYOSNFAOC-WHFBIAKZSA-N (2s)-n-[(2s)-1-amino-1-oxopropan-2-yl]-5-oxopyrrolidine-2-carboxamide Chemical compound NC(=O)[C@H](C)NC(=O)[C@@H]1CCC(=O)N1 CLNSLBYOSNFAOC-WHFBIAKZSA-N 0.000 description 2
- UICDNADSGVMHKL-ZETCQYMHSA-N (2s)-n-butyl-5-oxopyrrolidine-2-carboxamide Chemical compound CCCCNC(=O)[C@@H]1CCC(=O)N1 UICDNADSGVMHKL-ZETCQYMHSA-N 0.000 description 2
- ADFXKUOMJKEIND-UHFFFAOYSA-N 1,3-dicyclohexylurea Chemical compound C1CCCCC1NC(=O)NC1CCCCC1 ADFXKUOMJKEIND-UHFFFAOYSA-N 0.000 description 2
- AZCKRPCBIRVBHR-AHXFUIDQSA-N 4-amino-2-[(2S)-5-oxopyrrolidine-2-carbonyl]pentanoic acid Chemical compound CC(N)CC(C(O)=O)C(=O)[C@@H]1CCC(=O)N1 AZCKRPCBIRVBHR-AHXFUIDQSA-N 0.000 description 2
- SJTNUDPSFMEUGP-UHFFFAOYSA-N 4-amino-2-phenylmethoxycarbonylbutanoic acid Chemical compound NCCC(C(O)=O)C(=O)OCC1=CC=CC=C1 SJTNUDPSFMEUGP-UHFFFAOYSA-N 0.000 description 2
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 2
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 2
- QOSSAOTZNIDXMA-UHFFFAOYSA-N Dicylcohexylcarbodiimide Chemical compound C1CCCCC1N=C=NC1CCCCC1 QOSSAOTZNIDXMA-UHFFFAOYSA-N 0.000 description 2
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- 108010010803 Gelatin Proteins 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
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- 229940124277 aminobutyric acid Drugs 0.000 description 2
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- 229940097496 nasal spray Drugs 0.000 description 1
- 239000002674 ointment Substances 0.000 description 1
- BARWIPMJPCRCTP-UHFFFAOYSA-N oleic acid oleyl ester Natural products CCCCCCCCC=CCCCCCCCCOC(=O)CCCCCCCC=CCCCCCCCC BARWIPMJPCRCTP-UHFFFAOYSA-N 0.000 description 1
- 125000000636 p-nitrophenyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)[N+]([O-])=O 0.000 description 1
- 238000007911 parenteral administration Methods 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- 239000008363 phosphate buffer Substances 0.000 description 1
- 239000002504 physiological saline solution Substances 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 229920000191 poly(N-vinyl pyrrolidone) Polymers 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 230000002335 preservative effect Effects 0.000 description 1
- 150000003141 primary amines Chemical class 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 125000006239 protecting group Chemical group 0.000 description 1
- 208000020016 psychiatric disease Diseases 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- DTSWLLBBGHRXQH-XPUUQOCRSA-N pyroglutamylvaline Chemical compound CC(C)[C@@H](C(O)=O)NC(=O)[C@@H]1CCC(=O)N1 DTSWLLBBGHRXQH-XPUUQOCRSA-N 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 230000007017 scission Effects 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- DOMTZTVJNZKUNX-UHFFFAOYSA-N tert-butyl 3-aminopropanoate;hydrochloride Chemical compound Cl.CC(C)(C)OC(=O)CCN DOMTZTVJNZKUNX-UHFFFAOYSA-N 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 1
- 230000001646 thyrotropic effect Effects 0.000 description 1
- PZSJOBKRSVRODF-UHFFFAOYSA-N vanillin acetate Chemical compound COC1=CC(C=O)=CC=C1OC(C)=O PZSJOBKRSVRODF-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/06—Dipeptides
- C07K5/06139—Dipeptides with the first amino acid being heterocyclic
- C07K5/06173—Dipeptides with the first amino acid being heterocyclic and Glp-amino acid; Derivatives thereof
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/18—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member
- C07D207/22—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member 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
- C07D207/24—Oxygen or sulfur atoms
- C07D207/26—2-Pyrrolidones
- C07D207/273—2-Pyrrolidones 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 other ring carbon atoms
- C07D207/277—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D207/28—2-Pyrrolidone-5- carboxylic acids; Functional derivatives thereof, e.g. esters, nitriles
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Medicinal Chemistry (AREA)
- Molecular Biology (AREA)
- Biochemistry (AREA)
- Biophysics (AREA)
- General Health & Medical Sciences (AREA)
- Genetics & Genomics (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Pyridine Compounds (AREA)
