DK200000691A - Pyrrolderivater - Google Patents
Pyrrolderivater Download PDFInfo
- Publication number
- DK200000691A DK200000691A DK200000691A DKPA200000691A DK200000691A DK 200000691 A DK200000691 A DK 200000691A DK 200000691 A DK200000691 A DK 200000691A DK PA200000691 A DKPA200000691 A DK PA200000691A DK 200000691 A DK200000691 A DK 200000691A
- Authority
- DK
- Denmark
- Prior art keywords
- formula
- compound
- xii
- lower alkyl
- carbon atoms
- Prior art date
Links
- KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 title 2
- 150000001875 compounds Chemical class 0.000 description 20
- 125000000217 alkyl group Chemical group 0.000 description 10
- 125000004432 carbon atom Chemical group C* 0.000 description 7
- 125000005843 halogen group Chemical group 0.000 description 5
- 229910052739 hydrogen Inorganic materials 0.000 description 5
- 239000001257 hydrogen Substances 0.000 description 5
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 5
- 150000003839 salts Chemical class 0.000 description 5
- 239000002253 acid Substances 0.000 description 4
- 125000002941 2-furyl group Chemical group O1C([*])=C([H])C([H])=C1[H] 0.000 description 3
- 125000000175 2-thienyl group Chemical group S1C([*])=C([H])C([H])=C1[H] 0.000 description 3
- 125000003682 3-furyl group Chemical group O1C([H])=C([*])C([H])=C1[H] 0.000 description 3
- -1 3-pyrryl Chemical group 0.000 description 3
- 125000001541 3-thienyl group Chemical group S1C([H])=C([*])C([H])=C1[H] 0.000 description 3
- 125000003545 alkoxy group Chemical group 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 3
- 150000001408 amides Chemical class 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 239000000010 aprotic solvent Substances 0.000 description 2
- 150000005690 diesters Chemical class 0.000 description 2
- 229910052736 halogen Inorganic materials 0.000 description 2
- HEOZYYOUKGGSBJ-UHFFFAOYSA-N 5-(4-methoxybenzoyl)-2,3-dihydro-1h-pyrrolizine-1-carboxylic acid Chemical compound C1=CC(OC)=CC=C1C(=O)C1=CC=C2N1CCC2C(O)=O HEOZYYOUKGGSBJ-UHFFFAOYSA-N 0.000 description 1
- 0 C[C@@](CC1*)[n]2c1ccc2*[Al] Chemical compound C[C@@](CC1*)[n]2c1ccc2*[Al] 0.000 description 1
- 230000000911 decarboxylating effect Effects 0.000 description 1
- OZWKMVRBQXNZKK-UHFFFAOYSA-N ketorolac Chemical compound OC(=O)C1CCN2C1=CC=C2C(=O)C1=CC=CC=C1 OZWKMVRBQXNZKK-UHFFFAOYSA-N 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/18—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member
- C07D207/22—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/30—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members
- C07D207/34—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Rheumatology (AREA)
- Pharmacology & Pharmacy (AREA)
- Pain & Pain Management (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pyrrole Compounds (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
hvor R er lavere alkyl med 1-6 carbonatomer, og X er halogen, cycliseres med en lithiumhindret amin i et aprot opløsningsmiddel til dannelse af en diester med formlen (XII):
(XII) (b) en divalent ester med formlen (XII) opnået i trin (a) forsæbes til dannelse af den tilsvarende divalente syre med formlen (XII):
(XM) hvor R er hydrogen, (c) den divalente syre med formlen (XII) opnået i trin (b) forestres til dannelse afen forbindelse med formlen (XVIII):
(XVIII) hvor R-gruppen i 1 -stillingen er lavere alkyl med 1-6 carbonatomer, (d) en forbindelse med formlen (XVIII) opnået i trin (c) decarboxyleres til dannelse af en forbindelse med formlen (XIX):
(XIX) hvor R har den ovenfor anførte betydning; (e) en forbindelse med formlen (XIX) opnået i trin (d) aroyleres med en amid elleret morpholid til dannelse af en forbindelse med formlen (I), hvor Ar er substitueret eller usubstitueret phenyl, 2- eller 3-furyl, 2- eller 3-thienyl eller 2- eller 3-pyrryl, som, når den er substitueret, kan have en eller flere lavere alkyl-, lavere alkoxy- eller halogengrupper i en hvilken som helst stilling, der er til rådighed, på ringen, og R er hydrogen eller lavere alkyl med 1-6 carbonatomer, og eventuelt (f) en forbindelse med formlen (I) omdannes til et farmaceutisk acceptabelt salt deraf.
