ES2031974T3 - Procedimiento para la obtencion de 3-amino-1-bencil piprolidinas. - Google Patents
Procedimiento para la obtencion de 3-amino-1-bencil piprolidinas.Info
- Publication number
- ES2031974T3 ES2031974T3 ES198888115370T ES88115370T ES2031974T3 ES 2031974 T3 ES2031974 T3 ES 2031974T3 ES 198888115370 T ES198888115370 T ES 198888115370T ES 88115370 T ES88115370 T ES 88115370T ES 2031974 T3 ES2031974 T3 ES 2031974T3
- Authority
- ES
- Spain
- Prior art keywords
- bencil
- formula
- amino
- dionas
- different
- 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.)
- Expired - Lifetime
Links
- KLSJWNVTNUYHDU-UHFFFAOYSA-N Amitrole Chemical compound NC1=NC=NN1 KLSJWNVTNUYHDU-UHFFFAOYSA-N 0.000 abstract 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 2
- SLRMQYXOBQWXCR-UHFFFAOYSA-N 2154-56-5 Chemical class [CH2]C1=CC=CC=C1 SLRMQYXOBQWXCR-UHFFFAOYSA-N 0.000 abstract 1
- 101100244083 Arabidopsis thaliana PKL gene Proteins 0.000 abstract 1
- -1 CARBONYL GROUPS Chemical group 0.000 abstract 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical class [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical class [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 abstract 1
- 239000001257 hydrogen Substances 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 238000004519 manufacturing process Methods 0.000 abstract 1
- 229910052757 nitrogen Inorganic materials 0.000 abstract 1
- 230000017105 transposition Effects 0.000 abstract 1
Classifications
-
- 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
- C07D207/04—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 no double bonds between ring members or between ring members and non-ring members
- C07D207/10—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 no 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
- C07D207/14—Nitrogen atoms not forming part of a nitro radical
-
- 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)
- Pyrrole Compounds (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Peptides Or Proteins (AREA)
Abstract
PROCESO DE PRODUCCION DE 3 - AMINO - 1 - BENCIL - PIRROLIDINAS DE FORMULA(I), DONDE R1 Y R2 SON IGUALES O DIFERENTES Y SON RESPECTIVAMENTE H O ALQUILO, MEDIANTE REACCION DE 1 - BENCIL - 3 PIRROLIN - 2,5 - DIONAS DE FORMULA(II) CON NUCLEOFILOS DE NITROGENO DE FORMULA (III) PARA CONSEGUIR 3 - AMINO - 1 - BENCIL - PIRROLIDIN - 2,5 - DIONAS, SUSTITUIDAS EN SU CASO, DE FORMULA (IV), SIENDO EN LA FORMULA (III) R3 Y R4 (IGUALES O DISTINTOS) H O ALQUILO, R5 H, BENCILO, NAFTILMETILO O UN SUSTITUYENTE FENIL CHR6, CON R6 ES C1 C6 - ALQUILO O FENILO, TENIENDO R1 Y R2 EL SIGNIFICADO DADO ANTERIORMENTE, Y POSTERIOR DIVISION DEL GRUPO PROTECTOR R5 PARA EL CASO DE QUE R5 SEA DISTINTO DE HIDROGENO EN 3 - AMINO - 1 BENCIL - PIRROLIDIN - 2,5 - DIONAS DE FORMULA (IVA)Y TRANSPOSICION A LA 3 - AMINO - 1 - BENCIL - PIRROLIDINA DE FORMULA (I) MEDIANTE REDUCCION COMPLETA DE LOS GRUPOS CARBONILO
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19873733289 DE3733289A1 (de) | 1987-10-02 | 1987-10-02 | Verfahren zur herstellung von 3-amino-1-benzyl-pyrrolidinen |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2031974T3 true ES2031974T3 (es) | 1993-01-01 |
Family
ID=6337440
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES198888115370T Expired - Lifetime ES2031974T3 (es) | 1987-10-02 | 1988-09-20 | Procedimiento para la obtencion de 3-amino-1-bencil piprolidinas. |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US4910319A (es) |
| EP (1) | EP0310854B1 (es) |
| JP (1) | JP2505550B2 (es) |
| KR (1) | KR970004595B1 (es) |
| AT (1) | ATE76403T1 (es) |
| CA (1) | CA1331623C (es) |
| DE (2) | DE3733289A1 (es) |
| ES (1) | ES2031974T3 (es) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4859776A (en) * | 1988-03-11 | 1989-08-22 | Abbott Laboratories | (S)-7-(3-aminopyrrolidin-1-yl)-1-(ortho, para-difluorophenyl)-1,4-dihydro-6-fluoro-4-oxo-1,8-naphthyridine-3-carboxylic acid and method for its preparation |
| JP2002284761A (ja) * | 2001-01-17 | 2002-10-03 | Toray Ind Inc | 光学活性３−アミノピロリジン−２，５−ジオン誘導体および光学活性３−アミノピロリジン誘導体の製造方法 |
| WO2003082815A1 (fr) * | 2002-03-29 | 2003-10-09 | Kaneka Corporation | Procede d'amelioration de la purete optique de 1-benzyl-3- aminopyrrolidine et sel utilise dans ce procede |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3433801A (en) * | 1966-03-22 | 1969-03-18 | Robins Co Inc A H | 1-aryl-3-(n-lower alkyl amino) pyrrolidines |
| US3433802A (en) * | 1968-06-25 | 1969-03-18 | Robins Co Inc A H | 3-(n-lower-alkylanilino)pyrrolidines |
| JPS593474B2 (ja) * | 1976-08-25 | 1984-01-24 | 山之内製薬株式会社 | ３−アミノ−１−ベンジルピロリジン誘導体の製法 |
| JPS5522699A (en) * | 1979-08-10 | 1980-02-18 | Yamanouchi Pharmaceut Co Ltd | Novel 3-amino-1-benzylpyrrolidine derivative |
-
1987
- 1987-10-02 DE DE19873733289 patent/DE3733289A1/de not_active Withdrawn
-
1988
- 1988-09-20 EP EP88115370A patent/EP0310854B1/de not_active Expired - Lifetime
- 1988-09-20 ES ES198888115370T patent/ES2031974T3/es not_active Expired - Lifetime
- 1988-09-20 AT AT88115370T patent/ATE76403T1/de not_active IP Right Cessation
- 1988-09-20 DE DE8888115370T patent/DE3871316D1/de not_active Expired - Lifetime
- 1988-09-28 JP JP63241165A patent/JP2505550B2/ja not_active Expired - Fee Related
- 1988-09-28 US US07/250,294 patent/US4910319A/en not_active Expired - Lifetime
- 1988-09-30 CA CA000578933A patent/CA1331623C/en not_active Expired - Fee Related
- 1988-09-30 KR KR1019880012774A patent/KR970004595B1/ko not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| DE3733289A1 (de) | 1989-04-20 |
| KR890006583A (ko) | 1989-06-14 |
| KR970004595B1 (ko) | 1997-03-29 |
| EP0310854A1 (de) | 1989-04-12 |
| DE3871316D1 (de) | 1992-06-25 |
| JP2505550B2 (ja) | 1996-06-12 |
| US4910319A (en) | 1990-03-20 |
| CA1331623C (en) | 1994-08-23 |
| ATE76403T1 (de) | 1992-06-15 |
| JPH01106862A (ja) | 1989-04-24 |
| EP0310854B1 (de) | 1992-05-20 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FG2A | Definitive protection |
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