- Peptides Or Proteins (AREA)
- Plural Heterocyclic Compounds (AREA)
Priority Applications (11)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2423389A DE2423389A1 (de) | 1974-05-14 | 1974-05-14 | Arzneimittel mit psychotroper wirkung und verfahren zu ihrer herstellung |
| NL7505479A NL7505479A (nl) | 1974-05-14 | 1975-05-09 | Werkwijze voor het bereiden van geneesmiddelen met psychotrope werking. |
| DK207575A DK207575A (da) | 1974-05-14 | 1975-05-12 | Legemiddel med psykotrop virkning dets anveldelse samt fremgangsmade til fremstilling deraf og af de aktive forbindelser deri |
| LU72449A LU72449A1 (enExample) | 1974-05-14 | 1975-05-12 | |
| US05/576,715 US4053588A (en) | 1974-05-14 | 1975-05-12 | Pharmaceutical preparations having psychotropic activity and process for their manufacture |
| GB19839/75A GB1503680A (en) | 1974-05-14 | 1975-05-12 | Pharmaceutical preparations having psychotropic activity and process for their manufacture |
| CA227,257A CA1067410A (en) | 1974-05-14 | 1975-05-13 | Pharmaceutical preparations having psychotropic activity and process for their manufacture |
| IE1068/75A IE41055B1 (en) | 1974-05-14 | 1975-05-13 | Pharmaceutical preparations having psycotropic activity and process for their manufacture |
| FR7515027A FR2270867B1 (enExample) | 1974-05-14 | 1975-05-14 | |
| JP50056231A JPS50157361A (enExample) | 1974-05-14 | 1975-05-14 | |
| BE156336A BE829058A (fr) | 1974-05-14 | 1975-05-14 | Medicament ayant un effet psychotrope, a base de derive de l'pyroglutamyle |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2423389A DE2423389A1 (de) | 1974-05-14 | 1974-05-14 | Arzneimittel mit psychotroper wirkung und verfahren zu ihrer herstellung |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE2423389A1 true DE2423389A1 (de) | 1975-12-04 |
Family
ID=5915522
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE2423389A Withdrawn DE2423389A1 (de) | 1974-05-14 | 1974-05-14 | Arzneimittel mit psychotroper wirkung und verfahren zu ihrer herstellung |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US4053588A (enExample) |
| JP (1) | JPS50157361A (enExample) |
| BE (1) | BE829058A (enExample) |
| CA (1) | CA1067410A (enExample) |
| DE (1) | DE2423389A1 (enExample) |
| DK (1) | DK207575A (enExample) |
| FR (1) | FR2270867B1 (enExample) |
| GB (1) | GB1503680A (enExample) |
| IE (1) | IE41055B1 (enExample) |
| LU (1) | LU72449A1 (enExample) |
| NL (1) | NL7505479A (enExample) |
Families Citing this family (27)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1492640A (en) * | 1975-07-08 | 1977-11-23 | Ucb Sa | L-pyroglutamyl-l-prolinamide |
| AU600259B2 (en) * | 1986-02-28 | 1990-08-09 | Hafslund Nycomed As | Pharmaceutical preparation containing a dipeptide with cell growth regulating effect |
| IT1244548B (it) * | 1991-02-06 | 1994-07-15 | Poli Ind Chimica Spa | Derivati della 5-oxo-l-prolina e loro applicazioni farmaceutiche |
| WO2005018556A2 (en) | 2003-08-12 | 2005-03-03 | 3M Innovative Properties Company | Hydroxylamine substituted imidazo-containing compounds |
| RU2006105101A (ru) | 2003-08-27 | 2007-10-10 | 3М Инновейтив Пропертиз Компани (US) | Арилокси и арилалкиленокси замещенные имидазохинолины |
| WO2005023190A2 (en) | 2003-09-05 | 2005-03-17 | 3M Innovative Properties Company | Treatment for cd5+ b cell lymphoma |
| US7544697B2 (en) | 2003-10-03 | 2009-06-09 | Coley Pharmaceutical Group, Inc. | Pyrazolopyridines and analogs thereof |
| US8871782B2 (en) | 2003-10-03 | 2014-10-28 | 3M Innovative Properties Company | Alkoxy substituted imidazoquinolines |
| US8598192B2 (en) | 2003-11-14 | 2013-12-03 | 3M Innovative Properties Company | Hydroxylamine substituted imidazoquinolines |
| CA2545774A1 (en) | 2003-11-14 | 2005-06-02 | 3M Innovative Properties Company | Oxime substituted imidazo ring compounds |
| AR046781A1 (es) | 2003-11-25 | 2005-12-21 | 3M Innovative Properties Co | Derivados de imidazoquinolinas. composiciones farmaceuticas. |
| WO2005066170A1 (en) | 2003-12-29 | 2005-07-21 | 3M Innovative Properties Company | Arylalkenyl and arylalkynyl substituted imidazoquinolines |