PATENTKRAV 1. Fremgangsmåde til fremstilling af en forbindelse med den generelle formel (I):
(0 hvor
Ar er substitueret eller usubstitueret phenyl, 2- eller 3-furyl, 2- eller 3-thienyl eller 2- eller 3-pyrryl, som, når den er substitueret, kan have en eller flere lavere alkyl-, lavere alkoxy- eller halogengrupper i en hvilken som helst stilling, der er til rådighed, på ringen, og R er hydrogen eller lavere alkyl med 1-6 carbonatomer, elleret farmaceutisk acceptabelt salt af denne, kendetegnet ved, at (a) en forbindelse med formlen (XVI):
(XVI) hvor R er lavere alkyl med 1-6 carbonatomer, og X er halogen, cycliseres med en lithiumhindret amin i et aprot opløsningsmiddel til dannelse afen diester med formlen (XII):
(XII) (b) en divalent ester med formlen (XII) opnået i trin (a) forsæbes til dannelse af den tilsvarende divalente syre med formlen (XII):
(XII) hvor R er hydrogen, (c) den divalente syre med formlen (XII) opnået i trin (b) forestres til dannelse af en forbindelse med formlen (XVIII):
(XVIII) hvor R-gruppen i 1-stillingen er lavere alkyl med 1-6 carbonatomer, (d) en forbindelse med formlen (XVIII) opnået i trin (c) decarboxyleres til dannelse af en forbindelse med formlen (XIX);
(XIX) hvor R har den ovenfor anførte betydning; (e) en forbindelse med formlen (XIX) opnået i trin (d) aroyleres med en amid eller et morpholid til dannelse af en forbindelse med formlen (I), hvor Ar er substitueret eller usubstitueret phenyl, 2- eller 3-furyl, 2- eller 3-thienyl eller 2- eller 3-pyrryl, som, når den er substitueret, kan have en eller flere lavere alkyl-, lavere alkoxy- eller halogengrupper i en hvilken som helst stilling, der er til rådighed, på ringen, og R er hydrogen eller lavere alkyl med 1-6 carbonatomer, og eventuelt (f) en forbindelse med formlen (I) omdannes til et farmaceutisk acceptabelt salt deraf. 2. Fremgangsmåde ifølge krav 1, kendetegnet ved, at (a) en forbindelse med formlen (I) omdannes til den tilsvarende frie forbindelse med formlen (I), eller (b) en forbindelse med formlen (I) esterificeres, eller (c) en ester med formlen (I) omdannes til den tilsvarende frie forbindelse med formlen (l). 3. Fremgangsmåde ifølge krav 1 eller 2, hvor den dannede forbindelse er 5- benzoyl-1,2-dihydro-3H-pyrrolo[1,2-a]pyrrol-1-carboxylsyre eller et farmaceutisk acceptabelt salt af denne. 4. Fremgangsmåde ifølge krav 1 eller 2, hvor den dannede forbindelse er 5-p- anisoyl-1,2-dihydro-3H-pyrrolo[1,2-a]pyrrol-1-carboxylsyre eller et farmaceutisk acceptabelt salt af denne.
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US07/003,162 US4835288A (en) | 1987-01-14 | 1987-01-14 | Process for preparing (+)-2,3-dihydro-1H-pyrrolo[1,2-a]pyrrole-1,7-dicarboxylates |
| US07/003,104 US4849526A (en) | 1987-01-14 | 1987-01-14 | Process for preparing (±)-2,3-dihydro-1H-pyrrolo[1,2-A]pyrrole-1,7-dicarboxylates |
| US316287 | 1987-01-14 | ||
| US310487 | 1987-01-14 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| DK200000691A true DK200000691A (da) | 2000-04-27 |
| DK175516B1 DK175516B1 (da) | 2004-11-15 |
Family
ID=26671322
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DK198800143A DK174999B1 (da) | 1987-01-14 | 1988-01-13 | Pyrrolderivater |
| DK200000691A DK175516B1 (da) | 1987-01-14 | 2000-04-27 | Fremgangsmåde til fremstilling af pyrrolderivater |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DK198800143A DK174999B1 (da) | 1987-01-14 | 1988-01-13 | Pyrrolderivater |
Country Status (16)
| Country | Link |
|---|---|
| EP (1) | EP0275092B1 (da) |
| JP (1) | JP2665342B2 (da) |
| KR (1) | KR960001475B1 (da) |
