CZ295713B6 - Způsob výroby 1,4,7,10-tetraazacyklododekanu - Google Patents
Způsob výroby 1,4,7,10-tetraazacyklododekanu Download PDFInfo
- Publication number
- CZ295713B6 CZ295713B6 CZ19993818A CZ381899A CZ295713B6 CZ 295713 B6 CZ295713 B6 CZ 295713B6 CZ 19993818 A CZ19993818 A CZ 19993818A CZ 381899 A CZ381899 A CZ 381899A CZ 295713 B6 CZ295713 B6 CZ 295713B6
- Authority
- CZ
- Czechia
- Prior art keywords
- formula
- compound
- process according
- hydrolysis
- preparation
- Prior art date
Links
- QBPPRVHXOZRESW-UHFFFAOYSA-N 1,4,7,10-tetraazacyclododecane Chemical compound C1CNCCNCCNCCN1 QBPPRVHXOZRESW-UHFFFAOYSA-N 0.000 title claims abstract description 7
- 238000004519 manufacturing process Methods 0.000 title 1
- 150000001875 compounds Chemical class 0.000 claims abstract description 31
- 238000000034 method Methods 0.000 claims abstract description 18
- 230000007062 hydrolysis Effects 0.000 claims abstract description 14
- 238000006460 hydrolysis reaction Methods 0.000 claims abstract description 14
- 150000004985 diamines Chemical class 0.000 claims abstract description 13
- 238000002360 preparation method Methods 0.000 claims abstract description 10
- 125000004054 acenaphthylenyl group Chemical group C1(=CC2=CC=CC3=CC=CC1=C23)* 0.000 claims abstract description 5
- HXGDTGSAIMULJN-UHFFFAOYSA-N acetnaphthylene Natural products C1=CC(C=C2)=C3C2=CC=CC3=C1 HXGDTGSAIMULJN-UHFFFAOYSA-N 0.000 claims abstract description 5
- 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 claims description 25
- 238000006243 chemical reaction Methods 0.000 claims description 12
- VILCJCGEZXAXTO-UHFFFAOYSA-N 2,2,2-tetramine Chemical compound NCCNCCNCCN VILCJCGEZXAXTO-UHFFFAOYSA-N 0.000 claims description 11
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 10
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 claims description 9
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical group NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 claims description 7
- 238000002425 crystallisation Methods 0.000 claims description 3
- 230000008025 crystallization Effects 0.000 claims description 3
- 239000012452 mother liquor Substances 0.000 claims description 3
- FKLJPTJMIBLJAV-UHFFFAOYSA-N Compound IV Chemical compound O1N=C(C)C=C1CCCCCCCOC1=CC=C(C=2OCCN=2)C=C1 FKLJPTJMIBLJAV-UHFFFAOYSA-N 0.000 claims description 2
- 239000007864 aqueous solution Substances 0.000 claims description 2
- 239000011261 inert gas Substances 0.000 claims description 2
- RTWNYYOXLSILQN-UHFFFAOYSA-N methanediamine Chemical compound NCN RTWNYYOXLSILQN-UHFFFAOYSA-N 0.000 claims description 2
- HQJLFRMMLKYIJX-UHFFFAOYSA-N 1,2,3,4,4a,5,6,7,8,8a-decahydropyrazino[2,3-b]pyrazine Chemical compound N1CCNC2NCCNC21 HQJLFRMMLKYIJX-UHFFFAOYSA-N 0.000 claims 1
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 33
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 12
- LEQAOMBKQFMDFZ-UHFFFAOYSA-N glyoxal Chemical compound O=CC=O LEQAOMBKQFMDFZ-UHFFFAOYSA-N 0.000 description 10
- 229960001124 trientine Drugs 0.000 description 9
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 7
- 239000000243 solution Substances 0.000 description 7
- HTSGKJQDMSTCGS-UHFFFAOYSA-N 1,4-bis(4-chlorophenyl)-2-(4-methylphenyl)sulfonylbutane-1,4-dione Chemical compound C1=CC(C)=CC=C1S(=O)(=O)C(C(=O)C=1C=CC(Cl)=CC=1)CC(=O)C1=CC=C(Cl)C=C1 HTSGKJQDMSTCGS-UHFFFAOYSA-N 0.000 description 5
- 239000006227 byproduct Substances 0.000 description 5
- 229940015043 glyoxal Drugs 0.000 description 5
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- 239000002585 base Substances 0.000 description 4
- 230000003647 oxidation Effects 0.000 description 4
