BRPI9813001A - processo de fabricação de derivados de camptotecina. - Google Patents
processo de fabricação de derivados de camptotecina.Info
- Publication number
- BRPI9813001A BRPI9813001A BRPI9813001A BRPI9813001A BRPI9813001A BR PI9813001 A BRPI9813001 A BR PI9813001A BR PI9813001 A BRPI9813001 A BR PI9813001A BR PI9813001 A BRPI9813001 A BR PI9813001A BR PI9813001 A BRPI9813001 A BR PI9813001A
- Authority
- BR
- Brazil
- Prior art keywords
- group
- hydrogen atom
- camptothecin derivatives
- alkyl group
- hydroxyl
- Prior art date
Links
- 238000004519 manufacturing process Methods 0.000 title abstract 3
- VSJKWCGYPAHWDS-FQEVSTJZSA-N camptothecin Chemical class C1=CC=C2C=C(CN3C4=CC5=C(C3=O)COC(=O)[C@]5(O)CC)C4=NC2=C1 VSJKWCGYPAHWDS-FQEVSTJZSA-N 0.000 title abstract 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 5
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 3
- 150000001875 compounds Chemical class 0.000 abstract 2
- 238000000034 method Methods 0.000 abstract 2
- -1 methylene-dioxy Chemical group 0.000 abstract 2
- 125000006699 (C1-C3) hydroxyalkyl group Chemical group 0.000 abstract 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical group [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 abstract 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 abstract 1
- KLWPJMFMVPTNCC-UHFFFAOYSA-N Camptothecin Natural products CCC1(O)C(=O)OCC2=C1C=C3C4Nc5ccccc5C=C4CN3C2=O KLWPJMFMVPTNCC-UHFFFAOYSA-N 0.000 abstract 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical group [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 abstract 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical group FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 abstract 1
- 125000006242 amine protecting group Chemical group 0.000 abstract 1
- 150000001412 amines Chemical group 0.000 abstract 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 1
- 125000001584 benzyloxycarbonyl group Chemical group C(=O)(OCC1=CC=CC=C1)* 0.000 abstract 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 abstract 1
- 229910052794 bromium Inorganic materials 0.000 abstract 1
- 229940127093 camptothecin Drugs 0.000 abstract 1
- 229910052801 chlorine Inorganic materials 0.000 abstract 1
- 239000000460 chlorine Chemical group 0.000 abstract 1
- 125000004122 cyclic group Chemical group 0.000 abstract 1
- VSJKWCGYPAHWDS-UHFFFAOYSA-N dl-camptothecin Natural products C1=CC=C2C=C(CN3C4=CC5=C(C3=O)COC(=O)C5(O)CC)C4=NC2=C1 VSJKWCGYPAHWDS-UHFFFAOYSA-N 0.000 abstract 1
- 229910052731 fluorine Inorganic materials 0.000 abstract 1
- 239000011737 fluorine Chemical group 0.000 abstract 1
- 239000001257 hydrogen Substances 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 229910052740 iodine Inorganic materials 0.000 abstract 1
- 239000011630 iodine Chemical group 0.000 abstract 1
- UYWQUFXKFGHYNT-UHFFFAOYSA-N phenylmethyl ester of formic acid Natural products O=COCC1=CC=CC=C1 UYWQUFXKFGHYNT-UHFFFAOYSA-N 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/22—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed systems contains four or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/22—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains four or more hetero rings
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/55—Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Abstract
"processo de fabricação de derivados de camptotecina", o qual relaciona-se a um processo de fabricação de um composto de fórmula geral (1) a partir do composto de fórmula geral (2) : no qual y e z são o mesmo ou diferente e cada um representa um átomo de hidrogênio, o grupo alquil c~ 1~-c~ 6~, um grupo hidroxialquil c~ 1~-c~ 3~, ou um grupo de proteção geral de amina como benziloxicarbonil, benzil, etc.; r~ 1~ é um átomo de hidrogênio, um grupo alquil c~ 1~-c~ 6~, ou um grupo hidroxil; r~ 2~ e r~ 3~ são os mesmos ou diferentes e cada um representa um átomo de hidrogênio ou um grupo de hidroxil, ou podem ser unidos juntos para formar uma metade primária cíclica, que é um grupo metileno-dióxil ou etilenodioxil; r~ 4~ é um átomo de hidrogênio ou um grupo alquil c~ 1~-c~ 6~; e r~ 5~ é hidrogênio, hidroxil, flúor, cloro, bromo, iodo ou amina. segue abaixo a representação das fórmulas quais 1 e 2.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| KR19970031710 | 1997-07-09 | ||
| PCT/KR1998/000199 WO1999002530A1 (en) | 1997-07-09 | 1998-07-08 | A process of manufacturing camptothecin derivatives |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| BRPI9813001A true BRPI9813001A (pt) | 2000-08-15 |
