CO5700810A2 - Procedimiento para la sintesis de peptidos que contienen una sub-estructura de 4-hidroxi-prolina - Google Patents
Procedimiento para la sintesis de peptidos que contienen una sub-estructura de 4-hidroxi-prolinaInfo
- Publication number
- CO5700810A2 CO5700810A2 CO05057286A CO05057286A CO5700810A2 CO 5700810 A2 CO5700810 A2 CO 5700810A2 CO 05057286 A CO05057286 A CO 05057286A CO 05057286 A CO05057286 A CO 05057286A CO 5700810 A2 CO5700810 A2 CO 5700810A2
- Authority
- CO
- Colombia
- Prior art keywords
- compound
- formula
- carbon atoms
- hydroxy
- salt
- Prior art date
Links
- PMMYEEVYMWASQN-BKLSDQPFSA-N 4-hydroxy-L-proline Chemical compound OC1C[NH2+][C@H](C([O-])=O)C1 PMMYEEVYMWASQN-BKLSDQPFSA-N 0.000 title 1
- 230000015572 biosynthetic process Effects 0.000 title 1
- 238000000034 method Methods 0.000 title 1
- 102000004196 processed proteins & peptides Human genes 0.000 title 1
- 108090000765 processed proteins & peptides Proteins 0.000 title 1
- 238000003786 synthesis reaction Methods 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 9
- 125000004432 carbon atom Chemical group C* 0.000 abstract 7
- 125000001424 substituent group Chemical group 0.000 abstract 5
- 150000003839 salts Chemical class 0.000 abstract 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 3
- 239000002184 metal Substances 0.000 abstract 2
- 230000000269 nucleophilic effect Effects 0.000 abstract 2
- 125000003545 alkoxy group Chemical group 0.000 abstract 1
- 125000003282 alkyl amino group Chemical group 0.000 abstract 1
- 125000005115 alkyl carbamoyl group Chemical group 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 abstract 1
- 125000004663 dialkyl amino group Chemical group 0.000 abstract 1
- 125000005117 dialkylcarbamoyl group Chemical group 0.000 abstract 1
- 239000012039 electrophile Substances 0.000 abstract 1
- 125000001188 haloalkyl group Chemical group 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 150000002367 halogens Chemical class 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 239000001257 hydrogen Substances 0.000 abstract 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 1
- 230000003301 hydrolyzing effect Effects 0.000 abstract 1
- -1 hydroxy, amino Chemical group 0.000 abstract 1
- 238000004519 manufacturing process Methods 0.000 abstract 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
- 239000007790 solid phase Substances 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/347—Preparation of carboxylic acids or their salts, halides or anhydrides by reactions not involving formation of carboxyl groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/15—Preparation of carboxylic acids or their salts, halides or anhydrides by reaction of organic compounds with carbon dioxide, e.g. Kolbe-Schmitt synthesis
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C65/00—Compounds having carboxyl groups bound to carbon atoms of six—membered aromatic rings and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups
- C07C65/01—Compounds having carboxyl groups bound to carbon atoms of six—membered aromatic rings and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups containing hydroxy or O-metal groups
-
- 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)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Peptides Or Proteins (AREA)
- Pyrrole Compounds (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
1.- Un procedimiento para preparar un compuesto de la fórmula I: en donde R1 es un substituyente reactivo o una unión a una fase sólida;R2 es un substituyente reactivo; yR3, R4 y R5 son cada uno independientemente hidrógeno o uno o más substituyentes unidos a cada anillo benceno y seleccionados de hidroxi, amino, alquilo de 1 a 10 átomos de carbono, alcoxi de 1 a 10 átomos de carbono, alquilamino de 1 a 10 átomos de carbono, dialquilamino de 1 a 10 átomos de carbono, carbamoilo, alquilcarbamoilo de 1 a 10 átomos de carbono, dialquilcarbamoilo de 1 a 10 átomos de carbono, haloalquilo de 1 a 10 átomos de carbono, halógeno y nitro;en forma libre o de sal; que comprende:(a) hacer reaccionar un compuesto de la fórmula VI con un electrófilo: en donde R3, R4 y R5 son como se definieron anteriormente;R9 es -OH, -OM o -OMX, en donde M es un metal y X es un substituyente nucleofílico;R10 es -M o -MX, en donde M es un metal y X es un substituyente nucleofílico;en forma líbre o de sal;e hidrolizar el compuesto resultante para formar un compuesto de la fórmula I, en donde R2 es hidroxi;(b) opcionalmente convertir un compuesto de la fórmula I, en donde R2 es hidroxi a un compuesto de la fórmula I, en donde R2 es distinto a hidroxi;(c) opcionalmente convertir R1 en un compuesto de la fórmula I a un grupo R1 alternativo;(d) opcionalmente desproteger el compuesto de la fórmula I en forma protegida; y(e) cuando se requiera, convertir un compuesto de la fórmula I obtenido en forma libre a la forma de sal deseada, o viceversa.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB0229020A GB0229020D0 (en) | 2002-12-12 | 2002-12-12 | Organic compounds |