- 238000007254 oxidation reaction Methods 0.000 description 4
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- AVXURJPOCDRRFD-UHFFFAOYSA-N Hydroxylamine Chemical compound ON AVXURJPOCDRRFD-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 239000000284 extract Substances 0.000 description 3
- 238000002955 isolation Methods 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 239000008188 pellet Substances 0.000 description 3
- UYBWIEGTWASWSR-UHFFFAOYSA-N 1,3-diaminopropan-2-ol Chemical compound NCC(O)CN UYBWIEGTWASWSR-UHFFFAOYSA-N 0.000 description 2
- BMYNFMYTOJXKLE-UHFFFAOYSA-N 3-azaniumyl-2-hydroxypropanoate Chemical compound NCC(O)C(O)=O BMYNFMYTOJXKLE-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 2
- 239000000920 calcium hydroxide Substances 0.000 description 2
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 2
- 238000009833 condensation Methods 0.000 description 2
- 230000005494 condensation Effects 0.000 description 2
- 230000003301 hydrolyzing effect Effects 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 238000010992 reflux Methods 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- AMQJEAYHLZJPGS-UHFFFAOYSA-N N-Pentanol Chemical compound CCCCCO AMQJEAYHLZJPGS-UHFFFAOYSA-N 0.000 description 1
- -1 Triethylene tetramine monohydrate Chemical class 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- 229940100198 alkylating agent Drugs 0.000 description 1
- 239000002168 alkylating agent Substances 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 239000011260 aqueous acid Substances 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 239000012458 free base Substances 0.000 description 1
- 238000004817 gas chromatography Methods 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 239000000383 hazardous chemical Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 239000012074 organic phase Substances 0.000 description 1
- 238000007248 oxidative elimination reaction Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 150000003458 sulfonic acid derivatives Chemical class 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D257/00—Heterocyclic compounds containing rings having four nitrogen atoms as the only ring hetero atoms
- C07D257/02—Heterocyclic compounds containing rings having four nitrogen atoms as the only ring hetero atoms not condensed with other rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IT97MI000982A IT1291673B1 (it) | 1997-04-28 | 1997-04-28 | Processo per la preparazione di 1,4,7,10 - tetraazaciclododecano |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CZ381899A3 CZ381899A3 (cs) | 2000-04-12 |
| CZ295713B6 true CZ295713B6 (cs) | 2005-10-12 |
Family
ID=11377020
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CZ19993818A CZ295713B6 (cs) | 1997-04-28 | 1998-04-16 | Způsob výroby 1,4,7,10-tetraazacyklododekanu |
Country Status (15)
| Country | Link |
|---|---|
| US (1) | US5886174A (en, 2012) |
| EP (1) | EP0980360B1 (en, 2012) |
| JP (1) | JP4308327B2 (en, 2012) |
| CN (1) | CN1122664C (en, 2012) |
| AT (1) | ATE220668T1 (en, 2012) |
| AU (1) | AU7335598A (en, 2012) |
| CA (1) | CA2288148C (en, 2012) |
| CZ (1) | CZ295713B6 (en, 2012) |
| DE (1) | DE69806592T2 (en, 2012) |
| ES (1) | ES2181213T3 (en, 2012) |
| HU (1) | HU228519B1 (en, 2012) |
| IT (1) | IT1291673B1 (en, 2012) |
| NO (1) | NO313139B1 (en, 2012) |
| WO (1) | WO1998049151A1 (en, 2012) |
| ZA (1) | ZA983483B (en, 2012) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| IT1293778B1 (it) * | 1997-07-25 | 1999-03-10 | Bracco Spa | 1,4,7,10-tetraazabiciclo(8.2.2.)tetradecan-2 one, sua preparazione e suo uso per la preparazione di tetraazamacrocicli |
