NO322795B1 - Fremgangsmate for fremstilling av iohexol - Google Patents
Fremgangsmate for fremstilling av iohexol Download PDFInfo
- Publication number
- NO322795B1 NO322795B1 NO19990889A NO990889A NO322795B1 NO 322795 B1 NO322795 B1 NO 322795B1 NO 19990889 A NO19990889 A NO 19990889A NO 990889 A NO990889 A NO 990889A NO 322795 B1 NO322795 B1 NO 322795B1
- Authority
- NO
- Norway
- Prior art keywords
- iohexol
- solvent
- isopropanol
- methoxyethanol
- dihydroxypropyl
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims abstract description 26
- 238000002360 preparation method Methods 0.000 title description 3
- NTHXOOBQLCIOLC-UHFFFAOYSA-N iohexol Chemical compound OCC(O)CN(C(=O)C)C1=C(I)C(C(=O)NCC(O)CO)=C(I)C(C(=O)NCC(O)CO)=C1I NTHXOOBQLCIOLC-UHFFFAOYSA-N 0.000 claims abstract description 55
- 229960001025 iohexol Drugs 0.000 claims abstract description 54
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 claims abstract description 50
- 239000002904 solvent Substances 0.000 claims abstract description 41
- XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 claims abstract description 21
- 238000004519 manufacturing process Methods 0.000 claims abstract description 12
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 7
- 238000006243 chemical reaction Methods 0.000 claims description 11
- 239000007787 solid Substances 0.000 claims description 11
- 239000007810 chemical reaction solvent Substances 0.000 claims description 10
- 229910052757 nitrogen Inorganic materials 0.000 claims description 10
- 238000005406 washing Methods 0.000 claims description 9
- 239000011541 reaction mixture Substances 0.000 claims description 5
- 238000000746 purification Methods 0.000 claims description 4
- 150000003839 salts Chemical class 0.000 claims description 4
- CTKINSOISVBQLD-UHFFFAOYSA-N Glycidol Chemical compound OCC1CO1 CTKINSOISVBQLD-UHFFFAOYSA-N 0.000 claims description 3
- DGIJJAHTRAQISB-UHFFFAOYSA-N 4-acetamido-1-n,2-n-bis(2,3-dihydroxypropyl)-1,3,5-triiodocyclohexa-3,5-diene-1,2-dicarboxamide Chemical compound CC(=O)NC1=C(I)C(C(=O)NCC(O)CO)C(I)(C(=O)NCC(O)CO)C=C1I DGIJJAHTRAQISB-UHFFFAOYSA-N 0.000 abstract 1
- 238000002425 crystallisation Methods 0.000 description 16
- 230000008025 crystallization Effects 0.000 description 16
- 239000000047 product Substances 0.000 description 7
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 6
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 238000004128 high performance liquid chromatography Methods 0.000 description 5
- -1 2 ,3-dihydroxypropyl group Chemical group 0.000 description 4
- SSZWWUDQMAHNAQ-UHFFFAOYSA-N 3-chloropropane-1,2-diol Chemical compound OCC(O)CCl SSZWWUDQMAHNAQ-UHFFFAOYSA-N 0.000 description 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 239000000725 suspension Substances 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 229940100198 alkylating agent Drugs 0.000 description 3
- 239000002168 alkylating agent Substances 0.000 description 3
- 239000002585 base Substances 0.000 description 3
- 239000006227 byproduct Substances 0.000 description 3
- 239000002872 contrast media Substances 0.000 description 3
- 239000012043 crude product Substances 0.000 description 3
- 238000001704 evaporation Methods 0.000 description 3
- 230000008020 evaporation Effects 0.000 description 3
- 238000007126 N-alkylation reaction Methods 0.000 description 2
- 238000010934 O-alkylation reaction Methods 0.000 description 2
- WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 description 2
- 238000007792 addition Methods 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 150000007529 inorganic bases Chemical class 0.000 description 2
- 150000007522 mineralic acids Chemical class 0.000 description 2
- 238000001953 recrystallisation Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- DLFVBJFMPXGRIB-UHFFFAOYSA-N Acetamide Chemical group CC(N)=O DLFVBJFMPXGRIB-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 238000010533 azeotropic distillation Methods 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 229940126534 drug product Drugs 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 150000007530 organic bases Chemical class 0.000 description 1
