CO5261523A1 - Procedimiento para la preparacion de esteres de acidos aril-iminometil-carbamicos - Google Patents
Procedimiento para la preparacion de esteres de acidos aril-iminometil-carbamicosInfo
- Publication number
- CO5261523A1 CO5261523A1 CO01001652A CO01001652A CO5261523A1 CO 5261523 A1 CO5261523 A1 CO 5261523A1 CO 01001652 A CO01001652 A CO 01001652A CO 01001652 A CO01001652 A CO 01001652A CO 5261523 A1 CO5261523 A1 CO 5261523A1
- Authority
- CO
- Colombia
- Prior art keywords
- group
- formula
- phenyl
- jpeg
- methoxy
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C271/00—Derivatives of carbamic acids, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C269/00—Preparation of derivatives of carbamic acid, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C271/00—Derivatives of carbamic acids, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
- C07C271/06—Esters of carbamic acids
- C07C271/08—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms
- C07C271/10—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms
- C07C271/20—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms to carbon atoms of hydrocarbon radicals substituted by nitrogen atoms not being part of nitro or nitroso groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C271/00—Derivatives of carbamic acids, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
- C07C271/62—Compounds containing any of the groups, X being a hetero atom, Y being any atom, e.g. N-acylcarbamates
- C07C271/64—Y being a hydrogen or a carbon atom, e.g. benzoylcarbamates
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pyrane Compounds (AREA)
- Indole Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
Procedimiento para la preparación de compuestos de la fórmula general (I)<EMI FILE="01001652_1" ID="1" IMF=JPEG >en la queR1 significa un radical seleccionado entre el grupo que consta de metilo, etilo propilo, ciclopentilo, ciclohexilo, fenilo, bencilo y -C(Me2)fenilo, que en cada caso puede estar sustituido una vez o dos o tres veces con hidroxi;R2 significa un radical seleccionado entre el grupo que consta de metilo, etilo, propilo y bencilo, caracterizado porque un compuesto de la fórmula general (II)<EMI FILE="01001652_2" ID="2" IMF=JPEG >en, la queR1´ significa un radical seleccionado entre el grupo que consta de metilo, etilo, propilo, ciclopentilo, ciclohexilo, fenilo, bencilo y -C(Me2)fenilo, que en cada caso puede estar sustituido una vez o dos o tres veces con un grupo -O-PG una función hidroxílica protegida que se selecciona entre el grupo que consta de metoxi-metiloxi, 2-metoxi-etoxi-metiloxi, 1-etoxi-etiloxi, 2-tetrahidropiraniloxi, 1-butoxi-etiloxi, terc.-butiloxi, benciloxi y 4-metoxi-benciloxi,se hace reaccionar en primer lugar, en el seno de un disolvente etéreo o aromático, con un hexaalquil-disilazano de metal alcalino y a continuación se trata con un compuesto de la fórmula (III) R2-O-COXAND#39 (III)en la queR2 representa el significado precedentemente mencionado yXAND#39 significa cloro, bromo o -O-R2, después del tratamiento se aisla mediante un ácido de la fórmula HY un componente de la fórmula (IV) y/o su forma tautómera <EMI FILE="01001652_3" ID="3" IMF=JPEG >en la que los radicales R1 y R2 presentan los significados precedentemente mencionados, e Y significa un radical deácido cualquiera, y a partir de éste se pone en libertad el compuesto de la fórmula (I).
