JP2002541263A5 - - Google Patents
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- Publication number
- JP2002541263A5 JP2002541263A5 JP2000610861A JP2000610861A JP2002541263A5 JP 2002541263 A5 JP2002541263 A5 JP 2002541263A5 JP 2000610861 A JP2000610861 A JP 2000610861A JP 2000610861 A JP2000610861 A JP 2000610861A JP 2002541263 A5 JP2002541263 A5 JP 2002541263A5
- Authority
- JP
- Japan
- Prior art keywords
- pta
- solvent
- cis
- amine
- platinum
- 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.)
- Granted
Links
- 238000000034 method Methods 0.000 description 50
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 41
- 229910052697 platinum Inorganic materials 0.000 description 22
- 239000002904 solvent Substances 0.000 description 16
- 150000001412 amines Chemical class 0.000 description 9
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical group CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 7
- 229910052736 halogen Inorganic materials 0.000 description 7
- 150000002367 halogens Chemical class 0.000 description 7
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 7
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 6
- 239000000010 aprotic solvent Substances 0.000 description 6
- 125000003118 aryl group Chemical group 0.000 description 6
- -1 carbonate ester Chemical class 0.000 description 6
- 150000004820 halides Chemical class 0.000 description 6
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 5
- 125000006615 aromatic heterocyclic group Chemical group 0.000 description 5
- BSKHPKMHTQYZBB-UHFFFAOYSA-N 2-methylpyridine Chemical compound CC1=CC=CC=N1 BSKHPKMHTQYZBB-UHFFFAOYSA-N 0.000 description 4
- KXDHJXZQYSOELW-UHFFFAOYSA-M Carbamate Chemical compound NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 0.000 description 3
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- 150000007942 carboxylates Chemical class 0.000 description 3
- 150000001733 carboxylic acid esters Chemical class 0.000 description 3
- 229910052739 hydrogen Inorganic materials 0.000 description 3
- 239000001257 hydrogen Substances 0.000 description 3
- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 3
- 125000004433 nitrogen atom Chemical group N* 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical group C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- 239000000908 ammonium hydroxide Substances 0.000 description 2
- 239000003125 aqueous solvent Substances 0.000 description 2
- 125000004429 atom Chemical group 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 238000001704 evaporation Methods 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 239000007800 oxidant agent Substances 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 125000001309 chloro group Chemical group Cl* 0.000 description 1
- XQRLCLUYWUNEEH-UHFFFAOYSA-L diphosphonate(2-) Chemical compound [O-]P(=O)OP([O-])=O XQRLCLUYWUNEEH-UHFFFAOYSA-L 0.000 description 1
- 239000012458 free base Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- ZJAOAACCNHFJAH-UHFFFAOYSA-N phosphonoformic acid Chemical compound OC(=O)P(O)(O)=O ZJAOAACCNHFJAH-UHFFFAOYSA-N 0.000 description 1
- 150000003057 platinum Chemical class 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US12893999P | 1999-04-13 | 1999-04-13 | |
| US60/128,939 | 1999-04-13 | ||