- 239000000825 pharmaceutical preparation Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 239000013557 residual solvent Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C231/00—Preparation of carboxylic acid amides
- C07C231/08—Preparation of carboxylic acid amides from amides by reaction at nitrogen atoms of carboxamide groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Glass Compositions (AREA)
- Iron Core Of Rotating Electric Machines (AREA)
- Saccharide Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GBGB9618056.7A GB9618056D0 (en) | 1996-08-29 | 1996-08-29 | Process |
| PCT/GB1997/002332 WO1998008804A1 (en) | 1996-08-29 | 1997-08-29 | Process for iohexol manufacture |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| NO990889D0 NO990889D0 (no) | 1999-02-25 |
| NO990889L NO990889L (no) | 1999-02-25 |
| NO322795B1 true NO322795B1 (no) | 2006-12-11 |
Family
ID=10799120
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO19990889A NO322795B1 (no) | 1996-08-29 | 1999-02-25 | Fremgangsmate for fremstilling av iohexol |
Country Status (26)
| Country | Link |
|---|---|
| US (2) | US5948940A (id) |
| EP (1) | EP0925275B1 (id) |
| JP (1) | JP3780002B2 (id) |
| KR (1) | KR100517588B1 (id) |
| CN (1) | CN1120148C (id) |
| AT (1) | ATE210631T1 (id) |
| AU (1) | AU723184B2 (id) |
| BG (1) | BG63663B1 (id) |
| BR (1) | BR9711381A (id) |
| CA (1) | CA2265047A1 (id) |
| CZ (1) | CZ295058B6 (id) |
| DE (1) | DE69709127T2 (id) |
| EE (1) | EE9900082A (id) |
| ES (1) | ES2173476T3 (id) |
| GB (1) | GB9618056D0 (id) |
| HK (1) | HK1020722A1 (id) |
| HU (1) | HU229253B1 (id) |
| IL (1) | IL128715A (id) |
| IN (1) | IN186429B (id) |
| NO (1) | NO322795B1 (id) |
| NZ (1) | NZ334817A (id) |
| PL (1) | PL190151B1 (id) |
| PT (1) | PT925275E (id) |
| SK (1) | SK26499A3 (id) |
| TR (1) | TR199900405T2 (id) |
| WO (1) | WO1998008804A1 (id) |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB9618056D0 (en) * | 1996-08-29 | 1996-10-09 | Nycomed Imaging As | Process |
| US6262303B1 (en) * | 1998-05-08 | 2001-07-17 | Dibra S.P.A. | Process for the preparation of S-N,N′-bis[2-hydroxy-1-(hydroxymethyl)ethyl]-5-[(2-hydroxy-1-oxopropyl)-amino]-2,4,6-triiodo-1,3-benzenedicarboxamide |
| ITMI20010773A1 (it) | 2001-04-11 | 2002-10-11 | Chemi Spa | Processo per la produzione di ioexolo ad elevata purezza |
| TWI288654B (en) * | 2001-05-17 | 2007-10-21 | Ind Tech Res Inst | Process for the purification of water-soluble non-ionic contrast agents |
| NO20033058D0 (no) * | 2003-07-03 | 2003-07-03 | Amersham Health As | Prosess |
| NO20053687D0 (no) * | 2005-07-29 | 2005-07-29 | Amersham Health As | Crystallisation Process. |
| NO20053676D0 (no) | 2005-07-29 | 2005-07-29 | Amersham Health As | Crystallisation Process |
| PT103391B (pt) * | 2005-11-24 | 2008-10-30 | Hovione Farmaciencia S A | Processo para fabrico de lohexol |
| WO2009091758A1 (en) * | 2008-01-14 | 2009-07-23 | Mallinckrodt Inc. | Process for the preparation of iosimenol |
| WO2015133651A1 (en) * | 2014-03-04 | 2015-09-11 | Otsuka Pharmaceutical Co., Ltd. | Iohexol powder and method of using the same |
| CN110054569B (zh) * | 2019-05-17 | 2022-05-17 | 浙江海洲制药有限公司 | 一种制备碘海醇的方法 |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1548594A (en) * | 1922-05-27 | 1925-08-04 | Helios Machine Company | Motion-converting mechanism |
| CH608189A5 (id) * | 1974-12-13 | 1978-12-29 | Savac Ag | |
| GB1548594A (en) * | 1976-06-11 | 1979-07-18 | Nyegaard & Co As | Triiodoisophthalic acid amides |
| IT1207226B (it) * | 1979-08-09 | 1989-05-17 | Bracco Ind Chimica Spa | Derivati dell'acido 2,4,6-triiodo-isoftalico, metodo per la loro preparazione e mezzi di contrasto che li contengono. |
| DK162045C (da) * | 1982-10-01 | 1992-02-10 | Nyegaard & Co As | Trijodbenzenderivater, fremgangsmaade til fremstilling deraf og radiologiske praeparater indeholdende saadanne forbindelser |
| NO161368C (no) * | 1982-11-08 | 1989-08-09 | Nyegaard & Co As | Roentgenkontrastmidler samt radiologiske preparater derav. |
| IL94718A (en) * | 1989-07-05 | 1994-10-21 | Schering Ag | Non-ionic carboxamide contrast agent and method of preparation |