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE10000907A DE10000907A1 (de) | 2000-01-12 | 2000-01-12 | Verfahren zur Herstellung von Aryl-iminomethyl-carbaminsäureestern |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CO5261523A1 true CO5261523A1 (es) | 2003-03-31 |
Family
ID=7627236
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CO01001652A CO5261523A1 (es) | 2000-01-12 | 2001-01-11 | Procedimiento para la preparacion de esteres de acidos aril-iminometil-carbamicos |
Country Status (31)
| Country | Link |
|---|---|
| EP (1) | EP1250318B1 (es) |
| JP (1) | JP2003523328A (es) |
| KR (1) | KR100681726B1 (es) |
| CN (2) | CN1187322C (es) |
| AR (1) | AR027208A1 (es) |
| AT (1) | ATE311360T1 (es) |
| AU (1) | AU2846401A (es) |
| BG (1) | BG106916A (es) |
| BR (1) | BR0107551A (es) |
| CA (1) | CA2399598C (es) |
| CO (1) | CO5261523A1 (es) |
| CZ (1) | CZ296784B6 (es) |
| DE (2) | DE10000907A1 (es) |
| EA (1) | EA005006B1 (es) |
| EE (1) | EE04960B1 (es) |
| ES (1) | ES2253388T3 (es) |
| HK (1) | HK1051851A1 (es) |
| HU (1) | HUP0300348A3 (es) |
| IL (1) | IL150621A (es) |
| MX (1) | MXPA02006846A (es) |
| MY (1) | MY117435A (es) |
| NO (1) | NO20023348D0 (es) |
| NZ (1) | NZ520713A (es) |
| PL (1) | PL356607A1 (es) |
| SK (1) | SK286709B6 (es) |
| TW (1) | TWI228119B (es) |
| UA (1) | UA71664C2 (es) |
| UY (1) | UY26524A1 (es) |
| WO (1) | WO2001051457A2 (es) |
| YU (1) | YU52602A (es) |
| ZA (1) | ZA200205746B (es) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP5262623B2 (ja) * | 2008-11-26 | 2013-08-14 | 株式会社豊田中央研究所 | スルホンアミド化合物の製造方法 |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0518818A3 (en) * | 1991-06-11 | 1993-04-28 | Ciba-Geigy Ag | Arylethers, their manufacture and use as medicament |
| JPH06279389A (ja) * | 1993-03-30 | 1994-10-04 | Terumo Corp | アミジノフェニルエーテル誘導体 |
| DE4424713A1 (de) * | 1994-07-13 | 1996-01-18 | Boehringer Ingelheim Kg | Substituierte Benzamidine, ihre Herstellung und Verwendung als Arnzneistoffe |
| AU1651201A (en) * | 1999-12-06 | 2001-06-18 | Ajinomoto Co., Inc. | Amidinophenylpyruvic acid derivative |
-
2000
- 2000-01-12 DE DE10000907A patent/DE10000907A1/de not_active Withdrawn
-
2001
- 2001-01-08 UY UY26524A patent/UY26524A1/es not_active Application Discontinuation
- 2001-01-10 MY MYPI20010104A patent/MY117435A/en unknown
- 2001-01-11 AU AU2846401A patent/AU2846401A/xx not_active Withdrawn
- 2001-01-11 IL IL150621A patent/IL150621A/en not_active IP Right Cessation
- 2001-01-11 NZ NZ520713A patent/NZ520713A/en unknown
- 2001-01-11 EE EEP200200392A patent/EE04960B1/xx not_active IP Right Cessation
- 2001-01-11 AT AT01942357T patent/ATE311360T1/de not_active IP Right Cessation
- 2001-01-11 BR BR0107551-9A patent/BR0107551A/pt not_active Expired - Fee Related
- 2001-01-11 CZ CZ20022283A patent/CZ296784B6/cs not_active IP Right Cessation
- 2001-01-11 CO CO01001652A patent/CO5261523A1/es not_active Application Discontinuation
- 2001-01-11 DE DE50108237T patent/DE50108237D1/de not_active Expired - Fee Related
- 2001-01-11 YU YU52602A patent/YU52602A/sh unknown
- 2001-01-11 WO PCT/EP2001/000262 patent/WO2001051457A2/de active IP Right Grant
- 2001-01-11 CA CA002399598A patent/CA2399598C/en not_active Expired - Fee Related
- 2001-01-11 ES ES01942357T patent/ES2253388T3/es not_active Expired - Lifetime
- 2001-01-11 TW TW090100613A patent/TWI228119B/zh not_active IP Right Cessation
- 2001-01-11 CN CNB018037283A patent/CN1187322C/zh not_active Expired - Fee Related
- 2001-01-11 EA EA200200741A patent/EA005006B1/ru not_active IP Right Cessation
- 2001-01-11 EP EP01942357A patent/EP1250318B1/de not_active Expired - Lifetime
- 2001-01-11 HU HU0300348A patent/HUP0300348A3/hu unknown
- 2001-01-11 JP JP2001551839A patent/JP2003523328A/ja active Pending
- 2001-01-11 CN CNB2004100335497A patent/CN1255378C/zh not_active Expired - Fee Related
- 2001-01-11 KR KR1020027008996A patent/KR100681726B1/ko not_active IP Right Cessation
- 2001-01-11 PL PL01356607A patent/PL356607A1/xx unknown
- 2001-01-11 SK SK1004-2002A patent/SK286709B6/sk not_active IP Right Cessation
- 2001-01-11 MX MXPA02006846A patent/MXPA02006846A/es active IP Right Grant
- 2001-01-12 AR ARP010100134A patent/AR027208A1/es not_active Suspension/Interruption
- 2001-11-01 UA UA2002086635A patent/UA71664C2/uk unknown
-
2002
- 2002-07-11 NO NO20023348A patent/NO20023348D0/no not_active Application Discontinuation
- 2002-07-12 BG BG106916A patent/BG106916A/xx active Pending
- 2002-07-18 ZA ZA200205746A patent/ZA200205746B/en unknown
-
2003
- 2003-06-11 HK HK03104093A patent/HK1051851A1/xx not_active IP Right Cessation
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FG | Application granted | ||
| FD | Application lapsed |