| PCT/CA2000/000385 WO2000061590A1 (en) | 1999-04-13 | 2000-04-11 | Process for preparing amine platinum complexes |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2002541263A JP2002541263A (ja) | 2002-12-03 |
| JP2002541263A5 true JP2002541263A5 (https=) | 2009-11-19 |
| JP4756669B2 JP4756669B2 (ja) | 2011-08-24 |
Family
ID=22437722
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2000610861A Expired - Fee Related JP4756669B2 (ja) | 1999-04-13 | 2000-04-11 | アミン白金錯体を調製するためのプロセス |
Country Status (32)
| Country | Link |
|---|---|
| US (1) | US6518428B1 (https=) |
| EP (1) | EP1165576B1 (https=) |
| JP (1) | JP4756669B2 (https=) |
| KR (1) | KR100711955B1 (https=) |
| CN (3) | CN1916009B (https=) |
| AR (1) | AR043084A1 (https=) |
| AT (1) | ATE309257T1 (https=) |
| AU (1) | AU770006B2 (https=) |
| BG (1) | BG65429B1 (https=) |
| BR (1) | BR0009780B1 (https=) |
| CA (1) | CA2368849C (https=) |
| CY (1) | CY1104965T1 (https=) |
| CZ (1) | CZ303156B6 (https=) |
| DE (1) | DE60023859T2 (https=) |
| DK (1) | DK1165576T3 (https=) |
| EE (1) | EE04747B1 (https=) |
| ES (1) | ES2253214T3 (https=) |
| HK (1) | HK1039336B (https=) |
| HU (1) | HUP0200748A3 (https=) |
| IL (1) | IL145671A0 (https=) |
| IS (1) | IS2711B3 (https=) |
| MX (1) | MXPA01010430A (https=) |
| MY (1) | MY122706A (https=) |
| NO (1) | NO330429B1 (https=) |
| NZ (1) | NZ514736A (https=) |
| PL (1) | PL202731B1 (https=) |
| RU (1) | RU2245340C2 (https=) |
| SK (1) | SK286374B6 (https=) |
| TW (1) | TWI289565B (https=) |
| UA (1) | UA71614C2 (https=) |
| WO (1) | WO2000061590A1 (https=) |
| ZA (1) | ZA200107965B (https=) |
Families Citing this family (30)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB9502799D0 (en) * | 1995-02-14 | 1995-04-05 | Johnson Matthey Plc | Improvements in platinum complexes |
| DK1165576T3 (da) | 1999-04-13 | 2006-03-27 | Anormed Inc | Fremgangsmåde til fremstilling af amin-platin-komplekser |
| US6413953B1 (en) * | 1999-04-13 | 2002-07-02 | Anormed Inc. | Pt(IV) antitumor agent |
| GB0011903D0 (en) * | 2000-05-18 | 2000-07-05 | Astrazeneca Ab | Combination chemotherapy |
| US6806289B1 (en) * | 2000-07-14 | 2004-10-19 | Stephen J. Lippard | Coordination complexes, and methods for preparing by combinatorial methods, assaying and using the same |
| US6894049B1 (en) * | 2000-10-04 | 2005-05-17 | Anormed, Inc. | Platinum complexes as antitumor agents |
| WO2005077385A2 (en) | 2004-02-18 | 2005-08-25 | Gpc Biotech Ag | Methods for treating resistant or refractory tumors |
| CZ2004964A3 (cs) * | 2004-09-14 | 2006-03-15 | Pliva-Lachema A. S. | Perorální farmaceutická kompozice pro cílený transport komplexu platiny do kolorektální oblasti, zpusob její prípravy a tato kompozice pro pouzití jako lécivo |
| ES2257178B1 (es) * | 2004-09-30 | 2007-08-16 | Universidad Autonoma De Madrid | Compuestos de platino de formula trans-(ptc12(isopropilamina)(4-(hidroximetil)-piridina)) y trans-(ptc12(isopropilamina)(3-hidroximetil)-piridina y su aplicacion como farmaco antitumoral. |
| RU2298556C1 (ru) * | 2005-11-17 | 2007-05-10 | Общество с ограниченной ответственностью "ЦитоСтарт" | Триметилоламинометановая соль цис-бис [4-нитраминопиридин-n] тетрахлороплатины (iv) и способ ее получения |
| RU2309158C1 (ru) * | 2006-03-27 | 2007-10-27 | Институт химии и химической технологии СО РАН (ИХХТ СО РАН) | Способ получения цис-дихлороамминизопропиламинплатины (ii) |