| CA2551399A1 (en) | 2003-12-30 | 2005-07-21 | 3M Innovative Properties Company | Imidazoquinolinyl, imidazopyridinyl, and imidazonaphthyridinyl sulfonamides |
| AU2005228150A1 (en) | 2004-03-24 | 2005-10-13 | 3M Innovative Properties Company | Amide substituted imidazopyridines, imidazoquinolines, and imidazonaphthyridines |
| WO2005123080A2 (en) | 2004-06-15 | 2005-12-29 | 3M Innovative Properties Company | Nitrogen-containing heterocyclyl substituted imidazoquinolines and imidazonaphthyridines |
| US8026366B2 (en) | 2004-06-18 | 2011-09-27 | 3M Innovative Properties Company | Aryloxy and arylalkyleneoxy substituted thiazoloquinolines and thiazolonaphthyridines |
| WO2006065280A2 (en) | 2004-06-18 | 2006-06-22 | 3M Innovative Properties Company | Isoxazole, dihydroisoxazole, and oxadiazole substituted imidazo ring compounds and methods |
| WO2006038923A2 (en) | 2004-06-18 | 2006-04-13 | 3M Innovative Properties Company | Aryl substituted imidazonaphthyridines |
| US20080119508A1 (en) * | 2004-12-30 | 2008-05-22 | 3M Innovative Properties Company | Multi-Route Administration Of Immune Response Modifier Compounds |
| EP1831226B1 (en) | 2004-12-30 | 2012-08-08 | 3M Innovative Properties Company | Chiral tetracyclic compounds inducing interferon biosynthesis |
| AU2005326708C1 (en) | 2004-12-30 | 2012-08-30 | 3M Innovative Properties Company | Substituted chiral fused [1,2]imidazo[4,5-c] ring compounds |
| AU2006210392A1 (en) | 2005-02-04 | 2006-08-10 | Coley Pharmaceutical Group, Inc. | Aqueous gel formulations containing immune response modifiers |
| CA2597587A1 (en) | 2005-02-11 | 2006-08-17 | Coley Pharmaceutical Group, Inc. | Oxime and hydroxylamine substituted imidazo[4,5-c] ring compounds and methods |
| US7943636B2 (en) | 2005-04-01 | 2011-05-17 | 3M Innovative Properties Company | 1-substituted pyrazolo (3,4-C) ring compounds as modulators of cytokine biosynthesis for the treatment of viral infections and neoplastic diseases |
| WO2006107853A2 (en) | 2005-04-01 | 2006-10-12 | Coley Pharmaceutical Group, Inc. | Pyrazolopyridine-1,4-diamines and analogs thereof |
| US7906506B2 (en) | 2006-07-12 | 2011-03-15 | 3M Innovative Properties Company | Substituted chiral fused [1,2] imidazo [4,5-c] ring compounds and methods |
| DE102014110783B4 (de) * | 2014-07-30 | 2025-12-24 | Licit Solutions Gmbh | Zusammensetzung zur Konservierung und Fixierung von Organen, Geweben, Ganzkör-perpräparaten und Leichen |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE63496C (de) * | B. A. DOBSON in Bolton, Grafsch. Lancaster, England, und E. APPENZELLER in Alost, Belgien | Krempel mit Verringerung der Geschwindigkeit des Abnehmers beim Zerreifsen des Bandes | ||
| US3002978A (en) * | 1958-05-06 | 1961-10-03 | Bocher Gustave Marie Joseph | Glyceryl pyrrolidone carboxylates |
| FR2207707A1 (en) * | 1972-11-27 | 1974-06-21 | Fabre Sa Pierre | 2-Pyrrolidone-5-carboxylic acid esters and amides - with sedative and hypnotic activity |
-
1974
- 1974-05-14 DE DE2423389A patent/DE2423389A1/de not_active Withdrawn
-
1975
- 1975-05-09 NL NL7505479A patent/NL7505479A/xx not_active Application Discontinuation
- 1975-05-12 DK DK207575A patent/DK207575A/da not_active Application Discontinuation
- 1975-05-12 US US05/576,715 patent/US4053588A/en not_active Expired - Lifetime
- 1975-05-12 LU LU72449A patent/LU72449A1/xx unknown
- 1975-05-12 GB GB19839/75A patent/GB1503680A/en not_active Expired
- 1975-05-13 IE IE1068/75A patent/IE41055B1/xx unknown
- 1975-05-13 CA CA227,257A patent/CA1067410A/en not_active Expired
- 1975-05-14 JP JP50056231A patent/JPS50157361A/ja active Pending
- 1975-05-14 FR FR7515027A patent/FR2270867B1/fr not_active Expired
- 1975-05-14 BE BE156336A patent/BE829058A/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| NL7505479A (nl) | 1975-11-18 |
| IE41055L (en) | 1975-11-14 |
| GB1503680A (en) | 1978-03-15 |
| LU72449A1 (enExample) | 1977-02-09 |
| FR2270867B1 (enExample) | 1978-08-04 |
| JPS50157361A (enExample) | 1975-12-19 |
| BE829058A (fr) | 1975-11-14 |
| US4053588A (en) | 1977-10-11 |
| CA1067410A (en) | 1979-12-04 |
| IE41055B1 (en) | 1979-10-10 |
| FR2270867A1 (enExample) | 1975-12-12 |
| DK207575A (da) | 1975-11-15 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| 8141 | Disposal/no request for examination |