| BRPI9813001B1 BRPI9813001B1 (pt) | 2011-11-01 |
| BRPI9813001B8 BRPI9813001B8 (pt) | 2021-07-06 |
Family
ID=19513816
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BRPI9813001 BRPI9813001B8 (pt) | 1997-07-09 | 1998-07-08 | processo de fabricação de derivados de camptotecina. |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US6310207B1 (pt) |
| KR (1) | KR100266743B1 (pt) |
| AU (1) | AU8244998A (pt) |
| BR (1) | BRPI9813001B8 (pt) |
| CH (1) | CH693877A8 (pt) |
| ES (1) | ES2163365B2 (pt) |
| IN (1) | IN189180B (pt) |
| RU (1) | RU2181122C2 (pt) |
| WO (1) | WO1999002530A1 (pt) |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7109165B2 (en) * | 2001-05-18 | 2006-09-19 | Sirna Therapeutics, Inc. | Conjugates and compositions for cellular delivery |
| AU2005233456A1 (en) * | 2004-04-12 | 2005-10-27 | Taisho Pharmaceutical Co., Ltd. | Cyclic amine compound |
| US7928235B2 (en) * | 2006-08-11 | 2011-04-19 | The Christus Stehlin Foundation For Cancer Research | Methods of making esters of camptothecins |
| LT3946464T (lt) | 2019-03-29 | 2022-11-10 | Medimmune Limited | Junginiai ir jų konjugatai |
| MX2022000450A (es) | 2019-07-10 | 2022-04-25 | Cybrexa 3 Inc | Conjugados peptídicos de agentes dirigidos a microtúbulos como terapéuticos. |
| PH12022550039A1 (en) | 2019-07-10 | 2023-06-26 | Cybrexa 3 Inc | Peptide conjugates of cytotoxins as therapeutics |
| CN121064209A (zh) * | 2022-09-09 | 2025-12-05 | 杭州爱科瑞思生物医药有限公司 | 喜树碱-7-乙基胺衍生物及其制备方法和应用 |
| CN116478051B (zh) * | 2023-04-13 | 2024-06-21 | 戊言医药科技（上海）有限公司 | 一种贝洛替康盐酸盐及其关键中间体的制备方法 |
| CN120058720A (zh) * | 2024-01-08 | 2025-05-30 | 杭州爱科瑞思生物医药有限公司 | 7-含羟胺结构取代的烷基喜树碱衍生物的制备及其应用 |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4939255A (en) | 1987-06-24 | 1990-07-03 | Daiichi Pharmaceutical Co., Ltd. | Hexa-cyclic camptothecin derivatives |
| HU213136B (en) | 1990-08-14 | 1997-02-28 | Kyorin Seiyaku Kk | Process for producing fluoroethyl camptothecin derivatives and pharmaceutical compositions containing them |
| JP3008226B2 (ja) * | 1991-01-16 | 2000-02-14 | 第一製薬株式会社 | 六環性化合物 |
| IS4152A (is) * | 1993-04-29 | 1994-10-30 | Glaxo Inc. | Vatnsuppleysanlegar Camptothecin afleiður og aðferð til framleiðslu þeirra |
| KR960029336A (ko) | 1995-01-09 | 1996-08-17 | 김충환 | 캄토테신 유도체, 그의 제조 방법 및 이를 함유하는 항암제 |
-
1998
- 1998-07-06 IN IN1921DE1998 patent/IN189180B/en unknown
- 1998-07-07 KR KR1019980027267A patent/KR100266743B1/ko not_active Expired - Lifetime
- 1998-07-08 RU RU2000100980/04A patent/RU2181122C2/ru active
- 1998-07-08 US US09/462,271 patent/US6310207B1/en not_active Expired - Lifetime
- 1998-07-08 BR BRPI9813001 patent/BRPI9813001B8/pt not_active IP Right Cessation
- 1998-07-08 AU AU82449/98A patent/AU8244998A/en not_active Abandoned
- 1998-07-08 ES ES009950083A patent/ES2163365B2/es not_active Expired - Fee Related
- 1998-07-08 CH CH00031/00A patent/CH693877A8/de not_active IP Right Cessation
- 1998-07-08 WO PCT/KR1998/000199 patent/WO1999002530A1/en not_active Ceased
Also Published As
| Publication number | Publication date |
|---|---|
| KR100266743B1 (ko) | 2000-12-01 |
| RU2181122C2 (ru) | 2002-04-10 |
| BRPI9813001B8 (pt) | 2021-07-06 |
| BRPI9813001B1 (pt) | 2011-11-01 |
| ES2163365B2 (es) | 2002-11-01 |
| AU8244998A (en) | 1999-02-08 |
| ES2163365A1 (es) | 2002-01-16 |
| IN189180B (pt) | 2003-01-04 |
| CH693877A8 (de) | 2004-05-28 |
| WO1999002530A1 (en) | 1999-01-21 |
| KR19990013649A (ko) | 1999-02-25 |
| CH693877A5 (de) | 2004-03-31 |
| US6310207B1 (en) | 2001-10-30 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| B16A | Patent or certificate of addition of invention granted [chapter 16.1 patent gazette] |
Free format text: PRAZO DE VALIDADE: 10 (DEZ) ANOS CONTADOS A PARTIR DE 01/11/2011, OBSERVADAS AS CONDICOES LEGAIS. ONDE DE LE: FORMALDEHYDE, PARAFORMALDEIDRO, DIMETHYLFORMAMIDE E DIMETHYL; LEIA-SE: FORMALDEIDO, PARAFORMALDEIDO, DIMETILFORMAMIDA E DIMETIL. |
|
| B25D | Requested change of name of applicant approved | ||
| B25G | Requested change of headquarter approved | ||
| B25A | Requested transfer of rights approved | ||
| B16C | Correction of notification of the grant [chapter 16.3 patent gazette] |
Free format text: PRAZO DE VALIDADE: 20 (VINTE) ANOS CONTADOS A PARTIR DE 08/07/98, OBSERVADAS AS CONDICOES LEGAIS. PATENTE CONCEDIDA CONFORME ADI 5.529/DF, QUE DETERMINA A ALTERACAO DO PRAZO DE CONCESSAO |
|
| B21A | Patent or certificate of addition expired [chapter 21.1 patent gazette] |
Free format text: PATENTE EXTINTA EM 08.07.2018 |