| US8168661B2 (en) * | 2006-11-06 | 2012-05-01 | Poniard Pharmaceuticals, Inc. | Use of picoplatin to treat colorectal cancer |
| US8178564B2 (en) * | 2006-11-06 | 2012-05-15 | Poniard Pharmaceuticals, Inc. | Use of picoplatin to treat colorectal cancer |
| US8168662B1 (en) | 2006-11-06 | 2012-05-01 | Poniard Pharmaceuticals, Inc. | Use of picoplatin to treat colorectal cancer |
| US8173686B2 (en) | 2006-11-06 | 2012-05-08 | Poniard Pharmaceuticals, Inc. | Use of picoplatin to treat colorectal cancer |
| US20110033528A1 (en) * | 2009-08-05 | 2011-02-10 | Poniard Pharmaceuticals, Inc. | Stabilized picoplatin oral dosage form |
| US20100260832A1 (en) * | 2007-06-27 | 2010-10-14 | Poniard Pharmaceuticals, Inc. | Combination therapy for ovarian cancer |
| TW200916094A (en) * | 2007-06-27 | 2009-04-16 | Poniard Pharmaceuticals Inc | Stabilized picoplatin dosage form |
| EP2178893A4 (en) * | 2007-07-16 | 2012-09-19 | Poniard Pharmaceuticals Inc | ORAL FORMULATIONS FOR PICOPLATIN |
| WO2009099649A1 (en) * | 2008-02-08 | 2009-08-13 | Poniard Pharmaceuticals, Inc. | Use of picoplatin and bevacizumab to treat colorectal cancer |
| US20120123121A1 (en) * | 2009-06-12 | 2012-05-17 | Poniard Pharmaceuticals, Inc. | Synthesis of picoplatin |
| RU2451010C1 (ru) * | 2011-01-11 | 2012-05-20 | Закрытое Акционерное Общество "Ива Фарм" | Палладиево-медные катализаторы гомогенного селективного окисления тиольных групп, комбинация и композиция на их основе и способ терапевтического воздействия |
| CN105254679B (zh) * | 2013-11-19 | 2018-05-15 | 辽宁大学 | 单6-(氮杂环取代)蒽醌二氯化铂配合物及其制备方法和应用 |
| CN103860539B (zh) * | 2014-04-14 | 2016-02-10 | 于迎涛 | 一种具有混合轴向配体的Pt（IV）类抗癌药物及制备方法 |
| CN104231000A (zh) * | 2014-08-20 | 2014-12-24 | 山东铂源药业有限公司 | 一种抗肿瘤药物甲啶铂的合成方法 |
| US10987353B2 (en) | 2016-05-04 | 2021-04-27 | The Wistar Institute Of Anatomy And Biology | Methods of treating cancers overexpressing CARM1 with EZH2 inhibitors and platinum-based antineoplastic drugs |
| KR102137669B1 (ko) * | 2019-08-05 | 2020-07-27 | 한국과학기술연구원 | 메탄올 또는 그 전구체 합성용 촉매, 이의 제조방법 및 이를 이용한 메탄올 또는 그 전구체의 제조방법 |
| CN115955962B (zh) | 2020-07-08 | 2024-07-12 | 代顿治疗股份公司 | 用于治疗淋巴肿瘤的沙铂 |
| CN113402565B (zh) * | 2021-06-16 | 2023-07-28 | 中国人民解放军空军军医大学 | 一类含有泊沙康唑的四价铂配合物、制备方法及其应用 |
| AU2022430214A1 (en) | 2022-01-07 | 2024-08-15 | Pharma& Schweiz Gmbh | Treating haematological malignancies by means of satraplatin |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4329299A (en) * | 1979-08-23 | 1982-05-11 | Johnson, Matthey & Co., Limited | Composition of matter containing platinum |
| US4533502A (en) * | 1983-02-22 | 1985-08-06 | Rochon Fernande D | Platinum (II) compounds and their preparation |
| DE3582961D1 (de) * | 1984-06-27 | 1991-07-04 | Johnson Matthey Plc | Platinkoordinationsverbindungen. |
| US5244919A (en) | 1988-02-02 | 1993-09-14 | Johnson Matthey, Inc. | Pt(IV) complexes as anti-tumor agents |
| SU1790190A1 (ru) * | 1990-08-08 | 1996-04-27 | Ленинградский химико-фармацевтический институт | Цис-хлордиаммин-1,3-диметилксантинплатины (ii) хлорид дигидрат, проявляющий противоопухолевую активность |
| GB9105037D0 (en) | 1991-03-09 | 1991-04-24 | Johnson Matthey Plc | Improvements in chemical compounds |