| US5527926A (en) * | 1990-11-26 | 1996-06-18 | Bracco International B.V. | Methods and compositions for using non-ionic contrast agents to reduce the risk of clot formation in diagnostic procedures |
| US5371278A (en) * | 1994-03-25 | 1994-12-06 | Mallinckrodt Medical Pmc | Synthesis of ioversol using a minimal excess of acetoxyacetylchloride |
| US5624957A (en) * | 1995-06-06 | 1997-04-29 | Bristol-Myers Squibb Company | Rary-specific retinobenzoic acid derivatives |
| GB9618056D0 (en) * | 1996-08-29 | 1996-10-09 | Nycomed Imaging As | Process |
| GB9618055D0 (en) * | 1996-08-29 | 1996-10-09 | Nycomed Imaging As | Process |
-
1996
- 1996-08-29 GB GBGB9618056.7A patent/GB9618056D0/en active Pending
-
1997
- 1997-08-21 IN IN2367DE1997 patent/IN186429B/en unknown
- 1997-08-29 CA CA002265047A patent/CA2265047A1/en not_active Abandoned
- 1997-08-29 PT PT97939000T patent/PT925275E/pt unknown
- 1997-08-29 DE DE69709127T patent/DE69709127T2/de not_active Expired - Lifetime
- 1997-08-29 KR KR10-1999-7001686A patent/KR100517588B1/ko active IP Right Grant
- 1997-08-29 PL PL97331706A patent/PL190151B1/pl unknown
- 1997-08-29 TR TR1999/00405T patent/TR199900405T2/xx unknown
- 1997-08-29 EE EEP199900082A patent/EE9900082A/xx unknown
- 1997-08-29 SK SK264-99A patent/SK26499A3/sk unknown
- 1997-08-29 WO PCT/GB1997/002332 patent/WO1998008804A1/en active IP Right Grant
- 1997-08-29 HU HU9904325A patent/HU229253B1/hu unknown
- 1997-08-29 CZ CZ1999669A patent/CZ295058B6/cs not_active IP Right Cessation
- 1997-08-29 BR BR9711381A patent/BR9711381A/pt not_active IP Right Cessation
- 1997-08-29 CN CN97197524A patent/CN1120148C/zh not_active Expired - Lifetime
- 1997-08-29 EP EP97939000A patent/EP0925275B1/en not_active Expired - Lifetime
- 1997-08-29 IL IL12871597A patent/IL128715A/en not_active IP Right Cessation
- 1997-08-29 AT AT97939000T patent/ATE210631T1/de active
- 1997-08-29 JP JP51139998A patent/JP3780002B2/ja not_active Expired - Lifetime
- 1997-08-29 ES ES97939000T patent/ES2173476T3/es not_active Expired - Lifetime
- 1997-08-29 AU AU41236/97A patent/AU723184B2/en not_active Expired
- 1997-08-29 NZ NZ334817A patent/NZ334817A/xx unknown
-
1998
- 1998-07-23 US US09/120,724 patent/US5948940A/en not_active Expired - Lifetime
-
1999
- 1999-02-25 NO NO19990889A patent/NO322795B1/no not_active IP Right Cessation
- 1999-03-26 BG BG103289A patent/BG63663B1/bg unknown
- 1999-05-17 US US09/312,956 patent/US6153796A/en not_active Expired - Lifetime
- 1999-12-20 HK HK99105985A patent/HK1020722A1/xx not_active IP Right Cessation
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| RU2135462C1 (ru) | Способ кристаллизации иопамидола | |
| NO322795B1 (no) | Fremgangsmate for fremstilling av iohexol | |
| KR920000648B1 (ko) | α-L-아스파르틸-L-페닐알라닌 메틸 에스테르의 분리방법 | |
| US20060135777A1 (en) | Method for the production of d-threo-2-phenyl-2-piperidine-2-yl acetates | |
| EP1641743B1 (en) | Process for iohexol manufacture | |
| ES2977123T3 (es) | Procedimiento para la separación de ácidos dibásicos y aminoácidos de cadena larga | |
| US4340751A (en) | Method of optical resolution of (±)-2-amino-1-butanol and/or (±)-mandelic acid | |
| JPH07285919A (ja) | アスパラギン酸アンモニウムからｌ−アスパラギン酸を製造する方法 | |
| US3397231A (en) | Refining of alpha-6-deoxy-5-oxytetracycline | |
| RU2173315C2 (ru) | Способ получения иогексола | |
| JPS63425B2 (id) | ||
| NO331657B1 (no) | Fremgangsmate for fremstilling av iohexol | |
| JPS62138443A (ja) | ビスクレゾ−ルの製造方法 | |
| KR100654923B1 (ko) | 고순도의 광학활성아미드를 연속적으로 제조하는 방법 | |
| JPH0217544B2 (id) | ||
| JP3316917B2 (ja) | 新規フェニルアラニン塩結晶とその製造法 | |
| RU2054411C1 (ru) | Способ получения бисфенолов | |
| RU2030387C1 (ru) | Способ получения 2-метокси-5-хлорбензойной кислоты | |
| JP2641022B2 (ja) | ４，４’−ジヒドロキシジフェニルスルホンの精製法 | |
| CN115991653A (zh) | 一种普拉西坦关键中间体n,n-二异丙基乙二胺的制备方法 | |
| JP2009518325A (ja) | 医薬目的のために適切なイオプロミドの母液からの回収方法 | |
| KR20000053467A (ko) | 1,3-비스(아미노페녹시 벤젠) 재결정화 방법 | |
| JPH0621120B2 (ja) | クロロアルキルアミン塩酸塩の製造方法 | |
| JPH07224023A (ja) | トランス−１，４−シクロヘキサンジメタノールジアルキルスルホネートの精製方法 |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MK1K | Patent expired |