| AU (1) | AU613334B2 (da) |
| CA (1) | CA1340404C (da) |
| DE (1) | DE3871533T2 (da) |
| DK (2) | DK174999B1 (da) |
| ES (1) | ES2041703T3 (da) |
| FI (1) | FI90344C (da) |
| GR (1) | GR3004788T3 (da) |
| HK (1) | HK39097A (da) |
| HU (8) | HU198927B (da) |
| IE (1) | IE62987B1 (da) |
| IL (1) | IL85094A (da) |
| NO (1) | NO169124C (da) |
| NZ (1) | NZ223175A (da) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR0140134B1 (ko) * | 1994-11-16 | 1998-06-01 | 강재헌 | 피롤리진 유도체의 제조방법 |
| CN112898307A (zh) * | 2021-02-07 | 2021-06-04 | 贵州省中国科学院天然产物化学重点实验室(贵州医科大学天然产物化学重点实验室) | 一种酮咯酸杂质c及其制备方法与应用 |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS539789A (en) * | 1976-07-14 | 1978-01-28 | Syntex Inc | Production of 55*22floyl** * 55*22thenoyl** * 55*33 floyl** and 55*33thenoyl** 1*22dihydroo3hhpyroro * 1*22a*pyrolee11carboxylic acid derivative |
| US4089969A (en) * | 1976-07-14 | 1978-05-16 | Syntex (U.S.A.) Inc. | 5-Aroyl-1,2-dihydro-3H-pyrrolo[1,2-a]pyrrole-1-carboxylic acid derivatives and process for the production thereof |
| US4097579A (en) * | 1977-03-31 | 1978-06-27 | Syntex (U.S.A.) Inc. | 5-(2-Pyrroyl)-1,2-dihydro-3H-pyrrolo 1,2-a!pyrrole-1-carboxylic acid derivatives and process for the production thereof |
| US4344943A (en) * | 1980-06-09 | 1982-08-17 | Syntex (U.S.A.) Inc. | 6-Chloro- or 6-bromo-1,2-dihydro-3H-pyrrolo[1,2-a]-pyrrole-1-carboxylic acids and derivatives thereof |
| US4353829A (en) * | 1980-11-21 | 1982-10-12 | Syntex (U.S.A.) Inc. | Process for 5-aroylation of 1,2-dihydro-3H-pyrrolo[1,2-a]pyrrole-1-carboxylic esters |
| US4560699A (en) * | 1983-01-17 | 1985-12-24 | Syntex (U.S.A.) Inc. | 5-(4-Vinylbenzoyl)-1,2-dihydro-3H-pyrrolo-[1,2-a]-pyrrole-1-carboxylic acids and derivatives thereof and use as analgesics and anti-inflammatories |
-
1987
- 1987-12-14 HU HU875631A patent/HU198927B/hu not_active IP Right Cessation
-
1988
- 1988-01-13 HU HU895355A patent/HUT52045A/hu unknown
- 1988-01-13 FI FI880133A patent/FI90344C/fi not_active IP Right Cessation
- 1988-01-13 IL IL85094A patent/IL85094A/xx not_active IP Right Cessation
- 1988-01-13 HU HU88117A patent/HU200606B/hu unknown
- 1988-01-13 KR KR1019880000169A patent/KR960001475B1/ko not_active Expired - Fee Related
- 1988-01-13 HU HU895354A patent/HUT51595A/hu unknown
- 1988-01-13 HU HU895356A patent/HU203721B/hu unknown
- 1988-01-13 AU AU10240/88A patent/AU613334B2/en not_active Expired
- 1988-01-13 DK DK198800143A patent/DK174999B1/da not_active IP Right Cessation
- 1988-01-13 ES ES198888100390T patent/ES2041703T3/es not_active Expired - Lifetime
- 1988-01-13 DE DE8888100390T patent/DE3871533T2/de not_active Expired - Lifetime
- 1988-01-13 EP EP88100390A patent/EP0275092B1/en not_active Expired - Lifetime
- 1988-01-13 HU HU895355A patent/HU203532B/hu unknown
- 1988-01-13 IE IE8388A patent/IE62987B1/en not_active IP Right Cessation
- 1988-01-13 HU HU895356A patent/HUT52046A/hu unknown
- 1988-01-13 HU HU895354A patent/HU201728B/hu unknown
- 1988-01-13 JP JP63006757A patent/JP2665342B2/ja not_active Expired - Lifetime
- 1988-01-13 NO NO880127A patent/NO169124C/no not_active IP Right Cessation
- 1988-01-13 NZ NZ223175A patent/NZ223175A/xx unknown
- 1988-01-13 CA CA000556465A patent/CA1340404C/en not_active Expired - Lifetime
-
1992
- 1992-06-04 GR GR920400600T patent/GR3004788T3/el unknown
-
1997
- 1997-03-27 HK HK39097A patent/HK39097A/en not_active IP Right Cessation
-
2000
- 2000-04-27 DK DK200000691A patent/DK175516B1/da not_active IP Right Cessation
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PUP | Patent expired |