| RU2050361C1 (ru) * | 1991-12-23 | 1995-12-20 | Юрий Михайлович Островский | Пентахлороплатинат (iv)-4- метил-3-[(2- метил-4- окси-5-пиримидинил) метил-]-5-(2 -оксиэтил)тиазолия, проявляющий противоопухолевую активность |
| GB9502799D0 (en) * | 1995-02-14 | 1995-04-05 | Johnson Matthey Plc | Improvements in platinum complexes |
| US5547982A (en) * | 1995-02-27 | 1996-08-20 | Johnson Matthey, Inc. | Anti-tumor platinum complexes |
| RU2089555C1 (ru) * | 1995-05-04 | 1997-09-10 | Новосибирский институт биоорганической химии СО РАН | Бисимидазол-(1,10)-фенантролинплатина (iii) дихлорид, проявляющий цитостатическую противоопухолевую активность |
| KR20010112343A (ko) | 1999-03-19 | 2001-12-20 | 추후제출 | 금속 착화합물을 포함하는 약제학적 조성물 |
| DK1165576T3 (da) | 1999-04-13 | 2006-03-27 | Anormed Inc | Fremgangsmåde til fremstilling af amin-platin-komplekser |
-
2000
- 2000-04-11 DK DK00918620T patent/DK1165576T3/da active
- 2000-04-11 CN CN2006101003981A patent/CN1916009B/zh not_active Expired - Lifetime
- 2000-04-11 KR KR1020017013049A patent/KR100711955B1/ko not_active Expired - Fee Related
- 2000-04-11 HU HU0200748A patent/HUP0200748A3/hu unknown
- 2000-04-11 CN CNB2006100093181A patent/CN100460412C/zh not_active Expired - Lifetime
- 2000-04-11 CZ CZ20013648A patent/CZ303156B6/cs not_active IP Right Cessation
- 2000-04-11 PL PL351612A patent/PL202731B1/pl not_active IP Right Cessation
- 2000-04-11 RU RU2001130457/04A patent/RU2245340C2/ru not_active IP Right Cessation
- 2000-04-11 CN CNB008076359A patent/CN1250559C/zh not_active Expired - Fee Related
- 2000-04-11 MX MXPA01010430A patent/MXPA01010430A/es active IP Right Grant
- 2000-04-11 AT AT00918620T patent/ATE309257T1/de active
- 2000-04-11 US US09/547,074 patent/US6518428B1/en not_active Expired - Lifetime
- 2000-04-11 WO PCT/CA2000/000385 patent/WO2000061590A1/en not_active Ceased
- 2000-04-11 ES ES00918620T patent/ES2253214T3/es not_active Expired - Lifetime
- 2000-04-11 JP JP2000610861A patent/JP4756669B2/ja not_active Expired - Fee Related
- 2000-04-11 HK HK02100835.7A patent/HK1039336B/en unknown
- 2000-04-11 AU AU39510/00A patent/AU770006B2/en not_active Expired
- 2000-04-11 CA CA2368849A patent/CA2368849C/en not_active Expired - Fee Related
- 2000-04-11 NZ NZ514736A patent/NZ514736A/xx not_active IP Right Cessation
- 2000-04-11 DE DE60023859T patent/DE60023859T2/de not_active Expired - Lifetime
- 2000-04-11 SK SK1468-2001A patent/SK286374B6/sk not_active IP Right Cessation
- 2000-04-11 EE EEP200100536A patent/EE04747B1/xx not_active IP Right Cessation
- 2000-04-11 EP EP00918620A patent/EP1165576B1/en not_active Expired - Lifetime
- 2000-04-11 BR BRPI0009780-2B1A patent/BR0009780B1/pt not_active IP Right Cessation
- 2000-04-11 IL IL14567100A patent/IL145671A0/xx not_active IP Right Cessation
- 2000-04-12 AR ARP000101696A patent/AR043084A1/es active IP Right Grant
- 2000-04-12 MY MYPI20001537A patent/MY122706A/en unknown
- 2000-06-23 TW TW089112556A patent/TWI289565B/zh not_active IP Right Cessation
- 2000-11-04 UA UA2001117756A patent/UA71614C2/uk unknown
-
2001
- 2001-09-27 ZA ZA200107965A patent/ZA200107965B/en unknown
- 2001-09-28 IS IS6092A patent/IS2711B3/is unknown
- 2001-10-12 NO NO20014957A patent/NO330429B1/no not_active IP Right Cessation
- 2001-11-08 BG BG106090A patent/BG65429B1/bg unknown
-
2006
- 2006-02-01 CY CY20061100130T patent/CY1104965T1/el unknown
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