| DE19809543A1 (de) * | 1998-03-05 | 1999-09-09 | Clariant Gmbh | Verfahren zur Herstellung von makropolycyclischen Polymaninen |
| DE19856481C1 (de) * | 1998-12-02 | 2000-07-06 | Schering Ag | Verfahren zur Herstellung von Cyclen |
| US6156890A (en) * | 1999-01-15 | 2000-12-05 | Schering Aktiengesellschaft | Process for the production of cyclene |
| IT1309601B1 (it) * | 1999-03-09 | 2002-01-24 | Bracco Spa | Processo per la preparazione di 1,4,7,10 tetraazaciclododecano. |
| US8877861B2 (en) * | 2008-11-04 | 2014-11-04 | Wei-Ho Ting | One-pot synthetic method for synthesizing silver-containing waterborne polyurethane |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2753278A1 (de) * | 1977-11-30 | 1979-05-31 | Basf Ag | Aralkylpiperidinone |
| EP0002987A1 (fr) * | 1977-12-30 | 1979-07-11 | Societe Generale Pour L'emballage | Procédé et machine pour la préparation sur le lieu de consommation de doses unitaires de boissons et produit utilisable dans le procédé |
| FR2654102B1 (fr) * | 1989-11-09 | 1992-01-10 | Air Liquide | Procede de synthese de derives polyazotes cycliques. |
| US5587451A (en) * | 1993-11-26 | 1996-12-24 | The Dow Chemical Company | Process for preparing polyazamacrocycles |
| GB9504922D0 (en) * | 1995-03-10 | 1995-04-26 | Nycomed As | Process |
| IT1284046B1 (it) * | 1996-06-21 | 1998-05-08 | Bracco Spa | Processo per la preparazione di tetraazamacrocicli |
-
1997
- 1997-04-28 IT IT97MI000982A patent/IT1291673B1/it active IP Right Grant
-
1998
- 1998-04-16 ES ES98920530T patent/ES2181213T3/es not_active Expired - Lifetime
- 1998-04-16 EP EP98920530A patent/EP0980360B1/en not_active Expired - Lifetime
- 1998-04-16 CA CA002288148A patent/CA2288148C/en not_active Expired - Lifetime
- 1998-04-16 CN CN98804587A patent/CN1122664C/zh not_active Expired - Lifetime
- 1998-04-16 JP JP54654098A patent/JP4308327B2/ja not_active Expired - Lifetime
- 1998-04-16 AT AT98920530T patent/ATE220668T1/de not_active IP Right Cessation
- 1998-04-16 HU HU0001751A patent/HU228519B1/hu unknown
- 1998-04-16 WO PCT/EP1998/002222 patent/WO1998049151A1/en active IP Right Grant
- 1998-04-16 CZ CZ19993818A patent/CZ295713B6/cs not_active IP Right Cessation
- 1998-04-16 AU AU73355/98A patent/AU7335598A/en not_active Abandoned
- 1998-04-16 DE DE69806592T patent/DE69806592T2/de not_active Expired - Lifetime
- 1998-04-24 ZA ZA983483A patent/ZA983483B/xx unknown
- 1998-04-27 US US09/066,714 patent/US5886174A/en not_active Expired - Lifetime
-
1999
- 1999-10-27 NO NO19995252A patent/NO313139B1/no not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| JP4308327B2 (ja) | 2009-08-05 |
| CZ381899A3 (cs) | 2000-04-12 |
| DE69806592D1 (de) | 2002-08-22 |
| IT1291673B1 (it) | 1999-01-19 |
| CN1122664C (zh) | 2003-10-01 |
| NO995252L (no) | 1999-12-17 |
| NO313139B1 (no) | 2002-08-19 |
| NO995252D0 (no) | 1999-10-27 |
| ITMI970982A0 (en, 2012) | 1997-04-28 |
| HUP0001751A3 (en) | 2001-02-28 |
| US5886174A (en) | 1999-03-23 |
| ATE220668T1 (de) | 2002-08-15 |
| DE69806592T2 (de) | 2002-12-19 |
| CA2288148A1 (en) | 1998-11-05 |
| HUP0001751A1 (hu) | 2000-09-28 |
| JP2001522362A (ja) | 2001-11-13 |
| EP0980360B1 (en) | 2002-07-17 |
| EP0980360A1 (en) | 2000-02-23 |
| ITMI970982A1 (it) | 1998-10-28 |
| AU7335598A (en) | 1998-11-24 |
| CA2288148C (en) | 2008-12-23 |
| HU228519B1 (en) | 2013-03-28 |
| CN1253552A (zh) | 2000-05-17 |
| WO1998049151A1 (en) | 1998-11-05 |
| ES2181213T3 (es) | 2003-02-16 |
| ZA983483B (en) | 1998-10-29 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PD00 | Pending as of 2000-06-30 in czech republic | ||
| MK4A | Patent expired |
Effective date: 20180416 |