| GB0229280A GB0229280D0 (en) | 2002-12-16 | 2002-12-16 | Organic compounds |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CO5700810A2 true CO5700810A2 (es) | 2006-11-30 |
Family
ID=32510405
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CO05057286A CO5700810A2 (es) | 2002-12-12 | 2005-06-14 | Procedimiento para la sintesis de peptidos que contienen una sub-estructura de 4-hidroxi-prolina |
Country Status (24)
| Country | Link |
|---|---|
| US (3) | US7294722B2 (es) |
| EP (1) | EP1572615B8 (es) |
| JP (2) | JP4796303B2 (es) |
| KR (1) | KR101018491B1 (es) |
| AT (1) | ATE461173T1 (es) |
| AU (1) | AU2003290019B2 (es) |
| BR (2) | BRPI0317176B1 (es) |
| CA (1) | CA2509363C (es) |
| CO (1) | CO5700810A2 (es) |
| CY (1) | CY1110639T1 (es) |
| DE (1) | DE60331770D1 (es) |
| DK (1) | DK1572615T3 (es) |
| EC (1) | ECSP055846A (es) |
| ES (1) | ES2341336T3 (es) |
| HK (1) | HK1085459A1 (es) |
| IL (1) | IL168866A (es) |
| MX (1) | MXPA05006267A (es) |
| NO (1) | NO331836B1 (es) |
| NZ (1) | NZ540441A (es) |
| PL (1) | PL206914B1 (es) |
| PT (1) | PT1572615E (es) |
| RU (1) | RU2392265C2 (es) |
| SI (1) | SI1572615T1 (es) |
| WO (1) | WO2004052817A1 (es) |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE4306839A1 (de) | 1993-03-05 | 1994-09-08 | Bayer Ernst Prof Dr | Tritylgruppe enthaltendes Festphasensystem, Verfahren zu seiner Herstellung und seine Verwendung in Festphasenreaktionen |
| MY147327A (en) * | 1995-06-29 | 2012-11-30 | Novartis Ag | Somatostatin peptides |
| GB9625167D0 (en) * | 1996-12-04 | 1997-01-22 | Sandoz Ltd | Organic compounds |
| CA2294988C (en) * | 1997-07-01 | 2015-11-24 | Isis Pharmaceuticals Inc. | Compositions and methods for the delivery of oligonucleotides via the alimentary canal |
| GB0018891D0 (en) | 2000-08-01 | 2000-09-20 | Novartis Ag | Organic compounds |
-
2003
- 2003-12-11 CA CA2509363A patent/CA2509363C/en not_active Expired - Lifetime
- 2003-12-11 WO PCT/EP2003/014082 patent/WO2004052817A1/en active Application Filing
- 2003-12-11 EP EP03782373A patent/EP1572615B8/en not_active Expired - Lifetime
- 2003-12-11 DE DE60331770T patent/DE60331770D1/de not_active Expired - Lifetime
- 2003-12-11 AU AU2003290019A patent/AU2003290019B2/en not_active Expired
- 2003-12-11 RU RU2005121664/04A patent/RU2392265C2/ru active
- 2003-12-11 NZ NZ540441A patent/NZ540441A/en not_active IP Right Cessation
- 2003-12-11 PL PL375821A patent/PL206914B1/pl unknown
- 2003-12-11 MX MXPA05006267A patent/MXPA05006267A/es active IP Right Grant
- 2003-12-11 KR KR1020057010600A patent/KR101018491B1/ko active IP Right Grant
- 2003-12-11 BR BRPI0317176-0A patent/BRPI0317176B1/pt unknown
- 2003-12-11 US US10/538,028 patent/US7294722B2/en not_active Expired - Lifetime
- 2003-12-11 AT AT03782373T patent/ATE461173T1/de active
- 2003-12-11 PT PT03782373T patent/PT1572615E/pt unknown
- 2003-12-11 DK DK03782373.9T patent/DK1572615T3/da active
- 2003-12-11 SI SI200331800T patent/SI1572615T1/sl unknown
- 2003-12-11 ES ES03782373T patent/ES2341336T3/es not_active Expired - Lifetime
- 2003-12-11 BR BR0317176-0A patent/BR0317176A/pt not_active IP Right Cessation
- 2003-12-11 JP JP2004558073A patent/JP4796303B2/ja not_active Expired - Lifetime
-
2005
- 2005-05-30 IL IL168866A patent/IL168866A/en active IP Right Grant
- 2005-06-09 EC EC2005005846A patent/ECSP055846A/es unknown
- 2005-06-14 CO CO05057286A patent/CO5700810A2/es active IP Right Grant
- 2005-07-11 NO NO20053374A patent/NO331836B1/no not_active IP Right Cessation
-
2006
- 2006-03-10 HK HK06103122.9A patent/HK1085459A1/xx not_active IP Right Cessation
-
2007
- 2007-08-16 US US11/839,565 patent/US7449587B2/en not_active Expired - Lifetime
-
2008
- 2008-08-25 US US12/197,657 patent/US20080312456A1/en not_active Abandoned
-
2010
- 2010-04-05 JP JP2010086682A patent/JP5249276B2/ja not_active Expired - Lifetime
- 2010-05-14 CY CY20101100426T patent/CY1110639T1/el unknown
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FG | Application granted |